CRISPRimmunity

Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP042435	Panacibacter ginsenosidivorans strain Gsoil1550 chromosome, complete genome	5 crisprs	csa3,PrimPol,WYL,cas3,cas6,cas8b2,cas7,cas5,cas4,cas1,cas2,RT,PD-DExK,DEDDh	0	19	0	0

1. NZ_CP042435

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP042435_1

• CRISPR_ID: NZ_CP042435_1
• CRISPR_location: 298038-298271
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers

Consensus repeat of NZ_CP042435_1

Consensus_repeat	Method
NNGCCACCACTTGTAGAT	CRT

spacers of NZ_CP042435_1

>1.1|298056|36|NZ_CP042435|CRT
GTTTCAAGTGTACCGCGAATATTTGAAAGATGCACA
>1.2|298110|36|NZ_CP042435|CRT
GCAGACAGCTTTCCTTTAACATTATCAGCATCAATT
>1.3|298164|36|NZ_CP042435|CRT
GCATCAATAGTGCCATCAAGTGCAGAAAGATGAACA
>1.4|298218|36|NZ_CP042435|CRT
AATTCAATGTTTCCTTTGCAATTATCTGCATTAATA

CRISPR arrays and Neighbor proteins around NZ_CP042435_1

CRISPR arrays

The CRISPR arrays of NZ_CP042435_1

>merge|NZ_CP042435|1|298038-298271|CRT
CTGCCACCACTTGTAGATGTTTCAAGTGTACCGCGAATATTTGAAAGATGCACACTGCCACCACTTGTAGATGCAGACAGCTTTCCTTTAACATTATCAGCATCAATTCTGCCACCACTTGTAGATGCATCAATAGTGCCATCAAGTGCAGAAAGATGAACAGAGCCGCCACTTGTAGATAATTCAATGTTTCCTTTGCAATTATCTGCATTAATAGAACCACCACTTGTAGCA

>NZ_CP042435|1|1|298038-298271|CRT
CTGCCACCACTTGTAGAT	GTTTCAAGTGTACCGCGAATATTTGAAAGATGCACA
CTGCCACCACTTGTAGAT	GCAGACAGCTTTCCTTTAACATTATCAGCATCAATT
CTGCCACCACTTGTAGAT	GCATCAATAGTGCCATCAAGTGCAGAAAGATGAACA
GAGCCGCCACTTGTAGAT	AATTCAATGTTTCCTTTGCAATTATCTGCATTAATA
GAACCACCACTTGTAGCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042435.1|WP_147187779.1|284431_286873_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187781.1|289815_292239_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187793.1|309676_311038_+|response-regulator	unknown	unknown	gnl|CDD|225114
NZ_CP042435.1|WP_147187790.1|305900_306845_+|tyrosine-type-recombinase/integrase	unknown	unknown	gnl|CDD|271185
NZ_CP042435.1|WP_147187782.1|292458_294858_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187777.1|279201_281553_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187783.1|295047_297471_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187789.1|304619_305258_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147187787.1|302119_302797_-|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213222
NZ_CP042435.1|WP_147192989.1|307521_307791_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378935
NZ_CP042435.1|WP_147187774.1|273304_273763_+|DUF1801-domain-containing-protein	unknown	unknown	gnl|CDD|378058
NZ_CP042435.1|WP_147187785.1|299262_301626_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187775.1|273955_276388_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187786.1|301866_302085_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147187788.1|302847_304104_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl|CDD|273776
NZ_CP042435.1|WP_147187780.1|287229_289611_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187791.1|308244_308514_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147187792.1|308517_309060_+|transposase	unknown	unknown	unknown
NZ_CP042435.1|WP_147187778.1|281781_284217_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP042435.1|WP_147187776.1|276602_279011_-|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042435.1|WP_147187779.1|284431_286873_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	5.4373e-77
NZ_CP042435.1|WP_147187781.1|289815_292239_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	5.59627e-73
NZ_CP042435.1|WP_147187793.1|309676_311038_+|response-regulator	gnl|CDD|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	7.52447e-163
NZ_CP042435.1|WP_147187790.1|305900_306845_+|tyrosine-type-recombinase/integrase	gnl|CDD|271185	cd01185, INTN1_C_like, Integrase IntN1 of Bacteroides mobilizable transposon NBU1 and similar proteins, C-terminal catalytic domain. IntN1 is a tyrosine recombinase for the integration and excision of Bacteroides mobilizable transposon NBU1 from the host chromosome. IntN1 does not require strict homology between the recombining sites seen with other tyrosine recombinases. This family belongs to the superfamily of DNA breaking-rejoining enzymes, which share the same fold in their catalytic domain and the overall reaction mechanism. The catalytic domain contains six conserved active site residues. Their overall reaction mechanism involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA.	1.59877e-20
NZ_CP042435.1|WP_147187782.1|292458_294858_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	6.19875e-63
NZ_CP042435.1|WP_147187777.1|279201_281553_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	9.5797e-53
NZ_CP042435.1|WP_147187783.1|295047_297471_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	2.44328e-73
NZ_CP042435.1|WP_147187787.1|302119_302797_-|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	2.98932e-115
NZ_CP042435.1|WP_147192989.1|307521_307791_+|helix-turn-helix-domain-containing-protein	gnl|CDD|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	8.18673e-10
NZ_CP042435.1|WP_147187774.1|273304_273763_+|DUF1801-domain-containing-protein	gnl|CDD|378058	pfam08818, DUF1801, Domain of unknown function (DU1801). This large family of bacterial proteins is uncharacterized. They contain a presumed domain about 110 amino acids in length.	4.75831e-16
NZ_CP042435.1|WP_147187785.1|299262_301626_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	5.80664e-54
NZ_CP042435.1|WP_147187775.1|273955_276388_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	4.29371e-69
NZ_CP042435.1|WP_147187788.1|302847_304104_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	gnl|CDD|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	3.6015e-22
NZ_CP042435.1|WP_147187780.1|287229_289611_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	1.05137e-55
NZ_CP042435.1|WP_147187778.1|281781_284217_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	2.78236e-64
NZ_CP042435.1|WP_147187776.1|276602_279011_-|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	1.9421e-71

Protein sequences

>NZ_CP042435.1|WP_147187783.1|295047_297471_-|FtsX-like-permease-family-protein
MVRNYIKTAWRTLLRNKTYTAINSSGLAAGIAACLLIFVVVQFELSYDTFQNNYDRIYRIVSTEKHTDGSIARNPGIPCPAYDALKTDFPQLEKIVPLVISSGNQVTVLGTDANSDVAASKKFIEDNKISFTVPAYFDMFSAKWISGNAATLKDPGNVVLTKKNAQKYFGDYKNAVGKFIKIDNSVLLKVSGIIGDAPLNSDMNMGVFISYESFKTNPDNFGYSTEWGNLSSNHQIFVLLPKNVSAASIQSQLPAFVKKYYKQNDSRKAQVLQPFKDIHFDAGYGSLGDHSTDKNVLWTLAFIGVLIIVMASINFINLSTAQAIGRSKEVGIRKVLGSKRSQLIAQVMGETFLIVLFASILAVFIAKLAMPFLSNVASVPEGIALITAQTIIFLLAVLVVVTLLSGIYPALIVSGFKPVLALKSRITSASVGGISLRRVLVVTQFAISQMLIIGTIVAVSQMNHVRNADLGFNKEALLIMPAYTDSTDLARMEPLRQQMLQNPGVTSVSFGSDEVSSNNNWASNFAFDHKEDEGYPVFHKFGDAEYLKTYGVQLLAGRNYAASDTTNEIIINETLLHKLGFTDAQKIIGKDLRIGGGHWLPIVGVVKDFKTNSLKEETKPLTIAARKDFYFTIAVKINTANLSKTTAQIQKLWEKAYPEFAFSSHFADETIESFYRQETQLSLLYKIFAGIAIFISCLGLYGLVSFMASQKTKEVGIRKVLGASVSSIVVMFSKEFTILISIAFIIAVPVAWYFMNGWLQDFQYRISIGVGVFALAIVVSLIVAWVTVGYKAVRAALVNPVKSLRSE
>NZ_CP042435.1|WP_147187782.1|292458_294858_-|FtsX-like-permease-family-protein
MFRNYFKTALRNLQKNKLYSAINIFGLTIGLTACLLIGVYINHELSYDKFNTNANRIVRVTMTYGSAGTDNAVATTGTKVGPQFKRMFPSVEEYARTFISHNVVKSGDKIFDEPRILYADEPFFKMFSFHLVEGDASTALNAPDKIVITQSMAKKYFGKEDALNKTLTSGGKDLRVSAVIEDVPQNSQLKFDFVTQFMNLGNNVKEETWWTANWVTYMLVRDEKNIAQLQQQINDYTKSTALRTDAGLKDNDYLRYTLEPLAKVHLYSSLPGFEPNSSITYIYMFALIALLILIIACANYTNLATAQSAGRSGEIGMRKVMGASKRMVFMQFMGESSVITCIAAILAFVLSILLIPYFNNITGKQFTAEVLLQLLPIIALILFSLAVSFFAGLYPALVLSGTKISGVLKKGFSFTGGSNILRKTLIVAQFGISVFLIIYTIIILQQMHYMQTKNLGYDKDHLVVLPIGGNMTQNFQSLKDAFLQVKGVESVTASYDTPEYVGWGDGITATDEKGKHEISLNAMPVDLDFTKTTKMQLVAGRDFLQSDFALMDTTNNYANYQQPYIINETLAKKIGWTPQESIGRIIENRAMGPVVGVVKDFNFSSLHDPIGPMLIFLGRDFSRNFIIRVNDNDVQSVLARLEMVWKQRVTDRPFNYHFLDDSYNKLYLAEQRTSVLFSMAAALAIILACLGLFGLAAFTTVQRTKEIGIRRVLGANLSSITLLVAKNFLQLVGIAILIAAPLAWWAGNKWLQDYAFRVPIEVYVFIATAIVTVLIALITVSYHSLKAALMNPVKSLRTE
>NZ_CP042435.1|WP_147187781.1|289815_292239_-|FtsX-like-permease-family-protein
MFKNFLKIAWRNLAKYKLYSFLNISGLTIGILCAGFIFLFVTNELSYDNYHKAADRIYRLNFYGKIGDQLANTAQSPAPAGPELQRALPQIETMCRLKPNGRSVVKFDNVSFNEQNVLYADSTLFQVFNFPLLRGNPATALTMPGSVVISAATAKKYFGNSDPMGKTMQVDNDKLYIVSGVMKDIPVNTHFKCDLFLSMSSVEDSRVENWGSTNYQTYFVVKPGTDAAKLSKAATDLFVKKMTIVVKQYLNTSWDEFTKAGNYVKVEMFPVTKIHLYSELDDELAVNSNIKYVYIFSIVGLLILALACINFMNLATARAATRLKEVGVRKVSGALRFDLIRQFLGESLLLSFTAWLFAFVLLCFMLPALNQLSGKTFEIKDLLTMHFLLPSLALGFITGFAAGIYPALFLSAFAPIKVLKGSVAIRSKNTLRSGLVVFQFFITTVLLISSLIVYQQMQYIRNKNVGFNKEEVVAINDAYLLQDKFPVLKQKLLELPAVKSVTSANILPVGDERNTTSIIKGRNPSTENTVLVSNFWVDPDYVKAMGISIAAGRDFSKEITSDSSSVLINETLAQSFGYPGKPVVGQELSLPGEDAEHLRTFRIVGIMKDFHYNSLRDKIGPLAVFEGTSPLYVCVRFQTKDASSLIKNLQKVWNETVPAQPFSYNFLSEKFAQVYESETRIAQITDVFTAIAVMIACLGLLGLVTFVAQQRTKEIGIRKVLGASAMNITSLLAKDFIKLVLISIVLAFPVAYYFMHQWLQDFAYRINIEWWMFAVIAIAALVIAMLTLSFQAIKAAVANPVKSLRSE
>NZ_CP042435.1|WP_147187780.1|287229_289611_-|FtsX-like-permease-family-protein
MIKNYLKIAWRNLRKSKAYSAINILGLSIGMAVAILIGLWIWDELTFNEYHTNHAQLAQVMTTQTFNGHTGTGEAVAMPLGNELRTKYGSDFKAVSMASWNFGHILAVGDKKINSEGMWVEAVFPSMFSLKMIKGDKNSLKDPSSILLSASIAKTLFGNDDAMNKMVKLDNKDSYKVTGVYEDLPRNTTLYTTKILLPWEKYITTEDWMKNAMTQWGNHSWQAFVQVNDHVDIAKTTQKIKNASMIHLKEAEDGKEELVLQPMDKWRLYNKFENGKVVGGRIEFVWLFGVIGVFVLLLACINFMNLATARSEKRAKEVGIRKTVGSLRQQLIGQFLSESILVAFIAFIVSIGLVQLMLSFFNSIADKEMSIPWSNVWFWVLTIGFTFFTGLISGSYPAFYLSGFEPIKVLKGTFRVGRFASLPRKVLVVIQFTVSIALIIGTIIVFRQIQFAKDRPVGYTREGLITIDMSTPDIYGHYDAIRGDLIATGAVENMAQSSSPVTNVWSNQIGFNWEGKDPNSLPLFGIVATTYDFGKTIGWQIKEGRDFSKDFATDSTALIFNESAVKLTGLKNIVGKNIKWNDKNYNVVGVIKDMVMESPYTPVKPTIFTLNMDWASVITVRIKPTVPAREALAKIETVFKKYNPGAPFDYKFTDEEYAKKFEDEERIGNIATFFAILAIFISCLGLFGLASFVAEQRTKEIGVRKVLGASVFNLWGMLSKDFVVLVVISCFIAIPIAWYYLYEWLQRYEYRTPIAWWVFAAAAMGALLITLLTVSFQAIKAALANPVKSLRTE
>NZ_CP042435.1|WP_147187779.1|284431_286873_-|FtsX-like-permease-family-protein
MVKNYFKIAFRNLWKNKGYSTINILGLAIGLATCLLITLYVTDELSYDRYNVNADRIYRINADIRFGGGDLHMTQTSDMMGQVLKKDYPQVEEYTRIYGNEGAKLIKKGNEFITEKNIAYVDSTFFNVFTLPAIEGDAKTALNQPNTVVITASTAKKYFNSTNVLGKTIEVKNGETTTPFKITAVIKDIPHNSHFQLDFMLSMKNADYQWGQYTSHNFNTYLLLKKGTDYKAFEKSFEQYITKYVLPYVQQFIKINSMDEFRKSGNKLEYSLIPLTKIHLYSDYSFELSPSGNIQYVYIFSAVALFILIIACINFMNLSTARSASRAKEVGIRKVLGTERKTLIAQFLVESTITAFISLIIAVAIAYFVLPLFNDVAAKSLSVKDLLNIHILPFLILVPFVVGLLAGSYPALFLSGFKPIVVLKGSANTGFKKSNLRNVLVVFQFATSVMLIIGTIIVYSQLHYIQTTKLGFSKDQVLVVDGAYALNNNVQAFKNDVLAMNGVSSATVSAYLPVTNSSRSDNTYSKEAVMDFKNGIDMQTWRIDYDYIKTMGMEIVKGRNFSKEFGSDSSAMLITETTAKLLGYSDPIGKMMYVPSNIQGDNSMIPIKIIGVVKDFHFESLRQNIGPLCMLLGNSTGLISFKINVANADGLIKQIENKWKAMAPGMPFSYRFMDDSFNEMYRSEQRAGYIAITFAVLAIVIACLGLFGLVTYMAEQRTKEIGIRKVLGASTGNVVTMLSKDFLVLVIIACVIAFPVAWLAMSNWLKDYAYRINIEWWVFFVAGFTALAIALITVSFQAIKAALANPVKSLRTE
>NZ_CP042435.1|WP_147187778.1|281781_284217_-|FtsX-like-permease-family-protein
MIRNYFKIAWRNLMKYKFISFVNLFGLTVGLTCCLLIATYIINELSYDKYNKNAENIYRVTRSFNNQDGVVSLNLSTVSPPFGYYLPGDFPEIKKMTRLLNTGTLAIKYGEKIINEPNVYFADENLFNVFTLDVLKGDPNTALKDPFSVMLSEDVAKKYFGNEDPINKVLRVSNKYDVKVTGIYKGFPANSHMHPGTLLSFNTLKDSAIYGAENLRTNWGNNSFFTYLLLPDHYDPQKMVARFPAFIDAHMNRADYNGQLPSKFTTLGLQKLTDIHLYSHTDYEAEPNGDINRVYIFSAIALFILLIACINYMNLSSARSALRAREIGIRKVMGAGKKGLIFQFLSESVLIAWVAILMAFALLYFTLPLLNQLSGLELSVEMLLKWQVIVPLLLTPFVVGILSGLYPALFMSSFQPVKTLKGLFKIDGSNISFRKILVVAQFTISIVLIITTIIVFQQLKYMQNTSLGYDKDHIITLPYINDLNPSYETFRNELLQSNAVKNVTRSSRVPTGRLLDAMGASTFTGDSAMPVTSDIKFVVADYDFVSTYDIQIAAGRNFSRQYGTDTSNFILNEAAVKAIGWKSAQDALGKDFRYASIKGKIIGVVKDFHFESLHQQIVPMVLVNPANAATDGYFNFLSLQVAGNNIQSTLKTIEKTWKKYLPEVPYQATFLDETYSQLYVAEQKQGTIFTIFSCIAIFIACLGLFGLSAFAITQRVKEIGVRKVLGASTSTIVSLLSKDFLKLVLIAAVIAFPVAWYAMYNWLQDFAYRINIQWWVFIIAALLALIIALATISFQAIKAAIANPVKSLRSE
>NZ_CP042435.1|WP_147187777.1|279201_281553_-|FtsX-like-permease-family-protein
MIRNYLKIAWRNLFRNKGFSITNILGLTIGITCTMLILLWVYDELTYDKFQKNYDNIYQVIANRDFNNQVFTDRSMVLPLASELEHSSPQIKHAVVTTYQQQRVLAHGEDKIKKEGYIVSDHFFDMFSWKFIKGSAATALKDPNSIVLSESAAKAFFGNEDPINKVIRFDNSQDVKVTAVVEDAPGNSTFRFDWITPFNYNDPDTKNAMGEWVNSSWNVFVQTVPNVDTSLLNKTITKVKRAHGKDEISTYFAFPMSHWHLYSDFDNGVNTGGMIEYVHLFSVIAIIILLIACINFMNLSTARSEKRAKEVGIRKTLGSNKKRLILQFFFESMILTLIAFVIAIIAVLLLLPSFNQLVDKHLSLNATQPLFWLSATVIILFTGLVAGSYPALYLSSFNPVKVLKGTLSSGKKTVMPRHILVVSQFVISILLISATIIVYQQIQHVKDRDMGYNPNNLVMIPSTPDTDKSYDVIKQELLSTGLISNVTRTSSPITEVWWNTGAPDYDGKPANSQIIMGGLAVDVDFTKTMGIKMLQGRDFSGTPADSTSMILNKAAVDAMKLKNPVGMQMRYGRNYTVIGVSDNVIMTSPFEPAYPMLMVYDGNGSSMNTLRLKDGVAPQKAMASIETIFKKYNPTVPFEYQFVDQEFQKKFLTEDLIGKLTNIFSGLAIFICCLGLAGLASFTIEKRIREIGVRKVLGASVQQLLLLISKEFLKLVTIAFVIAVPLTYWAMTNWLSKYDYRISISIWLFVLVGIAMFLLTLVVVCMNTIRVAMSNPVKSLRTE
>NZ_CP042435.1|WP_147187776.1|276602_279011_-|FtsX-like-permease-family-protein
MIRNYLKIAFRNLRKNKIFSVINIVGLAIGLTCFMLITVFVYDELSYDKYADEADNIYRINLSATGNGDVAVYPNVDVAVGEGMKNAFPEIKASTRISPASDFVKYNDKQFKEQKLAFADSNFLQMFSIPLIEGDNKTALVQPNSVVISKAFAKKYFGNEDALGKSLTIGLHNALYKVTGVIDKVPDNTHFHFDAFLSLTTFHITRATWSNVGFYTYLLLNKNANAKALEAKFPQLVAKYVVPEVQHDMGVSLAEAQKSVNTFRFSLQPVTDIHLHANTKYELEPNGDIQYVYIFSALAIFILLLACVNFTNLSTARAVKRSREVGIRKVMGSIKKQLIFQFLTESVLFTFFSMLCAYALIFFLLPYFNELSNKNIDFIFFLSWQSILVLFSVSFIAGILAGIYPAFFLSSFNTIKVLKGASLQGSQRKPLRSSLIVFQFFISTALIIATIIVYQQLHYMQNKKLGYDKDQVLYLPDARLLGSNQFAFEQQILKDSRVVSASISRYVPGGIMMDGTEIYPKNETGNGTEIHTNIYHIDYDYLRTLGIRVVQGRDFSKAFSTDSAGVLINEEAARELGWTNSNAVGKTIVRSGQQEYKVVGVVADFNYASVKQKISPMMMMLGNNFGGLIVKINTKDIQGFLGDLKKQWTLFNPDGPLEYNFLDENFAKLYASEEHTQQIFSAFAVLAIIIASLGLFGLSAFVIEQRTKEIGIRKVLGASVKNVLLLVSKEFLLLVMIAFLISIPVTWWAMHTWLQDFAYRIDITAWVFAIAGIAVIFIAFLTISFQAIKAAIANPVKSLRTE
>NZ_CP042435.1|WP_147187775.1|273955_276388_-|FtsX-like-permease-family-protein
MFKNYFKIAVRQLRKQRMYSAVKIGGFALSIAACLLIALYIKDELSYDKNWTNADRIYRIIGEYNINGKMLSGAAWPAPMAKALKEDFPEVEKAGRFMDAPLFYGAGSNQLRKVDEEQNTFEQGFSYADQDMLDMLEIPMVYGDRAHALSEPNTMVISKSKADKYFPNQNPVGKVMILNNDVKNPYKIGGVINDFPATSHIHYDFLLTMTRHQLWDGEQTTWMASNYPTYVLLKPGADPVQFQNKLKLIMTKYYLPALRQNGNKEAETVLKNAKILIQPIADVHLYSANIDDRLDKGDIRFVWLFGAIAVFILVIACINFINLSTAKSANRAKEVGLRKVVGSHRSSLIKQFLTESLLYSVLSFVLGLLIAIILLPYFNTLAAKHLLIPWAAWWLLPLMITAAIIIGIVAGLYPSFYLSSFKPIQVLKGQVSKGSKNSLLRNGLVVFQFTTSIILIIGTIVIYNQTQYILNKKIGFDKDQVLLIQGTNTLEDKREAFKNELLKSSEIKTVSISDYLPIAGTKRDGNPFWKEGRTKEDPSVGGQKWQVDYDYLKTMGMHMIEGRYFSKDMASDSAAAVINNTMATKLGLKNPVGQRIENGWQKFTVIGVMEDFNFESMRQDVTPLCLVLGNYNSSIISVKISGADTKTAINYVSSVWKNFSPNQPFRYTFLDESFANMYADVQRTGSIFTSFAMLAVIIACLGLFALSAFMAEQRNKEIGIRKVLGASVSGITTMLSKDFVKLVLFSIVIASPVAWWAMSKWLQDFAYRISMSWWMIAAAALVAIVIALITISFQSIKAALMNPVKSLRSE
>NZ_CP042435.1|WP_147187774.1|273304_273763_+|DUF1801-domain-containing-protein
MQSTVLTPEAYIAGVPEERRAVFLKLRNEIKKNLPKGFQEIMGYGMIGYVVPHKLYPAGYHCDPKLPLPFMNLASQKNFIAVYHMGIYAKPSLLKWFIEEFAKQSSAKLDMGKSCIRFKKPENIPIKLMGELASKMTVDEWIDCYEKGFKRK
>NZ_CP042435.1|WP_147187785.1|299262_301626_-|FtsX-like-permease-family-protein
MIKNFFKIAYRNLLRNKGFSVINILGLAVGMASAMLILMWIQSEVSYDQFHEKKDRIYEAWNRAEFSGKLQCWNTTPKVLARTLERDLPEVEQAVRVDWKQNHLFSIGEKRLTVGGNIVDSNFLQVFSFPLVKGNATTVLKDMHSIVLTETLARKIYGNEDPMGKVIKIDNKESFTVTGVVKDLPLDTRFDFEYLLPWSYKRFLGDDDEYWGNNSTRTYVLLKPHASEASANAKLKVLKPKYEKDEPKWEMFIYPMSKWRLYSSFTNGKEDGGGRIEFVKLFGIIAAFILLIACINFMNLSTARSEKRAKEVGIRKVVGANKGSLIGQFIGESILLSFLAGILAVILVQISLPAFNSLTDKHLAIEYGNIYFWLAALGFIIFTGVLAGSYPAFFLSSFKPVKVLKGTFKKANALVTPRKVLVVLQFTFAIILIICTIIVKQQIDYAQNRETGYNKNNLIYHLFTGDIEKNYTLIKNELLNSGAASSVTKTSAPLTQSWSDGWGQEWEGKDPNDKTDFYRYNEDEGLGKTAGLTFVQGRDFDLTKFPTDSTGMIINESALKVMKFKDPIGKIVKDNGTEWHIVGVIKDFILTSPYEPTRPMLIAGSKAWFQTILIKLNSNVATGESLKKAEAIFKKYNTEYPFEYKFVDEEYAQKFEDEQRQGTLAALFAGLTIFISCLGLFGLATYMAENRIKEIGVRKVLGASVAGIATLLSKDFLKLVIVSFIIAAPISWWAMNAWLQDYNYRVTIEWWVFAMAAILSIVIAIITVSYQAIKAAVANPVRSLRTE
>NZ_CP042435.1|WP_147187786.1|301866_302085_-|hypothetical-protein
MKSISIHIVRAMLLLTLYVCCSSVVCCEASKPAVLESTSPGKMFEHSGYNKESLDEDITPLQMISVRITELL
>NZ_CP042435.1|WP_147187787.1|302119_302797_-|ATP-binding-cassette-domain-containing-protein
MIKITDLEKVYRTEEVETVALNKLTVEVKEGEFVAVMGPSGCGKSTLLNILGLLDDPDAGSFIFNGIEVAKFNERKRADLRKHNIGFVFQSFNLIDELTVFENVELPLIYTGIKPAERKKRVEAVLDKVQIMHRRNHYPQQLSGGQQQRVAVARAVVNNPKLILADEPTGNLDSSNGNEVMQLLTELNEQGTTIVMVTHSEHDARYSHRIVRMLDGQTVTENILI
>NZ_CP042435.1|WP_147187788.1|302847_304104_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MDRVIEKKTWTKKRILTIVGIAALAGLIIASYYYTSGGSKLNVDTERITISEVKKGVFQETIPVNGIVLPETTIYLDAVEGGRVEEKYVEDGAVMKKGQPILKLSNTDLQLNLVNQETSVYNLLTQMQISRNAAQQNTVNKLNQMTDAESQLKEAERVYLLDKHLYDQKAIGSQEYKKAENDYNYYLQKKKLTEQILKQDSVSNQQQLTQAQQSYEGSQNALAVMREKVGDLIVRAPVDGQLTSLDAEVGQNKNKGERLGQLDVVGGYKVRVDVDEHYISRIYAGLKGHFDFAGKTYELIIKKVYTQVVNGRFQVDMIFTGKVPDGIRRGQTLQILLALSDERQSLLLAKGGFYQQTGGNWIFKVSKDGSTAYKVDIQLGNQNPDYYEVLSGLEPGDKVVTSSYENYGTMQELVLKGK
>NZ_CP042435.1|WP_147187789.1|304619_305258_-|hypothetical-protein
MGTINKGILGGFSGTVGTVIGGSWKGIDYMRSQPSRKSGTTSQPQLEQQAKFSLIVKFLQSMTGLVMVTFHNYAVKMTGFNSALSYNIKNVITGTYPSYAIDYTKVLVSRGDLPNAGGPAAVAGTAGNINFTWTDNSGMGKAAATDNAVLVAYSSTMNLTIYDLEAATRNAAAATLNAATFSGETVEVYIGFMSEDGREVASSIYLGQVTVA
>NZ_CP042435.1|WP_147187790.1|305900_306845_+|tyrosine-type-recombinase/integrase
MVLLLICAFEKFTNTKLRIKRLPHYNSNLFFKEAEYWKNFYAAFTDFLFTEKKCFDNYVGTVIRIIRAFFRYLSNEQQINIGNFYERFYVLEEQIPVISLLPEQVSFLINNKDFENSLSVSLRRTKDIFVFGCLLALRYSDLFNIKVTDIEEACGNKYLGIKTQKTGATVKLKLTGYTLLIIDKLIAKAGKRKILIPYISKNQFNHNIKRIAEKAGWTKPMPKTRNRRGKQKMLYRPGTTQAYRFCDLLSSHCMRRTAITMMLMFGVPEHIVRMISGHTKNSKSFYRYISLVQSYLDTYMEKMSAKLSPAQTIL
>NZ_CP042435.1|WP_147192989.1|307521_307791_+|helix-turn-helix-domain-containing-protein
MQDPAPDNKNNNNQPIKKIVSAAENKNETATISDDIWLDKQDVLQRLHISARTLQNWRSSGLLPYSKIKGKIYYKETDIEILLLQHRNK
>NZ_CP042435.1|WP_147187791.1|308244_308514_+|hypothetical-protein
MNIFHRRQGQMHTDTCYFYTQTIQDFKHLLSDDYLKLLLSVGVYNLSRSGGWRHTAGSTQNVQPGQPVTLLRSIGWCPHLPKCYTKSLS
>NZ_CP042435.1|WP_147187792.1|308517_309060_+|transposase
MNIFHRRQGQMHTDTCYFYTQTIQDFKHLLSDDYLKLIVIRSLQYLVNNKLVKIYGYVIMPNHIHLLWCMLRQNGNESPAESFSKFTAHQFKKYLAKDKTFLIQYKSKKEDRDYQFWKRDPLAVPISTDNILIDKLHYIHHNPVKPKWALCKLPEEYKWSSAKFYASGEDEYKILTHFRE
>NZ_CP042435.1|WP_147187793.1|309676_311038_+|response-regulator
MSLKKYSILAIDDDPDVLTAVRLLLKPEAKEIVTEKNPENIPALLSKQSPDLVLLDMNFKASINTGNEGIYWLKRVKELKPDVAVIMITAYGDIDLAVRSLKEGASDFVVKPWHNEKLLTTIDDALRRKGAAKNKGDFSIRGDSVIGKELLGESEVMEDIFFKIDKIAPTDANVLILGENGTGKDLIAKAIHQKSLRANKPFIKVDVGALTETLFESELFGHKKGAFTDAKEDRMGRIESANEGTLFLDEIGNISLTQQAKLLTVLQNRFITRLGSNQPVPVDIRLICATNLPLVELANESKFRKDLVYRINTVEITVPPLRKRGEDIIMLAKHFLKLYASKYMKPVIKFDDAALHKLMQYHYPGNVRELQYIIERAIIMSDGDVLEPKDLIYSPIESAPPENNDADDLNLSSIEKNTILRVIEKHNGNITKAAKELGLTRTALYRRLSKYDI

Crispr_ID: NZ_CP042435_2

• CRISPR_ID: NZ_CP042435_2
• CRISPR_location: 2561424-2561521
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042435_2

Consensus_repeat	Method
GCAAAACCTGCCCATAAGCCCGT	CRISPRCasFinder

spacers of NZ_CP042435_2

>2.1|2561447|52|NZ_CP042435|CRISPRCasFinder
TGCAAAAGCAGCGACGCCAAAGAAAGCAGTTAAAGCAGCTCCTAAACCAGCT

CRISPR arrays and Neighbor proteins around NZ_CP042435_2

CRISPR arrays

The CRISPR arrays of NZ_CP042435_2

>merge|NZ_CP042435|2|2561424-2561521|CRISPRCasFinder
GCAAAACCTGCCCATAAGCCCGTTGCAAAAGCAGCGACGCCAAAGAAAGCAGTTAAAGCAGCTCCTAAACCAGCTGCAAAACCTGCCCATAAGCCTGT

>NZ_CP042435|2|1|2561424-2561521|CRISPRCasFinder
GCAAAACCTGCCCATAAGCCCGT	TGCAAAAGCAGCGACGCCAAAGAAAGCAGTTAAAGCAGCTCCTAAACCAGCT
GCAAAACCTGCCCATAAGCCTGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042435.1|WP_147189560.1|2557073_2557661_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147189563.1|2562522_2565801_-|TonB-dependent-receptor-plug-domain-containing-protein	unknown	unknown	gnl|CDD|379297
NZ_CP042435.1|WP_147189567.1|2574111_2574648_-|hypoxanthine-phosphoribosyltransferase	unknown	unknown	gnl|CDD|223707
NZ_CP042435.1|WP_147189553.1|2546890_2547271_+|glycine-cleavage-system-protein-GcvH	unknown	unknown	gnl|CDD|234918
NZ_CP042435.1|WP_147189559.1|2554211_2556824_-|T9SS-type-B-sorting-domain-containing-protein	unknown	unknown	gnl|CDD|372639
NZ_CP042435.1|WP_147189552.1|2546087_2546798_+|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|365914
NZ_CP042435.1|WP_158638350.1|2549119_2549842_+|outer-membrane-beta-barrel-protein	unknown	unknown	gnl|CDD|372635
NZ_CP042435.1|WP_147189564.1|2566212_2568255_+|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl|CDD|275036
NZ_CP042435.1|WP_147189566.1|2572066_2573800_-|DUF3520-domain-containing-protein	unknown	unknown	gnl|CDD|238742
NZ_CP042435.1|WP_147189557.1|2549921_2551367_-|DUF1501-domain-containing-protein	unknown	unknown	gnl|CDD|369346
NZ_CP042435.1|WP_147189554.1|2547579_2548122_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|237125
NZ_CP042435.1|WP_147189570.1|2576395_2577856_-|sodium:solute-symporter	unknown	unknown	gnl|CDD|271361
NZ_CP042435.1|WP_147189569.1|2575754_2576396_-|O-methyltransferase	unknown	unknown	gnl|CDD|226607
NZ_CP042435.1|WP_147189571.1|2578174_2578711_+|TIGR00730-family-Rossman-fold-protein	unknown	unknown	gnl|CDD|129813
NZ_CP042435.1|WP_158638351.1|2568674_2571905_+|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl|CDD|275036
NZ_CP042435.1|WP_147189558.1|2551736_2554064_-|DUF1553-domain-containing-protein	unknown	unknown	gnl|CDD|377872
NZ_CP042435.1|WP_147189561.1|2557912_2561302_+|isoleucine--tRNA-ligase	unknown	unknown	gnl|CDD|235681
NZ_CP042435.1|WP_147189568.1|2574672_2575755_-|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl|CDD|224619
NZ_CP042435.1|WP_147189572.1|2578691_2579405_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147189555.1|2548122_2548959_+|anti-sigma-factor	unknown	unknown	gnl|CDD|378389

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042435.1|WP_147189563.1|2562522_2565801_-|TonB-dependent-receptor-plug-domain-containing-protein	gnl|CDD|379297	pfam13620, CarboxypepD_reg, Carboxypeptidase regulatory-like domain.	2.30962e-16
NZ_CP042435.1|WP_147189567.1|2574111_2574648_-|hypoxanthine-phosphoribosyltransferase	gnl|CDD|223707	COG0634, Hpt, Hypoxanthine-guanine phosphoribosyltransferase [Nucleotide transport and metabolism].	2.04103e-61
NZ_CP042435.1|WP_147189553.1|2546890_2547271_+|glycine-cleavage-system-protein-GcvH	gnl|CDD|234918	PRK01202, PRK01202, glycine cleavage system protein GcvH.	1.20952e-65
NZ_CP042435.1|WP_147189559.1|2554211_2556824_-|T9SS-type-B-sorting-domain-containing-protein	gnl|CDD|372639	pfam13585, CHU_C, C-terminal domain of CHU protein family. The function of this C-terminal domain is not known; there are several conserved tryptophan and asparagine residues.	3.95069e-16
NZ_CP042435.1|WP_147189552.1|2546087_2546798_+|peptidylprolyl-isomerase	gnl|CDD|365914	pfam00160, Pro_isomerase, Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD. The peptidyl-prolyl cis-trans isomerases, also known as cyclophilins, share this domain of about 109 amino acids. Cyclophilins have been found in all organisms studied so far and catalyze peptidyl-prolyl isomerisation during which the peptide bond preceding proline (the peptidyl-prolyl bond) is stabilized in the cis conformation. Mammalian cyclophilin A (CypA) is a major cellular target for the immunosuppressive drug cyclosporin A (CsA). Other roles for cyclophilins may include chaperone and cell signalling function.	5.42198e-53
NZ_CP042435.1|WP_158638350.1|2549119_2549842_+|outer-membrane-beta-barrel-protein	gnl|CDD|372635	pfam13568, OMP_b-brl_2, Outer membrane protein beta-barrel domain. This domain is found in a wide range of outer membrane proteins. This domain assumes a membrane bound beta-barrel fold.	1.05533e-08
NZ_CP042435.1|WP_147189554.1|2547579_2548122_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|237125	PRK12519, PRK12519, RNA polymerase sigma factor; Provisional.	3.58146e-31
NZ_CP042435.1|WP_147189566.1|2572066_2573800_-|DUF3520-domain-containing-protein	gnl|CDD|238742	cd01465, vWA_subgroup, VWA subgroup: Von Willebrand factor type A (vWA) domain was originally found in the blood coagulation protein von Willebrand factor (vWF). Typically, the vWA domain is made up of approximately 200 amino acid residues folded into a classic a/b para-rossmann type of fold. The vWA domain, since its discovery, has drawn great interest because of its widespread occurrence and its involvement in a wide variety of important cellular functions. These include basal membrane formation, cell migration, cell differentiation, adhesion, haemostasis, signaling, chromosomal stability, malignant transformation and in immune defenses In integrins these domains form heterodimers while in vWF it forms multimers. There are different interaction surfaces of this domain as seen by the various molecules it complexes with. Ligand binding in most cases is mediated by the presence of a metal ion dependent adhesion site termed as the MIDAS motif that is a characteristic feature of most, if not all A domains. Not much is known about the function of the VWA domain in these proteins. The members do have a conserved MIDAS motif. The biochemical function however is not known.	5.0817e-61
NZ_CP042435.1|WP_147189557.1|2549921_2551367_-|DUF1501-domain-containing-protein	gnl|CDD|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	6.83866e-176
NZ_CP042435.1|WP_147189564.1|2566212_2568255_+|T9SS-type-A-sorting-domain-containing-protein	gnl|CDD|275036	TIGR04183, hypothetical_protein, Por secretion system C-terminal sorting domain. Species that include Porphyromonas gingivalis, Fibrobacter succinogenes, Flavobacterium johnsoniae, Cytophaga hutchinsonii, Gramella forsetii, Prevotella intermedia, and Salinibacter ruber average twenty or more copies of a C-terminal domain, represented by this model, associated with sorting to the outer membrane and covalent modification.	5.7134e-07
NZ_CP042435.1|WP_147189570.1|2576395_2577856_-|sodium:solute-symporter	gnl|CDD|271361	cd10326, SLC5sbd_NIS-like, Na(+)/iodide (NIS) and Na(+)/multivitamin (SMVT) cotransporters, and related proteins; solute binding domain. NIS (product of the SLC5A5 gene) transports I-, and other anions including ClO4-, SCN-, and Br-. SMVT (product of the SLC5A6 gene) transports biotin, pantothenic acid and lipoate. This subfamily also includes SMCT1 and 2. SMCT1(the product of the SLC5A8 gene) is a high-affinity transporter of various monocarboxylates including lactate and pyruvate, short-chain fatty acids, ketone bodies, nicotinate and its structural analogs, pyroglutamate, benzoate and its derivatives, and iodide. SMCT2 (product of the SLC5A12 gene) is a low-affinity transporter for short-chain fatty acids, lactate, pyruvate, and nicotinate. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	0
NZ_CP042435.1|WP_147189569.1|2575754_2576396_-|O-methyltransferase	gnl|CDD|226607	COG4122, COG4122, Predicted O-methyltransferase [General function prediction only].	9.89064e-49
NZ_CP042435.1|WP_147189571.1|2578174_2578711_+|TIGR00730-family-Rossman-fold-protein	gnl|CDD|129813	TIGR00730, LOG_family_protein_YJL055W, TIGR00730 family protein. This model represents one branch of a subfamily of proteins of unknown function. Both PSI-BLAST and weak hits by this model show a low level of similarity to and suggest an evolutionary relationship of the subfamily to the DprA/Smf family of DNA-processing proteins involved in chromosomal transformation with foreign DNA. Both Aquifex aeolicus and Mycobacterium leprae have one member in each of two branches of this subfamily, suggesting that the branches may have distinct functions. [Hypothetical proteins, Conserved].	1.7584e-50
NZ_CP042435.1|WP_158638351.1|2568674_2571905_+|T9SS-type-A-sorting-domain-containing-protein	gnl|CDD|275036	TIGR04183, hypothetical_protein, Por secretion system C-terminal sorting domain. Species that include Porphyromonas gingivalis, Fibrobacter succinogenes, Flavobacterium johnsoniae, Cytophaga hutchinsonii, Gramella forsetii, Prevotella intermedia, and Salinibacter ruber average twenty or more copies of a C-terminal domain, represented by this model, associated with sorting to the outer membrane and covalent modification.	1.85315e-07
NZ_CP042435.1|WP_147189558.1|2551736_2554064_-|DUF1553-domain-containing-protein	gnl|CDD|377872	pfam07583, PSCyt2, Protein of unknown function (DUF1549). A family of paralogues in the planctomyces.	6.74681e-127
NZ_CP042435.1|WP_147189561.1|2557912_2561302_+|isoleucine--tRNA-ligase	gnl|CDD|235681	PRK06039, ileS, isoleucyl-tRNA synthetase; Reviewed.	0
NZ_CP042435.1|WP_147189568.1|2574672_2575755_-|LysM-peptidoglycan-binding-domain-containing-protein	gnl|CDD|224619	COG1705, FlgJ, Muramidase (flagellum-specific) [Cell motility and secretion / Intracellular trafficking and secretion].	2.11529e-25
NZ_CP042435.1|WP_147189555.1|2548122_2548959_+|anti-sigma-factor	gnl|CDD|378389	pfam10099, RskA, Anti-sigma-K factor rskA. This domain, formerly known as DUF2337, is the anti-sigma-K factor, RskA. In Mycobacterium tuberculosis the protein positively regulates expression of the antigenic proteins MPB70 and MPB83.	9.89569e-21

Protein sequences

>NZ_CP042435.1|WP_147189561.1|2557912_2561302_+|isoleucine--tRNA-ligase
MSAKYKEFSGLNLPAIEQEILAKWNESQAFEKSVELREGAVPFVFYEGPPSANGMPGIHHVISRTLKDLVCRYKTMRGFQVKRKGGWDTHGLPIELGVEKELGITKEDIGKKISVEEYNQKCREAVLRYKDKWDELTMKMGYWVDLNNPYITFDNKYIETLWWMLSELYKKGLLYESVSIQPYSPAAGTGLSSHELNQPGTYKDVKDTSAVAMFKAVKNEKSKFLFDAAKDEDVFFLAWTTTPWTLPSNLGLTVGANIDYVLVKTFNPYLHNSVNVILAKPLLGKYFKEEGENGDFDNYNEKTKILPWKILTSFKGKEIEGCSYEQLLAFEANKIDNPNSFKVLLGDFVTTEDGTGIVHTAPAFGADDFRVGKKYDIGILTMVDRQGKFVDGLGEFSNRYVKDYKDEPNYQDVNVDIAVKLKKENRAFKVEKYEHSYPHCWRTDKPVLYYPLDAWFIKTTALKDRMIELNKTINWKPKSTGEGRFGNWLENMVDWNLSRSRFWGTPLPVWRTEDGQEEVCVGSIQELNDGIKKASEILGGNVNKGYLHEGILDLHKPYVDEIILVSASGKPMKRVPDLIDVWFDSGAMPYAQWHFPFENIDIFENSYPADFIAEGVDQTRGWFYTLHALGSLMKESVHEQLSETGLQADELEKRYPGVAYKTVVSNGLVLDKNGVKMSKRLGNLVNPFETIEKYGADATRWYLITNASPWDNLKFDLAGIQEVQRKFFGTLYNTYQFFALYANVDGFAFKEAYIPIEERPEIDRWILSSLNTLIKKVTVAMDDYEPTIAGRSIEVFVDEHLSNWYVRLCRRRFWKGEYEHDKICAYQTLYECLETLVRLIAPVSPFFSDAVFQNLEAVTGRLQAASVHHANFPVANEKVIDTDLEERMQLAQDASSLVLSLRKKVNIKVRQPLQKVLIPVLDVKMKHQLEKVEDLLKAEVNVKAIEYITETEGFINKKIKPNFKSLGSKLGPKMKAVNAALSQFSQQQIIQFEKDGNYTLTIDGGLIELSLSDVEIAAEDIPGWSVASKGSLTVALDIIITEDLKQEGEARELVNRIQNIRKENGFELTDRIFVELLENDLLKLSINKFKNYICAEILAENLTWVPEMQDGTEIEINDILLKVRVNKKG
>NZ_CP042435.1|WP_147189560.1|2557073_2557661_-|hypothetical-protein
MKTILILFITAFLGINASAQQDGYCGLERLFALNKNLSKEAIADSVKNIYGAEALNINTAGNSAPKELLIYHIRNSECFNGNNIRLRFEFLNNKLVKAYMQTEFARTDYYQMLDNFNALRNFLRLHWEKEKEIKFSSTDLISTGFDFTKPKQSITISDKIALQYINTRPDKGYGIYLLRLSWVNSNNADIENIVY
>NZ_CP042435.1|WP_147189559.1|2554211_2556824_-|T9SS-type-B-sorting-domain-containing-protein
MKKIIYFYIILTSLANNARADHIKGGEISYILKSVAGSDYTYTVTVKMYMECNSYREFYNPTFVSVFNRKTGIRVRDLSVPITKIEVTSLTDNDDCITNPPQVCNRIGYYIFDVTLPASPDGYLLTTEVFFRVNNMSNLMPGYQNIGATYTAEIPGTFNITTGPKNNSAKFADSDLVIVCAGHEFNYSFAAEDNDGDALAYSMTYAYRSDNFMFGIDLTPAAPPPYGSVPYGPEYSGGKPLGNNVKIDEHTGMISGIAPSPGTYVIAVSVEERRNGQYIATQRKDLQINVASCSFTSASLADTYLLCGNTNTVNLENLSVSELIQTYKWSITNNVGETIFSSASPTVNYTFADTGVYNVNLKINENAKCADSTDSQIKVYPGFKPDFNYKGVCLDKATQFTDATSSVYGTINSWQWNFTGDILSDAVSNTQNPVYNYTSLGNKSVSLIVTDSKGCIDTVYKNIEIFEKPPIQLAFTDTLICKPDTLQLIANAVGIYNWTPANEILNANTSNPTIIPTHTTKYYVDLDRDGCTNRDSVTVNVVDHVTMQAMKDTTICKGDAIQLHNISDALHYTWQPANQLNDATIQQPFATTSSNTKYTVTANIGSCTASDEINVVTVPYPVSLAGNDTIICFGTNVSLNGVTDGNRFEWSPSVGLFNYTSLHTIANPTTTTTYILTTYDIKGCPKPGIDSVTVTVLPKINVYAGHDTAIVINQPLQLNGSGGSTYTWSPPNNLSSPFIASPVAQFYYPSDGNRYKLIVNNEAGCADSAFITIKVYKTLPSVFVPTGFTPNRDGKNDILKPILAGIQRIQMFNVYNRLGQLIFSTSTEGRGWDGTIDGIPQNTGTYVWMVKAVDYNGVPYFNKGTVTLIR
>NZ_CP042435.1|WP_147189558.1|2551736_2554064_-|DUF1553-domain-containing-protein
MKKIFITILLLSSAAVFFMNACNTNEVAADGTTMPDSISYNFNIRPILSDKCFACHGPDANKRKAQLRLDIADSAFKALKETKGAYALVPFKPNESELYKRVSSTDTSYMMPPPISHLASLSPFEVQLIKKWIEQGAKYEKHWAFTAPKKVALPKVSDEKWAKNEIDYFVLSKLEKIGLKPNEEADKERLLKRVSFDLTGLPPTIEMMDAFNADNSPTAYEKIVDKLIASPQYGEHMAVHWLDIARYADSYGYQDDNIRTQWPWRDWVIHAFNENLPYDKFITWQIAGDMLPNATKEEILATGFLRNHKYTEEGGVVPEEYRVEYLIDKTKTYGKGILGITIECAQCHDHKYDPFPQKDYYSLLAFFNNTQEVGYEGDVSVSQPAKHPILTLNDTDIVRTMQFINKKDTGKLTVSVMGELKDSVRKTYVLNRGQYGSPTDEVKPHAPTAILPYDTTKYPRNRLGLAAWTVDKNNPLTARVFVNQLWQEIFGRGLVKTSGDFGMQGELPSHPELLDWLAVDFMEHNWDIKRLVKQMVMSATYRQSDVANKEQLEKDPENKYYARGPRNRLPAESIRDMILASSGLLNKSIGGPSVKPYQPKGLWEGATSGRGVLATYKQDHKEDLYRRGMYTFIKLTVPPPSMIMFDASNRDQCQVYRPKTNTPLQALIMENDPTMLEASRVLAQNLALQQSSAQDKITKAFRLIVCRRPSENENKILNEYYTEQLVAFQQKKLSADTTLKVGEYPMNDKADKTESAALMKVIEMIYNLEESITKT
>NZ_CP042435.1|WP_147189557.1|2549921_2551367_-|DUF1501-domain-containing-protein
MSKEFIEHRLNMNRRRFLSRLSLGVGSVALGSLLIPDLFSGKEEDAVMAGLPHFAPKAKRVIYLFQNGAPSQLDLFDYKPLLQQMHGQDLPASIRMGQRLTGMTADQKKFPLAGTVFKFDRYGQAGAYISELLPHTAKIADDLCIVKTIFTEAINHDPALTFFQTGAQVGNRPSMGAWVSYGLGTENKNLPSFCVLLSKGKGNGQGVYSKLWTNGFLDSTYQGVQFSSGEHPVLYLNDADGITREDRRKMLDKLGELNEESYKEFGDPEIAAKIQQYELAYRMQTAVPEITDLTKEPESIVKMYGPECLVPGTYAANCLLARKLSENGVRFVQLYHQGWDGHNNLPGEIVGQCKDVDQASAALITDLKQRGLLDETLVIWGGEFGRTNYCQGELTKDNYGRDHHPRCFTVWMAGGGIKPGVYGETDEFGYNIAKDPVHVHDFHATILNQLGLDHEKLTFKHLGRRYRLTDVSGKVVQGIIT
>NZ_CP042435.1|WP_158638350.1|2549119_2549842_+|outer-membrane-beta-barrel-protein
MKKKALSLLMIGVVISGALIAQQTEPKVNPGGIYIKGGYNAANISVNKDGSTNDAKTLSTFHIGAIADIPLAPVLSFQTGLLLTGKGAKSTFYADASDHSDNYVKSTFNPLYLELPANLVVKFPLGSDVRLYAGAGPYAAMGIGGNSKTESSLLGVKSSTSEAIKFNNDNPLTDQQEGARYDRLKRFDVGINALAGMEISRFALGVNYGWGLTKINSTQTNNSTDNNKYRTFSVGIGVRL
>NZ_CP042435.1|WP_147189555.1|2548122_2548959_+|anti-sigma-factor
MDTKAYIESGVIESYVLGLASADEAAELELLCMQHADIKNAVDEFAALIEANAFNNAVTPPPTVKDKVMLALSEEFEKEKNKIVPVIPLHTGNTDAETVTVAPKPTWRYLAAASIILLVVSTALNFYFYSNYKTSNEKYVALLEERNSLQAKNDVNLTRLNDYEESMHIIQNPDVQKIDLPGIKGHENTFAAVYWDSKTKDVYLLPAKMDALPSDKQYQLWAIVDGKPVSAGLVEDCNGLCKMSNVPKASMFAITVEPKGGSQSPHLDAMVVAGAVKI
>NZ_CP042435.1|WP_147189554.1|2547579_2548122_+|sigma-70-family-RNA-polymerase-sigma-factor
MPEIVKYTEEELVTLLKERQQNAFSYLYDHYSGALYNVILAIVPEHEQASDVLQEVFVKIWRMSESYDATRGRLFTWMMNIARNASIDVIRSKSYQNNQQNRELTETVYESGGSTATNIDKIGLRKLVHTLKDDYKVLVELSYFEGFTQDEISKMLNIPLGTVKTRLRAALLQLRELVKN
>NZ_CP042435.1|WP_147189553.1|2546890_2547271_+|glycine-cleavage-system-protein-GcvH
MNFPSGLKYTKDHEWIKLVDGNIALIGITDFAQHELGDIVYVDVASIGKAMQAQEVFGTVEAVKTVSDLFLPVSGTVLELNAALEKQPELVNTDPYGEGWMVKLEVANVADIDALMDAAAYEALVG
>NZ_CP042435.1|WP_147189552.1|2546087_2546798_+|peptidylprolyl-isomerase
MKKAAFILLVLIAAQNSFAQNAKPKSTTAKPAATVSKGRLVQLTTDYGVMVLRLYDSTPLHRDNFIKLVKEGFYDSLMFHRIIQNFMIQGGDPDSKNAEAGQQLGAGSAPGAERIPAEFAPNLIHKKGALAAARDNNPDKASSNCQFYIVQGQTYNDTALNMMECNVRQENPGFRFTEAQRKVYKTIGGTPFLDQNYTVFGEVIKGLEVLDKIAAAEKDGNDRPLKDIRMKMKMLN
>NZ_CP042435.1|WP_147189563.1|2562522_2565801_-|TonB-dependent-receptor-plug-domain-containing-protein
MSKYLISFCSIIFLLSISTILTAQETTSDIIGTIISDQKPVVGATVTALHVPTGTVYATTTRADGRYNLPNLKIGGPYTITVTFIGYKEEKQENISLLLGQEYKADFVLVSSANTLTEVVVSSISQNKIFNNSRTGSQEIISRSQLERLPTINRSLQDFTKLTPSANGLSFGGRNGSFNNLTVDGANFNNAFGLSGTLGGQTNSQPISLDAIEQIQVNISPYDVRQGGFSGAGINSVTRSGTNVFKGSVYTYLKGPNTQGYRVGTVKVPNQDFSYNLRGFSFGGPVIKNKLFFFISGEQERVTAPATSYIASDAAHAPNASSVSLANADTLNQLKQFLIDKYGYDPGSFQGYSYDTYSDKITAKIDWNINRNNTFTIKYNYLKSYRDIAASNSGAPGGNRQPGSTSLPFSGSGYRINNNFNILIAELNTRFGNRSSNKLQFGYTALRDFRASLAGGDFPLVDIMNGQGQTYTSFGYEPFTYNNLLNTDIYQLSDIFTMYKGSHEITIGTQNYFKKFKNGFAPNYEGVYRFNTLTDFYNSANNGLANAVSYNLQYAVTKDGSFPFAEIGSTELGLFAQDKWRIGTHFTFTYGLRVDVPIFQDKFESNPYAKDLVFRDGKKYDVGQKPATNPLISPRAGFNWDVTGDQKTQLRGGIGLFSGPPPFVWISNQASNNGVQFGSFSTTGVAFNNDINAYRPNATAENVAYNLVFTDKDFKYPQALKASLAVDRKLPGNIVATLEATYSKDINGVYFQNVNLPSTGVAFNGSDPRLRYDSTKLYGGKPTATVTNPNISNAILMTNSNKGYAYNVTLQLQKTLRNFYFSAAYTLNKSKTLNDGGSIAASMWRDRPVMGDPNAEELGYANFYQPHRFIGSASYRKEYAKHFATSVGIIFEAAPAGVGSYTYSGDANNDGTGGNNDLIYIPKDQTDIVLVPVNTGGGTITDTRTAAQIWAQLNNFINQDPYLSKHRGEVAQRNAAVLPNFHRLDINITQDIYFFTGSKKDTKHTLRLSLDIINAGNLFNKNWGVVKNFTSTSFLKYEGLVPSTDVDNAGRPRFSFPYLDPANQIPVVNSYIDNTSILSRWQMQFGIRYLFN
>NZ_CP042435.1|WP_147189564.1|2566212_2568255_+|T9SS-type-A-sorting-domain-containing-protein
MSKFYKFFGISAALILYTLFSNAQTSSYQKATPGMWQTFGNPVDRSQFSFVNGRLCNFLWKDIEPSNNVWDFTTFDKDLTDRTKDGLPVIFMVYTKEDAPDWIYSAGVPKVTETDNNGKIVGYSPYFADTDYKYFFKRMIQKVHSHIESLPTTVRNGIVGVQGCYGSTGDYISYKGNVPSQYDLDSKQFLDLFKEFSQYYYNEYKNTSPKIYLMSNPRNQGNDAAIWVQDNCPGWQKTGTLGKGFQLNDEADKLTWLYDMINIPQNSGEYMRTRSEMTHGNVATGWWKRAPYKNMFAVMCYGISWGLDWSNQDYAQLNDNNYDSSFLFFSKYAGQKNPASSTNAMCALKDALDAADAKRFPASTYGTVSRTNQQRYINIANKYSSKGALLEDVKSATLAEMDNIRASGTNDVGWNLMPGNYDRFLHQLIPNKTSIGYWNIQSKDSNSMYGRFGRAFDVAHNKMGLYFDVDNAFFSNKPLKGQYTITIEVTYLDKGTGGWQLYYDAQTGPDKASGIISCTNTNKWKKATITIPDAYFGNKGPNASDFSIRSTSKKQDVIFSVVELSRPSNFAFSTKSAISMLSSNTNSQATSITNDTNVKDQLLINPNPATDHFYIQTKDSQLIRQVIIYNQSGQIILQKQVSAGLVVVVNRNEMAAATPGIYFIKVSTATALYTGKLMVL
>NZ_CP042435.1|WP_158638351.1|2568674_2571905_+|T9SS-type-A-sorting-domain-containing-protein
MFNYGVWQTFGDPINVVQYPEIKGRLCNFNWKDIEVANNVWAWDSFDIELTRRAQDSLPIIFLVYTEEGAPDWIYDLGVPKVAQNENGTITYAPYYANNRYKNLFKRMITTVHQHIETLPYPVRKFIIGVQGCFGSTGDYIGYKGTVDSQYALTDEQFFGLFTEFSQYYYNEYVNTDPKIYLLSNPQNNGQDQMNWLIQNCPNGWIKCGSIGKGFQLNDEVYKSGWLYNLLNYPQNGDYIRSRSELQFNPDESGWWSEYKYKNMFALITYDIFWGLDWSNQAPGQIFDQQYDYAFNFYNKYAGQKKPSTATNAMCALRDGLNAADTIRFPVSVYGKADRADTTRYKNIATRFAKFGARQEDPLTATLGELNNLAANGINDVGWDVFPGNYERYLHQLKANETSVGYWNVRALADSNTMYGKYARGINATNSKNALYFDVDSLFLNNAPVNGKYPIIVDITYLDSGFGGFRMFYDAKTSTNKSSLAVQLTNTNVWKKASVTLYDAYFGNRAFNASDFYIQAINNQNVLFSVVELSRPDSANPRLGLFTQESLLFDTICTKSTGSIKSFILNGYFLNGSNILISPLPGYSFSTAINGTFTDSLIISSYGTGINKSIYVKFSPLKTNVYSGNVFISGGGYKAISMALKGAGINSRPVLTANISNASCNNTKNGAIDLVVTGGAGPFSYSWTTDSFPFKSTTEDINGLSPANYSVTVNSFGGCTVTAEYIITQPSILSASIKKDSDIVCKGSTTTVTVSAVGGTTPYAGTGIFTVSSGNVSFVVTDANGCASETDKITILPGALVVPPKPDEIKGNDGGGLCDGGTFYYAASPVSSATSYTWTLPAGTVIKKTSAKKDSISLTVQAEFAEGTLLVTANNVCGSSLPASKTITAIPEKPVGISGPVSVFANQAGLIYSVINPKSVLTYTWSSSSGTRITTGQNTWQATINWGPVDGKVNVKANNNCGSSGPASIDVTVLSPALQNTLKTKVKNKSNIKSLSAIVMPNPANTLAIVGFIAEKTDVYEMELTDLTGKTLLRKKLTSIIGANTEKINMQPYSNGLYFITLTNNTGRVTLKVIRN
>NZ_CP042435.1|WP_147189566.1|2572066_2573800_-|DUF3520-domain-containing-protein
MQSHSQYYLRGEVKDENGQGIYNAKIFLSSKGTIPFYTGSSGAFGIPLSTPTDSIIFMADGYETIKTLTDARKYNTYTLKFASANALVAKHKLYSLVPQNADDVTETYYNQGETYTNLIENDFTFAEKYPETGFALNINRASYSNIRRFLNNNMTVPPDAVRIEEMLNYFDFADKANTDRDNFSCATQLTQSPWDVGKRLLFIKFKAPYINVDTAPPTNLVFLVDVSGSMENPNRLPLLKDAFKMLVNNLRDKDTIAMVIYGGIVGTYLQPISCKYKDSINRSIDKLEASGETPGEAAIRTAYALAERMYKKEANNRIILATDGDFNVGQTTDKELEDLVVTHRNSGIYLTCLGVGMGNYKDSKLEILAKKGNGNFAYIDNIYEAEKVLISEFSKTMYAVANDASVNVYFNPYYVKRYRLIGFDNRKELLENSVAELEGGEVGSGHSLMAVFEIEPVDAMYDSIMRNNPDVNIAQLQLHYKVPQSDQQVVKNFSVPNNFEDFNTCDSSIRFATSVIMFGGLLKQSELWENLNWEDIIKIARNSAMENDFSQKEFVALVGKAKIIYEPYRKKKKKEQE
>NZ_CP042435.1|WP_147189567.1|2574111_2574648_-|hypoxanthine-phosphoribosyltransferase
MAEIKVHDKYFVPWLSEEIIQQRVKEIATEINTDYAGKKPLFIGVLNGAFMFASDLFKNIHIEAEISFIKLASYKGTKSTGQVITAIGLDMDLTGRDIIIVEDIIDTGKTLTEFLPQIRNQQPASLKIAVLLHKPEAMVHPIHIDYCCFSIPNKFVVGYGLDYNGLGRNISSLYQVKE
>NZ_CP042435.1|WP_147189568.1|2574672_2575755_-|LysM-peptidoglycan-binding-domain-containing-protein
MKRFSLLIFPLFFLMTYVSAQTNDAVQQYIEKYKEIAINEEIRTGVPAAITLAQGIFESMAGQSDLALASNNHFGIKCKENWTGKKVYHDDDSRGECFRSYTTVEESYRDHSDFLKSRPNYTFLFTIDPSDYKAWAYGLKKAGYATNPVYAQAIIKKIEDNDLQQYTLIAMQRGSGVQPDVAVNNTPDKPVMNTVVAALPDVSAIAIQSAEKPSAQETVLAEYNGEGNYPIGMFTINQTKTIYAAAGTSLFALASNNNIALEKLLEFNEIDNSDDILAQGQLIYLEKKSKKSNTKDFHIVAPNETIETIAQREGIQLESLFEYNKMQKGLEPAPGEKVYLKPGRQTYYPKLLPKNNAKIG
>NZ_CP042435.1|WP_147189569.1|2575754_2576396_-|O-methyltransferase
MELVNILAEAYAEKYTSPEDAVLKQINEDTYANHTQPHMLSGHVQGKVLEFISCIMQPKYILEIGTFTGYSALCLAKGLQNDGELHAIELREEDAQLCAKNFSQSALHKKIHLHVGNALDIIPNLPYKWDLVFIDADKTGYIAYYEMLLSRLNDNGLIIADNVLFHGKVLEDNISGKSARAVDAFNRHVAEDERTEQVMLTVRDGLLFIKKKK
>NZ_CP042435.1|WP_147189570.1|2576395_2577856_-|sodium:solute-symporter
MSATFLFSFVIAYFLLLLGVAWYTSRNSNNDSFFIGNRSSNWMLVSFGMIGTSLSGVTFVSVPGTVGANAFGYFQVVIGYFIGYFVVAYVLLPLYYRLNLTSIYNYLLQRFGNTAYKTGAMFFILSRVLGATARLYLVINVLQLFILDNLHIPFPLTTFVILLMILLYTFEGGVKTIVFTDTLQTTFMLLGLIVCVFYIMYSLDLSFVSTLKLLSAQGYTKIINTDVNSAGFFLKQIIGGAFITIGMTGLDQEMMQKNISVKTLGGSQKNMVTFSFVLVVVNFLFLLLGGLLYLFASTNNIAIKGDDLFPTVALQYLPSFVSIIFIIGLISALFPSADGALTALTSSFCIDILGLKKRDDLDEKQRRTIRLKVHLTMAIIFFLCVMMFKWINDKSIINIILTVAGYTYGPLLALFAFGIFTKRKLPDNFAVIFVCLAAPLFCYFLSNNAVTWFNGYHIGVELLLINALVTIAGLYFISQPADKIAA
>NZ_CP042435.1|WP_147189571.1|2578174_2578711_+|TIGR00730-family-Rossman-fold-protein
MYKSIAVFCGSNSGNDPIYEQHAKDIGTLLAEKNIMLVYGGGNTGLMGIVANTVLQEGGKVIGVIPELLKNIERHHKGLTELHIVADMHTRKKMMYELSDAAIVLPGGNGTLDEMFEMITWNALTIHNKKIILLNTAGFYNALIGHINQMQVQGFLHTDLRDTFEIYDTPDAVIASMV
>NZ_CP042435.1|WP_147189572.1|2578691_2579405_-|hypothetical-protein
MTQHKIDTNNILNAGKIVDVDYSATFVINKLKMNNKHLLLAFGIMITTLVQAQRPATYDAEESKQSGFSTNRIFVGGSINLGFSSYSFQAGAVPEIGYSITDWLDAGLGINLNYSSERADYYYNGNVRYRNFNYGGGPFVRIYPIRFLFVQTQFEHNWLKQNAKDMNTGYEYKATYGSNSFIAGIGYTQRIVGQSSFYTMIGLDLLTDKNSPYRDYNGSAYPIIRAGFNFYLKPSKR

Crispr_ID: NZ_CP042435_3

• CRISPR_ID: NZ_CP042435_3
• CRISPR_location: 4241045-4241167
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042435_3

Consensus_repeat	Method
AAAACGCAAGCTGAAAAATATTATGATCATTTTGCGCATCGTCCTCT	CRISPRCasFinder

spacers of NZ_CP042435_3

>3.1|4241092|29|NZ_CP042435|CRISPRCasFinder
CTGAGAGACGATGCTAAACTGAAACCATG

CRISPR arrays and Neighbor proteins around NZ_CP042435_3

CRISPR arrays

The CRISPR arrays of NZ_CP042435_3

>merge|NZ_CP042435|3|4241045-4241167|CRISPRCasFinder
AAAACGCAAGCTGAAAAATATTATGATCATTTTGCGCATCGTCCTCTCTGAGAGACGATGCTAAACTGAAACCATGAAAACGCAAGTTGAAAAATATTATGATCATTTTGCGCATCGTCCTCT

>NZ_CP042435|3|2|4241045-4241167|CRISPRCasFinder
AAAACGCAAGCTGAAAAATATTATGATCATTTTGCGCATCGTCCTCT	CTGAGAGACGATGCTAAACTGAAACCATG
AAAACGCAAGTTGAAAAATATTATGATCATTTTGCGCATCGTCCTCT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042435.1|WP_147191787.1|4250089_4250482_+|WxcM-like-domain-containing-protein	unknown	unknown	gnl|CDD|377522
NZ_CP042435.1|WP_147191758.1|4235062_4236337_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|213187
NZ_CP042435.1|WP_158638399.1|4230616_4232035_+|hypothetical-protein	unknown	unknown	gnl|CDD|367953
NZ_CP042435.1|WP_147191768.1|4241297_4242413_+|lipopolysaccharide-biosynthesis-protein	unknown	unknown	gnl|CDD|211420
NZ_CP042435.1|WP_147191760.1|4236341_4236944_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379276
NZ_CP042435.1|WP_147191766.1|4238996_4239893_+|hypothetical-protein	unknown	unknown	gnl|CDD|250689
NZ_CP042435.1|WP_147191748.1|4229808_4230306_+|HAD-family-hydrolase	unknown	unknown	gnl|CDD|319769
NZ_CP042435.1|WP_147191762.1|4236974_4237790_+|glycosyltransferase	unknown	unknown	gnl|CDD|133055
NZ_CP042435.1|WP_147191764.1|4237804_4238980_+|glycosyltransferase	unknown	unknown	gnl|CDD|340831
NZ_CP042435.1|WP_147191782.1|4248058_4248955_+|glycosyltransferase	unknown	unknown	gnl|CDD|133055
NZ_CP042435.1|WP_158638401.1|4249016_4250027_+|acyltransferase-family-protein	unknown	unknown	gnl|CDD|224748
NZ_CP042435.1|WP_147191754.1|4233011_4233896_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_CP042435.1|WP_147191772.1|4243497_4244187_+|sulfotransferase-family-2-domain-containing-protein	unknown	unknown	gnl|CDD|367564
NZ_CP042435.1|WP_147191752.1|4232031_4232994_+|alpha-1,2-fucosyltransferase	unknown	unknown	gnl|CDD|211387
NZ_CP042435.1|WP_147191778.1|4246027_4247134_+|glycosyltransferase	unknown	unknown	gnl|CDD|366154
NZ_CP042435.1|WP_147191770.1|4242582_4243491_+|glycosyltransferase	unknown	unknown	gnl|CDD|366154
NZ_CP042435.1|WP_147191756.1|4233931_4234924_+|acyltransferase-family-protein	unknown	unknown	gnl|CDD|224748
NZ_CP042435.1|WP_147191774.1|4244209_4244932_+|sulfotransferase-family-2-domain-containing-protein	unknown	unknown	gnl|CDD|367564
NZ_CP042435.1|WP_158638400.1|4244976_4246038_+|glycosyltransferase	unknown	unknown	gnl|CDD|132997
NZ_CP042435.1|WP_147191780.1|4247140_4248022_+|FkbM-family-methyltransferase	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042435.1|WP_147191787.1|4250089_4250482_+|WxcM-like-domain-containing-protein	gnl|CDD|377522	pfam05523, FdtA, WxcM-like, C-terminal. This family includes FdtA from Aneurinibacillus thermoaerophilus, which has been characterized as a dtdp-6-deoxy-3,4-keto-hexulose isomerase. It also includes WxcM from Xanthomonas campestris (pv. campestris).	1.84967e-60
NZ_CP042435.1|WP_147191758.1|4235062_4236337_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	1.06965e-104
NZ_CP042435.1|WP_158638399.1|4230616_4232035_+|hypothetical-protein	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	0.00026273
NZ_CP042435.1|WP_147191768.1|4241297_4242413_+|lipopolysaccharide-biosynthesis-protein	gnl|CDD|211420	cd11579, Glyco_tran_WbsX, Glycosyl hydrolase family 99-like domain of WbsX-like glycosyltransferases. Members of this domain family are found in proteins within O-antigen biosynthesis clusters in Gram negative bacteria, where they may function as glycosyl hydrolases and typically co-occur with glycosyltransferase domains. They bear resemblance to GH71 and the GH99 family of alpha-1,2-mannosidases and may share a similar cataltyic site and mechanism. The O-antigens are essential lipopolysaccharides in gram-negative bacteria's outer membrane and have been linked to pathogenicity.	8.39232e-180
NZ_CP042435.1|WP_147191760.1|4236341_4236944_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|379276	pfam13578, Methyltransf_24, Methyltransferase domain. This family appears to be a methyltransferase domain.	4.56036e-18
NZ_CP042435.1|WP_147191766.1|4238996_4239893_+|hypothetical-protein	gnl|CDD|250689	pfam01531, Glyco_transf_11, Glycosyl transferase family 11. This family contains several fucosyl transferase enzymes.	3.52245e-05
NZ_CP042435.1|WP_147191748.1|4229808_4230306_+|HAD-family-hydrolase	gnl|CDD|319769	cd01630, HAD_KDO-like, haloacid dehalogenase-like (HAD) hydrolase, similar to Escherichia coli 3-deoxy-D-manno-octulosonate 8-phosphate (KDO 8-P) phosphatase KdsC, and rainbow trout N-acylneuraminate cytidylyltransferase. KDO 8-P phosphatase catalyzes the hydrolysis of KDO 8-P to KDO (3-deoxy-D-manno-octulosonate) and inorganic phosphate and is the last enzyme in the KDO biosynthetic pathway. KDO is an 8-carbon sugar that links the lipid A and polysaccharide moieties of the lipopolysaccharide region in Gram-negative bacteria. An interruption in KDO biosynthesis leads to the accumulation of lipid A precursors and subsequent arrest in cell growth. The KDO biosynthesis pathway involves five sequential enzymatic reactions. This family also includes rainbow trout CMP-sialic acid synthetase which effectively converts both deaminoneuraminic acid (KDN, 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid) and N-acetylneuraminic acid (Neu5Ac) to CMP-KDN and CMP-Neu5Ac, respectively. This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	1.25865e-58
NZ_CP042435.1|WP_147191762.1|4236974_4237790_+|glycosyltransferase	gnl|CDD|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	9.32517e-32
NZ_CP042435.1|WP_147191764.1|4237804_4238980_+|glycosyltransferase	gnl|CDD|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	4.33785e-36
NZ_CP042435.1|WP_147191782.1|4248058_4248955_+|glycosyltransferase	gnl|CDD|133055	cd06433, GT_2_WfgS_like, WfgS and WfeV are involved in O-antigen biosynthesis. Escherichia coli WfgS and Shigella dysenteriae WfeV are glycosyltransferase 2 family enzymes involved in O-antigen biosynthesis. GT-2 enzymes have GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	3.57875e-35
NZ_CP042435.1|WP_158638401.1|4249016_4250027_+|acyltransferase-family-protein	gnl|CDD|224748	COG1835, COG1835, Predicted acyltransferases [Lipid metabolism].	1.85284e-26
NZ_CP042435.1|WP_147191754.1|4233011_4233896_+|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	1.7195e-47
NZ_CP042435.1|WP_147191772.1|4243497_4244187_+|sulfotransferase-family-2-domain-containing-protein	gnl|CDD|367564	pfam03567, Sulfotransfer_2, Sulfotransferase family. This family includes a variety of sulfotransferase enzymes. Chondroitin 6-sulfotransferase catalyzes the transfer of sulfate to position 6 of the N-acetylgalactosamine residue of chondroitin. This family also includes Heparan sulfate 2-O-sulfotransferase (HS2ST) and Heparan sulfate 6-sulfotransferase (HS6ST). Heparan sulfate (HS) is a co-receptor for a number of growth factors, morphogens, and adhesion proteins. HS biosynthetic modifications may determine the strength and outcome of HS-ligand interactions. Mice that lack HS2ST undergo developmental failure only after midgestation,the most dramatic effect being the complete failure of kidney development. Heparan sulphate 6- O -sulfotransferase (HS6ST) catalyzes the transfer of sulphate from adenosine 3'-phosphate, 5'-phosphosulphate to the 6th position of the N -sulphoglucosamine residue in heparan sulphate.	6.26782e-13
NZ_CP042435.1|WP_147191752.1|4232031_4232994_+|alpha-1,2-fucosyltransferase	gnl|CDD|211387	cd11301, Fut1_Fut2_like, Alpha-1,2-fucosyltransferase. Alpha-1,2-fucosyltransferases (Fut1, Fut2) catalyze the transfer of alpha-L-fucose to the terminal beta-D-galactose residue of glycoconjugates via an alpha-1,2-linkage, generating carbohydrate structures that exhibit H-antigenicity for blood-group carbohydrates. These structures also act as ligands for morphogenesis, the adhesion of microbes, and metastasizing cancer cells. Fut1 is responsible for producing the H antigen on red blood cells. Fut2 is expressed in epithelia of secretory tissues, and individuals termed "secretors" have at least one functional copy of the gene; they secrete H antigen which is further processed into A and/or B antigens depending on the ABO genotype. O-fucosyltransferase-like proteins are GDP-fucose dependent enzymes with similarities to the family 1 glycosyltransferases (GT1). They are soluble ER proteins that may be proteolytically cleaved from a membrane-associated preprotein, and are involved in the O-fucosylation of protein substrates, the core fucosylation of growth factor receptors, and other processes.	1.09921e-61
NZ_CP042435.1|WP_147191778.1|4246027_4247134_+|glycosyltransferase	gnl|CDD|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	2.61798e-21
NZ_CP042435.1|WP_147191770.1|4242582_4243491_+|glycosyltransferase	gnl|CDD|366154	pfam00535, Glycos_transf_2, Glycosyl transferase family 2. Diverse family, transferring sugar from UDP-glucose, UDP-N-acetyl- galactosamine, GDP-mannose or CDP-abequose, to a range of substrates including cellulose, dolichol phosphate and teichoic acids.	1.60825e-36
NZ_CP042435.1|WP_147191756.1|4233931_4234924_+|acyltransferase-family-protein	gnl|CDD|224748	COG1835, COG1835, Predicted acyltransferases [Lipid metabolism].	6.25546e-24
NZ_CP042435.1|WP_147191774.1|4244209_4244932_+|sulfotransferase-family-2-domain-containing-protein	gnl|CDD|367564	pfam03567, Sulfotransfer_2, Sulfotransferase family. This family includes a variety of sulfotransferase enzymes. Chondroitin 6-sulfotransferase catalyzes the transfer of sulfate to position 6 of the N-acetylgalactosamine residue of chondroitin. This family also includes Heparan sulfate 2-O-sulfotransferase (HS2ST) and Heparan sulfate 6-sulfotransferase (HS6ST). Heparan sulfate (HS) is a co-receptor for a number of growth factors, morphogens, and adhesion proteins. HS biosynthetic modifications may determine the strength and outcome of HS-ligand interactions. Mice that lack HS2ST undergo developmental failure only after midgestation,the most dramatic effect being the complete failure of kidney development. Heparan sulphate 6- O -sulfotransferase (HS6ST) catalyzes the transfer of sulphate from adenosine 3'-phosphate, 5'-phosphosulphate to the 6th position of the N -sulphoglucosamine residue in heparan sulphate.	4.95653e-12
NZ_CP042435.1|WP_158638400.1|4244976_4246038_+|glycosyltransferase	gnl|CDD|132997	cd00761, Glyco_tranf_GTA_type, Glycosyltransferase family A (GT-A) includes diverse families of glycosyl transferases with a common GT-A type structural fold. Glycosyltransferases (GTs) are enzymes that synthesize oligosaccharides, polysaccharides, and glycoconjugates by transferring the sugar moiety from an activated nucleotide-sugar donor to an acceptor molecule, which may be a growing oligosaccharide, a lipid, or a protein. Based on the stereochemistry of the donor and acceptor molecules, GTs are classified as either retaining or inverting enzymes. To date, all GT structures adopt one of two possible folds, termed GT-A fold and GT-B fold. This hierarchy includes diverse families of glycosyl transferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. The majority of the proteins in this superfamily are Glycosyltransferase family 2 (GT-2) proteins. But it also includes families GT-43, GT-6, GT-8, GT13 and GT-7; which are evolutionarily related to GT-2 and share structure similarities.	5.71066e-25

Protein sequences

>NZ_CP042435.1|WP_147191766.1|4238996_4239893_+|hypothetical-protein
MVVIDHKAGQLANRLFQFSYFIAHSLEHDYKLINPCFEEYRDLFETTSKSNFDTGNIQLAFSRNLFINKKLTQLINRLRRPASKNNSKLFFFEFHNIRQQYDQQHKVFDMSDASFVKKAKRKILFAKGWHYRDTAALIKHADTVRKIFTPCDIFMNQVKNVVAATKNYDVRIGVHLRKGDYENFFEGRWFYDDTVYAQKMQALQNTFAAQKKTCVFILFSNEIIDATSFAGLNILTGQRPAITDLYSMAACDYLVGPPSTFTMWASFYGSVPLLILKNKDTIPAVENFKIANGIEAFF
>NZ_CP042435.1|WP_147191764.1|4237804_4238980_+|glycosyltransferase
MNVLIAIGSFYDGGAEIFAIRLANALSESRQVVFVELQPYETDKKSQRKLLSPAVKVIQLGKNVPGFLLHKYLRKGRVRQRLKHYYNASVEQTFGKVLKEYNIQVVHSHCLQTDIYFTRLKSKYSFKLATTLHGHYELEQKEKLLGLFESNHMQERTDKYVWVTQQQNETLDNLKVPNKKRNKIYYGIPGDIAKACTVYTPDEPLKIVMAARGIPEKGWKETIDACLLLLKKFPGKLQLTLLGDGVFIDELRSLYNHTAIHFYGYIEDVLPFIEDAHIAVLPSYYKAESLPNSIIEYLFCGKPVIATSIGAVEEMISYNHERAGILIGLVHEKVAVQDIADAIQVYLENPELVAQHSVIALQAAQKFDMKQCVDSYTALYEEMLNEPVMQQ
>NZ_CP042435.1|WP_147191762.1|4236974_4237790_+|glycosyltransferase
MHHPLISVITPCYNQGQYVEDAIQSIPYEKVNFDIEHIIIDDGSTDSFSLQKFKELEESGTNIIHQENKGLATTRNIGISMAKGKYIIPLDADNKLNDVYFTKAIDILEQHDNIDVVYGDFTVFGTGQRTHETGDFDICNMIEWNKIDACAIFRKSAFDRVDGYDTNMVFGCEDWDLWLNLYFNGSNFYYLPEVAFYYRVTSQSMLQNITEPNKQVIRQYLYKKYHQQIIEVLLKRKNDAEAYSRQLLKYKNAEKQTIKATLKLLLKGSII
>NZ_CP042435.1|WP_147191760.1|4236341_4236944_+|class-I-SAM-dependent-methyltransferase
MLSFLQKQKKHIQYDQAGLATALARVTGQISHAELFTLYRHALQLSKGAVVVEIGSYRGKSSIALGLAARQSGARVYCIDPHDDYVGVAGGVFGPVDLKDKIANIQQFDLGDIIFPVCLSSFEVGKIWSKPIDLLWIDGDHSYTGVSTDFYQFSVHVKKNGILIFHDSHMEGIKQLMSEIDINSFRKIGEVDSMTIYERR
>NZ_CP042435.1|WP_147191758.1|4235062_4236337_+|ATP-binding-cassette-domain-containing-protein
MSNTVIKVESLSKQYRLGQVGRKSLSHDINRWWYGIRGKEDPYLKIGEENDRSKKGSTEYVWALQDINFAVQQGEVLGIIGRNGAGKSTLLKILSKVTAPTTGNVKIKGRIASLLEVGTGFHPDLSGRDNIFLNGAILGMTKKEITAKFDEIVDFAGVERYIDTPVKRYSSGMYVRLAFAVAAHLEPEILIVDEVLAVGDAEFQKKCLGKMKDVSEKDGRTVLFVSHNIAAVKTLCTQGLLLENGLLSVNATAEEAIRQYQQNTQSIISNEALTGHVMLEGPGLLELVCKSKSYDTATFLFGEAIQINMHWHFIDSLKSRVISLRIYNTADELMCGFNTLYDKYITSMEESGSYYIALDIVNTFAPGTYYISAGSYIRPHTNEFIYNKVAGFEISEEPKEKDILPNIMGGPKFYSPFSWVIKKQ
>NZ_CP042435.1|WP_147191756.1|4233931_4234924_+|acyltransferase-family-protein
MERNLTLDVLRGIAAMAVLLFHYTYGYREYYGHILDPKYDFIYGNLGVELFFMISGFVIFSSIAKVNNAGDFIFRRFSRIYPTFWFCMLVSFFLVIIFLPGTVKNYQLKWTATMISSFFGCKPTEGVYWTLLYEFFFYMQIALLLFFKQIDNIVWWGILQLSLVWINVFIYAFSDRFCMAANLNWGMLFFAGILFYKLKNADNKRRWSVHLLLMLCYFTSCITLHSAAERIAVFIFFTVFYLFCFGILDWVQWKPFVFLGSISYPLYLLHMSIGYIIMNAIKNYFTFSPFIFICIPVIVVILLAWLVHRFIEVPTNRYLRGNKYLVLLFS
>NZ_CP042435.1|WP_147191754.1|4233011_4233896_+|ABC-transporter-permease
MHNSFTEQQLQQETEQWTEIITPRNKLFDLRLKEVWHYRDLLGLFVKRDLAAQYKQTVLGPLWHIVQPVLTTIMFLVVFNKIAHIPTDGIPAVVFYMSGIAMWSYFSTCLTGTSNTFISNAGIFGKVYFPRLITPLSIITSNLIKFSIQFGLLVAAMLYYAYTGDMKIDIGMHTLLIPAVLFAMAGLGLGLGIIISSLTTKYRDLTVLVNFGVGLLMYATPVAYPLSYVEKSSYKTLILLNPLSSLIETFRYAVLGKGTFDPMLFGYSCLFMVVILFFGMIIFGKVEKTFMDTV
>NZ_CP042435.1|WP_147191752.1|4232031_4232994_+|alpha-1,2-fucosyltransferase
MIIVRISMGLGNQLFQYAAGKALSLEKNVPLKVDIASYGGYKLRNYELEKSFDINTPVATPTEIQHYYYPHPVKRVWNNLFPSRKMRVLGLRYDEPPLQKKLLQAHDLLLPPHKRTTYIEPHLNFDAHFFKANDDIYLQGYWMSWRYFEKYDETIRKIFTIHKPVVAHLENIVDDIHAQNSVSIHIRRTDYTSAAVIALKGQTTMGFYKNAIDIIEAKINNPVYYMFSDDIEWVKENFPMQDRMVHYIDNSISNSAIEDFYLMQQCRHNIITHSTFGWWAAYLNPNKEKMIIAPKKWFIKKSHNDKDICPPSWITIENNI
>NZ_CP042435.1|WP_158638399.1|4230616_4232035_+|hypothetical-protein
MSENKTKPRVIIPIVGQGSVIHVIRTGMLDRMSEFVTPVVAMLWEQPDLIEELKAKGYEVTLMPTYNVTAAYYALRAKITLWYSKYVLKSPTRIILRSYLDLYLPAKKVWKRKLKNALPEFLFATWPPYIKRLIKQEGVLIKQQPCYDAYYTWVRSLQADSIFTITPFLQEVELVARILKEQGKKVMASIHSFDNITTRQWPAFFFDHYLVWNNINKAELERINPQLKTNNAITICGAAQFDFHYKPNFTWSREEWLAKLGLPADKKIILYAGGPVSLFKDEPQYLAHLNEAFKAGKIDASEAVILFRSHPLDKKERWHALVGDSPYIIYDAAQSGKEKFDHTNVTEEDIRKLMSTVKHADVQINFTSTMTIDGSVFYRPQIGPYYTELDKARKEKLTRMMYMQEHYLPITKSGAINMPASKEAFIQMVSEALQNPARYTQHCDDCLDTMITYKDGQTTGRVIAALKRFYNA
>NZ_CP042435.1|WP_147191748.1|4229808_4230306_+|HAD-family-hydrolase
MVKIKLFLSDVDGVLTDAGMYYTESGDEFKKFNTHDGMGFTLLRKAGIKTGMITSENTKIVERRAAKLKVDYLYQGKEFGDKLSAALDICAKENISISEVAYIGDDINCISLLQAVGVAACPANALPKIKNIKGIIQLEKKGGDGAVREFIEMLFDKEWFNINAE
>NZ_CP042435.1|WP_147191768.1|4241297_4242413_+|lipopolysaccharide-biosynthesis-protein
MPRLIAYYLPQYHPIPENDAWWGTGFTEWTNVAKAKPLFNGHYQPHFPADLGYYDLRVPEVREQQEAMARQYGIEGFMYYHYWFGNGRVLLERPMQQMLRAKKNNFPFCLCWANESWKGVWHGVSTGKTLIEQTYPGKSDYEKHFYYLLDAFNDERYIKVDNKPVFNVYMPLNLPDIHEFANTFHELAIKEGFSGMYLIGSRCPIDWNPCQYGFSGVIGSEMANLRIKQRSYFSKKKIYLVKKIQSHTQQLAKKKMFAPNKIPLVTAYENIIDQLITDKTFSFDYYPCAVPNWDNTPRAGADGLVFHHSTPQLFGKHLQHALQKVSHLPAERQFVFIKSWNEWAEGNYLEPDQQFGYGYLEEIKQQLQAIA
>NZ_CP042435.1|WP_147191770.1|4242582_4243491_+|glycosyltransferase
MPAYNAAASVASGIKSLQEQTYSNWELIIVDDGSTDDTAAIIQSIAHTDKRIKYFYQQNSKQGKARNKGIKEAAGAFIAFIDADDVWMHNKLEKQIEFINLTNADLVFADVTAIDEKGDPYLDSWNVTDATYSGDEGLLAFMQENKAPLLSVLVKKEAVLKVNGFDEDRDMQYVEDYDLWLRMLQSGARFASSSEKLACYSFDTKKTTARKKTLINVVNTLKKVSVHDESLQQQKNLAMTLWTRKIIKRCTPAIEKADMKKIISLIPSPPVKFFLSIINNILGASVAGRIILLFTKNVSVQG
>NZ_CP042435.1|WP_147191772.1|4243497_4244187_+|sulfotransferase-family-2-domain-containing-protein
MSLIKNIKRLVKGSPPRKAYVAGNINYDHHYIFIHIPKNAGTSVYKALSFSNSTHAEAKQYKQMLGKSYEDFFSFCFVRNPFDRFISTYNYARLEESYYHSSIDPSKTKFGKHLDYDILKDASLEEAVDLLLEGKLIHDKAWNHWKPQVQWILDEDEKVIVDYIGRLENIQTDFSYICNKLQLPVHNSLPALNVSEAKKKDYRDLINPGMRAKLEHYYRKDLEILEYEF
>NZ_CP042435.1|WP_147191774.1|4244209_4244932_+|sulfotransferase-family-2-domain-containing-protein
MKGILTSNIQKAKRYIKENRRRKIAAAYYREHEALRPGNYYSTNCFDYYKCIFIHIPKTAGLSVSKSLFGNYAGGHLSYDSYVKKFGKATVDNYFKFTFVRNPWERLASAYFFLKKGGMNSADAAFAKKYLSSVNNFESFVNDWLSEDNLDLYYHIIPQYKYITSNNAERIMVDFVGKYENLQDDFRRICNSIFHTEKLLLDINSTEASKIKYKTLYTEDMKKKVAVLYAMDIQMFGYAF
>NZ_CP042435.1|WP_158638400.1|4244976_4246038_+|glycosyltransferase
MENREGVSVIICCYNSALRLPETLRHIYNQKVPEQIGWEIIVVDNNSTDNTSDVAMSEWRRYNNNIPFKVVHQEIQGLSFARSKGFENANYDILIFCDDDNWLRDDYIRYAFEIMQSNESIGILGGVSSGYFEVGKPFWFDAFMESYAVGKQMYETGIANSRTYLAGAAVVVRKAIYQKLNFLSYSLLLTGRIGKRLTSGEDTELCWLAMFLGFNLYYDERLRFVHFMPKQRLNWKYCVSMIAYGHSIPRIYFSLYHYLHNNIFNNREVSFDITYKTLMRRHLNYLRKHNPNLKSILNAVRSLFISTEGSEKEIQFKSDIHKLRYLLFNKSDLEKNFYAITSLMQKIKQQNVS
>NZ_CP042435.1|WP_147191778.1|4246027_4247134_+|glycosyltransferase
MYLKQSNGISVLICTYNGANRLGKTLAHLAAQVTVDSLKWEIILIDNNSNDNTSEISKNIWQQLSCKIPFYIFKEPRPGKSFALETGVSKSNYDILIICDDDNWLQENYVQYAYDFLQKNRTVGILGSFAEPYLDSAKPLWFDKYENVFAIGRQMPQTGIANKRNYLFGAGMVIRKEIYTTVAALNHEMFLTCRKGNELSSGGDSEICLLAMQLGYDLYYDEGLQFTHYISPGRLKWSYCVEMITKGFASPQIYYAIYDYCFNAVNKNEAADFENLYRWNMRKQKRILLNEISGAGNFFSSVAALLFSKPGNDKEIRIKTAINKLRYMQKNKKQLAADFEKILALAKRMQQVKALPMEQDKQQIIQQQ
>NZ_CP042435.1|WP_147191780.1|4247140_4248022_+|FkbM-family-methyltransferase
MKQRIYKMLGSLRRFFYEPVLLKFTSNHDSILDSRADEIKRNIALTMPDNIVLKGYKCYSAGEEDGMIEAIFEKITAGSKTFLEIGCERGLENNSHFLLLNGWQGMWVDGNPAFIKSISSFLGGENLAKLMVRQLFVDKENVRKLFDDVYAYYKVNEVDFFSLDIDGNDYHVMQSVLEYGVQPKMICVEYNAKWGKHANVKVSYDAGFVWAADDYMGVALAAWLQLFGQHGYTLLSCDMGGNNAFFIRNEYANLFTIYSPSLLYQPARYYLTRRRSGHPSTLKMLKNVLNKTV
>NZ_CP042435.1|WP_147191782.1|4248058_4248955_+|glycosyltransferase
MQIVSIIAVCYNQAAYVADTLNSIKAQTYPNIQLIVADDGSEDGSKEVIKNWIAQNDPSAIFIDHQKNLGLTKNINSALPYIKGDYFQVFGCDDIMLPDKIERQVALLQANKDAGIVYSDMQLIDKEGHDLPLTYFQKHAYKQPFSGDHYESLINRIIPAAPTVLIKKGVLEKTGYYNEKLDYEDYDYFLRAAKHYSFIYEPTITVKYRVLESSLSNHNVYPVKYFRNLFTVLYSNYDTRKQYRQQFNDRLLFCIKNLYSLKYKNAFGLFSKALLKTGDTRLLKYTIASIPFMFTGIK
>NZ_CP042435.1|WP_158638401.1|4249016_4250027_+|acyltransferase-family-protein
MKKRIDTLDALRGIAAFSVLLLHYTSGYRAHYKHSFNQDYDFVYGYLGVELFFMISGFVIFLTLIHSKNSIDFLYKRFSRIYPTFLFCLVTTFTIVFLFGLPMRERSLYQAAGNVLIATNIFGFKPVDGVYWTLEIEIFFYLFMALLLFCKQIKNILFWGVFFLAMTWVNAFFYTIPDKLSIILNVKYNCFFFAGILFYKIKFSQDRIDWKIHLLIASCLITSLIVIGPWPAKAIASCFFVLFYLFSYGLINLHAKPLLFLGKISYPLYLLHQNIGYVIMNNTKPYLGNYPFIFIGTTAMTMIFIAFLVHKFIEQPSIRFFRNLYSNKFNLKVIAK
>NZ_CP042435.1|WP_147191787.1|4250089_4250482_+|WxcM-like-domain-containing-protein
MELLHFPKILDQRGNLSFLQSNKEVPFEIKRVYWIYDVPGGEMRGGHAYKNLNEVIIALSGSYDVVLHDGEKEYRYHLNRSYYGLYVPKMMWRHIENFSTNSLALILTDDLYKEDEYIRDFDAFKAMKGI

Crispr_ID: NZ_CP042435_4

• CRISPR_ID: NZ_CP042435_4
• CRISPR_location: 4543931-4552312
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 128 spacers
• Cas_protein_info: cas2,cas1,cas4,cas3,cas5,cas7,cas8b2,cas6

Consensus repeat of NZ_CP042435_4

Consensus_repeat	Method
CTTGTAATCGTATCATTGAGGAATTGAAAT	PILER-CR
CTTGTAATCGTATCATTGAGGAATTGAAAT	CRISPRCasFinder
CTTGTAATCGTATCATTGAGGAATTGAAAT	CRT
CTTGTAATCGTATCATTGAGGAATTGAAAT	PILER-CR

spacers of NZ_CP042435_4

>4.1|4543961|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAGCAAAGTGCGTATGGCCATTGGCAAAGGTTTGG
>4.2|4544027|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATCATTACAGCAATTCAGATGGACGACGGACGCAG
>4.3|4544092|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAAGAACAGAATGATAGGAAAGAACGACAACTGG
>4.4|4544157|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TGTAGATTAAACCATGCAGTTTTATAAGCAGATGAA
>4.5|4544223|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
GTATGAGCGAAGAGTTACCGGAAATGAAGGATATG
>4.6|4544288|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTTTGTCTATTGGATTGCCACCCAGCAATTCCA
>4.7|4544352|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTAATTAAAGCATGGCAAAAATCGTGGGGGACGTA
>4.8|4544417|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAGATAGGAATTATACAGACGAACAGCACAAAGA
>4.9|4544482|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTAAGTTCTTTAATCAATCTGTTTATACATTCAGTA
>4.10|4544548|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
CAGGCAACAGGTGTAAGACAGATATGGAAGTTTAAT
>4.11|4544614|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTGGCTTTATACAGGCAGGCACTAATGTAACTATA
>4.12|4544679|37|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTATTCTAAAAAAACTTTTGCGTGGAGGGGCGCCCA
>4.13|4544746|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TGGGATTTAAACTATGACTTTGATAAAGATGGTGTA
>4.14|4544812|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTGCTATTCAATATTATAACCTCACAGGCCATAGA
>4.15|4544878|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TAGTATTGATTTTCGAGTGATGGCATGGCTGTAAA
>4.16|4544943|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATAAATATTTCGCTATCGACACAGCTAATACAGCT
>4.17|4545008|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TAGAAAAGATAACCCATTGCTTTAATGCCCATAA
>4.18|4545072|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTGAAAAAAGATATTTCGGCTTTTGAAGTTTTAAAA
>4.19|4545138|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
CTTGTTCCTGTTCTATAACCAATACTTGTAAGCGT
>4.20|4545203|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTAACTAAGACAGAAATAGAAAGCGTGAACAATGC
>4.21|4545268|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TGTTCTGTAATAATAAATATCGCCGATGTAACAGGT
>4.22|4545334|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AGATTTCCCTGGAGTACCGCATTTCTTGATCGCAA
>4.23|4545399|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTGAAACAGTTTCACAAACTGCATTTGAACATGGC
>4.24|4545464|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTAAATGCTTTGTGGATATAACAACCAACAGCAA
>4.25|4545528|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTGATTGACTTAGCAGATCATTGATGCCTAAAGA
>4.26|4545592|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAATAACGCTGCTCGGCCTGGTAAAAGAAACTTGCC
>4.27|4545658|37|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAATTAGCCCAAAAGTCCCGAAGGCGAAAAGGCTAA
>4.28|4545725|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATAAAATAATCACATTGCTTTGTTTTCAGGTCGTAA
>4.29|4545791|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAATAAGCAACGTGCCCAGCCGATTGAGTAAATTC
>4.30|4545856|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
CAGTTTATTTGCGCAAACAGTTTATTACCCTTGCCA
>4.31|4545922|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATAGAATTGAAATTGGTAAACGTATTCAGGAGGTA
>4.32|4545987|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTAATGCAAATGCCTGTGTGCCATCGCCATCCCA
>4.33|4546052|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAATAAACAACAAAAATGAAACGCTTAATCAATTT
>4.34|4546117|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
CAAATTGCTTTATTCGCATCTGTTACAAAACGATGT
>4.35|4546183|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTGATAGAATAGATGTAATTGTTCTTACTACCGG
>4.36|4546248|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AGTCCTTTATCAACGCCATTAAACTTTGGAAGTATT
>4.37|4546314|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TAATAAAGAGGAGCGCGGATTACTCCGCCGCTGCCT
>4.38|4546380|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTGATCGGGAATACTTTATTTGCAGCGGTTTTTGT
>4.39|4546445|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AATAAACTGTTCCAGTCTCTTTTTCGGTCCTGCCA
>4.40|4546510|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATCATTGCAAAAAGCTGCTCAATCTCTTGTATTA
>4.41|4546574|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TAGTAGGCAGTAACAATTTTTGGTACGATACTTTTG
>4.42|4546640|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTATTGATGCGGATGGGTTTGAAAGGCCTGTTAA
>4.43|4546705|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTATTTATGTGAATTCGAAATGATCATTGTTCTT
>4.44|4546769|37|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTCGCTATATACAATAACCGTATTGGTGGAAGTTATG
>4.45|4546836|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TAACTTCAAAGAAGGTGTAGCCAAAACAGCAGTAG
>4.46|4546901|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATAATTCCTGCCGGTTATCTTTCGAGAAGTCAAAT
>4.47|4546966|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAGAAACATTACTACCATGTGTTATTAACAGAAAT
>4.48|4547032|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTTTAGATGGATGAAATACAGTTATTATTTTGG
>4.49|4547096|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTAATTTATCCACTAAGACAATCCTTTACAACAAAA
>4.50|4547162|37|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAACTTCCCTCTATAGATCCTATATGGAAGGATGCCG
>4.51|4547229|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATATTTATAACCCAATTGATAAGCCTGCAATTGATA
>4.52|4547295|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTGGTATGCCGTTTTCTTTCCAGCAAAAAGCCAT
>4.53|4547360|38|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAGATTGGCAACTGAATTATTTACAGCGTCGCAGCTTG
>4.54|4547428|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAATCTATCTGGGGCTTTAAACCTGTGCTGTCCGA
>4.55|4547493|38|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AGTAAAAGTAATTCAATTGTTTCATCCGAAGCATCAGT
>4.56|4547561|37|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATCCATGCATTGGCTGTTTGCTTGCTGGCATACTAGT
>4.57|4547628|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
CCGTTAAGGAAGCGTTGATAACGTAGCTCTATTAGC
>4.58|4547694|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ACAATTTTATACAAGTCGCCGTCTGCTTTCCATT
>4.59|4547758|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTAAAAAACGCATCGCAGCACGAACTTCTACTA
>4.60|4547822|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTGCTGCACTATCATCCTGCCACATAGCCATTGT
>4.61|4547887|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATATATCATGCCCCTCAGCTTTTAACTGTGTAATGA
>4.62|4547953|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTCCTTGCGGATAGCTGTTTAGCTGCAACATTTACA
>4.63|4548019|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAATTAAACTCTATAACCTACCAATGGAATAAGGT
>4.64|4548085|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
GCAACAATTCTACCTGCAGCACTATCAGTTGCACT
>4.65|4548150|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ACAATAGAATTTGGTGCAAAGCTGCAGGGCGATGTT
>4.66|4548216|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AGTGTTGCAGTCGTTAATATTGAAATCTCTTATTT
>4.67|4548281|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATAACTGATTATCATTGCCAGGATTGAAACGCATTT
>4.68|4548347|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAACATATTGCAGCATGCGCTCTAATGCAAAGCAG
>4.69|4548413|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTCATGATAGAATCTACCTTCCATGTAAATTCTGA
>4.70|4548478|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTTCCTAATTTGGTAAAAACAGAAAGGGAACTTACC
>4.71|4548544|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATATTTACCCATTCAAGGCCATCTATTGTACCCT
>4.72|4548608|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AACTTTAAAATATCATCTTCTGTTGGATTGTCCG
>4.73|4548672|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTGTAGCCGTGCTGATAATAATGTGCACCGTTCTG
>4.74|4548737|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TCATTTCCGGATATCCTCCACAGGAAGAACTTATA
>4.75|4548802|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAAAATATTGCTCGTAGAGCGTTTTAAATTTCTC
>4.76|4548866|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TGAATTCCTGTTTCACGATTCCATCTTAATATCA
>4.77|4548930|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AGTATTTGGACGAAGGAACATTTACCTGGAAACTAA
>4.78|4548996|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TCATAGAACCAATAAGATATTCTCCAGGGTAGTTTT
>4.79|4549062|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TGGATTCTACCATGCCAAACGGCGTTGATGTGAA
>4.80|4549126|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AGAATCACTATCGAAGTGGACTTCGACAATGGAA
>4.81|4549190|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AATCTTACAGCAGGCGATGAGGGTTGGATTTTAGTA
>4.82|4549256|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATTTAAATCCATGTGTACTTTACTTCATTAAATTA
>4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TGAAAAAAATAATTGTATTTCTGTTTTTAATAAAC
>4.84|4549386|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TGGCTTTGCCGGCTGCCTGCCCTTGTGTAATTTTT
>4.85|4549451|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AACATATCCATTAACAGATGTAACCACAGGTGAG
>4.86|4549515|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
>4.87|4549581|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAGATAAGTAATACAATGTATTACACAAAATATAT
>4.88|4549646|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TCCCCTTCCCCTGTTACAACAATGCGGTAAAGAGT
>4.89|4549711|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TAATAAAATTGGATAAAATTCGAAGCTGCATTTC
>4.90|4549775|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
GAACTTGACCCTTACAACGCATACGTAACAACAA
>4.91|4549839|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTATAATTACCGGACGCATCTTTTACCGTTCCCAC
>4.92|4549904|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TTAGTAACAAGCATTTTTCCTTCGCCAGTAAGAAG
>4.93|4549969|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
TAATAGAAAACTCCACACAAAACATCACTGGGTTT
>4.94|4550034|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
>4.95|4550100|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT
AAGCTTCAGTAAACGTATCGGCAATCGGCATGCACG
>4.96|4550166|35|NZ_CP042435|PILER-CR
ACATTTTATTGATTACGAAGTTGGCACGGTAAAGA
>4.97|4550231|36|NZ_CP042435|PILER-CR
TTATCAGCTTCACTATCTGTTGTGTCTTTTTCAAAG
>4.98|4550297|36|NZ_CP042435|PILER-CR
AATACTTTGAATGTTGTGTAAGCTGATGTACTGTAA
>4.99|4550363|35|NZ_CP042435|PILER-CR
ATATCTGCAGGGCTGAATAATTGCCTTCCCATGTT
>4.100|4550428|34|NZ_CP042435|PILER-CR
AATGATCCGTTTGTTTTAAATCGTTACAGCAATG
>4.101|4550492|37|NZ_CP042435|PILER-CR
ATCATAACCGGCTTTTATATTTATAACCCTGTCAAAA
>4.102|4550559|36|NZ_CP042435|PILER-CR
TGTGCTAACATGTCATTTACCATTTGTGTAATGCTT
>4.103|4550625|35|NZ_CP042435|PILER-CR
TACTGTCTGTAACATTACCCGTTTGCGGTTCGTAA
>4.104|4550690|35|NZ_CP042435|PILER-CR
CTATAACCGTTTGGATTGCCCGGCTGTGGCATCTT
>4.105|4550755|35|NZ_CP042435|PILER-CR
TTTATTGCTTTATTGCCTATCTGTCCCGCTTTCTT
>4.106|4550820|34|NZ_CP042435|PILER-CR
AGGTTATCGAATTTAAAATAAGATGTTCCGCTAA
>4.107|4550884|33|NZ_CP042435|PILER-CR
AGGTTATCGAATTAAAATAAGATGTTCCGCTAA
>4.108|4550947|36|NZ_CP042435|PILER-CR
ACGCCCGTTAAGGCTGAATACTCTAAGCTATTATAA
>4.109|4551013|36|NZ_CP042435|PILER-CR
TTATTTTTCTTAATATTCCATCTTTGGATTTATAAA
>4.110|4551079|34|NZ_CP042435|PILER-CR
TTATTTGGTTCTGCAGTTTCCGGAACAAATTCTA
>4.111|4551143|35|NZ_CP042435|PILER-CR
TACTGGAACTGATAAAAAAGGCGGAAATGTTATTA
>4.112|4551208|35|NZ_CP042435|PILER-CR
GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
>4.113|4551273|35|NZ_CP042435|PILER-CR
GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
>4.114|4551338|36|NZ_CP042435|PILER-CR
ATAGCTAATCCTGCATCAATTAATCCGAAAAGGTCA
>4.115|4551404|35|NZ_CP042435|PILER-CR
TTATTTTGTTATATGCGTTCATTGTTAAATATTAA
>4.116|4551469|35|NZ_CP042435|PILER-CR
ATCATTGCAGCAATTCAGATGGACGACGGACGCAG
>4.117|4551534|35|NZ_CP042435|PILER-CR
TTGTAACCATGTTGGTAATAGTGAGCGCCATTTTG
>4.118|4551599|35|NZ_CP042435|PILER-CR
TCGGTTAAAGTAGCTAAATTATTACGAGGAAAACC
>4.119|4551664|33|NZ_CP042435|PILER-CR
TCAACAGCTGGATCGCTTATCGTTGCTGTCCCG
>4.120|4551727|34|NZ_CP042435|PILER-CR
AATACTATTGTGCCCTATAATTCAAGTGCATTAA
>4.121|4551791|35|NZ_CP042435|PILER-CR
TTTTCACGATCACGCTGCAATAACTGTAGCTGATT
>4.122|4550166|34|NZ_CP042435|CRISPRCasFinder,CRT
CATTTTATTGATTACGAAGTTGGCACGGTAAAGA
>4.123|4550230|36|NZ_CP042435|CRISPRCasFinder,CRT
TTATCAGCTTCACTATCTGTTGTGTCTTTTTCAAAG
>4.124|4550296|36|NZ_CP042435|CRISPRCasFinder,CRT
AATACTTTGAATGTTGTGTAAGCTGATGTACTGTAA
>4.125|4550362|35|NZ_CP042435|CRISPRCasFinder,CRT
ATATCTGCAGGGCTGAATAATTGCCTTCCCATGTT
>4.126|4550427|34|NZ_CP042435|CRISPRCasFinder,CRT
AATGATCCGTTTGTTTTAAATCGTTACAGCAATG
>4.127|4550491|37|NZ_CP042435|CRISPRCasFinder,CRT
ATCATAACCGGCTTTTATATTTATAACCCTGTCAAAA
>4.128|4550558|36|NZ_CP042435|CRISPRCasFinder,CRT
TGTGCTAACATGTCATTTACCATTTGTGTAATGCTT
>4.129|4550624|35|NZ_CP042435|CRISPRCasFinder,CRT
TACTGTCTGTAACATTACCCGTTTGCGGTTCGTAA
>4.130|4550689|35|NZ_CP042435|CRISPRCasFinder,CRT
CTATAACCGTTTGGATTGCCCGGCTGTGGCATCTT
>4.131|4550754|35|NZ_CP042435|CRISPRCasFinder,CRT
TTTATTGCTTTATTGCCTATCTGTCCCGCTTTCTT
>4.132|4550819|34|NZ_CP042435|CRISPRCasFinder,CRT
AGGTTATCGAATTTAAAATAAGATGTTCCGCTAA
>4.133|4550883|33|NZ_CP042435|CRISPRCasFinder,CRT
AGGTTATCGAATTAAAATAAGATGTTCCGCTAA
>4.134|4550946|36|NZ_CP042435|CRISPRCasFinder,CRT
ACGCCCGTTAAGGCTGAATACTCTAAGCTATTATAA
>4.135|4551012|36|NZ_CP042435|CRISPRCasFinder,CRT
TTATTTTTCTTAATATTCCATCTTTGGATTTATAAA
>4.136|4551078|34|NZ_CP042435|CRISPRCasFinder,CRT
TTATTTGGTTCTGCAGTTTCCGGAACAAATTCTA
>4.137|4551142|35|NZ_CP042435|CRISPRCasFinder,CRT
TACTGGAACTGATAAAAAAGGCGGAAATGTTATTA
>4.138|4551207|35|NZ_CP042435|CRISPRCasFinder,CRT
GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
>4.139|4551272|35|NZ_CP042435|CRISPRCasFinder,CRT
GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
>4.140|4551337|36|NZ_CP042435|CRISPRCasFinder,CRT
ATAGCTAATCCTGCATCAATTAATCCGAAAAGGTCA
>4.141|4551403|35|NZ_CP042435|CRISPRCasFinder,CRT
TTATTTTGTTATATGCGTTCATTGTTAAATATTAA
>4.142|4551468|35|NZ_CP042435|CRISPRCasFinder,CRT
ATCATTGCAGCAATTCAGATGGACGACGGACGCAG
>4.143|4551533|35|NZ_CP042435|CRISPRCasFinder,CRT
TTGTAACCATGTTGGTAATAGTGAGCGCCATTTTG
>4.144|4551598|35|NZ_CP042435|CRISPRCasFinder,CRT
TCGGTTAAAGTAGCTAAATTATTACGAGGAAAACC
>4.145|4551663|33|NZ_CP042435|CRISPRCasFinder,CRT
TCAACAGCTGGATCGCTTATCGTTGCTGTCCCG
>4.146|4551726|34|NZ_CP042435|CRISPRCasFinder,CRT
AATACTATTGTGCCCTATAATTCAAGTGCATTAA
>4.147|4551790|35|NZ_CP042435|CRISPRCasFinder,CRT
TTTTCACGATCACGCTGCAATAACTGTAGCTGATT
>4.148|4551855|35|NZ_CP042435|CRISPRCasFinder,CRT
AAATGTTTTAATGATAGATTCAAACGGTATAATAA
>4.149|4551920|35|NZ_CP042435|CRISPRCasFinder,CRT
AAATGTTTTAATGATAGATTCAAACGGTATAATAA
>4.150|4551985|36|NZ_CP042435|CRISPRCasFinder,CRT
TAGCATTGATCATTGGCCTTAAGACAAGTAAGCATA
>4.151|4552051|35|NZ_CP042435|CRISPRCasFinder,CRT,PILER-CR
TAAACAAATGGTGGCAACTATTCACAAGTTTTATG
>4.152|4552116|37|NZ_CP042435|CRISPRCasFinder,CRT,PILER-CR
GCATTAAAGACACTGTGAAAATGTTGCGTGAAAAGAA
>4.153|4552183|35|NZ_CP042435|CRISPRCasFinder,CRT,PILER-CR
ATAACATAAATAGCATAAGTTGACTGTCCGCATAT
>4.154|4552248|35|NZ_CP042435|CRISPRCasFinder,CRT
TAAACATGACCAAGTGAATCTATGCCTGTTAAAGT

CRISPR arrays and Neighbor proteins around NZ_CP042435_4

CRISPR arrays

The CRISPR arrays of NZ_CP042435_4

>merge|NZ_CP042435|4|4543931-4552312|PILER-CR,CRISPRCasFinder,CRT,PILER-CR
CTTGTAATCGTATCATTGAGGAATTGAAATAAAGCAAAGTGCGTATGGCCATTGGCAAAGGTTTGGCTTGTAATCGTATCATTGAGGAATTGAAATATCATTACAGCAATTCAGATGGACGACGGACGCAGCTTGTAATCGTATCATTGAGGAATTGAAATAAAAGAACAGAATGATAGGAAAGAACGACAACTGGCTTGTAATCGTATCATTGAGGAATTGAAATTGTAGATTAAACCATGCAGTTTTATAAGCAGATGAACTTGTAATCGTATCATTGAGGAATTGAAATGTATGAGCGAAGAGTTACCGGAAATGAAGGATATGCTTGTAATCGTATCATTGAGGAATTGAAATTTTTTGTCTATTGGATTGCCACCCAGCAATTCCACTTGTAATCGTATCATTGAGGAATTGAAATTTAATTAAAGCATGGCAAAAATCGTGGGGGACGTACTTGTAATCGTATCATTGAGGAATTGAAATAAAGATAGGAATTATACAGACGAACAGCACAAAGACTTGTAATCGTATCATTGAGGAATTGAAATTTAAGTTCTTTAATCAATCTGTTTATACATTCAGTACTTGTAATCGTATCATTGAGGAATTGAAATCAGGCAACAGGTGTAAGACAGATATGGAAGTTTAATCTTGTAATCGTATCATTGAGGAATTGAAATTTGGCTTTATACAGGCAGGCACTAATGTAACTATACTTGTAATCGTATCATTGAGGAATTGAAATTTTATTCTAAAAAAACTTTTGCGTGGAGGGGCGCCCACTTGTAATCGTATCATTGAGGAATTGAAATTGGGATTTAAACTATGACTTTGATAAAGATGGTGTACTTGTAATCGTATCATTGAGGAATTGAAATTTTGCTATTCAATATTATAACCTCACAGGCCATAGACTTGTAATCGTATCATTGAGGAATTGAAATTAGTATTGATTTTCGAGTGATGGCATGGCTGTAAACTTGTAATCGTATCATTGAGGAATTGAAATATAAATATTTCGCTATCGACACAGCTAATACAGCTCTTGTAATCGTATCATTGAGGAATTGAAATTAGAAAAGATAACCCATTGCTTTAATGCCCATAACTTGTAATCGTATCATTGAGGAATTGAAATTTGAAAAAAGATATTTCGGCTTTTGAAGTTTTAAAACTTGTAATCGTATCATTGAGGAATTGAAATCTTGTTCCTGTTCTATAACCAATACTTGTAAGCGTCTTGTAATCGTATCATTGAGGAATTGAAATTTAACTAAGACAGAAATAGAAAGCGTGAACAATGCCTTGTAATCGTATCATTGAGGAATTGAAATTGTTCTGTAATAATAAATATCGCCGATGTAACAGGTCTTGTAATCGTATCATTGAGGAATTGAAATAGATTTCCCTGGAGTACCGCATTTCTTGATCGCAACTTGTAATCGTATCATTGAGGAATTGAAATTTGAAACAGTTTCACAAACTGCATTTGAACATGGCCTTGTAATCGTATCATTGAGGAATTGAAATTTAAATGCTTTGTGGATATAACAACCAACAGCAACTTGTAATCGTATCATTGAGGAATTGAAATTTGATTGACTTAGCAGATCATTGATGCCTAAAGACTTGTAATCGTATCATTGAGGAATTGAAATAAATAACGCTGCTCGGCCTGGTAAAAGAAACTTGCCCTTGTAATCGTATCATTGAGGAATTGAAATAAAATTAGCCCAAAAGTCCCGAAGGCGAAAAGGCTAACTTGTAATCGTATCATTGAGGAATTGAAATATAAAATAATCACATTGCTTTGTTTTCAGGTCGTAACTTGTAATCGTATCATTGAGGAATTGAAATAAATAAGCAACGTGCCCAGCCGATTGAGTAAATTCCTTGTAATCGTATCATTGAGGAATTGAAATCAGTTTATTTGCGCAAACAGTTTATTACCCTTGCCACTTGTAATCGTATCATTGAGGAATTGAAATATAGAATTGAAATTGGTAAACGTATTCAGGAGGTACTTGTAATCGTATCATTGAGGAATTGAAATTTTAATGCAAATGCCTGTGTGCCATCGCCATCCCACTTGTAATCGTATCATTGAGGAATTGAAATAAATAAACAACAAAAATGAAACGCTTAATCAATTTCTTGTAATCGTATCATTGAGGAATTGAAATCAAATTGCTTTATTCGCATCTGTTACAAAACGATGTCTTGTAATCGTATCATTGAGGAATTGAAATTTTGATAGAATAGATGTAATTGTTCTTACTACCGGCTTGTAATCGTATCATTGAGGAATTGAAATAGTCCTTTATCAACGCCATTAAACTTTGGAAGTATTCTTGTAATCGTATCATTGAGGAATTGAAATTAATAAAGAGGAGCGCGGATTACTCCGCCGCTGCCTCTTGTAATCGTATCATTGAGGAATTGAAATTTGATCGGGAATACTTTATTTGCAGCGGTTTTTGTCTTGTAATCGTATCATTGAGGAATTGAAATAATAAACTGTTCCAGTCTCTTTTTCGGTCCTGCCACTTGTAATCGTATCATTGAGGAATTGAAATATCATTGCAAAAAGCTGCTCAATCTCTTGTATTACTTGTAATCGTATCATTGAGGAATTGAAATTAGTAGGCAGTAACAATTTTTGGTACGATACTTTTGCTTGTAATCGTATCATTGAGGAATTGAAATTTTATTGATGCGGATGGGTTTGAAAGGCCTGTTAACTTGTAATCGTATCATTGAGGAATTGAAATTTATTTATGTGAATTCGAAATGATCATTGTTCTTCTTGTAATCGTATCATTGAGGAATTGAAATTTCGCTATATACAATAACCGTATTGGTGGAAGTTATGCTTGTAATCGTATCATTGAGGAATTGAAATTAACTTCAAAGAAGGTGTAGCCAAAACAGCAGTAGCTTGTAATCGTATCATTGAGGAATTGAAATATAATTCCTGCCGGTTATCTTTCGAGAAGTCAAATCTTGTAATCGTATCATTGAGGAATTGAAATAAAGAAACATTACTACCATGTGTTATTAACAGAAATCTTGTAATCGTATCATTGAGGAATTGAAATTTTTTAGATGGATGAAATACAGTTATTATTTTGGCTTGTAATCGTATCATTGAGGAATTGAAATTTAATTTATCCACTAAGACAATCCTTTACAACAAAACTTGTAATCGTATCATTGAGGAATTGAAATAAACTTCCCTCTATAGATCCTATATGGAAGGATGCCGCTTGTAATCGTATCATTGAGGAATTGAAATATATTTATAACCCAATTGATAAGCCTGCAATTGATACTTGTAATCGTATCATTGAGGAATTGAAATTTTGGTATGCCGTTTTCTTTCCAGCAAAAAGCCATCTTGTAATCGTATCATTGAGGAATTGAAATAAGATTGGCAACTGAATTATTTACAGCGTCGCAGCTTGCTTGTAATCGTATCATTGAGGAATTGAAATAAATCTATCTGGGGCTTTAAACCTGTGCTGTCCGACTTGTAATCGTATCATTGAGGAATTGAAATAGTAAAAGTAATTCAATTGTTTCATCCGAAGCATCAGTCTTGTAATCGTATCATTGAGGAATTGAAATATCCATGCATTGGCTGTTTGCTTGCTGGCATACTAGTCTTGTAATCGTATCATTGAGGAATTGAAATCCGTTAAGGAAGCGTTGATAACGTAGCTCTATTAGCCTTGTAATCGTATCATTGAGGAATTGAAATACAATTTTATACAAGTCGCCGTCTGCTTTCCATTCTTGTAATCGTATCATTGAGGAATTGAAATTTTAAAAAACGCATCGCAGCACGAACTTCTACTACTTGTAATCGTATCATTGAGGAATTGAAATTTTGCTGCACTATCATCCTGCCACATAGCCATTGTCTTGTAATCGTATCATTGAGGAATTGAAATATATATCATGCCCCTCAGCTTTTAACTGTGTAATGACTTGTAATCGTATCATTGAGGAATTGAAATTTCCTTGCGGATAGCTGTTTAGCTGCAACATTTACACTTGTAATCTTATCATTGAGGAATTGAAATAAAATTAAACTCTATAACCTACCAATGGAATAAGGTCTTGTAATCGTATCATTGAGGAATTGAAATGCAACAATTCTACCTGCAGCACTATCAGTTGCACTCTTGTAATCGTATCATTGAGGAATTGAAATACAATAGAATTTGGTGCAAAGCTGCAGGGCGATGTTCTTGTAATCGTATCATTGAGGAATTGAAATAGTGTTGCAGTCGTTAATATTGAAATCTCTTATTTCTTGTAATCGTATCATTGAGGAATTGAAATATAACTGATTATCATTGCCAGGATTGAAACGCATTTCTTGTAATCGTATCATTGAGGAATTGAAATAAAACATATTGCAGCATGCGCTCTAATGCAAAGCAGCTTGTAATCGTATCATTGAGGAATTGAAATTTCATGATAGAATCTACCTTCCATGTAAATTCTGACTTGTAATCGTATCATTGAGGAATTGAAATTTTCCTAATTTGGTAAAAACAGAAAGGGAACTTACCCTTGTAATCGTATCATTGAGGAATTGAAATATATTTACCCATTCAAGGCCATCTATTGTACCCTCTTGTAATCGTATCATTGAGGAATTGAAATAACTTTAAAATATCATCTTCTGTTGGATTGTCCGCTTGTAATCGTATCATTGAGGAATTGAAATTTGTAGCCGTGCTGATAATAATGTGCACCGTTCTGCTTGTAATCGTATCATTGAGGAATTGAAATTCATTTCCGGATATCCTCCACAGGAAGAACTTATACTTGTAATCGTATCATTGAGGAATTGAAATAAAAATATTGCTCGTAGAGCGTTTTAAATTTCTCCTTGTAATCGTATCATTGAGGAATTGAAATTGAATTCCTGTTTCACGATTCCATCTTAATATCACTTGTAATCGTATCATTGAGGAATTGAAATAGTATTTGGACGAAGGAACATTTACCTGGAAACTAACTTGTAATCGTATCATTGAGGAATTGAAATTCATAGAACCAATAAGATATTCTCCAGGGTAGTTTTCTTGTAATCGTATCATTGAGGAATTGAAATTGGATTCTACCATGCCAAACGGCGTTGATGTGAACTTGTAATCGTATCATTGAGGAATTGAAATAGAATCACTATCGAAGTGGACTTCGACAATGGAACTTGTAATCGTATCATTGAGGAATTGAAATAATCTTACAGCAGGCGATGAGGGTTGGATTTTAGTACTTGTAATCGTATCATTGAGGAATTGAAATATTTAAATCCATGTGTACTTTACTTCATTAAATTACTTGTAATCGTATCATTGAGGAATTGAAATTGAAAAAAATAATTGTATTTCTGTTTTTAATAAACCTTGTAATCGTATCATTGAGGAATTGAAATTGGCTTTGCCGGCTGCCTGCCCTTGTGTAATTTTTCTTGTAATCGTATCATTGAGGAATTGAAATAACATATCCATTAACAGATGTAACCACAGGTGAGCTTGTAATCGTATCATTGAGGAATTGAAATATGATTGTACCACCAACTTTAGCAAGACTTCCTGTTCTTGTAATCGTATCATTGAGGAATTGAAATAAGATAAGTAATACAATGTATTACACAAAATATATCTTGTAATCGTATCATTGAGGAATTGAAATTCCCCTTCCCCTGTTACAACAATGCGGTAAAGAGTCTTGTAATCGTATCATTGAGGAATTGAAATTAATAAAATTGGATAAAATTCGAAGCTGCATTTCCTTGTAATCGTATCATTGAGGAATTGAAATGAACTTGACCCTTACAACGCATACGTAACAACAACTTGTAATCGTATCATTGAGGAATTGAAATTTATAATTACCGGACGCATCTTTTACCGTTCCCACCTTGTAATCGTATCATTGAGGAATTGAAATTTAGTAACAAGCATTTTTCCTTCGCCAGTAAGAAGCTTGTAATCGTATCATTGAGGAATTGAAATTAATAGAAAACTCCACACAAAACATCACTGGGTTTCTTGTAATCGTATCATTGAGGAATTGAAATATGATTGTACCACCAACTTTAGCAAGACTTCCTGTTCTTGTAATCGTATCATTGAGGAATTGAAATAAGCTTCAGTAAACGTATCGGCAATCGGCATGCACGCTTGTAATCGTATCATTGAGAATTGAAATACATTTTATTGATTACGAAGTTGGCACGGTAAAGACTTGTAATCGTATCATTGAGGAATTGAAATTTATCAGCTTCACTATCTGTTGTGTCTTTTTCAAAGCTTGTAATCGTATCATTGGGGAATTGAAATAATACTTTGAATGTTGTGTAAGCTGATGTACTGTAACTTGTAATCGTATCATTGAGGAATTGAAATATATCTGCAGGGCTGAATAATTGCCTTCCCATGTTCTTGTAATCGTATCATTGAGGAATTGAAATAATGATCCGTTTGTTTTAAATCGTTACAGCAATGCTTGTAATCGTATCATTGAGGAATTGAAATATCATAACCGGCTTTTATATTTATAACCCTGTCAAAACTTGTAATCGTATCATTGAGGAATTGAAATTGTGCTAACATGTCATTTACCATTTGTGTAATGCTTCTTGTAATCGTATCATTGAGGAATTGAAATTACTGTCTGTAACATTACCCGTTTGCGGTTCGTAACTTGTAATCGTATCATTGAGGAATTGAAATCTATAACCGTTTGGATTGCCCGGCTGTGGCATCTTCTTGTAATCGTATCATTGAGGAATTGAAATTTTATTGCTTTATTGCCTATCTGTCCCGCTTTCTTCTTGTAATCGTATCATTGAGGAATTGAAATAGGTTATCGAATTTAAAATAAGATGTTCCGCTAACTTGTAATCGTATCATTGAGGAATTGAAATAGGTTATCGAATTAAAATAAGATGTTCCGCTAACTTGTAATCGTATCATTGAGGAATTGAAATACGCCCGTTAAGGCTGAATACTCTAAGCTATTATAACTTGTAATCGTATCATTGAGGAATTGAAATTTATTTTTCTTAATATTCCATCTTTGGATTTATAAACTTGTAATCGTATCATTGAGGAATTGAAATTTATTTGGTTCTGCAGTTTCCGGAACAAATTCTACTTGTAATCGTATCATTGAGGAATTGAAATTACTGGAACTGATAAAAAAGGCGGAAATGTTATTACTTGTAATCGTATCATTGAGGAATTGAAATGTAATTCCTGCCAGCCATCTGGTGTGTAATCTAATCTTGTAATCGTATCATTGAGGAATTGAAATGTAATTCCTGCCAGCCATCTGGTGTGTAATCTAATCTTGTAATCGTATCATTGAGGAATTGAAATATAGCTAATCCTGCATCAATTAATCCGAAAAGGTCACTTGTAATCGTATCATTGAGGAATTGAAATTTATTTTGTTATATGCGTTCATTGTTAAATATTAACTTGTAATCGTATCATTGAGGAATTGAAATATCATTGCAGCAATTCAGATGGACGACGGACGCAGCTTGTAATCGTATCATTGAGGAATTGAAATTTGTAACCATGTTGGTAATAGTGAGCGCCATTTTGCTTGTAATCGTATCATTGAGGAATTGAAATTCGGTTAAAGTAGCTAAATTATTACGAGGAAAACCCTTGTAATCGTATCATTGAGGAATTGAAATTCAACAGCTGGATCGCTTATCGTTGCTGTCCCGCTTGTAATCGTATCATTGAGGAATTTAAATAATACTATTGTGCCCTATAATTCAAGTGCATTAACTTGTAATCGTATCATTGAGGAATTGAAATTTTTCACGATCACGCTGCAATAACTGTAGCTGATTCTTGTAATCGTATCATTGAGGAATTGAAATAAATGTTTTAATGATAGATTCAAACGGTATAATAACTTGTAATCGTATCATTGAGGAATTGAAATAAATGTTTTAATGATAGATTCAAACGGTATAATAACTTGTAATCGTATCATTGAGGAATTGAAATTAGCATTGATCATTGGCCTTAAGACAAGTAAGCATACTTGTAATCGTATCATTGAGGAATTGAAATTAAACAAATGGTGGCAACTATTCACAAGTTTTATGCTTGTAATCGTATCATTGAGGAATTGAAATGCATTAAAGACACTGTGAAAATGTTGCGTGAAAAGAACTTGTAATCGTATCATTGAGGAATTGAAATATAACATAAATAGCATAAGTTGACTGTCCGCATATCTTGTAATCGTATCATTGAGGAATTGAAATTAAACATGACCAAGTGAATCTATGCCTGTTAAAGTCTTGTAATCGTATCATTGAGGAATGGTCTT

>NZ_CP042435|4|1|4543931-4551854|PILER-CR
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGCAAAGTGCGTATGGCCATTGGCAAAGGTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTACAGCAATTCAGATGGACGACGGACGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAGAACAGAATGATAGGAAAGAACGACAACTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTAGATTAAACCATGCAGTTTTATAAGCAGATGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTATGAGCGAAGAGTTACCGGAAATGAAGGATATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTGTCTATTGGATTGCCACCCAGCAATTCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTAAAGCATGGCAAAAATCGTGGGGGACGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGATAGGAATTATACAGACGAACAGCACAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAGTTCTTTAATCAATCTGTTTATACATTCAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGGCAACAGGTGTAAGACAGATATGGAAGTTTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGGCTTTATACAGGCAGGCACTAATGTAACTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTCTAAAAAAACTTTTGCGTGGAGGGGCGCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGGATTTAAACTATGACTTTGATAAAGATGGTGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTATTCAATATTATAACCTCACAGGCCATAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTATTGATTTTCGAGTGATGGCATGGCTGTAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAATATTTCGCTATCGACACAGCTAATACAGCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGAAAAGATAACCCATTGCTTTAATGCCCATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAAAAAGATATTTCGGCTTTTGAAGTTTTAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CTTGTTCCTGTTCTATAACCAATACTTGTAAGCGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAACTAAGACAGAAATAGAAAGCGTGAACAATGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTTCTGTAATAATAAATATCGCCGATGTAACAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGATTTCCCTGGAGTACCGCATTTCTTGATCGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAACAGTTTCACAAACTGCATTTGAACATGGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAATGCTTTGTGGATATAACAACCAACAGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATTGACTTAGCAGATCATTGATGCCTAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAACGCTGCTCGGCCTGGTAAAAGAAACTTGCC
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAATTAGCCCAAAAGTCCCGAAGGCGAAAAGGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAAATAATCACATTGCTTTGTTTTCAGGTCGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAGCAACGTGCCCAGCCGATTGAGTAAATTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGTTTATTTGCGCAAACAGTTTATTACCCTTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAGAATTGAAATTGGTAAACGTATTCAGGAGGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAATGCAAATGCCTGTGTGCCATCGCCATCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAACAACAAAAATGAAACGCTTAATCAATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAAATTGCTTTATTCGCATCTGTTACAAAACGATGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGATAGAATAGATGTAATTGTTCTTACTACCGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTCCTTTATCAACGCCATTAAACTTTGGAAGTATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAGAGGAGCGCGGATTACTCCGCCGCTGCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATCGGGAATACTTTATTTGCAGCGGTTTTTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATAAACTGTTCCAGTCTCTTTTTCGGTCCTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTGCAAAAAGCTGCTCAATCTCTTGTATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTAGGCAGTAACAATTTTTGGTACGATACTTTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTGATGCGGATGGGTTTGAAAGGCCTGTTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTATGTGAATTCGAAATGATCATTGTTCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCGCTATATACAATAACCGTATTGGTGGAAGTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAACTTCAAAGAAGGTGTAGCCAAAACAGCAGTAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAATTCCTGCCGGTTATCTTTCGAGAAGTCAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGAAACATTACTACCATGTGTTATTAACAGAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTAGATGGATGAAATACAGTTATTATTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTTATCCACTAAGACAATCCTTTACAACAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAACTTCCCTCTATAGATCCTATATGGAAGGATGCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTATAACCCAATTGATAAGCCTGCAATTGATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGGTATGCCGTTTTCTTTCCAGCAAAAAGCCAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATTGGCAACTGAATTATTTACAGCGTCGCAGCTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATCTATCTGGGGCTTTAAACCTGTGCTGTCCGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTAAAAGTAATTCAATTGTTTCATCCGAAGCATCAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCCATGCATTGGCTGTTTGCTTGCTGGCATACTAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CCGTTAAGGAAGCGTTGATAACGTAGCTCTATTAGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATTTTATACAAGTCGCCGTCTGCTTTCCATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAAAAAACGCATCGCAGCACGAACTTCTACTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTGCACTATCATCCTGCCACATAGCCATTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATATCATGCCCCTCAGCTTTTAACTGTGTAATGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCCTTGCGGATAGCTGTTTAGCTGCAACATTTACA
CTTGTAATCTTATCATTGAGGAATTGAAAT	AAAATTAAACTCTATAACCTACCAATGGAATAAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCAACAATTCTACCTGCAGCACTATCAGTTGCACT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATAGAATTTGGTGCAAAGCTGCAGGGCGATGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTGTTGCAGTCGTTAATATTGAAATCTCTTATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACTGATTATCATTGCCAGGATTGAAACGCATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAACATATTGCAGCATGCGCTCTAATGCAAAGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCATGATAGAATCTACCTTCCATGTAAATTCTGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTCCTAATTTGGTAAAAACAGAAAGGGAACTTACC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTACCCATTCAAGGCCATCTATTGTACCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACTTTAAAATATCATCTTCTGTTGGATTGTCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGTAGCCGTGCTGATAATAATGTGCACCGTTCTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATTTCCGGATATCCTCCACAGGAAGAACTTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAATATTGCTCGTAGAGCGTTTTAAATTTCTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAATTCCTGTTTCACGATTCCATCTTAATATCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTATTTGGACGAAGGAACATTTACCTGGAAACTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATAGAACCAATAAGATATTCTCCAGGGTAGTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGATTCTACCATGCCAAACGGCGTTGATGTGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGAATCACTATCGAAGTGGACTTCGACAATGGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATCTTACAGCAGGCGATGAGGGTTGGATTTTAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATTTAAATCCATGTGTACTTTACTTCATTAAATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAAAAAAATAATTGTATTTCTGTTTTTAATAAAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGCTTTGCCGGCTGCCTGCCCTTGTGTAATTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACATATCCATTAACAGATGTAACCACAGGTGAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATAAGTAATACAATGTATTACACAAAATATAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCCCCTTCCCCTGTTACAACAATGCGGTAAAGAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAATTGGATAAAATTCGAAGCTGCATTTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	GAACTTGACCCTTACAACGCATACGTAACAACAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATAATTACCGGACGCATCTTTTACCGTTCCCAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAGTAACAAGCATTTTTCCTTCGCCAGTAAGAAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAGAAAACTCCACACAAAACATCACTGGGTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGCTTCAGTAAACGTATCGGCAATCGGCATGCACG
CTTGTAATCGTATCATTGAGAATTGAAATA	CATTTTATTGATTACGAAGTTGGCACGGTAAAGAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATCAGCTTCACTATCTGTTGTGTCTTTTTCAAAGC
TTGTAATCGTATCATTGGGGAATTGAAATA	ATACTTTGAATGTTGTGTAAGCTGATGTACTGTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	TATCTGCAGGGCTGAATAATTGCCTTCCCATGTTC
TTGTAATCGTATCATTGAGGAATTGAAATA	ATGATCCGTTTGTTTTAAATCGTTACAGCAATGC
TTGTAATCGTATCATTGAGGAATTGAAATA	TCATAACCGGCTTTTATATTTATAACCCTGTCAAAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	GTGCTAACATGTCATTTACCATTTGTGTAATGCTTC
TTGTAATCGTATCATTGAGGAATTGAAATT	ACTGTCTGTAACATTACCCGTTTGCGGTTCGTAAC
TTGTAATCGTATCATTGAGGAATTGAAATC	TATAACCGTTTGGATTGCCCGGCTGTGGCATCTTC
TTGTAATCGTATCATTGAGGAATTGAAATT	TTATTGCTTTATTGCCTATCTGTCCCGCTTTCTTC
TTGTAATCGTATCATTGAGGAATTGAAATA	GGTTATCGAATTTAAAATAAGATGTTCCGCTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	GGTTATCGAATTAAAATAAGATGTTCCGCTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	CGCCCGTTAAGGCTGAATACTCTAAGCTATTATAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATTTTTCTTAATATTCCATCTTTGGATTTATAAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATTTGGTTCTGCAGTTTCCGGAACAAATTCTAC
TTGTAATCGTATCATTGAGGAATTGAAATT	ACTGGAACTGATAAAAAAGGCGGAAATGTTATTAC
TTGTAATCGTATCATTGAGGAATTGAAATG	TAATTCCTGCCAGCCATCTGGTGTGTAATCTAATC
TTGTAATCGTATCATTGAGGAATTGAAATG	TAATTCCTGCCAGCCATCTGGTGTGTAATCTAATC
TTGTAATCGTATCATTGAGGAATTGAAATA	TAGCTAATCCTGCATCAATTAATCCGAAAAGGTCAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATTTTGTTATATGCGTTCATTGTTAAATATTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	TCATTGCAGCAATTCAGATGGACGACGGACGCAGC
TTGTAATCGTATCATTGAGGAATTGAAATT	TGTAACCATGTTGGTAATAGTGAGCGCCATTTTGC
TTGTAATCGTATCATTGAGGAATTGAAATT	CGGTTAAAGTAGCTAAATTATTACGAGGAAAACCC
TTGTAATCGTATCATTGAGGAATTGAAATT	CAACAGCTGGATCGCTTATCGTTGCTGTCCCGC
TTGTAATCGTATCATTGAGGAATTTAAATA	ATACTATTGTGCCCTATAATTCAAGTGCATTAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TTTCACGATCACGCTGCAATAACTGTAGCTGATTC
TTGTAATCGTATCATTGAGGAATTGAAATAAATGTTTTAATGATAGATTCAAACGGTATAATAACTTGTAATCGTATCATTGAGGAATTGAAATAAATGTTTTAATGATAGATTCAAACGGTATAATAACTTGTAATCGTATCATTGAGGAATTGAAATTAGCATTGATCATTGGCCTTAAGACAAGTAAGCATACTTGTAATCGTATCATTGAGGAATTGAAAT	TAAACAAATGGTGGCAACTATTCACAAGTTTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCATTAAAGACACTGTGAAAATGTTGCGTGAAAAGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACATAAATAGCATAAGTTGACTGTCCGCATAT


>NZ_CP042435|4|3|4543931-4552312|CRISPRCasFinder
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGCAAAGTGCGTATGGCCATTGGCAAAGGTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTACAGCAATTCAGATGGACGACGGACGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAGAACAGAATGATAGGAAAGAACGACAACTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTAGATTAAACCATGCAGTTTTATAAGCAGATGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTATGAGCGAAGAGTTACCGGAAATGAAGGATATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTGTCTATTGGATTGCCACCCAGCAATTCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTAAAGCATGGCAAAAATCGTGGGGGACGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGATAGGAATTATACAGACGAACAGCACAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAGTTCTTTAATCAATCTGTTTATACATTCAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGGCAACAGGTGTAAGACAGATATGGAAGTTTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGGCTTTATACAGGCAGGCACTAATGTAACTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTCTAAAAAAACTTTTGCGTGGAGGGGCGCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGGATTTAAACTATGACTTTGATAAAGATGGTGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTATTCAATATTATAACCTCACAGGCCATAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTATTGATTTTCGAGTGATGGCATGGCTGTAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAATATTTCGCTATCGACACAGCTAATACAGCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGAAAAGATAACCCATTGCTTTAATGCCCATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAAAAAGATATTTCGGCTTTTGAAGTTTTAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CTTGTTCCTGTTCTATAACCAATACTTGTAAGCGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAACTAAGACAGAAATAGAAAGCGTGAACAATGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTTCTGTAATAATAAATATCGCCGATGTAACAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGATTTCCCTGGAGTACCGCATTTCTTGATCGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAACAGTTTCACAAACTGCATTTGAACATGGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAATGCTTTGTGGATATAACAACCAACAGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATTGACTTAGCAGATCATTGATGCCTAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAACGCTGCTCGGCCTGGTAAAAGAAACTTGCC
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAATTAGCCCAAAAGTCCCGAAGGCGAAAAGGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAAATAATCACATTGCTTTGTTTTCAGGTCGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAGCAACGTGCCCAGCCGATTGAGTAAATTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGTTTATTTGCGCAAACAGTTTATTACCCTTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAGAATTGAAATTGGTAAACGTATTCAGGAGGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAATGCAAATGCCTGTGTGCCATCGCCATCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAACAACAAAAATGAAACGCTTAATCAATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAAATTGCTTTATTCGCATCTGTTACAAAACGATGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGATAGAATAGATGTAATTGTTCTTACTACCGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTCCTTTATCAACGCCATTAAACTTTGGAAGTATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAGAGGAGCGCGGATTACTCCGCCGCTGCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATCGGGAATACTTTATTTGCAGCGGTTTTTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATAAACTGTTCCAGTCTCTTTTTCGGTCCTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTGCAAAAAGCTGCTCAATCTCTTGTATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTAGGCAGTAACAATTTTTGGTACGATACTTTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTGATGCGGATGGGTTTGAAAGGCCTGTTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTATGTGAATTCGAAATGATCATTGTTCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCGCTATATACAATAACCGTATTGGTGGAAGTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAACTTCAAAGAAGGTGTAGCCAAAACAGCAGTAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAATTCCTGCCGGTTATCTTTCGAGAAGTCAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGAAACATTACTACCATGTGTTATTAACAGAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTAGATGGATGAAATACAGTTATTATTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTTATCCACTAAGACAATCCTTTACAACAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAACTTCCCTCTATAGATCCTATATGGAAGGATGCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTATAACCCAATTGATAAGCCTGCAATTGATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGGTATGCCGTTTTCTTTCCAGCAAAAAGCCAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATTGGCAACTGAATTATTTACAGCGTCGCAGCTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATCTATCTGGGGCTTTAAACCTGTGCTGTCCGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTAAAAGTAATTCAATTGTTTCATCCGAAGCATCAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCCATGCATTGGCTGTTTGCTTGCTGGCATACTAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CCGTTAAGGAAGCGTTGATAACGTAGCTCTATTAGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATTTTATACAAGTCGCCGTCTGCTTTCCATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAAAAAACGCATCGCAGCACGAACTTCTACTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTGCACTATCATCCTGCCACATAGCCATTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATATCATGCCCCTCAGCTTTTAACTGTGTAATGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCCTTGCGGATAGCTGTTTAGCTGCAACATTTACA
CTTGTAATCTTATCATTGAGGAATTGAAAT	AAAATTAAACTCTATAACCTACCAATGGAATAAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCAACAATTCTACCTGCAGCACTATCAGTTGCACT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATAGAATTTGGTGCAAAGCTGCAGGGCGATGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTGTTGCAGTCGTTAATATTGAAATCTCTTATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACTGATTATCATTGCCAGGATTGAAACGCATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAACATATTGCAGCATGCGCTCTAATGCAAAGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCATGATAGAATCTACCTTCCATGTAAATTCTGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTCCTAATTTGGTAAAAACAGAAAGGGAACTTACC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTACCCATTCAAGGCCATCTATTGTACCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACTTTAAAATATCATCTTCTGTTGGATTGTCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGTAGCCGTGCTGATAATAATGTGCACCGTTCTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATTTCCGGATATCCTCCACAGGAAGAACTTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAATATTGCTCGTAGAGCGTTTTAAATTTCTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAATTCCTGTTTCACGATTCCATCTTAATATCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTATTTGGACGAAGGAACATTTACCTGGAAACTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATAGAACCAATAAGATATTCTCCAGGGTAGTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGATTCTACCATGCCAAACGGCGTTGATGTGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGAATCACTATCGAAGTGGACTTCGACAATGGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATCTTACAGCAGGCGATGAGGGTTGGATTTTAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATTTAAATCCATGTGTACTTTACTTCATTAAATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAAAAAAATAATTGTATTTCTGTTTTTAATAAAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGCTTTGCCGGCTGCCTGCCCTTGTGTAATTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACATATCCATTAACAGATGTAACCACAGGTGAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATAAGTAATACAATGTATTACACAAAATATAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCCCCTTCCCCTGTTACAACAATGCGGTAAAGAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAATTGGATAAAATTCGAAGCTGCATTTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	GAACTTGACCCTTACAACGCATACGTAACAACAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATAATTACCGGACGCATCTTTTACCGTTCCCAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAGTAACAAGCATTTTTCCTTCGCCAGTAAGAAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAGAAAACTCCACACAAAACATCACTGGGTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGCTTCAGTAAACGTATCGGCAATCGGCATGCACG
CTTGTAATCGTATCATTGAGAATTGAAATA	CATTTTATTGATTACGAAGTTGGCACGGTAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATCAGCTTCACTATCTGTTGTGTCTTTTTCAAAG
CTTGTAATCGTATCATTGGGGAATTGAAAT	AATACTTTGAATGTTGTGTAAGCTGATGTACTGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATCTGCAGGGCTGAATAATTGCCTTCCCATGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATGATCCGTTTGTTTTAAATCGTTACAGCAATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATAACCGGCTTTTATATTTATAACCCTGTCAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTGCTAACATGTCATTTACCATTTGTGTAATGCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TACTGTCTGTAACATTACCCGTTTGCGGTTCGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CTATAACCGTTTGGATTGCCCGGCTGTGGCATCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTGCTTTATTGCCTATCTGTCCCGCTTTCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGGTTATCGAATTTAAAATAAGATGTTCCGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGGTTATCGAATTAAAATAAGATGTTCCGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACGCCCGTTAAGGCTGAATACTCTAAGCTATTATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTTTCTTAATATTCCATCTTTGGATTTATAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTGGTTCTGCAGTTTCCGGAACAAATTCTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TACTGGAACTGATAAAAAAGGCGGAAATGTTATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAGCTAATCCTGCATCAATTAATCCGAAAAGGTCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTTGTTATATGCGTTCATTGTTAAATATTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTGCAGCAATTCAGATGGACGACGGACGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGTAACCATGTTGGTAATAGTGAGCGCCATTTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCGGTTAAAGTAGCTAAATTATTACGAGGAAAACC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCAACAGCTGGATCGCTTATCGTTGCTGTCCCG
CTTGTAATCGTATCATTGAGGAATTTAAAT	AATACTATTGTGCCCTATAATTCAAGTGCATTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTCACGATCACGCTGCAATAACTGTAGCTGATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATGTTTTAATGATAGATTCAAACGGTATAATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATGTTTTAATGATAGATTCAAACGGTATAATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGCATTGATCATTGGCCTTAAGACAAGTAAGCATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAAACAAATGGTGGCAACTATTCACAAGTTTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCATTAAAGACACTGTGAAAATGTTGCGTGAAAAGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACATAAATAGCATAAGTTGACTGTCCGCATAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAAACATGACCAAGTGAATCTATGCCTGTTAAAGT
CTTGTAATCGTATCATTGAGGAATGGTCTT

>NZ_CP042435|4|2|4543931-4552312|CRT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGCAAAGTGCGTATGGCCATTGGCAAAGGTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTACAGCAATTCAGATGGACGACGGACGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAGAACAGAATGATAGGAAAGAACGACAACTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTAGATTAAACCATGCAGTTTTATAAGCAGATGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTATGAGCGAAGAGTTACCGGAAATGAAGGATATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTGTCTATTGGATTGCCACCCAGCAATTCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTAAAGCATGGCAAAAATCGTGGGGGACGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGATAGGAATTATACAGACGAACAGCACAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAGTTCTTTAATCAATCTGTTTATACATTCAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGGCAACAGGTGTAAGACAGATATGGAAGTTTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGGCTTTATACAGGCAGGCACTAATGTAACTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTCTAAAAAAACTTTTGCGTGGAGGGGCGCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGGATTTAAACTATGACTTTGATAAAGATGGTGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTATTCAATATTATAACCTCACAGGCCATAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTATTGATTTTCGAGTGATGGCATGGCTGTAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAATATTTCGCTATCGACACAGCTAATACAGCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGAAAAGATAACCCATTGCTTTAATGCCCATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAAAAAGATATTTCGGCTTTTGAAGTTTTAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CTTGTTCCTGTTCTATAACCAATACTTGTAAGCGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAACTAAGACAGAAATAGAAAGCGTGAACAATGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTTCTGTAATAATAAATATCGCCGATGTAACAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGATTTCCCTGGAGTACCGCATTTCTTGATCGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAACAGTTTCACAAACTGCATTTGAACATGGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAATGCTTTGTGGATATAACAACCAACAGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATTGACTTAGCAGATCATTGATGCCTAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAACGCTGCTCGGCCTGGTAAAAGAAACTTGCC
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAATTAGCCCAAAAGTCCCGAAGGCGAAAAGGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAAATAATCACATTGCTTTGTTTTCAGGTCGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAGCAACGTGCCCAGCCGATTGAGTAAATTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGTTTATTTGCGCAAACAGTTTATTACCCTTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAGAATTGAAATTGGTAAACGTATTCAGGAGGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAATGCAAATGCCTGTGTGCCATCGCCATCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAACAACAAAAATGAAACGCTTAATCAATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAAATTGCTTTATTCGCATCTGTTACAAAACGATGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGATAGAATAGATGTAATTGTTCTTACTACCGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTCCTTTATCAACGCCATTAAACTTTGGAAGTATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAGAGGAGCGCGGATTACTCCGCCGCTGCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATCGGGAATACTTTATTTGCAGCGGTTTTTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATAAACTGTTCCAGTCTCTTTTTCGGTCCTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTGCAAAAAGCTGCTCAATCTCTTGTATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTAGGCAGTAACAATTTTTGGTACGATACTTTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTGATGCGGATGGGTTTGAAAGGCCTGTTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTATGTGAATTCGAAATGATCATTGTTCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCGCTATATACAATAACCGTATTGGTGGAAGTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAACTTCAAAGAAGGTGTAGCCAAAACAGCAGTAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAATTCCTGCCGGTTATCTTTCGAGAAGTCAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGAAACATTACTACCATGTGTTATTAACAGAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTAGATGGATGAAATACAGTTATTATTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTTATCCACTAAGACAATCCTTTACAACAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAACTTCCCTCTATAGATCCTATATGGAAGGATGCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTATAACCCAATTGATAAGCCTGCAATTGATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGGTATGCCGTTTTCTTTCCAGCAAAAAGCCAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATTGGCAACTGAATTATTTACAGCGTCGCAGCTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATCTATCTGGGGCTTTAAACCTGTGCTGTCCGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTAAAAGTAATTCAATTGTTTCATCCGAAGCATCAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCCATGCATTGGCTGTTTGCTTGCTGGCATACTAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CCGTTAAGGAAGCGTTGATAACGTAGCTCTATTAGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATTTTATACAAGTCGCCGTCTGCTTTCCATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAAAAAACGCATCGCAGCACGAACTTCTACTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTGCACTATCATCCTGCCACATAGCCATTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATATCATGCCCCTCAGCTTTTAACTGTGTAATGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCCTTGCGGATAGCTGTTTAGCTGCAACATTTACA
CTTGTAATCTTATCATTGAGGAATTGAAAT	AAAATTAAACTCTATAACCTACCAATGGAATAAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCAACAATTCTACCTGCAGCACTATCAGTTGCACT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATAGAATTTGGTGCAAAGCTGCAGGGCGATGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTGTTGCAGTCGTTAATATTGAAATCTCTTATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACTGATTATCATTGCCAGGATTGAAACGCATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAACATATTGCAGCATGCGCTCTAATGCAAAGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCATGATAGAATCTACCTTCCATGTAAATTCTGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTCCTAATTTGGTAAAAACAGAAAGGGAACTTACC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTACCCATTCAAGGCCATCTATTGTACCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACTTTAAAATATCATCTTCTGTTGGATTGTCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGTAGCCGTGCTGATAATAATGTGCACCGTTCTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATTTCCGGATATCCTCCACAGGAAGAACTTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAATATTGCTCGTAGAGCGTTTTAAATTTCTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAATTCCTGTTTCACGATTCCATCTTAATATCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTATTTGGACGAAGGAACATTTACCTGGAAACTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATAGAACCAATAAGATATTCTCCAGGGTAGTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGATTCTACCATGCCAAACGGCGTTGATGTGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGAATCACTATCGAAGTGGACTTCGACAATGGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATCTTACAGCAGGCGATGAGGGTTGGATTTTAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATTTAAATCCATGTGTACTTTACTTCATTAAATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAAAAAAATAATTGTATTTCTGTTTTTAATAAAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGCTTTGCCGGCTGCCTGCCCTTGTGTAATTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACATATCCATTAACAGATGTAACCACAGGTGAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATAAGTAATACAATGTATTACACAAAATATAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCCCCTTCCCCTGTTACAACAATGCGGTAAAGAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAATTGGATAAAATTCGAAGCTGCATTTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	GAACTTGACCCTTACAACGCATACGTAACAACAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATAATTACCGGACGCATCTTTTACCGTTCCCAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAGTAACAAGCATTTTTCCTTCGCCAGTAAGAAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAGAAAACTCCACACAAAACATCACTGGGTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGCTTCAGTAAACGTATCGGCAATCGGCATGCACG
CTTGTAATCGTATCATTGAGAATTGAAATA	CATTTTATTGATTACGAAGTTGGCACGGTAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATCAGCTTCACTATCTGTTGTGTCTTTTTCAAAG
CTTGTAATCGTATCATTGGGGAATTGAAAT	AATACTTTGAATGTTGTGTAAGCTGATGTACTGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATCTGCAGGGCTGAATAATTGCCTTCCCATGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATGATCCGTTTGTTTTAAATCGTTACAGCAATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATAACCGGCTTTTATATTTATAACCCTGTCAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTGCTAACATGTCATTTACCATTTGTGTAATGCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TACTGTCTGTAACATTACCCGTTTGCGGTTCGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CTATAACCGTTTGGATTGCCCGGCTGTGGCATCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTGCTTTATTGCCTATCTGTCCCGCTTTCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGGTTATCGAATTTAAAATAAGATGTTCCGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGGTTATCGAATTAAAATAAGATGTTCCGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACGCCCGTTAAGGCTGAATACTCTAAGCTATTATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTTTCTTAATATTCCATCTTTGGATTTATAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTGGTTCTGCAGTTTCCGGAACAAATTCTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TACTGGAACTGATAAAAAAGGCGGAAATGTTATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTAATTCCTGCCAGCCATCTGGTGTGTAATCTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAGCTAATCCTGCATCAATTAATCCGAAAAGGTCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTTGTTATATGCGTTCATTGTTAAATATTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTGCAGCAATTCAGATGGACGACGGACGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGTAACCATGTTGGTAATAGTGAGCGCCATTTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCGGTTAAAGTAGCTAAATTATTACGAGGAAAACC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCAACAGCTGGATCGCTTATCGTTGCTGTCCCG
CTTGTAATCGTATCATTGAGGAATTTAAAT	AATACTATTGTGCCCTATAATTCAAGTGCATTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTCACGATCACGCTGCAATAACTGTAGCTGATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATGTTTTAATGATAGATTCAAACGGTATAATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATGTTTTAATGATAGATTCAAACGGTATAATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGCATTGATCATTGGCCTTAAGACAAGTAAGCATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAAACAAATGGTGGCAACTATTCACAAGTTTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCATTAAAGACACTGTGAAAATGTTGCGTGAAAAGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACATAAATAGCATAAGTTGACTGTCCGCATAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAAACATGACCAAGTGAATCTATGCCTGTTAAAGT
CTTGTAATCGTATCATTGAGGAATGGTCTT

>NZ_CP042435|4|2|4552021-4552247|PILER-CR
	AAAGCAAAGTGCGTATGGCCATTGGCAAAGGTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTACAGCAATTCAGATGGACGACGGACGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAGAACAGAATGATAGGAAAGAACGACAACTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTAGATTAAACCATGCAGTTTTATAAGCAGATGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	GTATGAGCGAAGAGTTACCGGAAATGAAGGATATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTGTCTATTGGATTGCCACCCAGCAATTCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTAAAGCATGGCAAAAATCGTGGGGGACGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGATAGGAATTATACAGACGAACAGCACAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAGTTCTTTAATCAATCTGTTTATACATTCAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGGCAACAGGTGTAAGACAGATATGGAAGTTTAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGGCTTTATACAGGCAGGCACTAATGTAACTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTCTAAAAAAACTTTTGCGTGGAGGGGCGCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGGATTTAAACTATGACTTTGATAAAGATGGTGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTATTCAATATTATAACCTCACAGGCCATAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTATTGATTTTCGAGTGATGGCATGGCTGTAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAATATTTCGCTATCGACACAGCTAATACAGCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGAAAAGATAACCCATTGCTTTAATGCCCATAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAAAAAGATATTTCGGCTTTTGAAGTTTTAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	CTTGTTCCTGTTCTATAACCAATACTTGTAAGCGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAACTAAGACAGAAATAGAAAGCGTGAACAATGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGTTCTGTAATAATAAATATCGCCGATGTAACAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGATTTCCCTGGAGTACCGCATTTCTTGATCGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGAAACAGTTTCACAAACTGCATTTGAACATGGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAAATGCTTTGTGGATATAACAACCAACAGCAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATTGACTTAGCAGATCATTGATGCCTAAAGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAACGCTGCTCGGCCTGGTAAAAGAAACTTGCC
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAATTAGCCCAAAAGTCCCGAAGGCGAAAAGGCTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAAAATAATCACATTGCTTTGTTTTCAGGTCGTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAGCAACGTGCCCAGCCGATTGAGTAAATTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAGTTTATTTGCGCAAACAGTTTATTACCCTTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAGAATTGAAATTGGTAAACGTATTCAGGAGGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAATGCAAATGCCTGTGTGCCATCGCCATCCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATAAACAACAAAAATGAAACGCTTAATCAATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CAAATTGCTTTATTCGCATCTGTTACAAAACGATGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGATAGAATAGATGTAATTGTTCTTACTACCGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTCCTTTATCAACGCCATTAAACTTTGGAAGTATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAGAGGAGCGCGGATTACTCCGCCGCTGCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGATCGGGAATACTTTATTTGCAGCGGTTTTTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATAAACTGTTCCAGTCTCTTTTTCGGTCCTGCCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCATTGCAAAAAGCTGCTCAATCTCTTGTATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAGTAGGCAGTAACAATTTTTGGTACGATACTTTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTATTGATGCGGATGGGTTTGAAAGGCCTGTTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATTTATGTGAATTCGAAATGATCATTGTTCTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCGCTATATACAATAACCGTATTGGTGGAAGTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAACTTCAAAGAAGGTGTAGCCAAAACAGCAGTAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAATTCCTGCCGGTTATCTTTCGAGAAGTCAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAGAAACATTACTACCATGTGTTATTAACAGAAAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTTTAGATGGATGAAATACAGTTATTATTTTGG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAATTTATCCACTAAGACAATCCTTTACAACAAAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAACTTCCCTCTATAGATCCTATATGGAAGGATGCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTATAACCCAATTGATAAGCCTGCAATTGATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGGTATGCCGTTTTCTTTCCAGCAAAAAGCCAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATTGGCAACTGAATTATTTACAGCGTCGCAGCTTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAATCTATCTGGGGCTTTAAACCTGTGCTGTCCGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTAAAAGTAATTCAATTGTTTCATCCGAAGCATCAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATCCATGCATTGGCTGTTTGCTTGCTGGCATACTAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	CCGTTAAGGAAGCGTTGATAACGTAGCTCTATTAGC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATTTTATACAAGTCGCCGTCTGCTTTCCATT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTAAAAAACGCATCGCAGCACGAACTTCTACTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTGCTGCACTATCATCCTGCCACATAGCCATTGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATATCATGCCCCTCAGCTTTTAACTGTGTAATGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCCTTGCGGATAGCTGTTTAGCTGCAACATTTACA
CTTGTAATCTTATCATTGAGGAATTGAAAT	AAAATTAAACTCTATAACCTACCAATGGAATAAGGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCAACAATTCTACCTGCAGCACTATCAGTTGCACT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ACAATAGAATTTGGTGCAAAGCTGCAGGGCGATGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTGTTGCAGTCGTTAATATTGAAATCTCTTATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACTGATTATCATTGCCAGGATTGAAACGCATTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAACATATTGCAGCATGCGCTCTAATGCAAAGCAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTCATGATAGAATCTACCTTCCATGTAAATTCTGA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTTCCTAATTTGGTAAAAACAGAAAGGGAACTTACC
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATATTTACCCATTCAAGGCCATCTATTGTACCCT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACTTTAAAATATCATCTTCTGTTGGATTGTCCG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTGTAGCCGTGCTGATAATAATGTGCACCGTTCTG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATTTCCGGATATCCTCCACAGGAAGAACTTATA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAAAATATTGCTCGTAGAGCGTTTTAAATTTCTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAATTCCTGTTTCACGATTCCATCTTAATATCA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGTATTTGGACGAAGGAACATTTACCTGGAAACTAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCATAGAACCAATAAGATATTCTCCAGGGTAGTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGATTCTACCATGCCAAACGGCGTTGATGTGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AGAATCACTATCGAAGTGGACTTCGACAATGGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	AATCTTACAGCAGGCGATGAGGGTTGGATTTTAGTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATTTAAATCCATGTGTACTTTACTTCATTAAATTA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGAAAAAAATAATTGTATTTCTGTTTTTAATAAAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TGGCTTTGCCGGCTGCCTGCCCTTGTGTAATTTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AACATATCCATTAACAGATGTAACCACAGGTGAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGATAAGTAATACAATGTATTACACAAAATATAT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TCCCCTTCCCCTGTTACAACAATGCGGTAAAGAGT
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAAAATTGGATAAAATTCGAAGCTGCATTTC
CTTGTAATCGTATCATTGAGGAATTGAAAT	GAACTTGACCCTTACAACGCATACGTAACAACAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTATAATTACCGGACGCATCTTTTACCGTTCCCAC
CTTGTAATCGTATCATTGAGGAATTGAAAT	TTAGTAACAAGCATTTTTCCTTCGCCAGTAAGAAG
CTTGTAATCGTATCATTGAGGAATTGAAAT	TAATAGAAAACTCCACACAAAACATCACTGGGTTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATGATTGTACCACCAACTTTAGCAAGACTTCCTGTT
CTTGTAATCGTATCATTGAGGAATTGAAAT	AAGCTTCAGTAAACGTATCGGCAATCGGCATGCACG
CTTGTAATCGTATCATTGAGAATTGAAATA	CATTTTATTGATTACGAAGTTGGCACGGTAAAGAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATCAGCTTCACTATCTGTTGTGTCTTTTTCAAAGC
TTGTAATCGTATCATTGGGGAATTGAAATA	ATACTTTGAATGTTGTGTAAGCTGATGTACTGTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	TATCTGCAGGGCTGAATAATTGCCTTCCCATGTTC
TTGTAATCGTATCATTGAGGAATTGAAATA	ATGATCCGTTTGTTTTAAATCGTTACAGCAATGC
TTGTAATCGTATCATTGAGGAATTGAAATA	TCATAACCGGCTTTTATATTTATAACCCTGTCAAAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	GTGCTAACATGTCATTTACCATTTGTGTAATGCTTC
TTGTAATCGTATCATTGAGGAATTGAAATT	ACTGTCTGTAACATTACCCGTTTGCGGTTCGTAAC
TTGTAATCGTATCATTGAGGAATTGAAATC	TATAACCGTTTGGATTGCCCGGCTGTGGCATCTTC
TTGTAATCGTATCATTGAGGAATTGAAATT	TTATTGCTTTATTGCCTATCTGTCCCGCTTTCTTC
TTGTAATCGTATCATTGAGGAATTGAAATA	GGTTATCGAATTTAAAATAAGATGTTCCGCTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	GGTTATCGAATTAAAATAAGATGTTCCGCTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	CGCCCGTTAAGGCTGAATACTCTAAGCTATTATAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATTTTTCTTAATATTCCATCTTTGGATTTATAAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATTTGGTTCTGCAGTTTCCGGAACAAATTCTAC
TTGTAATCGTATCATTGAGGAATTGAAATT	ACTGGAACTGATAAAAAAGGCGGAAATGTTATTAC
TTGTAATCGTATCATTGAGGAATTGAAATG	TAATTCCTGCCAGCCATCTGGTGTGTAATCTAATC
TTGTAATCGTATCATTGAGGAATTGAAATG	TAATTCCTGCCAGCCATCTGGTGTGTAATCTAATC
TTGTAATCGTATCATTGAGGAATTGAAATA	TAGCTAATCCTGCATCAATTAATCCGAAAAGGTCAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TATTTTGTTATATGCGTTCATTGTTAAATATTAAC
TTGTAATCGTATCATTGAGGAATTGAAATA	TCATTGCAGCAATTCAGATGGACGACGGACGCAGC
TTGTAATCGTATCATTGAGGAATTGAAATT	TGTAACCATGTTGGTAATAGTGAGCGCCATTTTGC
TTGTAATCGTATCATTGAGGAATTGAAATT	CGGTTAAAGTAGCTAAATTATTACGAGGAAAACCC
TTGTAATCGTATCATTGAGGAATTGAAATT	CAACAGCTGGATCGCTTATCGTTGCTGTCCCGC
TTGTAATCGTATCATTGAGGAATTTAAATA	ATACTATTGTGCCCTATAATTCAAGTGCATTAAC
TTGTAATCGTATCATTGAGGAATTGAAATT	TTTCACGATCACGCTGCAATAACTGTAGCTGATTC
TTGTAATCGTATCATTGAGGAATTGAAATAAATGTTTTAATGATAGATTCAAACGGTATAATAACTTGTAATCGTATCATTGAGGAATTGAAATAAATGTTTTAATGATAGATTCAAACGGTATAATAACTTGTAATCGTATCATTGAGGAATTGAAATTAGCATTGATCATTGGCCTTAAGACAAGTAAGCATACTTGTAATCGTATCATTGAGGAATTGAAAT	TAAACAAATGGTGGCAACTATTCACAAGTTTTATG
CTTGTAATCGTATCATTGAGGAATTGAAAT	GCATTAAAGACACTGTGAAAATGTTGCGTGAAAAGAA
CTTGTAATCGTATCATTGAGGAATTGAAAT	ATAACATAAATAGCATAAGTTGACTGTCCGCATAT
CTTGTAATCGTATCATTGAGGAATTGAAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042435.1|WP_147192207.1|4560848_4561157_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192200.1|4539287_4541600_+|CRISPR-associated-helicase-Cas3'	cas3	COG1203_cas3_CAS-I	gnl|CDD|187770
NZ_CP042435.1|WP_147192206.1|4554999_4560405_+|DUF4011-domain-containing-protein	unknown	unknown	gnl|CDD|350801
NZ_CP042435.1|WP_147192197.1|4536099_4537506_+|type-I-B-CRISPR-associated-protein-Cas8b1/Cst1	cas8b2	cls000029_cas8b2_CAS-I-B	gnl|CDD|187796
NZ_CP042435.1|WP_147192195.1|4533990_4534851_-|HEPN-domain-containing-protein	unknown	unknown	gnl|CDD|214800
NZ_CP042435.1|WP_147192196.1|4535272_4536076_+|CRISPR-associated-endoribonuclease-Cas6	cas6	cd09759_cas6_CAS-I-A	gnl|CDD|187889
NZ_CP042435.1|WP_147192213.1|4567975_4569775_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|226121
NZ_CP042435.1|WP_147192202.1|4542315_4543320_+|type-I-B-CRISPR-associated-endonuclease-Cas1	cas1	cd09722_cas1_CAS-I-B	gnl|CDD|187853
NZ_CP042435.1|WP_147192204.1|4552878_4553718_+|ion-transporter	unknown	unknown	gnl|CDD|366146
NZ_CP042435.1|WP_147192199.1|4538616_4539288_+|type-I-B-CRISPR-associated-protein-Cas5	cas5	COG1688_cas5_CAS-I	gnl|CDD|273860
NZ_CP042435.1|WP_147192201.1|4541602_4542106_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl|CDD|366863
NZ_CP042435.1|WP_147192198.1|4537524_4538613_+|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	cas7	cd09687_cas7_CAS-I-B	gnl|CDD|187818
NZ_CP042435.1|WP_147192211.1|4565351_4566257_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192205.1|4553757_4554954_+|M48-family-metalloprotease	unknown	unknown	gnl|CDD|320684
NZ_CP042435.1|WP_147192203.1|4543459_4543723_+|CRISPR-associated-endonuclease-Cas2	cas2	COG1343_cas2_CAS-I:CAS-II:CAS-III	gnl|CDD|187856
NZ_CP042435.1|WP_147192212.1|4566340_4567420_-|hypothetical-protein	unknown	unknown	gnl|CDD|272979
NZ_CP042435.1|WP_147192194.1|4533716_4533974_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_CP042435.1|WP_147192208.1|4561529_4563938_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192209.1|4563971_4564688_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192210.1|4564900_4565188_+|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP042435.1|WP_147192201.1|4541602_4542106_+|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	2.5e-52	172.0	3.0
NZ_CP042435.1|WP_147192202.1|4542315_4543320_+|type-I-B-CRISPR-associated-endonuclease-Cas1	cas1	cd09722_cas1_CAS-I-B	2.9e-130	428.8	2.4
NZ_CP042435.1|WP_147192198.1|4537524_4538613_+|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	cas7	cd09687_cas7_CAS-I-B	1.2e-55	183.6	3.3
NZ_CP042435.1|WP_147192197.1|4536099_4537506_+|type-I-B-CRISPR-associated-protein-Cas8b1/Cst1	cas8b2	cls000029_cas8b2_CAS-I-B	2e-26	87.4	3.2
NZ_CP042435.1|WP_147192203.1|4543459_4543723_+|CRISPR-associated-endonuclease-Cas2	cas2	COG1343_cas2_CAS-I:CAS-II:CAS-III	6.2e-30	98.2	1.3
NZ_CP042435.1|WP_147192200.1|4539287_4541600_+|CRISPR-associated-helicase-Cas3'	cas3	COG1203_cas3_CAS-I	1.1e-87	289.7	3.8
NZ_CP042435.1|WP_147192199.1|4538616_4539288_+|type-I-B-CRISPR-associated-protein-Cas5	cas5	COG1688_cas5_CAS-I	1.2e-16	55.8	0.2
NZ_CP042435.1|WP_147192196.1|4535272_4536076_+|CRISPR-associated-endoribonuclease-Cas6	cas6	cd09759_cas6_CAS-I-A	7e-27	89.6	0.2

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042435.1|WP_147192200.1|4539287_4541600_+|CRISPR-associated-helicase-Cas3'	gnl|CDD|187770	cd09639, Cas3_I, CRISPR/Cas system-associated protein Cas3. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; DEAD/DEAH box helicase DNA helicase cas3'; Often but not always is fused to HD nuclease domain; signature gene for Type I.	2.49358e-70
NZ_CP042435.1|WP_147192206.1|4554999_4560405_+|DUF4011-domain-containing-protein	gnl|CDD|350801	cd18043, DEXXQc_SF1, DEXXQ-box helicase domain of Superfamily 1 helicases. Superfamily 1 (SF1) helicases are nucleic acid motor proteins that couple ATP hydrolysis to translocation along with the concomitant unwinding of DNA or RNA. This is central to many aspects of cellular DNA and RNA metabolism and accordingly, they are implicated in a wide range of nucleic acid processing events including DNA replication, recombination, and repair as well as many aspects of RNA metabolism. Superfamily 1 helicases are members of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	2.8394e-28
NZ_CP042435.1|WP_147192197.1|4536099_4537506_+|type-I-B-CRISPR-associated-protein-Cas8b1/Cst1	gnl|CDD|187796	cd09665, Cas8a1_I-A, CRISPR/Cas system-associated protein Cas8a1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Large proteins, some contain Zn-finger domain; signature gene for I-A subtype; also known as CXXC_CXXC family.	2.58326e-11
NZ_CP042435.1|WP_147192195.1|4533990_4534851_-|HEPN-domain-containing-protein	gnl|CDD|214800	smart00748, HEPN, Higher Eukarytoes and Prokaryotes Nucleotide-binding domain.	5.85428e-13
NZ_CP042435.1|WP_147192196.1|4535272_4536076_+|CRISPR-associated-endoribonuclease-Cas6	gnl|CDD|187889	cd09759, Cas6_I-A, CRISPR/Cas system-associated RAMP superfamily protein Cas6. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas6 is an endoribonuclease that generates crRNAs, predicted subunit of Cascade complex; RAMP superfamily protein; Possesses double RRM/ferredoxin fold.	1.65332e-22
NZ_CP042435.1|WP_147192213.1|4567975_4569775_+|AAA-family-ATPase	gnl|CDD|226121	COG3593, COG3593, Predicted ATP-dependent endonuclease of the OLD family [DNA replication, recombination, and repair].	1.96264e-24
NZ_CP042435.1|WP_147192202.1|4542315_4543320_+|type-I-B-CRISPR-associated-endonuclease-Cas1	gnl|CDD|187853	cd09722, Cas1_I-B, CRISPR/Cas system-associated protein Cas1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas1 is the most universal CRISPR system protein thought to be involved in spacer integration; Cas1 is metal-dependent deoxyribonuclease, also binds RNA; Shown to possess a unique fold consisting of a N-terminal beta-strand domain and a C-terminal alpha-helical domain.	8.7518e-159
NZ_CP042435.1|WP_147192204.1|4552878_4553718_+|ion-transporter	gnl|CDD|366146	pfam00520, Ion_trans, Ion transport protein. This family contains sodium, potassium and calcium ion channels. This family is 6 transmembrane helices in which the last two helices flank a loop which determines ion selectivity. In some sub-families (e.g. Na channels) the domain is repeated four times, whereas in others (e.g. K channels) the protein forms as a tetramer in the membrane.	5.04652e-20
NZ_CP042435.1|WP_147192199.1|4538616_4539288_+|type-I-B-CRISPR-associated-protein-Cas5	gnl|CDD|273860	TIGR01895, conserved_hypothetical_protein, CRISPR-associated protein Cas5, subtype I-B/TNEAP. CRISPR is a term for Clustered Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This family is represented by TM1800 from Thermotoga maritima. It is related to TIGR01868 (CRISPR-associated protein, CT1976 family).	3.46682e-25
NZ_CP042435.1|WP_147192201.1|4541602_4542106_+|CRISPR-associated-protein-Cas4	gnl|CDD|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	6.15565e-58
NZ_CP042435.1|WP_147192198.1|4537524_4538613_+|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	gnl|CDD|187818	cd09687, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Cst2/DevR family.	5.67857e-49
NZ_CP042435.1|WP_147192205.1|4553757_4554954_+|M48-family-metalloprotease	gnl|CDD|320684	cd07325, M48_Ste24p_like, M48 Ste24 endopeptidase-like, integral membrane metallopeptidase. This family contains peptidase M48 family Ste24p-like proteins that are as yet uncharacterized, but probably function as intracellular, membrane-associated zinc metalloproteases; they all contain the HEXXH Zn-binding motif, which is critical for Ste24p activity. They likely remove the C-terminal three residues of farnesylated proteins proteolytically and are possibly associated with the endoplasmic reticulum and golgi. Some members also contain ankyrin domains which occur in very diverse families of proteins and mediate protein-protein interactions.	2.99641e-16
NZ_CP042435.1|WP_147192203.1|4543459_4543723_+|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	9.7227e-30
NZ_CP042435.1|WP_147192212.1|4566340_4567420_-|hypothetical-protein	gnl|CDD|272979	TIGR00237, exodeoxyribonuclease_VII_large_subunit, exodeoxyribonuclease VII, large subunit. This family consist of exodeoxyribonuclease VII, large subunit XseA which catalyses exonucleolytic cleavage in either the 5'->3' or 3'->5' direction to yield 5'-phosphomononucleotides. Exonuclease VII consists of one large subunit and four small subunits. [DNA metabolism, Degradation of DNA].	2.27643e-14
NZ_CP042435.1|WP_147192194.1|4533716_4533974_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	0.000376829

Protein sequences

>NZ_CP042435.1|WP_147192203.1|4543459_4543723_+|CRISPR-associated-endonuclease-Cas2
MYVILVYDIEEKRVAKMLKLCRRYLNWIQNSVFEGEITDVKLKELIHEARKIMDKEADSLIVFKSRQAKWLEKMVIGKEKNELDNIL
>NZ_CP042435.1|WP_147192202.1|4542315_4543320_+|type-I-B-CRISPR-associated-endonuclease-Cas1
MRKSYYLFNPGRLSRKDNTLKFTPLDEDGNEGTPKYIPIESVDNLYTFGSLDANSAMYNFLGKEQVSVHFFDYYEHYTGSFMPKDYLLAGKMLIAQSEAYSNKKKRKQIAQKLVDGAAFNMLKNLRYYNNRDKDTLTQIERIEALMLRIPFAEDIETLMGIEGNIRMSYYAAFNVIINDFEMGNRSKQPPGNEVNAMVSFVNSMCYTLSLDMIYHTQLNPTISFLHQPGERRYSLALDIAEIFKPLLADRLIFSLLNRKQVQQTDFDNRLNSCLLKDSGRKTVVKAWDEKLNETIKHRSLGRSVSYKHLVKLECYKLSKHILGIEEYKPFRAWW
>NZ_CP042435.1|WP_147192201.1|4541602_4542106_+|CRISPR-associated-protein-Cas4
MTITATLINLYHVCKREMWLHANGVRMEQTSETVADGKLLHETAYPQRSEKYSEIEIGGSKIDFYDAKNKVIHEIKKSDSFESAHEWQVKYYIWLLEQNGVEGVKGIIEYPKLRETKQVKLSAEDKTYLQQIVQQIEALVSADVCPPRIEKKFCKTCSYFDFCWIEE
>NZ_CP042435.1|WP_147192200.1|4539287_4541600_+|CRISPR-associated-helicase-Cas3'
MTLLAKSKDVKQNIKARTLKEHIDDCLLILDFLRRSFPRVASLTGMGDAYWEVLKICIICHDLGKAHLEFQNVLDGKPDNWKSQRHELFSLPFIEALSNIDKETSKIARLVVAGHHKDFETLRSFLNAYNNNDTFGSLEGLDEEQEDFETAFSKNVNILGVLNLLKDYPVTITTIHPKPIYGLIHGYNQKPYYQSNEGYFKLMMLFGGLKWCDHLGSALVNEIYQLENRDFDFLKRQQNELRAKYLDFYEHQKSSAKVNGHLILNAPTGSGKTESAFLWLKNQMINTGQGRAFYILPFTASINAMYERLNKAIGAEKGKVGMLHGKLSDYLNNYFEDLQYDINVKKDSIKEIKEKYKSIITPVKVATPFQLLKHLFGLKGYEQGIFEMAGCYLIFDEIHAYSPDVFAQIKVLLEFATKHLQAKVMIMTATMPRFLQAELEESLGKFSIVKANHELYESFKRHRIILKDGLLGGYINDIQKKLKDGKKVLVVCNTVKSAQNIFLQLKNSLNENEEILLHGSFTGMDRSRKERDLMKDHVKLLVGTQAIEVSLDIDYDMIFSEPAPIDALIQRFGRVNRKREKGICDCIIFKDSNKEDKYIYNPETVAKTLKAFENIIKEHQGIIDEALLQSAIDFVYCDWDENDRKEFEDKYQYLKDALQILSPMFKNKHTEEDFYSQFDGIKILPQSKKSDFEGHLNGFDFITAESLKVQIRKGRFMSWLKGQNIKKDIYAFDRGKKIYNVPYFITNKAYDSELGLLTDKEEVWQNTEII
>NZ_CP042435.1|WP_147192199.1|4538616_4539288_+|type-I-B-CRISPR-associated-protein-Cas5
MEVYKIDITSWTASFRYPNLISGVQPTLEVPPISTILGLINAAAGFYLEHKNLELGYYFEYEMEGEDLETIYQISSKYGKPTNNAKSNVINRKFLFNNFLRIYTTDKNIVDYLSQPYFPILLGRMNDLATVTNISQREILDKIEFATEIRGQVIPFKFHLPGQIQALPQYFTNDFPRKNIGTEPFSIISHKVKTFGTSVTAYRDILPNGKEVDIFFHQLSFEN
>NZ_CP042435.1|WP_147192198.1|4537524_4538613_+|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR
MNLKTQGFVLLDVDVVALNNAGKSTTSNFDNAVATKKIYKNGRAYTYVSGQAWRYWWREALKANHGWALSPITRDSKIAFTEANPIVYADDDVFGYMKAAKDVKRDDDGNPILDKKGKEAKEDVTVTRVSPLKNSAIISVASVGTVENWSSMARQEGDSVPYSKEEYSAIMKGMFSIDLFQIGTFATYNKTGYKNLTEKFKAGAMENGATEIEDPFVKTKNGEPQKLIQISKDIRTNRVVDTIAALKTISGGAMQTNNMADVTPKFIVLATMNSGNHPFSHIVKNDGVKSEKAVLNIEGLKEVLSDYKEQFKGIIFIGKRNGFMDEYNEELKTLEIEFPNVKILSINQAIDQYCEQVKNQIS
>NZ_CP042435.1|WP_147192197.1|4536099_4537506_+|type-I-B-CRISPR-associated-protein-Cas8b1/Cst1
MIENNQLEINWLTHPTGDSFADIGGFVIEYLQKKKPDKSILELIEEVTNIYVKKWDNNLHSFFLNSTITHNSNKGQKGINKTIAFYKGLFDGKDAEDGYCRITGQKGKVFQGTRDNHIMSGSATLINFHHGFESGIRLSKEALIRIFFVPLGVEQLGDKVAVLTSNNEGITRHFVQRNVDNNFRDIASGISKSIQRSEFSNPANALFEYANQCIENVKTVTFDEDTGRSKTQGTTLNLFHFTNFGASPTINLITLPASVFAFYAYCIREHKKEWQSFIFRQYSNSKFKNAQFDDVSKSWFNNKEEVDYSTFKVWRNSVFEALLNGNGQIIRKAFLAHSKSRILNFKIIEQYQINIQNMDKRTLTKIKELADFIVNDRSDDEIKKSMTRLNGSKSSNGLRYFLLKLADKNYKDGNDEPLFSIDEYVEYLFPDGTYWNEIRDLLLIAIYQKLHETNKKIEVELIENESEI
>NZ_CP042435.1|WP_147192196.1|4535272_4536076_+|CRISPR-associated-endoribonuclease-Cas6
MRFYLTLQATDSNSTITLNYQYPLSAAIYKIIQRADTAFSAFLHNTGYGLGHKNFKLFTFSDIDTPFKVIGDRMHMLSNTARVTICFYMPQAAEHFIRGLFMQQQLEIADKKSKATFVVQQIESLPHYVVSDIETTAIKNVLIQPLSPLVAGRKNEKGYYDYRSPLDADFTDCLLYNWLEKYKTVNDTYENTIQQIKEQTEIKVLLFSQPPKQRLITIKQGTSDETRVRGYTKFRLQLTAPEDMLQLAMDAGLGLYNSQGMGCVGVI
>NZ_CP042435.1|WP_147192195.1|4533990_4534851_-|HEPN-domain-containing-protein
MKTSLEHLPKTKQEQILQIVEIIKEVAVPEKIILFGSYATGKWVEDNYIEKGIKYEYISDYDFLVVTEDNEEKDYVLKDIIVNRSHDISKVPVNPIIHSISYVNEGLEFGQYFFADIIREGIILYNTQKSDFSNPKELTPTEMRIVAQRYFDQWFKSGEEFFIDANNAFKRNSLNHSAFYLHQSAERFYNTILLVITGYKPKTHNLDKLRRHAKNLSEELFLIFPYPTNDQHESHLFDLIKRGYIDARYKEDYVISKNEVSILISRIDEMRKTVGRVCAEKISLLK
>NZ_CP042435.1|WP_147192194.1|4533716_4533974_+|helix-turn-helix-transcriptional-regulator
MNAKKKEDIRKLFGMYLKKRREEYLKINSVRQLSFNSNIDQSKLSKIEKGQIDFRFDTLMEIAITYKLKPKQLFDFDISFWKEEE
>NZ_CP042435.1|WP_147192204.1|4552878_4553718_+|ion-transporter
MYAQVKHTVHLLLDPADGHTIWDRIINTIIVGLILLNTLAVIFETVDSIYLPNKALFNDFEIFSVSFFSIEYISRVWSCTAKKKYTHPIAGRLKYIVSAGAIIDLLAILPFYLPLLKIYDLRFLRILRLLRFFRFFKLGRYLNASKVIGSVFKSKKEELVLSFVITMFLIIVASSVMYYAEHDAQPDKFSSIPETMWWSVATLTTVGYGDEYPITGLGKFLTACISILGIGMFALPAGILASGFSDEFRKLKAIKIPARIVAVNCSEAYVQIIIKNKCY
>NZ_CP042435.1|WP_147192205.1|4553757_4554954_+|M48-family-metalloprotease
MLLPLQYHEATARFFQQQSQVWQFFVSNNHKEGQLKAFKTDLLKNTYKFDETADAQLYQKVNLAKEKLDMSIPVTLYQAQHTEDMNASIVYINDEAHIVFSGKIITLLSEDEMLAIIAHELSHVKLYTHLNGDVEVADRIVTAIGNHPGSTPAHYETARLFKLYTEIFCDRGAYIVTGNYAPIISSLVKISTGLQSVNADSYIKQAEEIFSVDAETKTTGVSHPENFIRARAIWLWHMKGHDAEPIIKQMIEGNINLDELDLFRQQQIATVTQQLIMLLLQPEWMQTAQTTALAKQYFGSIQLTEAPDITTLLAHVENVHSNLRDYLAYVLYDFATTDKTLEDVPLGYCFYLADDLKLDKPFAQAVKKERKLSDKKVTVLKKQTLAEFHKQQLQPTVN
>NZ_CP042435.1|WP_147192206.1|4554999_4560405_+|DUF4011-domain-containing-protein
MSTNTTFQQYLQSAFTTGPWSTDEVIEFVLPLFEEVLSFHDNGQVGSFEKPETIFLTDGRLDIDETFTHAPVSDLKTVKKLLEYQQIHGYTITERVLLDDDLGNNRTVAVNLHVQTNPNDELKHPVYLPGYQCYELKAGHHDAQTDIFCLGLILGSVVMGLDLYEVEDLNKFVVYRNQPAGLNSRMHPTICGLVTEMTELDRSQRSRDLQEIVQRLKYYRDYDPQKETDLSKLAAFQVKQPADRKTFILSKLRNRLFDTSRRNRLLYYKPNGRFVNLTVSSVPMVLHYQSINPQLLFTWNSEIAAQIIRQNDISLNKYLRFEDHPYLNAQLNGIRQHAENDKKEYGFSQLKLVVAFLHWHNLKEDSSERIQSPLLLLPVELDRKKSLKEEKFTLKITDNAALINPILANHLKDLYGIALPESIDFDDVSMTQFFEMLQEKINAAKQGVKLNYIDKPRIKIVHNIARQTINNYRKKLKLKGTPAFQQVDYSYSDENYKPLGLELFRQKVEPRQSTLQFLLSDNPVPAGTNNFAETSGTAVKSTFHLTDGESNAYSWDFDICNIVLGNFNYKKMSLVSDYNKVTDQGIEHPVFAELFTNEPKRRQEKVVPNDPAEWYHVITADPTQAKAVLHSRTGNSYIIQGPPGTGKSQTITNLIADFLAKGKTILFVCEKRAALDVVYYRLKQNKLAELCCYIHDSQGDKKEFIKDLKLVYDDFLKNKMDLTAITAKRKAVLDRLLAKINVLQTYHQQQREVDPAAGVSTRNLVETVVGTKAFVPKLDNLQKEAVPNYHQWLQYGDTIHQLGKALEDTGAEPQFSGHPFSNLGIEVIKAENPFSLMDSLTTHANASIQQISAVIGQNNIPSEHAAYLENIKNLIRDAVVLEPLAQSRNLRLVEKTNPESQEFEESYREYEEIINAYQHSLDANKRWVNKFDKQEVEQAIELAEKHEKSFFSFLNGNWRRLKNQLKQSYDFSAHQIKPAFSLVLKQLQDEYNINDQVIQNKKSLEKKYKVDNIENVYSGIEVLRGKQGDKEIDYLLEHPQANELVLQLSKLNNQLHQLELQLQQCLYGAKEKSLAQISDELSTLKSNMDVLKDLLPSLQKFIMLPENVQQFIRKIPVTPIQAESAMASKTLEILFRNRQTFAGINQKMLQETVKDIDALYRELLMLNSEYIRAERRQKFINNYELSNASSAVLTTEQKQGKKEYTDGRRILEHEMGKTMRFKSIREIASNESGNVLKDIKPVWLMSPLSVSDSLPLDTGFFDVVIFDEASQITLEEGIPALFRAPQTIIVGDDKQMPPSNFFSAKADDPEDLEVVDGEKEDEILSADADSLLVQGARKLDSTMLSWHYRSRYETLISYSNHAFYGAGLLTIPDKTVHHLEKQLTEIQQPEEGSEHAAELLNGSISFHYLPNSVYENRNNISEAKYIASMVKKLLLDNVRETIGIVAFSQEQQGIIEEAIENLAAGDRAFDEVLEKAYNRKDEGQFTGLFIKNLENVQGDERDIIIMSVCYGHDSNKKMLMNFGPINRKGGEKRLNVIFSRAKKHMAVVSSIRQHHITNDLNEGANYFKRFLSYAEMVSTGNMKAARNILDSLVTNEQKKTEIINGCAVTTLQIKNALETKGLIVEEQIGQSSFKCSLGIKRKLQDPDYALGILIDDELHYRNDDLMEQYYQRPAILQSFGWRVTNVFAKDWLEDPERVLSALLRLLQENPVSTEAEQTEKQTEVLAEKEEKELGTKLLSANGEKFWSVIQQEHQIQIRFGRSGTPGQVQIKTYATAEEATLARNKLIEEQLAAGFQHLIFS
>NZ_CP042435.1|WP_147192207.1|4560848_4561157_-|hypothetical-protein
MSIFNCSMLAEAALAIQSFFDTVIGHKEDVSLMQKTGGKDFITPIALQDKVRNLQQLIQQNKSMFILVTYSTVLIAVYRSESFGNSPYFSGSSIALFNEVDK
>NZ_CP042435.1|WP_147192208.1|4561529_4563938_+|hypothetical-protein
MATKLSKTHYFVFACLFLGILGSFIQGEFWSARALAESTLIICALSYLASKYYAGTIIRKYQDFYYNPGKGRRFWDTVIIESSFHIIMPVALALLYACCLLMLLKYLPQSSYKTVANLVNPVIDFNKHYIKYPLTLLVTVLGILTLTRYLSVKKYKSFQKASKYIGMPFKVAATLSFFLMQDKGISNNLLEYHFNANPVVAQFTTFNAATQQDVARQKEIKTALNAYLDYVIERLNNNYQSKEESDTSQIVVHPDAVKLKALVEQFPQVRDAVIDHIKRDPVYLIGDNDKTFTKYHEAIWTYNEHEVKTSNFYETVSKKESSFFEDFLSVIADERTSIKKKPLGENAEIIQKLMGDFWSEFIPADKLTESIPLHKILKDKAIDLLNDKLMNGIYTLFTKRRVTKNDIQELNTYIDDVVTDDYKAALNSVKNKFTVLGDYYSELSKTAATDYFNTIEKTADRSVVTYEEGIIQQRAYLEKIKAEWNTESDVKKNVEALKRRYPDRTDEELEDYVKVVRDEQLQNLDDRIGEIDAALRQKENLKDYTFIRDRFSAGGIFLGRSITPYGYTSPCGGRFYPALRDCPNALLTGNLLTLELNNNKLVVKTSTGSFESESAVSPGLLLAAYNYVYAENTYPVLIDGFFDNKGNEIFAYNRNFTYDAALLHTLFKSDNFIFDVLDDSIADTDLRSRFRDAVTTFHAERKDVSLSRIFDDAYFITTTKSGHFDINTQLTFSVVANDGDNTSTRYREMSDLSATFNSNYEWLLNRYPYLNDLVKFASYQALFRALPQNKVDITDLILKNKN
>NZ_CP042435.1|WP_147192209.1|4563971_4564688_+|hypothetical-protein
MVSVKDVADVIKMLGDVVKSTREIINAVNDGRKYLALKYPDAQRDFSSLIDQMQKAIEGMAKVTSVITNFRFVIAGNVDDSTIAYSELARFNDYIISQKADVAVLRNVARKLKADCGKVRTLRDKLDERTKERSWGSLFGLLGDKAQQRTVELHSTISNFYADDERMIELINQTLDLAESAIKDIEYVLGPAGVANPYNVPEAATILGIYAKLFEAPNKDLQHLANIMSEAQSALIIG
>NZ_CP042435.1|WP_147192210.1|4564900_4565188_+|hypothetical-protein
MEIRTITVHDGSKYFYTTSAFTAANPLGIVKATLIEYALYKPDNKEAPIGKLYKTNEGNWYDAPTDDVINTLLSASLKKAIDEAEKIHSATEVHS
>NZ_CP042435.1|WP_147192211.1|4565351_4566257_+|hypothetical-protein
MSKALNVLKNLIYIPIGITLIGMICYGIFYFIGSLYIGGRLAYIGTDKTIIVDSVWYTLEKIDPGKPSVKVNHIRFKNFTGSVSNLPPKLNLGDSVQILYYQKFNEGLTIEHTNKFIQIVDGLGGFIMAFVLASLMFIAFFVPFIYHTIEEFHFVKTAIAKSYQKPEFKSEQILETHKFLSYSIRFLPSILSVFINVLVLLVFLKTLLFVEKANEALCGVLVISILIYFAFISPKWVKWLYLLRYSNHWFLEALRIIVETVIGLKLIGELLFLFKKEDYYFGSLFDLFKETAVKLFDYLFG
>NZ_CP042435.1|WP_147192212.1|4566340_4567420_-|hypothetical-protein
MAANDTITPSALVNIFSNALSNDATRKPFTIKGIYVPGKGANYNGVYYDSLKDEYIDASITLVVPAILRVNLEAGQVIECSAYLTKKVQANGARIELQVNVMEVHSQEESKLTEEQIKTFEILQRKAAQGYKDVDGFIKTKIIQQQPVIVTIIIGRTGIIDSDTKHQLRDALAFFDFNFVRVSLSNEGEIVEALRAYDQKTDVLVVSRGGGENMSIFNRPVLAEAALELQSYFVTAIGHKEDVSLLQKIADKHFITPTALGQYFQELYTHTMEELQHSKARLIADVTTQLKGSYEVQLQNLQDKLKNANEFSEMQMKVKQDEIKSLQQLLDQKKGVPAYVWVLVVLAIIAAFLLGKLMT
>NZ_CP042435.1|WP_147192213.1|4567975_4569775_+|AAA-family-ATPase
MAKAKKTEVEASLVSSNPEITKPRLIKLIIKNYRCIGSTPVEIDLNDIVVLVGANNVGKSSILKAYELAMSQGSGKADLKREDFPNNTIDNDNLPEIELHTIVYDNSPGDKWIQVLENGEMLVRERWVWNGEGKPKREGWEVEASSWSENVPWGAPNVANARRPEPHRVDAFDSPEEQAKAIKKLLMQALNDRVKNLKAQNQEEGQEENDYKKLIAHVKALQKKIVLEAKDQIDAVNQELSDLVARVFPNYKIDFDAKPEDDLDSAINLFKADPQLLMGPADGYLSTIDRQGSGARRTLLWTAIKFISENNQKGKDNGAVVRPHLLLIDEPEICLHPNAIREACNLLYDLPSSDNWQVMVTTHSPIFIDFSKDNTTIIKVEKTSNGEIKGTTVFRPDKVQLDDDDKRNLKLLNICDPYVAEFFFGGKVIVVEGDTEYTAFNYIKRQKPEEYKDINIIRARGKATIVSLIKVLNHFGSDYAVLHDCDIPIITTKRGIEMANPAWGNNPNILNAMNAKPVGKSTRLLASLPNFELAYFGEVAENEKPYNALRTLEQDEVKFDTVEALLKALVDFASPPPINCTEWTSIEDLEQKLMDSLSG

Crispr_ID: NZ_CP042435_5

• CRISPR_ID: NZ_CP042435_5
• CRISPR_location: 4637339-4637500
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP042435_5

Consensus_repeat	Method
TTGTTGCGGTCTCCTGTTATCCTGTTGCGGCCTGTTCTCGTTTCTT	PILER-CR

spacers of NZ_CP042435_5

>5.1|4637385|29|NZ_CP042435|PILER-CR
CTGTCACCGCCACCTTGCTGGGGAGGTCC
>5.2|4637460|33|NZ_CP042435|PILER-CR
TTGATTTGGTCTGTTATCCGGAGGACGGTTAGG

CRISPR arrays and Neighbor proteins around NZ_CP042435_5

CRISPR arrays

The CRISPR arrays of NZ_CP042435_5

>merge|NZ_CP042435|5|4637339-4637500|PILER-CR
GGCCTGTTCTCGTTTCTTCTGTCACCGCCACCTTGCTGGGGAGGTCCTTGTTGCGGTCTCCTGTTATCCTGTTGCGGCCTGTTTTGATTTGGTCTGTTATCCGGAGGACGGTTAGGTTGTTGTGGTCTCCTGTTATCTTGTTGCGGCCTGTTCTCGTTTCTT

>NZ_CP042435|5|3|4637339-4637500|PILER-CR
GGCCTGTTCTCGTTTCTTCTGTCACCGCCACCTTGCTGGGGAGGTC	CTTGTTGCGGTCTCCTGTTATCCTGTTGC
GGCCTGTTTTGATTTGGTCTGTTATCCGGAGGACGGTTAGGTTGTT	GTGGTCTCCTGTTATCTTGTTGCGGCCTGTTCT
CGTTTCTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042435.1|WP_147192273.1|4636690_4637200_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192265.1|4629055_4630357_-|serine-hydrolase	unknown	unknown	gnl|CDD|379138
NZ_CP042435.1|WP_147192283.1|4650929_4652231_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|223234
NZ_CP042435.1|WP_147192275.1|4638925_4640146_-|hypothetical-protein	unknown	unknown	gnl|CDD|273213
NZ_CP042435.1|WP_147192276.1|4640240_4640810_-|redoxin-family-protein	unknown	unknown	gnl|CDD|223463
NZ_CP042435.1|WP_147192272.1|4635746_4636646_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192271.1|4634671_4635661_+|YihY-family-inner-membrane-protein	unknown	unknown	gnl|CDD|224214
NZ_CP042435.1|WP_147192279.1|4645196_4648298_+|SusC/RagA-family-TonB-linked-outer-membrane-protein	unknown	unknown	gnl|CDD|274948
NZ_CP042435.1|WP_147192278.1|4642467_4643169_-|ComF-family-protein	unknown	unknown	gnl|CDD|223970
NZ_CP042435.1|WP_147192267.1|4632851_4633259_-|aminoacyl-tRNA-hydrolase	unknown	unknown	gnl|CDD|181730
NZ_CP042435.1|WP_147192282.1|4650229_4650586_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192270.1|4634244_4634586_+|nucleotide-pyrophosphohydrolase	unknown	unknown	gnl|CDD|212138
NZ_CP042435.1|WP_147192281.1|4649835_4650225_-|hypothetical-protein	unknown	unknown	gnl|CDD|319905
NZ_CP042435.1|WP_147193285.1|4630451_4631939_-|oligosaccharide-flippase-family-protein	unknown	unknown	gnl|CDD|240533
NZ_CP042435.1|WP_147192266.1|4632215_4632836_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147192268.1|4633312_4633765_+|D-tyrosyl-tRNA(Tyr)-deacylase	unknown	unknown	gnl|CDD|376833
NZ_CP042435.1|WP_147192269.1|4633815_4634190_+|GxxExxY-protein	unknown	unknown	gnl|CDD|275083
NZ_CP042435.1|WP_147192280.1|4648327_4649692_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	unknown	unknown	gnl|CDD|185760
NZ_CP042435.1|WP_147192277.1|4640892_4642284_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042435.1|WP_147193286.1|4643208_4644582_-|DNA-repair-protein-RadA	unknown	unknown	gnl|CDD|236994

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042435.1|WP_147192265.1|4629055_4630357_-|serine-hydrolase	gnl|CDD|379138	pfam13354, Beta-lactamase2, Beta-lactamase enzyme family. This family is closely related to Beta-lactamase, pfam00144, the serine beta-lactamase-like superfamily, which contains the distantly related pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	2.88292e-10
NZ_CP042435.1|WP_147192283.1|4650929_4652231_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|223234	COG0156, BioF, 7-keto-8-aminopelargonate synthetase and related enzymes [Coenzyme metabolism].	4.57333e-111
NZ_CP042435.1|WP_147192275.1|4638925_4640146_-|hypothetical-protein	gnl|CDD|273213	TIGR00678, DNA_polymerase_III_subunit_delta', DNA polymerase III, delta' subunit. This model describes the N-terminal half of the delta' subunit of DNA polymerase III. Delta' is homologous to the gamma and tau subunits, which form an outgroup for phylogenetic comparison. The gamma/tau branch of the tree is much more tighly conserved than the delta' branch, and some members of that branch score more highly against this model than some proteins classisified as delta'. The noise cutoff is set to detect weakly scoring delta' subunits rather than to exclude gamma/tau subunits. At position 126-127 of the seed alignment, this family lacks the HM motif of gamma/tau; at 132 it has a near-invariant A vs. an invariant F in gamma/tau. [DNA metabolism, DNA replication, recombination, and repair].	1.54427e-27
NZ_CP042435.1|WP_147192276.1|4640240_4640810_-|redoxin-family-protein	gnl|CDD|223463	COG0386, BtuE, Glutathione peroxidase [Posttranslational modification, protein turnover, chaperones].	7.98937e-66
NZ_CP042435.1|WP_147192281.1|4649835_4650225_-|hypothetical-protein	gnl|CDD|319905	cd07241, VOC_BsYyaH, vicinal oxygen chelate (VOC) family protein similar to Bacillus subtilis YyaH. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	3.86749e-59
NZ_CP042435.1|WP_147192271.1|4634671_4635661_+|YihY-family-inner-membrane-protein	gnl|CDD|224214	COG1295, Rbn, Ribonuclease BN family enzyme [Replication, recombination, and repair].	1.31281e-47
NZ_CP042435.1|WP_147192279.1|4645196_4648298_+|SusC/RagA-family-TonB-linked-outer-membrane-protein	gnl|CDD|274948	TIGR04056, OMP_RagA_SusC, TonB-linked outer membrane protein, SusC/RagA family. This model describes a distinctive clade among the TonB-linked outer membrane proteins (OMP). Members of this family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 alone. Published descriptions of members of this family are available for RagA from Porphyromonas gingivalis, SusC from Bacteroides thetaiotaomicron, and OmpW from Bacteroides caccae. Members form pairs with members of the SusD/RagB family (pfam07980). Transporter complexes including these outer membrane proteins are likely to import large degradation products of proteins (e.g. RagA) or carbohydrates (e.g. SusC) as nutrients, rather than siderophores. [Transport and binding proteins, Unknown substrate].	0
NZ_CP042435.1|WP_147192278.1|4642467_4643169_-|ComF-family-protein	gnl|CDD|223970	COG1040, ComFC, Predicted amidophosphoribosyltransferases [General function prediction only].	1.05578e-33
NZ_CP042435.1|WP_147192267.1|4632851_4633259_-|aminoacyl-tRNA-hydrolase	gnl|CDD|181730	PRK09256, PRK09256, aminoacyl-tRNA hydrolase.	4.04673e-35
NZ_CP042435.1|WP_147192270.1|4634244_4634586_+|nucleotide-pyrophosphohydrolase	gnl|CDD|212138	cd11531, NTP-PPase_BsYpjD, Nucleoside Triphosphate Pyrophosphohydrolase (EC 3.6.1.8) MazG-like domain putative pyrophosphatase YpjD from Bacillus subtilis and its bacterial homologs. This family includes a putative pyrophosphatase Ypjd from Bacillus subtilis (BsYpjD) and its homologs. Although its biological role has not been described in detail, BsYpjD shows significant sequence similarity to the dimeric 2-deoxyuridine 5'-triphosphate nucleotidohydrolase (dUTP pyrophosphatase or dUTPase) and NTP-PPase MazG proteins. However, unlike typical tandem-domain MazG proteins, BsYpjD contains a single MazG-like domain.	3.50217e-39
NZ_CP042435.1|WP_147193285.1|4630451_4631939_-|oligosaccharide-flippase-family-protein	gnl|CDD|240533	cd13128, MATE_Wzx_like, Wzx, a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Escherichia coli Wzx and related proteins from other gram-negative bacteria are thought to act as flippases, assisting in the membrane translocation of lipopolysaccharides including those containing O-antigens. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).	5.53165e-25
NZ_CP042435.1|WP_147192268.1|4633312_4633765_+|D-tyrosyl-tRNA(Tyr)-deacylase	gnl|CDD|376833	pfam02580, Tyr_Deacylase, D-Tyr-tRNA(Tyr) deacylase. This family comprises of several D-Tyr-tRNA(Tyr) deacylase proteins. Cell growth inhibition by several d-amino acids can be explained by an in vivo production of d-aminoacyl-tRNA molecules. Escherichia coli and yeast cells express an enzyme, d-Tyr-tRNA(Tyr) deacylase, capable of recycling such d-aminoacyl-tRNA molecules into free tRNA and d-amino acid. Accordingly, upon inactivation of the genes of the above deacylases, the toxicity of d-amino acids increases. Orthologues of the deacylase are found in many cells.	1.2699e-85
NZ_CP042435.1|WP_147192269.1|4633815_4634190_+|GxxExxY-protein	gnl|CDD|275083	TIGR04256, conserved_hypothetical_protein, GxxExxY protein. Members of this protein family average about 130 residues in length and include an almost perfectly conserved motif GxxExxY. Members occur in a wide range of prokaryotes, including Proteobacteria, Perrucomicrobia, Cyanobacteria, Bacteriodetes, Archaea, etc.	6.9486e-47
NZ_CP042435.1|WP_147192280.1|4648327_4649692_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	gnl|CDD|185760	cd08977, SusD, starch binding outer membrane protein SusD. SusD-like proteins from Bacteroidetes, members of the human distal gut microbiota, are part of the starch utilization system (Sus). Sus is one of the large clusters of glycosyl hydrolases, called polysaccharide utilization loci (PULs), which play an important role in polysaccharide recognition and uptake, and it is needed for growth on amylose, amylopectin, pullulan, and maltooligosaccharides. SusD, together with SusC, a predicted beta-barrel porin, forms the minimum outer-membrane starch-binding complex. The adult human distal gut microbiota is essential for digestion of a large variety of dietary polysaccharides, for which humans lack the necessary glycosyl hydrolases.	2.66526e-49
NZ_CP042435.1|WP_147193286.1|4643208_4644582_-|DNA-repair-protein-RadA	gnl|CDD|236994	PRK11823, PRK11823, DNA repair protein RadA; Provisional.	0

Protein sequences

>NZ_CP042435.1|WP_147192273.1|4636690_4637200_-|hypothetical-protein
MMKYLTALTLLLLIDINLYCQNTSQWNPDNFSFSELTFHSTACNGTCPQVSLHLRKDKLIEVSRKIYKSKGVVDSSLSGNFIGVLDNKNYNSVLILLSTINWDTLSFSNSWCCDAPIKTILISYNGKYKKFKSMTPPEITYELFDDLIKLASKIKLTKYNKPLDFEDYN
>NZ_CP042435.1|WP_147192272.1|4635746_4636646_-|hypothetical-protein
MKKLFCCIIITISLAACKRDSSELLAGRWDFSALEMPGMPDFLYEIKQTGDDNALTLKKFLLDNKLILRKDSTFDLVLLKQYIHGSWHYEAATKYLFLKDSSASNLDITIHIDSITGSRLIFDIDEFALNKLVNRHAAINNYYDLLFNKSYCQFYLDIDNDRYSDLKDDPYSIENNKWRIKPFQQETDKQIKQRVLNHLDFWQNLFTDAQEKDRTYVAYTWFDSPLVVAENGVKLEFYDEHKKEWDQNFYDSTDANKGYQMMRKCFSKKLKFMETEDKYKRHEDVIRQLKANYTEALKD
>NZ_CP042435.1|WP_147192271.1|4634671_4635661_+|YihY-family-inner-membrane-protein
MTIKGLWQILKQTFKEFADLKITRMSAALAYYTVFSIAPMLIVIITLCDIFLGREAIEGQVFEQIRSFVGDSAALQIQELIKNATISKDISWASVVGIIALIFAATSVFAEIQDSINLIWRLKAKPRKGWLKLLINRVLSFSMVVSLGFILLVSLVVNAALNLLEDHLLSMFPGMQIYIAYALNILLQFITISFLFGTIFKVLPDAKIHWKNVRSGAFTTALLFMLGKFAVSYYLGKSHISSSYGAAGSLVIILLWVYYSAIILYFGAAFTRVYAQHTGNHIFPTSYAVFIQEIEVENKHALDEQSPEVKTIVKEDEIIIKHEDEKENI
>NZ_CP042435.1|WP_147192270.1|4634244_4634586_+|nucleotide-pyrophosphohydrolase
MTIQQAQTTVDNWIKTVGVRYFSELTNLGILMEEVGELSRLMVRTYGEQSFKESDKGKDIADEMADVLWVLICLANQTNVDLTAALQKNFEKKNIRDADRHKNNEKLGGGTIE
>NZ_CP042435.1|WP_147192269.1|4633815_4634190_+|GxxExxY-protein
MTEIIYKEESYKIIGLCMEVHKQLGMGFKEIIYKDALEIELNNAGISFIREQQYDIEYKGIILPHKYYADFVIEGKIIMEIKASSMIVNNFVSQTINYLKASGIHLGIIANFGEKSFTSKRIVF
>NZ_CP042435.1|WP_147192268.1|4633312_4633765_+|D-tyrosyl-tRNA(Tyr)-deacylase
MRAVIQRVSEASVTVDENITGNIGNGLLVLVGIEDADNDEDIQWLSSKIVNLRIFNDDEGVMNVSVKDCNGDILLVSQFTLHAATKKGNRPSYIKASKPDIAIPMYEKMITQLETDLGKKIYTGVFGADMKVRLLNDGPVTIVMDSKNKE
>NZ_CP042435.1|WP_147192267.1|4632851_4633259_-|aminoacyl-tRNA-hydrolase
MSITITNEIIFQTARSGGKGGQNVNKVETMVEGRWHVANSVLVSDEQKQSILQKLASKITTDGYLLVKSQTERTQLGNKEQVIKKMNQLIAQALIKKKSRIATKVPKVIKEKILEKKKQKSSVKATRRKLKPGDY
>NZ_CP042435.1|WP_147192266.1|4632215_4632836_+|hypothetical-protein
MQKKLLVILFLFTGFIALHAQVRDGRTTIDTTVRSAVIIESDLSQSEVENAIESYFDSMHIEKEKGKGFIIKKSMGYMLFRRAKVENVSDALDVYFVTENKKQKGKDASTVYITASRGLTNFLTPDNDQKVWSQLRDYASYMQSNYFEQYKLYVQLADVSKDMDKKKKKLDDVLKEKADLESNISNDSLQIVNFNEALLKLKIKKQ
>NZ_CP042435.1|WP_147193285.1|4630451_4631939_-|oligosaccharide-flippase-family-protein
MWYGVSSIAARFINYLLTPLLTYNLVNTEGLAHYGQIGLIYSAIPILNIIFTYGFETAYFRFASKEEYKKDIYNTSALSLIFSTLFFSILLWIFQHAFGVAIGLQDFPLIIQISIFIIALDALSTIPFAKLRQEQRPRKFAFIKIAGILINIFVTWFYVAWCPRHVDVHANSFLNIIYEPGTNPVVYVVLANLIQSAFTLLLLGSEIKQLRFNFNTRLWKEMMIYSLPLVIAGMGGMINETFDRLMLRWWLPGSVQHKEAEVGVYNACYKLSILITLFIQAFRLGAEPFFFKQAEGDNPQKTYARVMKFFVITVCVTFLIINLFIPIWKHFISPGYWEGLAVVPILVLANMCLGIYYNLSIWYKLSNRTGAGATITVIGAAITFLVNFLFIPHFSYMASAWATFSCYFSMMLISFVWGQKAYYVPYAWKKLLAYMVIVILLFFVHKGITHFYDNDIFSLAIGSIFTTAFIVFVLKVEKKEFIAMPVVGKYVARYI
>NZ_CP042435.1|WP_147192265.1|4629055_4630357_-|serine-hydrolase
MFLKRLTAVILVCFVNHIISFAQQKTGNLLATLLQKDTSAAVRKVISDPLTYRLQIIYTQIDRDKYNNPSFKNYYFNVDGNTYFNPASTVKLPLALLSLEKLNSIHINGVDKYATLLTDSTYSKQTTAYTDSTSKNYLPSLAHYIKKAFLISDNDAYNRMYEFVGQQTINRQLHNKGYTDIRITRRFTGMNEDENRHTNAIRFVDENNKLLYTQPAAYNTDSFDFSHIVKMGNAYYDRNDSLIHKPIDFTKANNLPLESLQQLLQSALFPASVPKQQRFNLSKDDYDFLYQYLSQYPSETNYPKYDTAHYYDSYVKFYFQNEGHQMPKDVRVFNKVGWAYGFMTDVSYVVDFSSKTEFMLTATIYVNSDGILNDNKYDYDSIGVPFMYRLGQLVYNYDKQRSREFKPDLKKFMINYEKRDPTDIRPLIKDADN
>NZ_CP042435.1|WP_147192275.1|4638925_4640146_-|hypothetical-protein
MLFKDIIGQQATKQQLCEMVENNRLSHALIFLGKEGCGALPLALTFAQYVSLNPHAKQTAKEATASLFGDVEEVAAPTIPSTPEEADAFMEKNTAYSKASKLIHPDIHFSYPVIPKKSGDKPKSTDYITEWREFISMHPYGNAFDWLQFIGAENKQGNITAEECNDIIHKLSLKSFESEYKILVMWMPEYLGKEGNKLLKLIEEPPANTLFILVAENEEQILPTILSRCQLVKIPLPETSEIQEALMQRAGATEDVALQTAAIAEGNYREALQLLQHSEEDWISLLSDWLKFVIRGMLQEQVKWVDDISKLGREKQKQLLLYFNHLLEQGIRLRVMGDSLTISPKEKDFAQRINKITSVSQQQVIIEELDKATYYIERNANAKMLFHALTIKMYHIIQDKALFLTD
>NZ_CP042435.1|WP_147192276.1|4640240_4640810_-|redoxin-family-protein
MKLLIASLLFIACTSATGKNSVDVKTTDNSNPGKNIYNFTIKALDGTTIDFSQFKGKKILIVNTASKCGFTPQYEGLEKLYEAHKDKLVIVGFPSDNFGGQEYQQDTAISAFCKKNYGVTFPLTTRVDVKGDNTTPVYKYLCNKSENGVLDATISWNFNKFVIDENGNLLVHFDSKVTPDSPELLKYLN
>NZ_CP042435.1|WP_147192277.1|4640892_4642284_-|hypothetical-protein
MKTRNLIFLLITAVAVFFVACKKTTFTDSPDALLFTSIDTIHFDTVFTSVGSITQSFKIFNANDQKLRISNIELAGGGSSVFKINVDGATGTSFNNIEIPPNDSIYVFVAATINPNNNTNPFLIQDSIKIEYNTNETFVQLDAYGQNANFLNNARVTKDTTWSNALPFVILGGLTVQEGKTLTIEKGTKIYSHAGATITVNGTLKAVGEKYDSTKIIFRNDRLDDYYKDLPASWNGILFTENSINNELAFASVLNATNAIVVRNPSFNSNPKLKIEESIIDNASGAGLYGIYSSIDATNCLVSNCTDNVKIVAGGDYNFNHCTVASYSNNFLTHNSPVLLITDVDDNNQSFPLTANFINSIFYGDDGLVTDEISLQQTGNNTFNINFENVLYKGNASNANFINSIQDQDPLFTTIDAFNNIFDFHLQDISPCVNTGKSTAVSIDLDGNERDEIPDIGCYEYKP
>NZ_CP042435.1|WP_147192278.1|4642467_4643169_-|ComF-family-protein
MTKILSETFHNLMHLFFPHVCEGCGTDILDNDALLCAICHTKLPETNFIEKENNLVEQKFYGQLKVDAAGAAFYFTKEGMLQHLIKQLKYHNNKQIGFYLGRQLGNFLAQTNRFNDVDVIIPLPLNPRKEKKRGYNQAAVIAEGVNSIWQKPVNTKAVERKIFTETQTHKDRINRWQSMRNVFEVTNADELSGKNILLIDDIITTGATLEACGEKILCVPNTKLFIATVAFTI
>NZ_CP042435.1|WP_147193286.1|4643208_4644582_-|DNA-repair-protein-RadA
MSKIKTAFFCGNCGYESTKWLGKCPSCNQWNTFIEEVIDKGNSKTQDNWKTYNTEKRSTAVIALTDVTSKEEKRITTNDPELNRVLGGGIVPGSIVLVAGEPGIGKSTLMLQDALELKNIVTLYISGEESEQQIKMRADRLKISNENFYLLTETSTHIIFQEIKKLKPDFVIVDSIQTLQSDIAESSPGSITQIRECAAAFQRFAKETDTPVFLIGHITKDGTIAGPKLLEHMVDTVLQFEGDRHYAYRILRTLKNRFGSTAELGIYEMTGDGMRAVLNPSEILINQKEEQLSGSAIAASMEGMRPLLIEVQALVTQSVYGTPQRTVTGFDLRRLQLLLAVLEKRGGFQFGVKDVFVNIAGGLKVEDPSIDLSVICALLSSYEDVPLPAHICFAGEVGLNGEIRAVNRIEQRIAEAEKLGFEKIVVSKFNKKGFDKNQFKIEIVALTRVDEVYRYLF
>NZ_CP042435.1|WP_147192279.1|4645196_4648298_+|SusC/RagA-family-TonB-linked-outer-membrane-protein
MRKLLLSCWGLFFLVISYAQTTTVTGKITDEKDGTPIIGATIKSKGGRAAAISQSDGAFSITVEPGIKVLVISFIGYLDKEVTIAGPNLSITLSQSSQSLSEVVVVGYGTRLKRDITGSVAKVGAKELNNTPVTSFESAIQGRASGVYVQQQNGKLGQGINIRIRGASSVSAGNEPLYVVDGVPVITADLSSNGAQTNPLSDLNINDIQSIEILKDASAAAIYGSRASNGVVLITTKKGATGTSKIELGYFTGFQKPTGKREFLDAKQFVDYTLRAADGAANYEYGLGYYETLDDAIADWRSYAESRLTRYSAGNEDWRDVKVNTNWQDQAFQDAPISQYDLNFSGGNEKTKFYASGQYLDQDGILVRNSYKRYNGRLNLDHKVKDWLSVGMNMSFSRSQNNRVSNDDQFSTPLQIVALSPITPIIDPRTGLPSGALDLETGAPNTNYPVYYNPLLSVDGSTYKTLVNRTLGNFYGNINIVKGLTFRTEFGIDQLNQTEEAYYGTVTARNTGVPNGSGFYSSNQLLNINTNNFFQYTKTFKEKHSLDVVAGMSFQKQTVASSLADGEVFPSDAYKKLASAASKVDATSASSEFSFLSYFLRANYKFNDKYLLALSGRYDGSSRFGENNRYGFFPAASVGWIISEEHFLENVNWLSFLKLKASYGLTGNAEIGNFASRGLYSGDGAYGGAAGQRPTQIANPDLKWETTNGVDFGIEGAIFNNRIGFEVDYYERNTKDLLLDVEIPGTSGFATQLKNIGNLKNKGVEFSINTTNISSKNFKWTSTLNFGANKNKITNLGGQVLGTDVNKAKEGQPLGVFFTKEFAGADPNNGDALYYLNTVKEDGSIDHSTTNDYNAAQDVVVGNPNPDFIYGFGNTVSYKGIDLDVLLQGVYGNQIYNNGGQYMSASGSNGFDNQTTDQLGYWDKPGDISMVPEPRMFYANGTNPSSRYISNGSYLRVKAVTLGYNLPSKLMNHLKIEKARIYIRAQNLFTITNYKGWDPEVNADWSVSNINQGQDFYSAPQLKTIVFGINISL
>NZ_CP042435.1|WP_147192280.1|4648327_4649692_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein
MQKKLINILSVTALLFFFSCSKQLDTQPTQSIDETIALQTSKDVEVALVGAYSDLGASAFYGGNIFVCADLLGDYNELNWSGTYQGMTQIKNKDIPVDNGFVSDSWLAGYRAINDVNNVLSAIDVVTDDKKDKVQGEAKFIRGAVYFDLVRLFAKAWNDGDPGSNPGVPIVLTPTRDITAESQVARSSVAAVYQQAISDLQDAESLLPEENGFFATKIAAAAMLARVYLQQGDYTNAADAANRAITMAEENGYALASSYYDEFPYVSPPAPQSNSSEDIFAMQVTTSSGANDFQTYYSADGRGDITIEDAHFALYEPNDDRLSIFYSISGSSYAGKFENVYGNVRIIRLAEMYLIRAEANFRLGTSVGAAPVDDINTIRTRVLLDPLDEESLTLDAILHERKLELAFEGFTLHDAKRLEQNIGPYSWNDPKLIYPIPQREIRVNANLTQNEGYE
>NZ_CP042435.1|WP_147192281.1|4649835_4650225_-|hypothetical-protein
MFIEHLAIWCTDLEKMKTFYCSWFNATANTKYFNPVKNFSSYFLSFEKGPRLELMEMPGISNNLNDLLKQYKGLIHFAVSVGSAEEVNRLTEAMRAKGITILGEPRFTGDGYYESVVADPEGNRIEITA
>NZ_CP042435.1|WP_147192282.1|4650229_4650586_-|hypothetical-protein
MPRKENTLRKTLLRTDDEFKLSAVKDNVPGDKERVPLIKRFSPFLILFCFLLLLFPYMMITGAGNIKSFWLLLFLFPFTEVNIFYADFAIWKYFTGKKILPIWLIELTFSILIVKMLI
>NZ_CP042435.1|WP_147192283.1|4650929_4652231_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MADIFERLVKNYGPIGEHRERAHGYYAFPKLDGPIGSRMKFRGQEMIVWSLNNYLGLANHPEVRKIDADAAAEYGLALPMGARMMSGNSNYHEQLERELAEFEGKEDVILMNYGYQGIMSAIDAICGRHDVIVYDAESHACIIDGLRLHPGHRYVYKHNDIDDCEKQLQRATKLIEEQGSGGILVITEGVFGMAGDQGKLKEIAALKAKYGFRLLVDDAHGFGTLGKTGAGAGEEQGCQDAIDLYFSTFAKSMASIGAFMAGPRVIIDYIRYNIRSQIFAKSLPMPIVLGNLKRLDMLRTMPELKEKLWSNAKKLQAGLKERGFDIGKTDSPVTPVYMKGGVEEATAMVRDLRENYHIFCSIVVYPVIPKGHIIYRLIPTAAHTDSDIQETLVAFSETKAKLDAGKYKVDEIPDMAEVTGKRFDYMLDKPRNK

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP042435_5	5.1|4637385|29|NZ_CP042435|PILER-CR	4637385-4637413	29	NZ_CP034999	Rhizobium acidisoli strain FH23 plasmid pRapFH23a, complete sequence	83040-83068	5	0.828
NZ_CP042435_4	4.4|4544157|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4544157-4544192	36	MG198570	Lake Baikal phage Baikal-20-5m-C28, complete genome	72281-72316	6	0.833
NZ_CP042435_4	4.24|4545464|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4545464-4545497	34	MN693747	Marine virus AFVG_250M949, complete genome	33015-33048	8	0.765
NZ_CP042435_4	4.36|4546248|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4546248-4546283	36	MH595538	Vibrio phage BONAISHI, complete genome	122840-122875	8	0.778
NZ_CP042435_4	4.71|4548544|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4548544-4548577	34	MK448718	Streptococcus phage Javan253, complete genome	20200-20233	8	0.765
NZ_CP042435_4	4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549321-4549355	35	NZ_CP019923	Borreliella burgdorferi strain PAbe plasmid p_lp28-1, complete sequence	14934-14968	8	0.771
NZ_CP042435_4	4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549321-4549355	35	NC_018988	Borrelia burgdorferi 297 plasmid 297_lp28-1, complete sequence	9849-9883	8	0.771
NZ_CP042435_4	4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549321-4549355	35	NC_011780	Borreliella burgdorferi ZS7 plasmid ZS7_lp28-1, complete sequence	10478-10512	8	0.771
NZ_CP042435_4	4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549321-4549355	35	NC_017404	Borreliella burgdorferi JD1 plasmid JD1 lp28-1, complete sequence	9843-9877	8	0.771
NZ_CP042435_4	4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549321-4549355	35	NZ_CP019762	Borreliella burgdorferi strain B31_NRZ isolate B31 plasmid p_lp28-1	13069-13103	8	0.771
NZ_CP042435_4	4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549321-4549355	35	NC_001851	Borreliella burgdorferi B31 plasmid lp28-1, complete sequence	13190-13224	8	0.771
NZ_CP042435_4	4.122|4550166|34|NZ_CP042435|CRISPRCasFinder,CRT	4550166-4550199	34	NZ_AP017297	Nostoc sp. NIES-3756 plasmid pNOS3756_2, complete sequence	22417-22450	8	0.765
NZ_CP042435_5	5.1|4637385|29|NZ_CP042435|PILER-CR	4637385-4637413	29	NZ_CP016463	Bosea sp. RAC05 plasmid pBSY19_1, complete sequence	371309-371337	8	0.724
NZ_CP042435_3	3.1|4241092|29|NZ_CP042435|CRISPRCasFinder	4241092-4241120	29	NC_022882	Bacillus thuringiensis YBT-1518 plasmid pBMB0233, complete sequence	26252-26280	9	0.69
NZ_CP042435_4	4.13|4544746|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4544746-4544781	36	AP014317	Uncultured Mediterranean phage uvMED isolate uvMED-GF-U-MedDCM-OCT-S32-C52, *** SEQUENCING IN PROGRESS ***	9014-9049	9	0.75
NZ_CP042435_4	4.23|4545399|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4545399-4545433	35	AP013398	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C38	23321-23355	9	0.743
NZ_CP042435_4	4.39|4546445|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4546445-4546479	35	KM359505	Prochlorococcus phage P-TIM68, complete genome	35949-35983	9	0.743
NZ_CP042435_4	4.79|4549062|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549062-4549095	34	NZ_CP032928	Agrobacterium tumefaciens strain 1D1460 plasmid pAt1D1460, complete sequence	294163-294196	9	0.735
NZ_CP042435_4	4.96|4550166|35|NZ_CP042435|PILER-CR	4550166-4550200	35	NZ_AP017297	Nostoc sp. NIES-3756 plasmid pNOS3756_2, complete sequence	22417-22451	9	0.743
NZ_CP042435_4	4.110|4551079|34|NZ_CP042435|PILER-CR	4551079-4551112	34	NZ_CP022992	Paraburkholderia aromaticivorans strain BN5 plasmid pBN2, complete sequence	275436-275469	9	0.735
NZ_CP042435_4	4.136|4551078|34|NZ_CP042435|CRISPRCasFinder,CRT	4551078-4551111	34	NZ_CP022992	Paraburkholderia aromaticivorans strain BN5 plasmid pBN2, complete sequence	275436-275469	9	0.735
NZ_CP042435_4	4.148|4551855|35|NZ_CP042435|CRISPRCasFinder,CRT	4551855-4551889	35	NC_014172	Bacillus thuringiensis BMB171 plasmid pBMB171, complete sequence	204090-204124	9	0.743
NZ_CP042435_4	4.148|4551855|35|NZ_CP042435|CRISPRCasFinder,CRT	4551855-4551889	35	NZ_CP010111	Bacillus thuringiensis serovar indiana strain HD521 plasmid pBTHD521-5, complete sequence	164957-164991	9	0.743
NZ_CP042435_4	4.148|4551855|35|NZ_CP042435|CRISPRCasFinder,CRT	4551855-4551889	35	NZ_CP010091	Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence	259938-259972	9	0.743
NZ_CP042435_4	4.149|4551920|35|NZ_CP042435|CRISPRCasFinder,CRT	4551920-4551954	35	NC_014172	Bacillus thuringiensis BMB171 plasmid pBMB171, complete sequence	204090-204124	9	0.743
NZ_CP042435_4	4.149|4551920|35|NZ_CP042435|CRISPRCasFinder,CRT	4551920-4551954	35	NZ_CP010111	Bacillus thuringiensis serovar indiana strain HD521 plasmid pBTHD521-5, complete sequence	164957-164991	9	0.743
NZ_CP042435_4	4.149|4551920|35|NZ_CP042435|CRISPRCasFinder,CRT	4551920-4551954	35	NZ_CP010091	Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence	259938-259972	9	0.743
NZ_CP042435_4	4.62|4547953|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4547953-4547988	36	NZ_CP015169	Acetobacter ascendens strain LMG 1591 plasmid unnamed1, complete sequence	221375-221410	10	0.722
NZ_CP042435_4	4.62|4547953|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4547953-4547988	36	NZ_CP021512	Acetobacter pasteurianus subsp. pasteurianus strain SRCM101342 plasmid pAP1342-3, complete sequence	123195-123230	10	0.722
NZ_CP042435_4	4.20|4545203|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4545203-4545237	35	NZ_CP016317	Bacillus cereus strain M3 plasmid pBCM301, complete sequence	144748-144782	11	0.686
NZ_CP042435_4	4.20|4545203|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4545203-4545237	35	NZ_CP022446	Bacillus cereus C1L plasmid pC1L1, complete sequence	472806-472840	11	0.686
NZ_CP042435_4	4.20|4545203|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4545203-4545237	35	NC_011777	Bacillus cereus AH820 plasmid pAH820_272, complete sequence	69868-69902	11	0.686
NZ_CP042435_4	4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT	4549321-4549355	35	AP013400	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C37	8794-8828	11	0.686

1. spacer 5.1|4637385|29|NZ_CP042435|PILER-CR matches to NZ_CP034999 (Rhizobium acidisoli strain FH23 plasmid pRapFH23a, complete sequence) position: , mismatch: 5, identity: 0.828

ctgtcac-cgccaccttgctggggaggtcc	CRISPR spacer
-ggtctcgcgccaccttgctgtggaggtcg	Protospacer
  *** * ************* ******* 

2. spacer 4.4|4544157|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to MG198570 (Lake Baikal phage Baikal-20-5m-C28, complete genome) position: , mismatch: 6, identity: 0.833

tgtagattaaaccatgcagttttataagca-gatgaa	CRISPR spacer
tctggatcgaaccatgcagttttataagcaccatga-	Protospacer
* *.***..*********************  **** 

3. spacer 4.24|4545464|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to MN693747 (Marine virus AFVG_250M949, complete genome) position: , mismatch: 8, identity: 0.765

ttaaatgctttgtggatataacaaccaacagcaa	CRISPR spacer
ttaaatgctttgtggataaaataatcttaatgaa	Protospacer
****************** **.**.*   *  **

4. spacer 4.36|4546248|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to MH595538 (Vibrio phage BONAISHI, complete genome) position: , mismatch: 8, identity: 0.778

agtcctttatcaacgccattaaactttggaagtatt	CRISPR spacer
agtcccttatcaacgccatgaaacttgttatccatt	Protospacer
*****.************* ******   *  .***

5. spacer 4.71|4548544|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to MK448718 (Streptococcus phage Javan253, complete genome) position: , mismatch: 8, identity: 0.765

-atatttacccattcaaggccatctattgtaccct	CRISPR spacer
gata-cagtctattcaagcccatctattgtatcct	Protospacer
 *** . ..*.******* ************.***

6. spacer 4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP019923 (Borreliella burgdorferi strain PAbe plasmid p_lp28-1, complete sequence) position: , mismatch: 8, identity: 0.771

tgaaaaaaataattgtatttctgtttttaataaac	CRISPR spacer
ctacatctataaatgtatttctatttttaataaac	Protospacer
. * *   **** *********.************

7. spacer 4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NC_018988 (Borrelia burgdorferi 297 plasmid 297_lp28-1, complete sequence) position: , mismatch: 8, identity: 0.771

tgaaaaaaataattgtatttctgtttttaataaac	CRISPR spacer
ctacatctataaatgtatttctatttttaataaac	Protospacer
. * *   **** *********.************

8. spacer 4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NC_011780 (Borreliella burgdorferi ZS7 plasmid ZS7_lp28-1, complete sequence) position: , mismatch: 8, identity: 0.771

tgaaaaaaataattgtatttctgtttttaataaac	CRISPR spacer
ctacatctataaatgtatttctatttttaataaac	Protospacer
. * *   **** *********.************

9. spacer 4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NC_017404 (Borreliella burgdorferi JD1 plasmid JD1 lp28-1, complete sequence) position: , mismatch: 8, identity: 0.771

tgaaaaaaataattgtatttctgtttttaataaac	CRISPR spacer
ctacatctataaatgtatttctatttttaataaac	Protospacer
. * *   **** *********.************

10. spacer 4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP019762 (Borreliella burgdorferi strain B31_NRZ isolate B31 plasmid p_lp28-1) position: , mismatch: 8, identity: 0.771

tgaaaaaaataattgtatttctgtttttaataaac	CRISPR spacer
ctacatctataaatgtatttctatttttaataaac	Protospacer
. * *   **** *********.************

11. spacer 4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NC_001851 (Borreliella burgdorferi B31 plasmid lp28-1, complete sequence) position: , mismatch: 8, identity: 0.771

tgaaaaaaataattgtatttctgtttttaataaac	CRISPR spacer
ctacatctataaatgtatttctatttttaataaac	Protospacer
. * *   **** *********.************

12. spacer 4.122|4550166|34|NZ_CP042435|CRISPRCasFinder,CRT matches to NZ_AP017297 (Nostoc sp. NIES-3756 plasmid pNOS3756_2, complete sequence) position: , mismatch: 8, identity: 0.765

cattttattgattacgaagttggcacggtaaaga	CRISPR spacer
ttttttatttactacgaagttggcacgaagaagc	Protospacer
. ******* *.***************. .*** 

13. spacer 5.1|4637385|29|NZ_CP042435|PILER-CR matches to NZ_CP016463 (Bosea sp. RAC05 plasmid pBSY19_1, complete sequence) position: , mismatch: 8, identity: 0.724

ctgtcaccgccaccttgctggggaggtcc	CRISPR spacer
gcttcaccgccaccttgccggggacgaag	Protospacer
 . ***************.***** *   

14. spacer 3.1|4241092|29|NZ_CP042435|CRISPRCasFinder matches to NC_022882 (Bacillus thuringiensis YBT-1518 plasmid pBMB0233, complete sequence) position: , mismatch: 9, identity: 0.69

ctgagagacgatgctaaactgaaaccatg	CRISPR spacer
tcgagagaggatgctaaactgaattggaa	Protospacer
..****** ************** . . .

15. spacer 4.13|4544746|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to AP014317 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-U-MedDCM-OCT-S32-C52, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 9, identity: 0.75

tgggatttaaactatgactttgataaagatggtgta	CRISPR spacer
ttcgaagaaaaatatgactttgatgaagatggtgat	Protospacer
*  **   *** ************.*********  

16. spacer 4.23|4545399|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to AP013398 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C38) position: , mismatch: 9, identity: 0.743

ttgaaacagtttcacaaactgcatttgaacatggc	CRISPR spacer
ttgcaacactttcacaaactgcattaccagatcca	Protospacer
*** **** ****************   * **   

17. spacer 4.39|4546445|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to KM359505 (Prochlorococcus phage P-TIM68, complete genome) position: , mismatch: 9, identity: 0.743

aataaactgttccagtctctttttcggtcctgcca	CRISPR spacer
caaaaactgttacagtctctttttgggtaaaagca	Protospacer
 * ******** ************ ***   . **

18. spacer 4.79|4549062|34|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP032928 (Agrobacterium tumefaciens strain 1D1460 plasmid pAt1D1460, complete sequence) position: , mismatch: 9, identity: 0.735

tggattctaccatgccaaacggcgttgatgtgaa	CRISPR spacer
tggcgaaatccatgccaaagggcgttgatgggag	Protospacer
***      ********** ********** **.

19. spacer 4.96|4550166|35|NZ_CP042435|PILER-CR matches to NZ_AP017297 (Nostoc sp. NIES-3756 plasmid pNOS3756_2, complete sequence) position: , mismatch: 9, identity: 0.743

acattttattgattacgaagttggcacggtaaaga	CRISPR spacer
tttttttatttactacgaagttggcacgaagaagc	Protospacer
 . ******* *.***************. .*** 

20. spacer 4.110|4551079|34|NZ_CP042435|PILER-CR matches to NZ_CP022992 (Paraburkholderia aromaticivorans strain BN5 plasmid pBN2, complete sequence) position: , mismatch: 9, identity: 0.735

ttatttggttctgcagtttccggaacaaattcta	CRISPR spacer
tgcccttggtctgccgtttccggaacagattctc	Protospacer
*  ..* * ***** ************.***** 

21. spacer 4.136|4551078|34|NZ_CP042435|CRISPRCasFinder,CRT matches to NZ_CP022992 (Paraburkholderia aromaticivorans strain BN5 plasmid pBN2, complete sequence) position: , mismatch: 9, identity: 0.735

ttatttggttctgcagtttccggaacaaattcta	CRISPR spacer
tgcccttggtctgccgtttccggaacagattctc	Protospacer
*  ..* * ***** ************.***** 

22. spacer 4.148|4551855|35|NZ_CP042435|CRISPRCasFinder,CRT matches to NC_014172 (Bacillus thuringiensis BMB171 plasmid pBMB171, complete sequence) position: , mismatch: 9, identity: 0.743

aaatgttttaatgatagattcaaacggtataataa	CRISPR spacer
tcctattttaacgattgattcaaacggtatcgtat	Protospacer
   *.******.*** ************** .** 

23. spacer 4.148|4551855|35|NZ_CP042435|CRISPRCasFinder,CRT matches to NZ_CP010111 (Bacillus thuringiensis serovar indiana strain HD521 plasmid pBTHD521-5, complete sequence) position: , mismatch: 9, identity: 0.743

aaatgttttaatgatagattcaaacggtataataa	CRISPR spacer
tcctattttaacgattgattcaaacggtatcgtat	Protospacer
   *.******.*** ************** .** 

24. spacer 4.148|4551855|35|NZ_CP042435|CRISPRCasFinder,CRT matches to NZ_CP010091 (Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence) position: , mismatch: 9, identity: 0.743

aaatgttttaatgatagattcaaacggtataataa	CRISPR spacer
tcctattttaacgattgattcaaacggtatcgtat	Protospacer
   *.******.*** ************** .** 

25. spacer 4.149|4551920|35|NZ_CP042435|CRISPRCasFinder,CRT matches to NC_014172 (Bacillus thuringiensis BMB171 plasmid pBMB171, complete sequence) position: , mismatch: 9, identity: 0.743

aaatgttttaatgatagattcaaacggtataataa	CRISPR spacer
tcctattttaacgattgattcaaacggtatcgtat	Protospacer
   *.******.*** ************** .** 

26. spacer 4.149|4551920|35|NZ_CP042435|CRISPRCasFinder,CRT matches to NZ_CP010111 (Bacillus thuringiensis serovar indiana strain HD521 plasmid pBTHD521-5, complete sequence) position: , mismatch: 9, identity: 0.743

aaatgttttaatgatagattcaaacggtataataa	CRISPR spacer
tcctattttaacgattgattcaaacggtatcgtat	Protospacer
   *.******.*** ************** .** 

27. spacer 4.149|4551920|35|NZ_CP042435|CRISPRCasFinder,CRT matches to NZ_CP010091 (Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence) position: , mismatch: 9, identity: 0.743

aaatgttttaatgatagattcaaacggtataataa	CRISPR spacer
tcctattttaacgattgattcaaacggtatcgtat	Protospacer
   *.******.*** ************** .** 

28. spacer 4.62|4547953|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP015169 (Acetobacter ascendens strain LMG 1591 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.722

ttccttgcggatagctgtttagctgcaacatttaca	CRISPR spacer
cagagtaacgatagctgtttagctgcaccattttca	Protospacer
.    *.  ****************** ***** **

29. spacer 4.62|4547953|36|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021512 (Acetobacter pasteurianus subsp. pasteurianus strain SRCM101342 plasmid pAP1342-3, complete sequence) position: , mismatch: 10, identity: 0.722

ttccttgcggatagctgtttagctgcaacatttaca	CRISPR spacer
cagagtaacgatagctgtttagctgcaccattttca	Protospacer
.    *.  ****************** ***** **

30. spacer 4.20|4545203|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP016317 (Bacillus cereus strain M3 plasmid pBCM301, complete sequence) position: , mismatch: 11, identity: 0.686

ttaactaagacagaaatagaaagcgtgaacaatgc	CRISPR spacer
cggatggttacagaaatagaaagagtgaataatgg	Protospacer
. .*. .  ************** *****.**** 

31. spacer 4.20|4545203|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP022446 (Bacillus cereus C1L plasmid pC1L1, complete sequence) position: , mismatch: 11, identity: 0.686

ttaactaagacagaaatagaaagcgtgaacaatgc	CRISPR spacer
cggatggttacagaaatagaaagagtgaataatgg	Protospacer
. .*. .  ************** *****.**** 

32. spacer 4.20|4545203|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to NC_011777 (Bacillus cereus AH820 plasmid pAH820_272, complete sequence) position: , mismatch: 11, identity: 0.686

ttaactaagacagaaatagaaagcgtgaacaatgc	CRISPR spacer
cggatggttacagaaatagaaagagtgaataatgg	Protospacer
. .*. .  ************** *****.**** 

33. spacer 4.83|4549321|35|NZ_CP042435|PILER-CR,CRISPRCasFinder,CRT matches to AP013400 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S30-C37) position: , mismatch: 11, identity: 0.686

tgaaaaaaataattgtatttctgtttttaataaac	CRISPR spacer
cttaccaaataattctacttctgtttttaatccta	Protospacer
.  *  ******** **.*************