CRISPRimmunity

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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_CP045118	Pseudomonas sp. SCB32 chromosome, complete genome	5 crisprs	DinG,DEDDh,cas3,csa3	0	1	5	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP045118_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP045118_1

169147-169329

Orphan

Consensus_repeat	Method
GGGGATCGGCTTGGGCGGCGGCGG	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP045118_1

>merge|NZ_CP045118|1|169147-169329|CRISPRCasFinder
GGTTTCGGCCTTGGGCGGCGTCGGTTGCTCAACCGGCTTGGACACGGGCTTGGGCTTGGCCACCGGTTTCGGCTTGGGTTTGGGGATCGGCTTGGGCGGCGGCGGTTGCACCGCGTTCTCGTCCACCACCGGAGGCGGCGGCTCCTGCACGATTGGCTCGGGGATCGGCTCGGGCGGCGGCGG

>NZ_CP045118|1|1|169147-169329|CRISPRCasFinder
GGTTTCGGCCTTGGGCGGCGTCGG	TTGCTCAACCGGCTTGGACACGGGCTTGGGCTTGGCCACCGGTTTCGGCTTGGGTTT
GGGGATCGGCTTGGGCGGCGGCGG	TTGCACCGCGTTCTCGTCCACCACCGGAGGCGGCGGCTCCTGCACGATTGGCTC
GGGGATCGGCTCGGGCGGCGGCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045118.1\|WP_152219053.1\|175337_176267_+\|zinc-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|226908
NZ_CP045118.1\|WP_152219025.1\|164475_165873_-\|amidase	unknown	unknown	gnl\|CDD\|235915
NZ_CP045118.1\|WP_152219026.1\|165974_166556_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|369095
NZ_CP045118.1\|WP_152219041.1\|171543_172554_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|236863
NZ_CP045118.1\|WP_152219044.1\|172762_173140_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP045118.1\|WP_152219028.1\|166675_167329_-\|gamma-glutamylcyclotransferase	unknown	unknown	gnl\|CDD\|226226
NZ_CP045118.1\|WP_152219031.1\|167644_168046_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|223917
NZ_CP045118.1\|WP_152219049.1\|173959_174760_-\|zinc-ABC-transporter-ATP-binding-protein-ZnuC	unknown	unknown	gnl\|CDD\|181939
NZ_CP045118.1\|WP_152219051.1\|174759_175266_-\|transcriptional-repressor	unknown	unknown	gnl\|CDD\|223806
NZ_CP045118.1\|WP_152219017.1\|158586_160011_-\|xanthine-dehydrogenase-small-subunit	unknown	unknown	gnl\|CDD\|274365
NZ_CP045118.1\|WP_152219033.1\|168047_168764_-\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|223881
NZ_CP045118.1\|WP_152219019.1\|160395_160959_+\|peroxiredoxin	unknown	unknown	gnl\|CDD\|211789
NZ_CP045118.1\|WP_152219039.1\|170881_171547_-\|methionine-ABC-transporter-permease-MetI	unknown	unknown	gnl\|CDD\|224922
NZ_CP045118.1\|WP_152219047.1\|173178_173967_-\|zinc-ABC-transporter-permease-subunit-ZnuB	unknown	unknown	gnl\|CDD\|181938
NZ_CP045118.1\|WP_152219056.1\|178999_179686_+\|NrdJb	unknown	unknown	gnl\|CDD\|236330
NZ_CP045118.1\|WP_152219015.1\|156254_158594_-\|xanthine-dehydrogenase-molybdopterin-binding-subunit	unknown	unknown	gnl\|CDD\|274367
NZ_CP045118.1\|WP_152219023.1\|162999_164433_-\|cardiolipin-synthase	unknown	unknown	gnl\|CDD\|234967
NZ_CP045118.1\|WP_152219037.1\|170057_170840_-\|methionine-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270315
NZ_CP045118.1\|WP_152219021.1\|161159_162725_+\|alkyl-hydroperoxide-reductase-subunit-F	unknown	unknown	gnl\|CDD\|237942
NZ_CP045118.1\|WP_152219055.1\|176833_178981_+\|adenosylcobalamin-dependent-ribonucleoside-diphosphate-reductase	unknown	unknown	gnl\|CDD\|274168

Protein	Function_ID	Function_description	E-value
NZ_CP045118.1\|WP_152219053.1\|175337_176267_+\|zinc-ABC-transporter-substrate-binding-protein	gnl\|CDD\|226908	COG4531, ZnuA, ABC-type Zn2+ transport system, periplasmic component/surface adhesin [Inorganic ion transport and metabolism].	7.5326e-135
NZ_CP045118.1\|WP_152219025.1\|164475_165873_-\|amidase	gnl\|CDD\|235915	PRK07042, PRK07042, amidase; Provisional.	0
NZ_CP045118.1\|WP_152219026.1\|165974_166556_-\|alpha/beta-hydrolase	gnl\|CDD\|369095	pfam06821, Ser_hydrolase, Serine hydrolase. Members of this family have serine hydrolase activity. They contain a conserved serine hydrolase motif, GXSXG/A, where the serine is a putative nucleophile. This family has an alpha-beta hydrolase fold. Eukaryotic members of this family have a conserved LXCXE motif, which binds to retinoblastomas. This motif is absent from prokaryotic members of this family.	1.39254e-75
NZ_CP045118.1\|WP_152219041.1\|171543_172554_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|236863	PRK11153, metN, DL-methionine transporter ATP-binding subunit; Provisional.	0
NZ_CP045118.1\|WP_152219028.1\|166675_167329_-\|gamma-glutamylcyclotransferase	gnl\|CDD\|226226	COG3703, ChaC, Uncharacterized protein involved in cation transport [Inorganic ion transport and metabolism].	2.1936e-53
NZ_CP045118.1\|WP_152219031.1\|167644_168046_-\|biopolymer-transporter-ExbD	gnl\|CDD\|223917	COG0848, ExbD, Biopolymer transport protein [Intracellular trafficking and secretion].	1.78247e-45
NZ_CP045118.1\|WP_152219049.1\|173959_174760_-\|zinc-ABC-transporter-ATP-binding-protein-ZnuC	gnl\|CDD\|181939	PRK09544, znuC, high-affinity zinc transporter ATPase; Reviewed.	2.55703e-117
NZ_CP045118.1\|WP_152219051.1\|174759_175266_-\|transcriptional-repressor	gnl\|CDD\|223806	COG0735, Fur, Fe2+/Zn2+ uptake regulation proteins [Inorganic ion transport and metabolism].	3.55154e-38
NZ_CP045118.1\|WP_152219017.1\|158586_160011_-\|xanthine-dehydrogenase-small-subunit	gnl\|CDD\|274365	TIGR02963, Includes:_Xanthine_dehydrogenase, xanthine dehydrogenase, small subunit. Members of this protein family are the small subunit (or, in eukaryotes, the N-terminal domain) of xanthine dehydrogenase, an enzyme of purine catabolism via urate. The small subunit contains both an FAD and a 2Fe-2S cofactor. Aldehyde oxidase (retinal oxidase) appears to have arisen as a neofunctionalization among xanthine dehydrogenases in eukaryotes and [Purines, pyrimidines, nucleosides, and nucleotides, Other].	0
NZ_CP045118.1\|WP_152219033.1\|168047_168764_-\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|223881	COG0811, TolQ, Biopolymer transport proteins [Intracellular trafficking and secretion].	4.63478e-55
NZ_CP045118.1\|WP_152219019.1\|160395_160959_+\|peroxiredoxin	gnl\|CDD\|211789	TIGR03137, AhpC, peroxiredoxin. This peroxiredoxin (AhpC, alkylhydroperoxide reductase subunit C) is one subunit of a two-subunit complex with subunit F(TIGR03140). Usually these are found as an apparent operon. The gene has been characterized in Bacteroides fragilis, where it is important in oxidative stress defense. This gene contains two invariant cysteine residues, one near the N-terminus and one near the C-terminus, each followed immediately by a proline residue. [Cellular processes, Detoxification, Cellular processes, Adaptations to atypical conditions].	6.62359e-124
NZ_CP045118.1\|WP_152219039.1\|170881_171547_-\|methionine-ABC-transporter-permease-MetI	gnl\|CDD\|224922	COG2011, AbcD, ABC-type metal ion transport system, permease component [Inorganic ion transport and metabolism].	1.18166e-106
NZ_CP045118.1\|WP_152219047.1\|173178_173967_-\|zinc-ABC-transporter-permease-subunit-ZnuB	gnl\|CDD\|181938	PRK09543, znuB, zinc ABC transporter permease subunit ZnuB.	3.97902e-95
NZ_CP045118.1\|WP_152219056.1\|178999_179686_+\|NrdJb	gnl\|CDD\|236330	PRK08665, PRK08665, vitamin B12-dependent ribonucleotide reductase.	5.50101e-11
NZ_CP045118.1\|WP_152219015.1\|156254_158594_-\|xanthine-dehydrogenase-molybdopterin-binding-subunit	gnl\|CDD\|274367	TIGR02965, xanthine_dehydrogenase, xanthine dehydrogenase, molybdopterin binding subunit. Members of the protein family are the molybdopterin-containing large subunit (or, in, eukaryotes, the molybdopterin-binding domain) of xanthine dehydrogenase, and enzyme that reduces the purine pool by catabolizing xanthine to urate. This model is based primarily on bacterial sequences; it does not manage to include all eukaryotic xanthine dehydrogenases and thereby discriminate them from the closely related enzyme aldehyde dehydrogenase. [Purines, pyrimidines, nucleosides, and nucleotides, Other].	0
NZ_CP045118.1\|WP_152219023.1\|162999_164433_-\|cardiolipin-synthase	gnl\|CDD\|234967	PRK01642, cls, cardiolipin synthetase; Reviewed.	0
NZ_CP045118.1\|WP_152219037.1\|170057_170840_-\|methionine-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270315	cd13597, PBP2_lipoprotein_Tp32, The substrate-binding domain of the 32-kilodalton lipoprotein (Tp32) from Treponema pallidum binds L-methionine; the type 2 periplasmic-binding protein fold. This group includes the lipoprotein Tp32, a periplasmic component of a methionine uptake transporter system, and its closely related homologs. The Tp32 has both structural and sequential homology to the MetQ family of substrate-binding protein, and thus it belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea.	1.595e-131
NZ_CP045118.1\|WP_152219021.1\|161159_162725_+\|alkyl-hydroperoxide-reductase-subunit-F	gnl\|CDD\|237942	PRK15317, PRK15317, alkyl hydroperoxide reductase subunit F; Provisional.	0
NZ_CP045118.1\|WP_152219055.1\|176833_178981_+\|adenosylcobalamin-dependent-ribonucleoside-diphosphate-reductase	gnl\|CDD\|274168	TIGR02504, ribonucleotide_reductase, ribonucleoside-diphosphate reductase, adenosylcobalamin-dependent. This model represents a group of adenosylcobalamin(B12)-dependent ribonucleotide reductases (Class II RNRs) related to the characterized species from Pyrococcus, Thermoplasma, Corynebacterium, and Deinococcus. RNR's are responsible for the conversion of the ribose sugar of RNA into the deoxyribose sugar of DNA. This is the rate-limiting step of DNA biosynthesis. This model identifies genes in a wide range of deeply branching bacteria. All are structurally related to the class I (non-heme iron dependent) RNRs. In most species this gene is known as NrdJ, while in mycobacteria it is called NrdZ. [Purines, pyrimidines, nucleosides, and nucleotides, 2'-Deoxyribonucleotide metabolism].	0

>NZ_CP045118.1|WP_152219033.1|168047_168764_-|MotA/TolQ/ExbB-proton-channel-family-protein
MSLPVSPLESVEGAAIWLLVGFSVATWALALVKGVQFTRQKSQDKRFQKQFWSATSLESAGDQAAGKPGAGARVAQAGFAAIQVQDNGQPDLAQSINHQDRLERALRQQIQRERRSLESGLAVLASIGSTSPFIGLFGTVWGIMEALKGISAAGSASLETVAGPIGSALIATGVGIAVAVPAVLVYNYFLRRLKLTAADLDDFAHDFYSLAQKSAFRVIALPTAARKPAAGANVKEAS
>NZ_CP045118.1|WP_152219031.1|167644_168046_-|biopolymer-transporter-ExbD
MAFSTQDSDEVLSEINVTPLVDVMLVLLVVFIVTAPLLTNAIPINLPKTEAVAPPEQKDPLVVSIDGAGKWFINKDEVQPEQLQTNLAAAKAKDAELRVQLQADEGVNYGQVAKAMASIEKAGITRLAVITAR
>NZ_CP045118.1|WP_152219028.1|166675_167329_-|gamma-glutamylcyclotransferase
MTSSPALDGPFYPPTLGVPERFTPQQLRASLDITMGEHGAGPVWLFAYGSLIWRPEFPVAEARRARVHGYHRGLYLWSLTHRGTPEAPGLVLGLDRGGSCSGFAFRLPEDNLDANLYALWEREMPYASYRPEWLSCRLDDGTRVRALGFVLERHLPSYAGALPDNIVQHVLDSAQGHFGTTRDYVEQTAKVLRDYAMPDLNLEGILARCCPLHRVQD
>NZ_CP045118.1|WP_152219026.1|165974_166556_-|alpha/beta-hydrolase
MRNERIRYLIVPGWHGSEDAHWQSHWQRALPNAARVQQRDWINPQRADWVAKLDHEIRREPGRVVLVAHSLGCVTVAAWAARADRRVLAQVSGALLVAPADVERETCHEALVNFAPIARQTLPFPTVLVGSDNDAACSPQRAMILGRAWGAETVILPSAGHINVKSGHGAWESGYRHLYRLQYLIDQQSRQRA
>NZ_CP045118.1|WP_152219025.1|164475_165873_-|amidase
MPPLHDLSAVELLALYRSHQLSPVEYLKHLIAHIERWEPQLCALYAFDPQRALEQARRSEARWIRCAPCGELDGVPVTIKELIATSGDPIPLGSAATLLQPATSDAPPAARMFEAGAILLGKTTVPDYGMLSSGLSSFHKLARNPWDLRMSPGGSSAGAASAAAAGYGPLHIGTDIGGSVRLPAGWCGLVGFKPSLGRIPIDPYYTGRCAGPMTRTLDDATLMMQHLSRPDWRDATALPAADLDWHIQPADVRGLRIGLQLDPGCGLQPEPEVRAAVEAAARRFAEAGAEIVEVRPILDRELLEGLDRFWRARLWAELENLPAERQAKVLPYIYQWAEGGASVSGTEAVRGFNRTFEMRRRAAEQFHGIDFLLSPTNQVAAFPAEFASPTNDPARPFEHIGFTVPWNMTEQPALSINCDFTAEGMPIGLQIVGPRFADVEVLRLGKAWERWRGPVPHWPQPPGTD
>NZ_CP045118.1|WP_152219023.1|162999_164433_-|cardiolipin-synthase
MQYSSYIAHLLVLIQLLGIVAAVHAVLTVRTAQGAIAWATSLVFMPLLTLVPYLVFGRSRFDAYIGARRQANEEMHVAAAELDWRPWVEEALAARQYDGYKGLKAMVGLARMPTLANNQVRLLVNGKASFDAMFEAISAAKKAVLVQFFIIRDDALGQRLAQLLLERAANGVDVFLLYDGIGSHALPGRYVEKLRNGGVQVHAFSTGSGMINRFQVNFRNHRKIVVVDGVRGFVGGHNVGVEYLGEKPPLSPWRDTHIELRGPAVACLQECFAEDWYWASHTLPTLILPKAYEDSGMLCQVVPSGPADPQETCSLFFVEAINAAMERIWITTPYFVPDEAVAAALRLAVLRGVDVRILLPSRPDHRTVYAASSLYALDAVRAGLRIFRYQPGFLHQKVVLIDHDTAAVGSANLDNRSFRLNFEIMVVTVDEGFAQEVEQMLEADFERSVEMTLDDRKRLHRLQQLGMRVARLVSPIL
>NZ_CP045118.1|WP_152219021.1|161159_162725_+|alkyl-hydroperoxide-reductase-subunit-F
MLDATLKTQLKAYLERVTQPFEIVASLDDGEKSRELSELLHEIVGLTDKITLREDGSDARVPSFALNRPGANIGLAFAGIPMGHEFTSLVLALLQVGGHPSKLEADVIEQIKGIQGSFEFETYFSLSCQNCPDVVQALNLMAVLNPNIRHVAIDGALFQDEVDRRQVMAVPSIYLNGEVFGQGRMGVEEILAKIDTGAAAREAEKLSAKEEFDVLVVGGGPAGAAAAIYAARKGIRTGVAAERFGGQVLDTMAIENFISVTETEGPKLARQLEEHVRHYDVDIMNLQRASALIPAKTAGGLHEVQFEGGGSLKAKSVILATGARWREMGVPGEKEYKAKGVCFCPHCDGPLFKGKRVAVIGGGNSGVEAAIDLAGIVSHVTLLEFDSKLRADAVLQRKLFSLPNVDVITSALTSEVKGDGQKVTGLVYKDRNSEEFKSVDLEGIFVQIGLLPNSDWLKGTLELTPRGEIIVDARGETSLPGIFAAGDVTTVPYKQIVIAVGEGAKASLSAFDHLIRSSAPA
>NZ_CP045118.1|WP_152219019.1|160395_160959_+|peroxiredoxin
MNLINTTVQPFKVNAFHNGKFIEVTEQSLKGKWSVLIFMPAAFTFNCPTEIEDAANNYAAFRDAGTEVYIVTTDTHFSHKVWHETSPAVGKAQFPLIGDPTHQLTNAFGVHIPEEGLALRGTFVINPEGVIKTVEIHSNEIARDVGETLRKLKAAQYTAAHPGEVCPAKWKEGEKTLAPSLDLVGKI
>NZ_CP045118.1|WP_152219017.1|158586_160011_-|xanthine-dehydrogenase-small-subunit
MILFLLGDELIRADGAAPETSLLDYLRGHLGRTGTKEGCASGDCGACTVVLVEADGEALRYRAVNACITLLGAVHGRQVLTVEHLSEGGALHPAQQAMVDCHGSQCGFCTPGIVMSLFAWRHSPPPHDRDTALTALSGNLCRCTGYRPILDAAAQIAAQPCADRFAQHAALTFARLRELPATGTLHEGEQQAWLPTSLEELDELLQRQPQARLIAGGTDLALEATQNLKAFPALIHLDRVSALQRLEAHPDHLLIGAARPYADCLEALAEFPGVAALLERLGSLQIRQRGTLGGNIANASPIGDMPPVLLALDARLRLRRAGSVREVPIDGFFTGYRKTLLQPGEYIESVLIPRLRAHQRLRVDKISKRRDDDISAVCMALRLDLDDAGIVTDARLACGGMAATPLRGARTEAALRGKPFDAAAVAAAQAAVPQDFQPIDDLRASAAYRLKVAQNLLQRALLEWTQSPAEVRHA
>NZ_CP045118.1|WP_152219015.1|156254_158594_-|xanthine-dehydrogenase-molybdopterin-binding-subunit
MRSLPPLASNGVAVAVHSAGQAREHDSAVLHVSGAARYVDDLKEPRELLHAAVGMTSIACGAVLSLDLDAVRAAPGVVAVLTLDDVPGHTDIGPVFPGDPLLAGDRVKYHGQALFAVAAETLIQARRAVRLAKVEYAEERALLDPLQAKAEERFVRPPHHMHRGDAEAALDTAPHVLEARQFVGGQEHFYLEGQASLALPADDGGMLVHTSSQHPSEVQKLVAEVLAIPLAKVTVEVRRMGGGFGGKETQAAPFACLAALLARKTGRAVKLRLPRADDMRLTGKRHPFHNRYRIGFDDEGRLLAAQLEVVGDCGHSPDLSDAIVDRAMFHADNAYFIPDVAISGYRSFTNIVSHTAFRGFGGPQGMMIIERAVDDIARAVGKDPLEIRKLNLYGGMGRELTPYHQKVEHNLLGELIARLEQSSDYHARRSAIHAVNASSPVLKKGLALTPVKFGISFTAQHLNQAGALIHLYTDGSIQLNHGGTEMGQGLNTKVAQIVAEEFQVPLECVAITATRTDKVPNTSPTAASSGTDLNGMAARDAARTLKKRLAEFLAERDGVKPQEVRFEHGGVTIGGQHLGFAEVIQAAYFARIQLSATGFYRTPKIFYDREKGQGHPFFYFAYGAAVSEVDVDTLTGEYRVRRVDILHDVGRSVNPAIDIGQIEGGFVQGMGWLTTEDLRWDEAGRLLTVGPATYKIPAVSDMPEDFRVALFDRPNEEDSVYLSKAVGEPPFMLAISVWSALRDAIASLADYRVSPDLDTPATPERVLWACEALRKEKRS
>NZ_CP045118.1|WP_152219037.1|170057_170840_-|methionine-ABC-transporter-substrate-binding-protein
MKKLLAACAAAAALSAPLAQAADSLTVAATPVPHAEILNFVKPILAKEGVELKVKEFTDYVQPNTQVAEKRLDANFFQHQPYLDEFNKTKGTHLVAVTGVHIEPLGAYSTKFKKLEELPSGATVVIPNDATNGGRALLLLDKAGVIKLKDNKSITATPKDIALNPKNIKVRELEAATLPRVLTQVDLALINTNYALEAKLNPTKDALAIEGSDSPYVNILVARPDNKDSAAMQKLAAALHSPEVKQFILEKYKGAVVPAF
>NZ_CP045118.1|WP_152219039.1|170881_171547_-|methionine-ABC-transporter-permease-MetI
MNEFFSNIDWSEILQASIDTFWMLGGSLLFTIVLGLPLGVLLFLTGPKQMFENRAVYALLSFVVNVLRSLPFIILLIVMIPFTVLITGTSLGVAGAIPPLVVGATPFFARLVETALREVDKGIIEATQAMGASTRQIIWNALLPEARPGIIAAITVTAITLVSYTAMAGVVGAGGLGDLAIRFGYQRFQTDVMVVTVVMLLVLVQILQTVGDKLVVHYSRK
>NZ_CP045118.1|WP_152219041.1|171543_172554_-|ATP-binding-cassette-domain-containing-protein
MIEFHDVHKTYRVAGRDIPALQPTRLTIEGGQVFGLIGHSGAGKSTLLRLINRLEEPSGGRIVIDGEDITALDADGLRRFRQRVGMIFQHFNLLASKTVADNIAMPMKLAGTYSAAEVTARVDELLDRVGLKDHARKYPAQLSGGQKQRVGIARALACRPKILLCDEATSALDPQTTGQVLQLLAEINRELKLTIVLITHEMDVIRRVCDQVAVMDAGRIVEQGDVADVFLHPQHETTRRFVFEAERVDEDEQHDDFAHVPGRILRLTFRGEATYAPLLGTVARQTGVDYSILAGRIDRIKDQPYGQLTLSLVGGDIEAAMAQLNAAEVHVEVLRA
>NZ_CP045118.1|WP_152219044.1|172762_173140_-|hypothetical-protein
MKSFVIRLFSLMALALALTACQSTASTPASSSGFETELAAGRLESAQLALGSEHEDAAQLAERRKRLADAYLERSRKALQNGDVNGASANLSRARSLMPRAPGVAADVSGLRKPATPASQPTCTP
>NZ_CP045118.1|WP_152219047.1|173178_173967_-|zinc-ABC-transporter-permease-subunit-ZnuB
MADFLLNALLAGLALALVAGPLGSFVVWRRMAYFGDTLSHAALLGVALGFLLDVSPTLAVTVGCILLAVLLVTLQQRQPLAADTLLGILAHSTLSLGLVTLSFMKEVRVDLMAYLFGDLLAVSQTDLLWIVAGSALVLGLICWLWRPLLAITVHEELARVEGLPVTAIRLALMLLIAIVIAVAMKIVGVLLITSLLIIPAAAAQRHARSPEQMAFGASLIGLIAVCAGLSLSWFKDTPAGPSIVVSAAALFLLSFVLPRRTV
>NZ_CP045118.1|WP_152219049.1|173959_174760_-|zinc-ABC-transporter-ATP-binding-protein-ZnuC
MSDTLIRLQGVGVSYAGQAVLLNVDLTIAPGEIVTLIGPNGAGKTTLVRSVLGLLKPDSGSVWRRPKLSIGYMPQKLHVDPTLPLTVLRFLRLVPGVQRSQALEALKEVGAAHVIDKPLQGVSGGELQRVLLARALLRKPELLVLDEPVQGVDVAGQAELYRLIGRLRDRLGCGVLMVSHDLHLVMSATDKVVCLNRHVCCSGHPEQVSGDPAFVELFGQDARSLAVYHHHHDHSHDLHGEVVKPAFPAGTRFTPVHQHGPDCNHG
>NZ_CP045118.1|WP_152219051.1|174759_175266_-|transcriptional-repressor
MYKIAPKTPLACRPHDHANCVASALADADALCARQGVRLTELRRRVLELVWQSHRPLGAYDILAVLSEEDGRKAAPPTVYRALDFLLENGLVHRIASLNAFIGCAHPEHAHEGQFLICRTCHTAIELEQPAISEAIVTGARSVGFSVETQTVEVVGLCGACAPGKREA
>NZ_CP045118.1|WP_152219053.1|175337_176267_+|zinc-ABC-transporter-substrate-binding-protein
MSFRPAALLITCCALLLSLPARAEVSVLTSIKPLQLIAAAIQDGEGTPDVLLPPGASPHSYSLRPSDIRRVRDAQLFYWVGPDLENFLPKVLESRKGPSVAVQDQAGMHLRKFADFSESNHPDQGDDTDHDHDHRPGMIDAHLWLLPANAQVIAARMAEDLAIADPTNASRYQANLKAFDERMEQLDARLKQRIDPLKGKPYFVFHEAFDYFEEAYGLRHTGVFAVSADVQPGARHVASMRAQLQKAGPSCIFSEPPIRPRLADTLSQGLPVRLAELDDLGVGVKVDAQGYENLLGNLAGEFAGCLEKL
>NZ_CP045118.1|WP_152219055.1|176833_178981_+|adenosylcobalamin-dependent-ribonucleoside-diphosphate-reductase
MAKTDARPRGADQGVLALQPASQDIWDSKYRLKQKSGKPIDGSVDETWQRVARALADVEADKALREHWYERFLWALRNGAIPAGRIISNAGAQGHKPATSTINCTVSGIIRDSMDDILQKVHEAGLTLKAGCGIGYEFSTLRPRGAYVSGAGAHTSGPLSFMDIYDKMCFTVSSAGGRRGAQMGTFDVSHPDVREFIRAKREDGRLRQFNLSLLITDDFMAAVEVDEDWPLIFPVHQKERDEVDLDDAEHVVWRDWPVHDEYLVREDGRVACRVYGRVKARHLWDMIMVSTYDYAEPGFILIDRVNELNNNWWCEAIRATNPCGEQPLPPYGSCLLGSVNLTCFVNDAFGAHARFDWERFREVVRVFTRMLDNVVEINGLPLEQQRAEILGKRRHGMGFLGLGSALTLLKLRYGSPEACVFTEEVAREMALVGWEVALELSREKGPAPVLAQDYDVTAEMLRKRPEMVDDGYKVGDKVAGRVLHAKYSRYMQRVAEYAPQLVEELAEQGARFTHHSSIAPTGTISLSLANNASNGIEPSFAHHYSRNLIRAGRKTKEKISVYSYELLAYRALVDNHAVPDAEEEKHRLPEYFITADDITPQQHVDIQAAAQKWIDSSISKTANVPTDYPFEDFKDIYLYAWRQGLKGCTTFRFNPAAFQGVLVKESDLEKTVYRFELEDGSVVELKGNEEVEYDGEMHTAANLFDALKEGYYGKY
>NZ_CP045118.1|WP_152219056.1|178999_179686_+|NrdJb
MSVKINQKIKGFQVVDVAEEKARAEAAQAAAVVKMDETLQRPEMLVGATYKIKSPLFEHALYVTINDMVLNPDTPYEQRRPFEIFINSKNMDHFQWIVALTRIMSAVFRKGGDCTFLVEEMKAVFDPRGGYLKRGGVYMPSIVAEIGAVVERHLVAIGLMEGAQIDEEQRLYLAEKRAAYEAAQGINKAEPGEGFPAGAQLCGKCNTMAVVQMDGCATCLNCGHSKCG

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Crispr_ID: NZ_CP045118_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP045118_2

209956-210032

Orphan

Consensus_repeat	Method
AAGCCCAAGCCGAAACCCAAGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP045118_2

>merge|NZ_CP045118|2|209956-210032|CRISPRCasFinder
AAGCCTGTGGAAAAGCCCAAGCCGAAACCCAAGCCGGTGGAAAGGGCCATCCCCAAGGTCGCGCCCAAGCCCAAGCC

>NZ_CP045118|2|2|209956-210032|CRISPRCasFinder
AAGCCTGTGGAAAAGCCCAAGCC	GAAACCCAAGCCGGTGGAAAGGGCCATCCCC
AAGGTCGCGCCCAAGCCCAAGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045118.1\|WP_152219103.1\|212598_213549_+\|adenosine-deaminase	unknown	unknown	gnl\|CDD\|236480
NZ_CP045118.1\|WP_152219081.1\|201875_203060_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|367049
NZ_CP045118.1\|WP_152219095.1\|208409_209372_+\|cobalamin-biosynthesis-protein-CobW	unknown	unknown	gnl\|CDD\|367104
NZ_CP045118.1\|WP_152219093.1\|207978_208332_-\|NADH:ubiquinone-oxidoreductase	unknown	unknown	unknown
NZ_CP045118.1\|WP_152219085.1\|205017_205419_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP045118.1\|WP_152219107.1\|214220_215864_-\|sulfate-permease	unknown	unknown	gnl\|CDD\|183265
NZ_CP045118.1\|WP_152219101.1\|211324_212407_-\|calcium:proton-antiporter	unknown	unknown	gnl\|CDD\|223464
NZ_CP045118.1\|WP_152219118.1\|219046_219364_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP045118.1\|WP_152219115.1\|218664_219063_+\|flagellar-export-chaperone-FliS	unknown	unknown	gnl\|CDD\|376819
NZ_CP045118.1\|WP_152227840.1\|200081_201500_-\|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|341045
NZ_CP045118.1\|WP_152219091.1\|207186_207819_+\|DUF1826-domain-containing-protein	unknown	unknown	gnl\|CDD\|378067
NZ_CP045118.1\|WP_152219114.1\|217324_218668_+\|flagellar-filament-capping-protein-FliD	unknown	unknown	gnl\|CDD\|224264
NZ_CP045118.1\|WP_152219111.1\|216687_217017_+\|multidrug/spermidine-efflux-SMR-transporter-subunit-MdtI	unknown	unknown	gnl\|CDD\|182618
NZ_CP045118.1\|WP_152227842.1\|203593_204049_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|273701
NZ_CP045118.1\|WP_152219087.1\|205548_205953_+\|RNA-polymerase-binding-protein-DksA	unknown	unknown	gnl\|CDD\|274124
NZ_CP045118.1\|WP_152219089.1\|205984_207187_+\|GTP-binding-protein	unknown	unknown	gnl\|CDD\|223597
NZ_CP045118.1\|WP_152219105.1\|213553_214219_-\|HAD-IA-family-hydrolase	unknown	unknown	gnl\|CDD\|319828
NZ_CP045118.1\|WP_152219109.1\|216334_216694_+\|QacE-family-quaternary-ammonium-compound-efflux-SMR-transporter	unknown	unknown	gnl\|CDD\|224987
NZ_CP045118.1\|WP_152219099.1\|210812_211322_-\|nucleoside-2-deoxyribosyltransferase	unknown	unknown	gnl\|CDD\|226140
NZ_CP045118.1\|WP_152219083.1\|203063_203516_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP045118.1\|WP_152219081.1\|201875_203060_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|367049	pfam02353, CMAS, Mycolic acid cyclopropane synthetase. This family consist of Cyclopropane-fatty-acyl-phospholipid synthase or CFA synthase EC:2.1.1.79 this enzyme catalyze the reaction: S-adenosyl-L-methionine + phospholipid olefinic fatty acid <=> S-adenosyl-L-homocysteine + phospholipid cyclopropane fatty acid.	1.17488e-129
NZ_CP045118.1\|WP_152219095.1\|208409_209372_+\|cobalamin-biosynthesis-protein-CobW	gnl\|CDD\|367104	pfam02492, cobW, CobW/HypB/UreG, nucleotide-binding domain. This domain is found in HypB, a hydrogenase expression / formation protein, and UreG a urease accessory protein. Both these proteins contain a P-loop nucleotide binding motif. HypB has GTPase activity and is a guanine nucleotide binding protein. It is not known whether UreG binds GTP or some other nucleotide. Both enzymes are involved in nickel binding. HypB can store nickel and is required for nickel dependent hydrogenase expression. UreG is required for functional incorporation of the urease nickel metallocenter. GTP hydrolysis may required by these proteins for nickel incorporation into other nickel proteins. This family of domains also contains P47K, a Pseudomonas chlororaphis protein needed for nitrile hydratase expression, and the cobW gene product, which may be involved in cobalamin biosynthesis in Pseudomonas denitrificans.	2.13397e-48
NZ_CP045118.1\|WP_152219101.1\|211324_212407_-\|calcium:proton-antiporter	gnl\|CDD\|223464	COG0387, ChaA, Ca2+/H+ antiporter [Inorganic ion transport and metabolism].	1.38498e-86
NZ_CP045118.1\|WP_152219107.1\|214220_215864_-\|sulfate-permease	gnl\|CDD\|183265	PRK11660, PRK11660, putative transporter; Provisional.	0
NZ_CP045118.1\|WP_152219103.1\|212598_213549_+\|adenosine-deaminase	gnl\|CDD\|236480	PRK09358, PRK09358, adenosine deaminase; Provisional.	4.64769e-166
NZ_CP045118.1\|WP_152219115.1\|218664_219063_+\|flagellar-export-chaperone-FliS	gnl\|CDD\|376819	pfam02561, FliS, Flagellar protein FliS. FliS is coded for by the FliD operon and is transcribed in conjunction with FliD and FliT, however this protein has no known function.	3.06754e-40
NZ_CP045118.1\|WP_152227840.1\|200081_201500_-\|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl\|CDD\|341045	cd17502, MFS_Azr1_MDR_like, Saccharomyces cerevisiae Azole resistance protein 1 (Azr1p), and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This subfamily is composed of multidrug resistance (MDR) transporters including various Saccharomyces cerevisiae proteins such as azole resistance protein 1 (Azr1p), vacuolar basic amino acid transporter 1 (Vba1p), vacuolar basic amino acid transporter 5 (Vba5p), and Sge1p (also known as Nor1p, 10-N-nonyl acridine orange resistance protein, and crystal violet resistance protein). MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. This subfamily belongs to the Methylenomycin A resistance protein (also called MMR peptide) and similar multidrug resistance (MDR) transporters (MMR-like MDR transporter) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.75128e-68
NZ_CP045118.1\|WP_152219091.1\|207186_207819_+\|DUF1826-domain-containing-protein	gnl\|CDD\|378067	pfam08856, DUF1826, Protein of unknown function (DUF1826). These proteins are functionally uncharacterized.	2.22546e-70
NZ_CP045118.1\|WP_152219114.1\|217324_218668_+\|flagellar-filament-capping-protein-FliD	gnl\|CDD\|224264	COG1345, FliD, Flagellar capping protein [Cell motility and secretion].	7.86347e-45
NZ_CP045118.1\|WP_152219111.1\|216687_217017_+\|multidrug/spermidine-efflux-SMR-transporter-subunit-MdtI	gnl\|CDD\|182618	PRK10650, PRK10650, multidrug/spermidine efflux SMR transporter subunit MdtI.	4.02663e-45
NZ_CP045118.1\|WP_152219087.1\|205548_205953_+\|RNA-polymerase-binding-protein-DksA	gnl\|CDD\|274124	TIGR02420, RNA_polymerase-binding_transcription_factor_DksA, RNA polymerase-binding protein DksA. The model that is the basis for this family describes a small, pleiotropic protein, DksA (DnaK suppressor A), originally named as a multicopy suppressor of temperature sensitivity of dnaKJ mutants. DksA mutants are defective in quorum sensing, virulence, etc. DksA is now understood to bind RNA polymerase directly and modulate its response to small molecules to control the level of transcription of rRNA. Nearly all members of this family are in the Proteobacteria. Whether the closest homologs outside the Proteobacteria function equivalently is unknown. The low value set for the noise cutoff allows identification of possible DksA proteins from outside the proteobacteria. TIGR02419 describes a closely related family of short sequences usually found in prophage regions of proteobacterial genomes or in known phage. [Transcription, Transcription factors, Regulatory functions, Small molecule interactions].	1.17141e-40
NZ_CP045118.1\|WP_152227842.1\|203593_204049_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|273701	TIGR01575, rimI, ribosomal-protein-alanine acetyltransferase. Members of this model belong to the GCN5-related N-acetyltransferase (GNAT) superfamily. This model covers prokarotes and the archaea. The seed contains a characterized accession for Gram negative E. coli. An untraceable characterized accession (PIR\|S66013) for Gram positive B. subtilis scores well (205.0) in the full alignment. Characterized members are lacking in the archaea. Noise cutoff (72.4) was set to exclude M. loti paralog of rimI. Trusted cutoff (80.0) was set at next highest scoring member in the mini-database. [Protein synthesis, Ribosomal proteins: synthesis and modification].	4.14499e-15
NZ_CP045118.1\|WP_152219089.1\|205984_207187_+\|GTP-binding-protein	gnl\|CDD\|223597	COG0523, COG0523, Putative GTPases (G3E family) [General function prediction only].	1.47622e-116
NZ_CP045118.1\|WP_152219109.1\|216334_216694_+\|QacE-family-quaternary-ammonium-compound-efflux-SMR-transporter	gnl\|CDD\|224987	COG2076, EmrE, Membrane transporters of cations and cationic drugs [Inorganic ion transport and metabolism].	3.85588e-30
NZ_CP045118.1\|WP_152219099.1\|210812_211322_-\|nucleoside-2-deoxyribosyltransferase	gnl\|CDD\|226140	COG3613, COG3613, Nucleoside 2-deoxyribosyltransferase [Nucleotide transport and metabolism].	3.93074e-54
NZ_CP045118.1\|WP_152219105.1\|213553_214219_-\|HAD-IA-family-hydrolase	gnl\|CDD\|319828	cd07526, HAD_BPGM_like, subfamily of beta-phosphoglucomutase-like family, similar to Escherichia coli 6-phosphogluconate phosphatase YieH. This subfamily includes Escherichia coli YieH/HAD3 an 6-phosphogluconate phosphatase, which can hydrolyzed purines and pyrimidines as secondary substrates. It belongs to the beta-phosphoglucomutase-like family whose other members include Lactococcus lactis beta-PGM, a mutase which catalyzes the interconversion of beta-D-glucose 1-phosphate (G1P) and D-glucose 6-phosphate (G6P), Saccharomyces cerevisiae phosphatases GPP1 and GPP2 that dephosphorylate DL-glycerol-3-phosphate, and DOG1 and DOG2 that dephosphorylate 2-deoxyglucose-6-phosphate. 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.	3.56439e-51

>NZ_CP045118.1|WP_152219095.1|208409_209372_+|cobalamin-biosynthesis-protein-CobW
MLKQIPTYLIAGPLGAGKTSLLRDLLGQRPADERWAVLVNEFGQVGLDAALLSRDEDGVALGEVAGGCLCCVNGAPFQVGLGRLLRKARPQRLFIEPSGLGHPSQLLAQLRAAPWQGVLAVQPLVMVLDAAALAAGQPLPEAQQNALAQAGLLLLNKSEDLDDAARAALLAGLPALPTRWTTQGHLALPELPTVPLTEPAAELPVLPRGVEGAVLLHRDQPLRQERIEDGRQAIGWRFHPDWRFRIGELDAWLATLPGLLRAKAVLHGEAGWMACNRTDRPVAWTDSAWRRDSRIELILATEVDAQPLQNALLRCAIAPV
>NZ_CP045118.1|WP_152219093.1|207978_208332_-|NADH:ubiquinone-oxidoreductase
MRQLLPFALACLPLFAHGEACVVHSQGANLDVKVCQQNRSIPAKLFREGFCQPQLKDQKVQVTYADSCPSGAFGVCENAQVQGMPYRQDIHYYGVASDARILQPFCEGQSNGQWRKP
>NZ_CP045118.1|WP_152219091.1|207186_207819_+|DUF1826-domain-containing-protein
MGALDSPAGPRQVLGDDPQVLAEVLKEDVNLAIWQRTLYPEISAFADRLGSRPLDLKQSLDVQGERVVLRELLPEHARLDGFSLFRADLEWLLEAFACLTGARRIGLRLRSLDRAMCPRFHVDHVPLRLVTTYIGPASQWLEEWAMARTRLADPTAEPNDAVQIRQMAAGDVGLFKGEKWAGNLGGGIVHRSSQPASGERRLLLTLDWLR
>NZ_CP045118.1|WP_152219089.1|205984_207187_+|GTP-binding-protein
MNQPLPVTVLSGFLGAGKSTLLNHVLKNRENLKVAVIVNDMSEINIDGREVQRDVSLNRGQERLVEMSNGCICCTLREDLLEEVSRLAREGRFDYLLIESTGISEPLPVAETFTFRDEQGRSLSDLARLDTLVTVVDGLNFLADYEGAESLAERGETLGEDDERSLSDLLVEQVEFADVILVSKIDLIGNAERDELLAILRKLNPDAYIQPMVMGQVPLARILDTGRFDFQRAARAPGWLKELRDEHLPETEAYGIASTVYRARRPFHPRRFHDFLAQPWSNGRLLRSKGFFWLASRYREAGSWSQAGGLMRHGLAGRWWRFVPRESWPQDTTELQAVLKHWDGDSGDCRQELVFIGQNLDFGRLFAELDRCLLDDAEMAAGASAWKQLPDPFEPWEVQA
>NZ_CP045118.1|WP_152219087.1|205548_205953_+|RNA-polymerase-binding-protein-DksA
MTEQELLAQPGEAYMSEAQQGYFRNLLLNQRGELQVRIDEQFHALQDGERPSDDADIASREEARQWQLRVLEREKKLLDKIDQALARLVRGDYGWCAETGEPIGLRRLLLRPTASLCIEAKERQERRELHVREA
>NZ_CP045118.1|WP_152219085.1|205017_205419_-|hypothetical-protein
MLRRALPLCLFAPLACASGQAPLPFPGEEPARCAWSAQVMACMDDAGNLYSVATQGHDTYLRGFDAASGRQWAQTGTRFGSLTFFSGVASDGQVWVGTSRGIGWTNISHFSSSSGDSTRLTCGRVSGCKQQAR
>NZ_CP045118.1|WP_152227842.1|203593_204049_+|GNAT-family-N-acetyltransferase
MTLRELDVDQAPWPLLLLADPSREQVQCYLRESCLLALLAGGRTLGVVVITPRSEGAAEITNLAVDEAWQGRGLGRRLLESAIARARVDGLQRLLIATGNSSLAQLGLYQRAGFRIVGIEPDYFVRHYPEPIFENGIQCRDQIRLALALNP
>NZ_CP045118.1|WP_152219083.1|203063_203516_-|hypothetical-protein
MSPKEWLYVWKQIPRSLQRDLFDAVPVLILGFFGLVFAAGIGIIIALMQLANYLRQHDSPYPGMSDAHFTYCLKISRDTLEARQALERLGPTPPAGVATDSAYARVDRLAGEYSQYCAERIWKKAFEAGLRERGVPPATSPEGWLAADRF
>NZ_CP045118.1|WP_152219081.1|201875_203060_+|methyltransferase-domain-containing-protein
MKANLPSELLSLQLPLRIRIGEAQAFDLGPDPQVTLVVRDPTLLTEISRPSLDVLGRAYVEKRMDIEGPIGEVIAMGDALSAALGDDDDSGEHVRESHDKATDAEAIHYHYDLSNEFYQLWLDPEMVYSCAYFETGSEGLATAQLAKLRHLCRKLRLQPGDSLLDVGCGWGGLARLAAKEFGAKVLGITLSEEQLRLGRERVKADGLQGQVRLERMDYRDLPRDGRFDKVVSVGMFEHVGHANLGMYFQHLFDVVRPGGLVMNHGITSRFTDGRPVGRGAGDFIDRYVFPHGELPHLSLAVARMSEAGLEVVDVEGLRLHYARTLDFWSASLEAKLAEAAKLVPEQALRIWRLYLAGCAYGFKKGWINLHQILASRPHADGSHEVPWNRRDIYA
>NZ_CP045118.1|WP_152227840.1|200081_201500_-|DHA2-family-efflux-MFS-transporter-permease-subunit
MLAIFLGALDQTIVAVSLPAISAGFGDFDLLAWVISGYMVAMTISMPIYGKLGDLYGRRVLMLFAIALFTAASLLCGAAQNMEQLVLARVLQGIGAGGMMSVSQAIIGEIVPPRERGRYQGYFSSMYAIASIAGPVLGGLLTEYLSWRWVFLINLPVGLVALAVSRRTLRGLPVPGRKPVIDYLGTALMIAGLGSLLLAITEVGQGARWSDPQMLGLFAAALALIALFVMQERQAPEPLVPMHLFRIRAATLSWLISFFASFQVISLSVLVPLRFQSVTGAGADSAALHLLPLAMGVPIGAYCCGRLTAILGRYKPQIVAGALLTPCAIAGLALASPGAYLLSGLCMLLTGIAAGTQFPTSLVAAQSAVDSRYLGVATSNITLFRSLGGAVGIALMSALLLAMLQPLAGNAGHGLSASALLASLGGPGHEAQRQTLDGVFRHLFLINAGFGALALLIALALPDHALRGRGSD
>NZ_CP045118.1|WP_152219099.1|210812_211322_-|nucleoside-2-deoxyribosyltransferase
MLKIYLAGPDVFRPDAFEQGERLKTLCAEFGLQGLYPLDHQVPEGIDQPQDQALWIYQANLALIAEADAVVANLNPFRGTEPDSGTAFELGYAAALGKPLYGYIREGGSCAERLPCEWKGQEPGRDRDGNQVEAFGLPLNLMLGVPVQIAVGGAREALELLKAELFQEE
>NZ_CP045118.1|WP_152219101.1|211324_212407_-|calcium:proton-antiporter
MLRALKDEKFLLLALLVAIAVYPLEHSLLGGGKMLAGITATALLAVIIGVSLRVAHHAEILAEKVGEPYGTMILTLAAVLVEVVILAIMMGHNHSPTLARDTIYAAVMLDMNGILGLAALLGGLKHGEQSYNDDSGKTYVTMILTAVGISMVVPELIPAEQWKLYSFFTIGCMVMLYALFLRMQTGQHSYFFSYNYAAHGEHAEGHEAAGNSKQSMGLLVVGVVLIGALAEVMSKALDVGLEGSGVPPIVPALLVAAISASPEILTALRAALANRMQPVVNIALGASLSTVILTVPVIEALALFKGQPIQMAMTPLQTGMMFITLMVAGFNLHDGKTNAIEGMTHFVLFATFLMLSLMGL
>NZ_CP045118.1|WP_152219103.1|212598_213549_+|adenosine-deaminase
MYDWLNALPKAELHLHLEGSLEPELLFALAERNKIALPWGDVESLRRAYAFNNLQEFLDLYYAGADVLRTEQDFYDLTWAYLQKCKAQNVIHVEPFFDPQTHTDRGIPFEVVLRGIQGALKDGEKQLGIRHGLILSFLRHLSEEEAFKTLEQALPFRDAFIAVGLDSSEVGHPPSKFQRVFDRARAEGFLTVAHAGEEGPPEYIWEALDLLKIQRIDHGVRAIEDERLMQRIIDEQIPLTVCPLSNTKLCVFDHMREHNILDMLERGVKVTVNSDDPAYFGGYVTENFQALHEHLGMTKEQAQRLAQNSLDARLVK
>NZ_CP045118.1|WP_152219105.1|213553_214219_-|HAD-IA-family-hydrolase
MAGRIDALIFDCDGTLVDSEQLSAELIVRLLGERGVHTSVEAILPIYRGERFQDVVEHLGRLYPQVAPSDFLANYRQRSLPWLRARLRPMPGAVALVRRLRVAKCVASNGPRDKIETSLDCAGLLDDFRGRVISAYDVGAWKPDPELIRHAARQLGVAAERCLVVDDSLPGLRAGLAAGARVVGFGELDFSGLGGEFARAKDMRELGRLLDGLGLLAPPSL
>NZ_CP045118.1|WP_152219107.1|214220_215864_-|sulfate-permease
MIALRDAWKAGLFGREHWTRNLVAGVIVGVVALPLAMAFAIASGVKPEQGIYTAILAGALVSLLGGSRVQIAGPTGAFIVILAGITARYGVDGLQIATLMAGAILVLLGVSRLGTIIRFIPAPVIVGFTAGIGVIIWVGQWKDFFGLPAVSGEHFHQKLWHLLQALPQLHLATTVLALLGLALVLFTPRIKALHRVPGPLVAMVVVTAIQSLFHFDGVATIGSAFGGIPQGLPSFSLPEVTLPRVLELIGPAFAIAMLGAIESLLSAVVADGMAGTRHDSNQELIGQGIANLVTPLFGGIAATGAIARTATNIRNGGSSPLAGVTHAVTLVLILLFLAPLASNIPLCALAAILFVVAWNMSEARHFLFMVRRAPRADVAILLITFLLTVFSDLVIAVNIGVILAMLHFMRRMASSVEVHADEGPELDVELRGRGLAELPPGVLVYSIEGPLFFGAVETFERALAQTHTDPKVLIIRLRRVPFMDITGLQTLQEVIEDLQRRGIEVRLCEANARVLGKLRKTGILDAPRAAGYHPDFPTALAATVAGA
>NZ_CP045118.1|WP_152219109.1|216334_216694_+|QacE-family-quaternary-ammonium-compound-efflux-SMR-transporter
MRSWIYLFAAIGFEVVGTTSMKLTHALYPVAGLLLMYLMVGLSYYFLSLAIKHVPVGVAYALWEGIGIVLISLVSAAWLGEDLTLEKALGLVVMIAGILLVKSGTRKSERETGMEAATC
>NZ_CP045118.1|WP_152219111.1|216687_217017_+|multidrug/spermidine-efflux-SMR-transporter-subunit-MdtI
MLNHDLIPMAWLGLAIVLEVIANLLLKYSDGFRKRILGVTSILFVLGAFTALSQAVRGIELSVAYAVWGGFGILATVAMGWALFGQRLAWRGWLGLVMLIVGMGLLKLA
>NZ_CP045118.1|WP_152219114.1|217324_218668_+|flagellar-filament-capping-protein-FliD
MSTIDSDYVKQMAQQLATYEVQNGLSKADRNKASYQSQLTAVTSLESALKTFASAVKGLNKATDASMLVNSATMSKDGYLTATVGSTAVAGKYDFFVEQLATSHQLSFSGLQAGDIDTQGTLTLSQNGKSFDIDLSKIDSDGDGSNSLDELAAAINKATDNTGVKATLVRSNGQVSLVLGADKSGAANAIGLSLSGTSTANSAFENALANPQELSKAQDARVRLGGESGMLMTNASNSFDNIIDGVSVTFTQAQKSGEQPISMTIAQDKSATTKKLQGFIDAYNALASQIDTLTASGDQNGNARGALAGDSSVRAIDNSLNQLLRTTFGGTNLINLGVSADRNGKLTLDTKRFEKAVASDPQGLDKLFLGKGNLLDSLDKNIALYTNSANGVMKSRKDTLNNGLRRVNDDYDTLQKQYDSYYARYLKQYTSMMQTMQSMSQTSGMFG
>NZ_CP045118.1|WP_152219115.1|218664_219063_+|flagellar-export-chaperone-FliS
MSGYAMNESYDSYRMVDLEAKAAASSPYELVLVLFDGLLDELARARGHIEHKRYQQKGRSLEKCLNILNGLSGALDYENGGEVVQGLARLYDYCIYRLSDVSVSLDVVGIDEVVRLLGILREGWEGVSATRG
>NZ_CP045118.1|WP_152219118.1|219046_219364_+|hypothetical-protein
MPHVDDRQRLLELYEQLGAALQRKDWSAMGQIDLAIRAQLVAMASQPGLAADVLLAKKRLKHLHEDASQACAAECERLRRLLLSHLEYAEGRSAYMQVDMLPEGR

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Crispr_ID: NZ_CP045118_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP045118_3

2641711-2641819

Orphan

Consensus_repeat	Method
GGCGGCGGCGGTGGTGGCCTGTACG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP045118_3

>merge|NZ_CP045118|3|2641711-2641819|CRISPRCasFinder
GGCGGCGGCGGTGGTGGCCTGTACGTCAGCTCTGGCAGCAGCCTGACCCTCCGCGATTCGGTGATCAGCAACAATACCGACACGGGCGGCGGCGGTGGCGGCCTGTACG

>NZ_CP045118|3|3|2641711-2641819|CRISPRCasFinder
GGCGGCGGCGGTGGTGGCCTGTACG	TCAGCTCTGGCAGCAGCCTGACCCTCCGCGATTCGGTGATCAGCAACAATACCGACACG
GGCGGCGGCGGTGGCGGCCTGTACG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045118.1\|WP_152223139.1\|2625896_2626679_+\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|273776
NZ_CP045118.1\|WP_152223147.1\|2630901_2631918_+\|sulfotransferase-family-protein	unknown	unknown	unknown
NZ_CP045118.1\|WP_152223137.1\|2625294_2625696_-\|GFA-family-protein	unknown	unknown	gnl\|CDD\|226314
NZ_CP045118.1\|WP_152223170.1\|2653110_2653455_+\|DUF861-domain-containing-protein	unknown	unknown	gnl\|CDD\|225981
NZ_CP045118.1\|WP_152223175.1\|2655378_2656008_-\|LysE-family-translocator	unknown	unknown	gnl\|CDD\|224199
NZ_CP045118.1\|WP_152223159.1\|2645962_2647450_+\|transporter	unknown	unknown	gnl\|CDD\|224455
NZ_CP045118.1\|WP_152223162.1\|2648651_2649953_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340874
NZ_CP045118.1\|WP_152223151.1\|2632554_2632875_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP045118.1\|WP_152223143.1\|2627994_2630088_+\|biotin/lipoyl-binding-protein	unknown	unknown	gnl\|CDD\|223914
NZ_CP045118.1\|WP_152223141.1\|2626675_2627995_+\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|273776
NZ_CP045118.1\|WP_152223145.1\|2630113_2630914_+\|Nif11-family-protein	unknown	unknown	gnl\|CDD\|377460
NZ_CP045118.1\|WP_152228058.1\|2653790_2654366_-\|damage-inducible-protein-DinB	unknown	unknown	gnl\|CDD\|225200
NZ_CP045118.1\|WP_152223166.1\|2651001_2651349_-\|RidA-family-protein	unknown	unknown	gnl\|CDD\|100007
NZ_CP045118.1\|WP_152223153.1\|2632939_2633518_+\|phage-tail-protein	unknown	unknown	gnl\|CDD\|227020
NZ_CP045118.1\|WP_152223149.1\|2632054_2632558_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|223532
NZ_CP045118.1\|WP_152223161.1\|2647577_2648597_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|227311
NZ_CP045118.1\|WP_152223164.1\|2649995_2650940_-\|D-2-hydroxyacid-dehydrogenase	unknown	unknown	gnl\|CDD\|240639
NZ_CP045118.1\|WP_152223168.1\|2651693_2653100_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|274522
NZ_CP045118.1\|WP_152223155.1\|2633625_2634489_+\|sulfotransferase	unknown	unknown	gnl\|CDD\|379204
NZ_CP045118.1\|WP_152223173.1\|2654481_2655327_-\|PhzF-family-phenazine-biosynthesis-isomerase	unknown	unknown	gnl\|CDD\|223461

Protein	Function_ID	Function_description	E-value
NZ_CP045118.1\|WP_152223139.1\|2625896_2626679_+\|efflux-RND-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].	9.59445e-32
NZ_CP045118.1\|WP_152223137.1\|2625294_2625696_-\|GFA-family-protein	gnl\|CDD\|226314	COG3791, COG3791, Uncharacterized conserved protein [Function unknown].	1.06499e-35
NZ_CP045118.1\|WP_152223170.1\|2653110_2653455_+\|DUF861-domain-containing-protein	gnl\|CDD\|225981	COG3450, COG3450, Predicted enzyme of the cupin superfamily [General function prediction only].	7.29779e-31
NZ_CP045118.1\|WP_152223175.1\|2655378_2656008_-\|LysE-family-translocator	gnl\|CDD\|224199	COG1280, RhtB, Putative threonine efflux protein [Amino acid transport and metabolism].	3.53165e-26
NZ_CP045118.1\|WP_152223159.1\|2645962_2647450_+\|transporter	gnl\|CDD\|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	4.6439e-17
NZ_CP045118.1\|WP_152223162.1\|2648651_2649953_-\|MFS-transporter	gnl\|CDD\|340874	cd17316, MFS_SV2_like, Metazoan Synaptic vesicle glycoprotein 2 (SV2) and related small molecule transporters of the Major Facilitator Superfamily. This family is composed of metazoan synaptic vesicle glycoprotein 2 (SV2) and related small molecule transporters including those that transport inorganic phosphate (Pht), aromatic compounds (PcaK and related proteins), proline/betaine (ProP), alpha-ketoglutarate (KgtP), citrate (CitA), shikimate (ShiA), and cis,cis-muconate (MucK), among others. SV2 is a transporter-like protein that serves as the receptor for botulinum neurotoxin A (BoNT/A), one of seven neurotoxins produced by the bacterium Clostridium botulinum. BoNT/A blocks neurotransmitter release by cleaving synaptosome-associated protein of 25 kD (SNAP-25) within presynaptic nerve terminals. Also included in this family is synaptic vesicle 2 (SV2)-related protein (SVOP) and similar proteins. SVOP is a transporter-like nucleotide binding protein that localizes to neurotransmitter-containing vesicles. The SV2-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.17946e-49
NZ_CP045118.1\|WP_152223161.1\|2647577_2648597_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|227311	COG4977, COG4977, Transcriptional regulator containing an amidase domain and an AraC-type DNA-binding HTH domain [Transcription].	1.95592e-79
NZ_CP045118.1\|WP_152223141.1\|2626675_2627995_+\|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].	1.90528e-14
NZ_CP045118.1\|WP_152223149.1\|2632054_2632558_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|223532	COG0456, RimI, Acetyltransferases [General function prediction only].	3.58748e-10
NZ_CP045118.1\|WP_152228058.1\|2653790_2654366_-\|damage-inducible-protein-DinB	gnl\|CDD\|225200	COG2318, DinB, Uncharacterized protein conserved in bacteria [Function unknown].	1.4144e-24
NZ_CP045118.1\|WP_152223166.1\|2651001_2651349_-\|RidA-family-protein	gnl\|CDD\|100007	cd06150, YjgF_YER057c_UK114_like_2, This group of proteins belong to a large family of YjgF/YER057c/UK114-like proteins present in bacteria, archaea, and eukaryotes with no definitive function. The conserved domain is similar in structure to chorismate mutase but there is no sequence similarity and no functional connection. Members of this family have been implicated in isoleucine (Yeo7, Ibm1, aldR) and purine (YjgF) biosynthesis, as well as threonine anaerobic degradation (tdcF) and mitochondrial DNA maintenance (Ibm1). This domain homotrimerizes forming a distinct intersubunit cavity that may serve as a small molecule binding site.	2.18013e-45
NZ_CP045118.1\|WP_152223153.1\|2632939_2633518_+\|phage-tail-protein	gnl\|CDD\|227020	COG4675, MdpB, Microcystin-dependent protein [Function unknown].	1.41278e-46
NZ_CP045118.1\|WP_152223145.1\|2630113_2630914_+\|Nif11-family-protein	gnl\|CDD\|377460	pfam05118, Asp_Arg_Hydrox, Aspartyl/Asparaginyl beta-hydroxylase. Iron (II)/2-oxoglutarate (2-OG)-dependent oxygenases catalyze oxidative reactions in a range of metabolic processes. Proline 3-hydroxylase hydroxylates proline at position 3, the first of a 2-OG oxygenase catalyzing oxidation of a free alpha-amino acid. The structure of proline 3-hydroxylase contains the conserved motifs present in other 2-OG oxygenases including a jelly roll strand core and residues binding iron and 2-oxoglutarate, consistent with divergent evolution within the extended family. This family represent the arginine, asparagine and proline hydroxylases. The aspartyl/asparaginyl beta-hydroxylase (EC:1.14.11.16) specifically hydroxylates one aspartic or asparagine residue in certain epidermal growth factor-like domains of a number of proteins.	1.32913e-14
NZ_CP045118.1\|WP_152223143.1\|2627994_2630088_+\|biotin/lipoyl-binding-protein	gnl\|CDD\|223914	COG0845, AcrA, Membrane-fusion protein [Cell envelope biogenesis, outer membrane].	1.92435e-10
NZ_CP045118.1\|WP_152223164.1\|2649995_2650940_-\|D-2-hydroxyacid-dehydrogenase	gnl\|CDD\|240639	cd12162, 2-Hacid_dh_4, Putative D-isomer specific 2-hydroxyacid dehydrogenases. 2-Hydroxyacid dehydrogenases catalyze the conversion of a wide variety of D-2-hydroxy acids to their corresponding keto acids. The general mechanism is (R)-lactate + acceptor to pyruvate + reduced acceptor. Formate/glycerate and related dehydrogenases of the D-specific 2-hydroxyacid dehydrogenase superfamily include groups such as formate dehydrogenase, glycerate dehydrogenase, L-alanine dehydrogenase, and S-adenosylhomocysteine hydrolase. Despite often low sequence identity, these proteins typically have a characteristic arrangement of 2 similar subdomains of the alpha/beta Rossmann fold NAD+ binding form. The NAD+ binding domain is inserted within the linear sequence of the mostly N-terminal catalytic domain, which has a similar domain structure to the internal NAD binding domain. Structurally, these domains are connected by extended alpha helices and create a cleft in which NAD is bound, primarily to the C-terminal portion of the 2nd (internal) domain. Some related proteins have similar structural subdomain but with a tandem arrangement of the catalytic and NAD-binding subdomains in the linear sequence. While many members of this family are dimeric, alanine DH is hexameric and phosphoglycerate DH is tetrameric.	1.58758e-129
NZ_CP045118.1\|WP_152223168.1\|2651693_2653100_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|274522	TIGR03329, Phn_aa_oxid, putative aminophosphonate oxidoreductase. This clade of sequences are members of the pfam01266 family of FAD-dependent oxidoreductases. Characterized proteins within this family include glycerol-3-phosphate dehydrogenase (1.1.99.5), sarcosine oxidase beta subunit (1.5.3.1) and a number of deaminating amino acid oxidases (1.4.-.-). These genes have been consistently observed in a genomic context including genes for the import and catabolism of 2-aminoethylphosphonate (AEP). If the substrate of this oxidoreductase is AEP itself, then it is probably acting in the manner of a deaminating oxidase, resulting in the same product (phosphonoacetaldehyde) as the transaminase PhnW (TIGR02326), but releasing ammonia instead of coupling to pyruvate:alanine. Alternatively, it is reasonable to suppose that the various ABC cassette transporters which are also associated with these loci allow the import of phosphonates closely related to AEP which may not be substrates for PhnW.	2.70987e-156
NZ_CP045118.1\|WP_152223155.1\|2633625_2634489_+\|sulfotransferase	gnl\|CDD\|379204	pfam13469, Sulfotransfer_3, Sulfotransferase family.	4.50789e-15
NZ_CP045118.1\|WP_152223173.1\|2654481_2655327_-\|PhzF-family-phenazine-biosynthesis-isomerase	gnl\|CDD\|223461	COG0384, COG0384, Predicted epimerase, PhzC/PhzF homolog [General function prediction only].	1.84375e-82

>NZ_CP045118.1|WP_152223155.1|2633625_2634489_+|sulfotransferase
MANSAPSFHFISGLPRSGSTLLAALLRQNPRFHAGMTSPVGSLFSALLNQFSADSEFGPVVTQEQRKRMLSGLFGNYYADQVGKDVVFDTNRQWCAKLPALLDLFPQAKVIACVRNVAWVMDSIERLYRANPYENTKLFNDDAERNTVYSRVDTLAQRNRLVGFAWAALKDAYYGEHANSLLLVEYDLLVTQPEKVLRLVYEFLGETWFEHDFEQVEYDAPEFDQALGLKGLHKVRPKIEATARRTILPPDLFEQYAQLDFWKDSQNSEANVIRTARNARAIDNGND
>NZ_CP045118.1|WP_152223153.1|2632939_2633518_+|phage-tail-protein
MSDPFIGEIRMLAFNFAPRGWALCQGQTLGIAQNAALFSLLGTTYGGNGVSTFQLPNLSGRTPLGAGNGPGLPPVVQGEVGGTPTVTLNLNQMPIHNHVASGTSSMNVGGTPASPALAPTATNNILGGSVGGSPQAAAIWSSELSGPVALGNPISTSVTVQNAGGSQPVSIQSPYLGMNFAIALEGVFPSRN
>NZ_CP045118.1|WP_152223151.1|2632554_2632875_+|hypothetical-protein
MSALPGREEFQRYLEQEWQLAWEGGSLPVTLVEVNQGTAMNARYECFNLVFAQPAGYQMPQHTYSLRGPDNQQLPELLLCPIGPEEDGERHLLQAVFHLRRPTQSP
>NZ_CP045118.1|WP_152223149.1|2632054_2632558_+|GNAT-family-N-acetyltransferase
MATLELNLRPMEDADLAFLRELYASTRAAEMERIPWDKATKDAFLTQQFNAQHQYYQAHYEGADFSLICHDDQPIGRLYVFRGPTTHNLIDISLMPQWHRRGIGTGFIADLTREADALGRSIRLFVEPENPALRLYERFGFRETGRRQHYLQMNREAVAALAQESQP
>NZ_CP045118.1|WP_152223147.1|2630901_2631918_+|sulfotransferase-family-protein
MASVTPMDDFSGWLPIRVWRQAGDWRVDWCWFGERRLARPFFRDDVDDALRLPFNQAFRRETGIQALFDWQAASPGLQPAALIFHASRCGSTLMAQMLAALPGNIVLSEPPPLDSLLRAHFLDAAATDWQGRGVQALLSAYGQRRLGLEQRLLVKLDAWSVFEAPLLAALYPQVPRIFLYRDPLEIVVSQLRQPGMHRVPGLLGPSALDQRLPGAQGMTPLEYSCRMIGEIFQGGLELCRRHGGIALNYSELPGALWARLASLLGVEDEDRAPLQAVAAFDAKQPSMTFSADGQAKRESAGEDVRQAVERWVRAPYLELESLRQKVGFGSLASFHTIV
>NZ_CP045118.1|WP_152223145.1|2630113_2630914_+|Nif11-family-protein
MTARSLPRCSRLALAFEVPPLLEALSRVDAGAWQTHFNTGYYEGDWSGIALVAPEDAPLPLAPGQGAPVRSGWWLGEPAWGALLDRFHTVVRSARLLRLGPGARIHEHCDPDLGQPDGDLRLHVPLLSPSGVEFLVDGLQVPMVVGECWFIDLSRPHRVDNPGPGERIHLVLDCVPNPWLLGLLEQGLAGTPPLQPGRAGQAFAAFRQRVATEPALAAALQALGDSRDFLRETVRLGAELGLVFSEAEVRGAMHQGRQAWSEQWRA
>NZ_CP045118.1|WP_152223143.1|2627994_2630088_+|biotin/lipoyl-binding-protein
MLPALRPDLQLSPAAPGLDGAPQWTLADPLRGRYFKLGSAAVRLLRHWALGDPQRVLQAANAEPGQLLGAAEVEEMLRFLRGHDLIAALDAEQRASYAMKAAAMRQSLWQKVLHQYLFFRIPLWRPDAFLNRAWPVLQRNGGWLLRWGLPLVFALGLFLVARDWQRFIATFPHLFSLGGALAFGVALGFAKLCHEFGHAFMAKRAGCRVQSMGVAFMVMLPMFYTDVSDAWRVSDRRSRLLIGAGGVLAEMVLAVLALLAWSLLPDGPARTSAFMLASATWVTTVLINLNPFMRFDGYFLVSDLLGVENLQARAFALCRWRLRETLFGYGEPAPEPWSPVMERRLLTWGFGSWIWRAVLFFGIALAVYHLFFKVLGIFLMLVELVWFIGLPIWRELREWWQRRDQAEPRKVLLVGVGLLALLALLAVPWRASVEVPALLEASRTTTLHAPVAGRLKAVLVADGQAVEQGALLLELESPDLEAKQAIARREIEILQLQLRRQAARSETVGDTGILEQQLAEAVAEYRGLAAQRERLQIRAPQAGVVRDLLPDLAVGRWLSPRELLARVVEPGQRLRGYLAEENLWRVQPGAEGRFIADDPARPALAVRLDEVDATGVSYLELEALASDHYGPIAVRRDEQRRAEPVQAQYGVRLSQLDAAFHPAQPLRGVVVLDGEGQSLLGSVWRRLAALGVRESGF
>NZ_CP045118.1|WP_152223141.1|2626675_2627995_+|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MNAPQVGMLERVFAQFLGLEQQARAAATVEQLAYHMVNDSQALFGFRHAALLIAGKVRALTGISVVEPNSPFVAFVEQACAQLQTRGALGTARPVDFQVLGAQQQADWQALSAGEVFWLPLLDRQGALFGGLWLAREQAWNDAEQALLTQLGNTYAHAWLALQPRKPWRLRWPKKKLLMIAGGLCLLLLVPVRQSVLAPADVVPLGGRVVAAPLDGVIAEFLVKPNQTVAAGDLLVRFDATSLKAQADVADRALGVAEAELKTSTQRAFADAESSARVDLLAARVEQKRAERDYARQLLARSEVRAERAGIAVFADAERLTGKPVQTGERLMQIADPAQAELRIELPVGDAISLAPGAEVALFLDSDPLNRHDAKLERAAYEAQPTAAGQLAYRLDAAFMNAPPRIGLRGTAKLFGDRAPLAYYLLRRPLAALRQSLGL
>NZ_CP045118.1|WP_152223139.1|2625896_2626679_+|efflux-RND-transporter-periplasmic-adaptor-subunit
MRGWAWLGLGLSVYGACAAQGSEQATDDPLLAAPRSSAAGAGDVRGVLRARDQAMLSSELSGRILEMPFAEGQTFHKGDVLVRFDCSAYQAQLSAAQAGAKAASEQLGHNRQLAALNSVGRFEVALAEAKLAEAQAQAQVYKVQVGRCAVVAPFDGQVVQRKAQPFESVSGGAPLLEIVDNRSLEIRLLVPSRWVSQLKVGQSFTFVPDETGQPLQVEVKRLGARIDEGSQMLPLIAALPADAKGLLAGMSGTARFADAP
>NZ_CP045118.1|WP_152223137.1|2625294_2625696_-|GFA-family-protein
MAESFQGSCLCGAISYKLLSPPRSLSHCHCSQCRKGHGAAFASYASVPRSDLRILKGAEALKSYASSELVLRQFCTHCGSSLFWSRSQGEFSDWISIALGTLDSTFTAHKQRHIQLASKAPWYELSDHWTQTD
>NZ_CP045118.1|WP_152223159.1|2645962_2647450_+|transporter
MKRQMTLLGVSLLALAVSGCAVTTQPIDRSVSEQRARNDLKAMFKDQEPLSGPLTLHDAMARAVKYNLESRLKVMEEALSRRQLDLATFDMLPRMALEAGYVGRNNVSASSSQSVQTGTQSLEPSTSQDRDRNVADLTMVWNVLDFGVSYVSAKQQADQRLIVQERRRKVVQTIIQDVRSAYWRAIAAQRLLGQIDSLMARVDGARKDSQQMSQQRIGDPVQALNYQRALIEASRQLEEQRRALSLAKTELATLINLPMGTELTLAVPEGYDVPELKADFDSLEQQALASRPELREQDYQARISAAETKKAMLRMLPGLEFSAGGHYDSNSFLVNDRWADYGVKVTWNLFNVLSAPAAIDVAKAGEDVTAARRQAMSMAVLAQLYVANANYSEARRQFLTTQELASLDNQIVGQLRNRQQAQGIGELELIQGELNALQADLRRDLAYAELRNSYGQIFASAGIDPLPGGLADTQLKTLANGLAERERQLDGGQLK
>NZ_CP045118.1|WP_152223161.1|2647577_2648597_+|helix-turn-helix-domain-containing-protein
MNPSQPVPDEDSLEHVLKPDLRVAIVLIDQFTLTPVAGFVDALRFAADRSFESRQILCQWEWLSVTGEPVSASCGLPIAPTKRLDPDAEYDYVVLAGGLLSGVMNPAPELLDYIRRLHARKVPLVALCASYFTLGLAGILEGRRCAVHFTVQEQFAALFPQTQAVVDKSYIEDSGVFSCPGGSAFELAAEIIGRHCGKRRAQKSLEYLLVADEDVRRGTDNSVAHVYQDPLVHRALDYMRAHLDSHCTIRELAQQLGSNERQLNRAFLANAGQPPAQFWRKLRLQEARKLLSDTSLHVTQIAYATGFSDASHFIQQFRKSYGETPHLFRKLRHNAERLQ
>NZ_CP045118.1|WP_152223162.1|2648651_2649953_-|MFS-transporter
MQSIDISNSPADLHSPIRPLHIQAAVGGVGGQFCDGYVLGIIGIAISLATTPLGLDALWLGLLGGAALIGLFLGSLLTGPLADRYGRKHIYRWNMALFFGASIAQFFVQDAQQLLILRLLLGFALGSDFVVGVSLVAELVPRRFRGPLLALMAVSWTLGFTLSYIVGYLMQSWGDDAWRWILASSAVPSLLVLLVRQGTPESPLWLMKQGRHGEARRVIERLGGTDLPAEEGGKAKASWGQLFSPEHRRRTLVGMVFYTCQVIPYFAMSTFIPRILEALKIEDSYTGGLIYNIFLLAGSVVGLLLINLLTRRTFLIGTFSINAVALFVLAIWSGMPGLYVVGVFAVFAFVMAASGVLEFAYTSELFPTELRASGVGISVAASRIGAASCTFILPVVMERFGASAAIGICVTALVIGAVVCQRWAPETNPRYVG
>NZ_CP045118.1|WP_152223164.1|2649995_2650940_-|D-2-hydroxyacid-dehydrogenase
MLHDVVFLDRDAFPASVKIRELPFPHRWSCHDYTAPEDMVARLSTATVAITGGVPISVAQLEQLPALRMISLAMTGTDVVDLEYCRQRGIHVTNVPGYGTHAVAEHALAMIFELLRNVGRYHRLLMDERQRGQPLNPTYFDYPIRDLRGKVLGIIGHGPIAQRLADLASRLEMEVYFHDRDGHYQGERYLPLQALLTRSDVVSLNCPLTPQTRGLLGRQQFQWMKKDAVLINTARGAVINEPELIRALQDGEIAGAALDVVTNEPLTLDEPLLHLAATHNLVLNPHVAWSSAEAMQGLMDSALENVAAFVAQKP
>NZ_CP045118.1|WP_152223166.1|2651001_2651349_-|RidA-family-protein
MDIQRKGRNARYSQCVRFNECIETSGIVARDPDQDIAEQTRDVLEQLEAVLDLAGVDKSRLIRVQIWLADMAEFDAMNSVYDAWVDPQHPPARACVGAALADSRYRLEIQASAVA
>NZ_CP045118.1|WP_152223168.1|2651693_2653100_+|FAD-dependent-oxidoreductase
MKFPAVPPLKRSFWMLSAEPDLQLPSPLSGNHRADVAIVGGGFVGLWTALTIKEHEPDCRVIVLEQDICGGGASGRNGGFVMSWWPKIQSLTSFCSTEQATFLATSAERAISELGEFCERHRIDASFKQKGWLWTATCKAHVDSWNATLAACERLGFHPFERLSREEVARRSGSDVHIAGVLERSNATVQPAALVRGMRRVALEAGIEIFENTPVSEIQPGRPVSLVTAGGRVEADRVVLATNAWSAAIPELSKLFVPVGSSIVVTEPLGPRLESLGWSGAEAITDSQLLVDYYRTTPDERIAFGKGTGSLSYGSKMGPVFSEDREGIALTEADLRRAYPMLHDALVTHSWSGPIDRTYDSLPVFGQIAGSDNIHYGIGWSGNGVGPSRLGGRILASLALGRKDPWSGCALVGRRCKPFPPEPVRYLGGSMVRKAVIRKERAELNGKPANQFDVLMARFAPAGLEDKA
>NZ_CP045118.1|WP_152223170.1|2653110_2653455_+|DUF861-domain-containing-protein
MTPVLFRLDNAQFTEPAPAGIPIGEPIPMASTAAHQELASQNASSGFWECSPGRLRRAIMQAEYSYFIEGRGVFTPDGGEPIAFKAGDSIYFAANTHGEWEIIEKVRKAYLILG
>NZ_CP045118.1|WP_152228058.1|2653790_2654366_-|damage-inducible-protein-DinB
MSATSESQPESAATTRPAAPPTAATDSLKMLVRYKAWANELTFESVMNLPEGEALRPRQTRFGNMVHTLNHVYVVDDIFRHHLQDKKHHYTARNTEHPSPLGDLWSAVQAMDRWYIELVDTWSAKDLSKVVHFEFVGGGKGVMTQEEIVLHLVNHATYHRGFVGDMIYQIPVTPPSNDLPVFIRDHYRKAR
>NZ_CP045118.1|WP_152223173.1|2654481_2655327_-|PhzF-family-phenazine-biosynthesis-isomerase
MTYEFQMIDVFGAEPLSGNPLAVVMGADALKTDEMQRLTRWFNLSETAFLLSPTHPAADYRVRIFTLEREMPFAGHPTLGSCHAWLSTGRAPINENEIVQECGVGLVTIRREPGLLSFAAPPLIRSGPPSQEELAEAIQFLGIDLQDVIDAAWIDNGPGWLGIRLTSAEQVLALSPQRSWPRRIDIGVVGAHSHGDAAFEVRAFFNNHLGTIVEDPVTGSLNASLAQWLFSTGVVEEAYIAAQGTRLDRKGRIHVARDNAGQFWIGGKTQTQVTGRLQGLA
>NZ_CP045118.1|WP_152223175.1|2655378_2656008_-|LysE-family-translocator
MIGSPIALAYCSYFLAAASPGPSNMAIMGTAMRDGRMPALILACGVMTGSLAWAVLAATGISTLLATTAKALVVIKVLGGLYLLYLAMRAGSSALRPVPDVPRVDTARGTARYLPLYRQGVLMHIANPKAIMSWMAIMSLGLREDAPGGTLPAIIGGCAVLGIGIFGGYAILFSTARIIAFYSRVGRWIQGLFSALFAIAGVKLLVSPG

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Crispr_ID: NZ_CP045118_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP045118_4

5727694-5727794

Orphan

Consensus_repeat	Method
TCGCGGACAAAGTCCGCTCCTACG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP045118_4

>merge|NZ_CP045118|4|5727694-5727794|CRISPRCasFinder
TCGCGGACAAAGTCCGCTCCTACGCGGGCGCTATAGTCCGTGTTTACCTGTGGTAGTAATTTCATTCGCTATGGATTTCGCGGACAAGGTCCGCTCCTACG

>NZ_CP045118|4|4|5727694-5727794|CRISPRCasFinder
TCGCGGACAAAGTCCGCTCCTACG	CGGGCGCTATAGTCCGTGTTTACCTGTGGTAGTAATTTCATTCGCTATGGATT
TCGCGGACAAGGTCCGCTCCTACG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045118.1\|WP_152226895.1\|5728311_5728566_-\|outer-membrane-protein-assembly-factor-BamE	unknown	unknown	gnl\|CDD\|367908
NZ_CP045118.1\|WP_152226889.1\|5724803_5725394_-\|HutD-family-protein	unknown	unknown	gnl\|CDD\|377578
NZ_CP045118.1\|WP_152226901.1\|5730401_5730932_-\|lactoylglutathione-lyase	unknown	unknown	gnl\|CDD\|319900
NZ_CP045118.1\|WP_152226897.1\|5728639_5729245_-\|DUF924-family-protein	unknown	unknown	gnl\|CDD\|377592
NZ_CP045118.1\|WP_152226891.1\|5725390_5726161_-\|histidine-utilization-repressor	unknown	unknown	gnl\|CDD\|188194
NZ_CP045118.1\|WP_152226885.1\|5722645_5723668_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223836
NZ_CP045118.1\|WP_152226883.1\|5721770_5722565_+\|transporter-substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|270347
NZ_CP045118.1\|WP_152226903.1\|5731059_5732967_-\|autotransporter-domain-containing-protein	unknown	unknown	gnl\|CDD\|225780
NZ_CP045118.1\|WP_152226912.1\|5742145_5743555_+\|glutamate--ammonia-ligase	unknown	unknown	gnl\|CDD\|181884
NZ_CP045118.1\|WP_152226910.1\|5740359_5741814_-\|tRNA-4-thiouridine(8)-synthase-ThiI	unknown	unknown	gnl\|CDD\|234932
NZ_CP045118.1\|WP_152226875.1\|5714852_5716253_-\|amino-acid-permease	unknown	unknown	gnl\|CDD\|182566
NZ_CP045118.1\|WP_152226887.1\|5723660_5724395_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224051
NZ_CP045118.1\|WP_152226881.1\|5719519_5721196_-\|urocanate-hydratase	unknown	unknown	gnl\|CDD\|235448
NZ_CP045118.1\|WP_152226893.1\|5726239_5727604_+\|formimidoylglutamate-deiminase	unknown	unknown	gnl\|CDD\|236420
NZ_CP045118.1\|WP_152226879.1\|5717982_5719395_-\|cytosine-permease	unknown	unknown	gnl\|CDD\|224374
NZ_CP045118.1\|WP_152226906.1\|5734436_5738168_-\|DUF2339-domain-containing-protein	unknown	unknown	gnl\|CDD\|227665
NZ_CP045118.1\|WP_152226908.1\|5738371_5740189_-\|translational-GTPase-TypA	unknown	unknown	gnl\|CDD\|224138
NZ_CP045118.1\|WP_152226899.1\|5729244_5730258_-\|class-1-fructose-bisphosphatase	unknown	unknown	gnl\|CDD\|236458
NZ_CP045118.1\|WP_152226877.1\|5716351_5717881_-\|histidine-ammonia-lyase	unknown	unknown	gnl\|CDD\|236484
NZ_CP045118.1\|WP_152226905.1\|5733072_5734440_-\|DUF3999-family-protein	unknown	unknown	gnl\|CDD\|372507

Protein	Function_ID	Function_description	E-value
NZ_CP045118.1\|WP_152226895.1\|5728311_5728566_-\|outer-membrane-protein-assembly-factor-BamE	gnl\|CDD\|367908	pfam04355, SmpA_OmlA, SmpA / OmlA family. Lipoprotein Bacterial outer membrane lipoprotein, possibly involved in in maintaining the structural integrity of the cell envelope. Lipid attachment site is a conserved N terminal cysteine residue. Sometimes found adjacent to the OmpA domain (pfam00691).	4.52061e-07
NZ_CP045118.1\|WP_152226889.1\|5724803_5725394_-\|HutD-family-protein	gnl\|CDD\|377578	pfam05962, HutD, HutD. HutD from Pseudomonas fluorescens SBW25 is a component of the histidine uptake and utilisation operon. HutD is operonic with the well characterized repressor protein HutC. Genetic analysis using transcriptional fusions (lacZ) and deletion mutants shows that hutD is necessary to maintain fitness in environments replete with histidine. Evidence outlined by Zhang & Rainey (2007) suggests that HutD functions as a governor that sets an upper bound on the level of hut operon transcription. The mechanistic basis is unknown, but in silico molecular docking studies based on the crystal structure of PA5104 (HutD from Pseudomonas aeruginosa) show that urocanate (the first breakdown product of histidine) docks with the active site of HutD.	4.82254e-68
NZ_CP045118.1\|WP_152226901.1\|5730401_5730932_-\|lactoylglutathione-lyase	gnl\|CDD\|319900	cd07233, GlxI_Zn, Glyoxalase I that uses Zn(++) as cofactor. This family includes eukaryotic glyoxalase I that prefers the divalent cation zinc as cofactor. Glyoxalase I (also known as lactoylglutathione lyase; EC 4.4.1.5) is part of the glyoxalase system, a two-step system for detoxifying methylglyoxal, a side product of glycolysis. This system is responsible for the conversion of reactive, acyclic alpha-oxoaldehydes into the corresponding alpha-hydroxyacids and involves 2 enzymes, glyoxalase I and II. Glyoxalase I catalyses an intramolecular redox reaction of the hemithioacetal (formed from methylglyoxal and glutathione) to form the thioester, S-D-lactoylglutathione. This reaction involves the transfer of two hydrogen atoms from C1 to C2 of the methylglyoxal, and proceeds via an ene-diol intermediate. Glyoxalase I has a requirement for bound metal ions for catalysis. Eukaryotic glyoxalase I prefers the divalent cation zinc as cofactor, whereas Escherichia coil and other prokaryotic glyoxalase I uses nickel. However, eukaryotic Trypanosomatid parasites also use nickel as a cofactor, which could possibly be explained by acquiring their GLOI gene by horizontal gene transfer. Human glyoxalase I is a two-domain enzyme and it has the structure of a domain-swapped dimer with two active sites located at the dimer interface. In yeast, in various plants, insects and Plasmodia, glyoxalase I is four-domain, possibly the result of a further gene duplication and an additional gene fusing event.	1.00344e-83
NZ_CP045118.1\|WP_152226897.1\|5728639_5729245_-\|DUF924-family-protein	gnl\|CDD\|377592	pfam06041, DUF924, Bacterial protein of unknown function (DUF924). This family consists of several hypothetical bacterial proteins of unknown function. Structurally, this family resembles TPR-like repeats.	1.15055e-81
NZ_CP045118.1\|WP_152226891.1\|5725390_5726161_-\|histidine-utilization-repressor	gnl\|CDD\|188194	TIGR02018, Histidine_utilization_repressor, histidine utilization repressor, proteobacterial. This model represents a proteobacterial histidine utilization repressor. It is usually found clustered with the enzymes HutUHIG so that it can regulate its own expression as well. A number of species have several paralogs and may fine-tune the regulation according to levels of degradation intermediates such as urocanate. This family belongs to the larger GntR family of transcriptional regulators. [Energy metabolism, Amino acids and amines, Regulatory functions, DNA interactions].	4.64509e-129
NZ_CP045118.1\|WP_152226885.1\|5722645_5723668_+\|ABC-transporter-permease-subunit	gnl\|CDD\|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	9.8977e-86
NZ_CP045118.1\|WP_152226883.1\|5721770_5722565_+\|transporter-substrate-binding-domain-containing-protein	gnl\|CDD\|270347	cd13629, PBP2_Dsm1740, Amino acid-binding domain of the type 2 periplasmic binding fold superfamily. This subfamily includes the periplasmic binding protein type II (BPBII). This domain is found in solute binding proteins that serve as initial receptors in the ABC transport, signal transduction and channel gating. The PBPII proteins share the same architecture as periplasmic binding proteins type I (PBPI), but have a different topology. They are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBPII proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the family includes ionotropic glutamate receptors and unorthodox sensor proteins involved in signal transduction.	2.29296e-116
NZ_CP045118.1\|WP_152226903.1\|5731059_5732967_-\|autotransporter-domain-containing-protein	gnl\|CDD\|225780	COG3240, COG3240, Phospholipase/lecithinase/hemolysin [Lipid metabolism / General function prediction only].	1.26753e-78
NZ_CP045118.1\|WP_152226912.1\|5742145_5743555_+\|glutamate--ammonia-ligase	gnl\|CDD\|181884	PRK09469, glnA, glutamate--ammonia ligase.	0
NZ_CP045118.1\|WP_152226910.1\|5740359_5741814_-\|tRNA-4-thiouridine(8)-synthase-ThiI	gnl\|CDD\|234932	PRK01269, PRK01269, tRNA s(4)U8 sulfurtransferase; Provisional.	0
NZ_CP045118.1\|WP_152226875.1\|5714852_5716253_-\|amino-acid-permease	gnl\|CDD\|182566	PRK10580, proY, putative proline-specific permease; Provisional.	0
NZ_CP045118.1\|WP_152226887.1\|5723660_5724395_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224051	COG1126, GlnQ, ABC-type polar amino acid transport system, ATPase component [Amino acid transport and metabolism].	3.3116e-153
NZ_CP045118.1\|WP_152226881.1\|5719519_5721196_-\|urocanate-hydratase	gnl\|CDD\|235448	PRK05414, PRK05414, urocanate hydratase; Provisional.	0
NZ_CP045118.1\|WP_152226893.1\|5726239_5727604_+\|formimidoylglutamate-deiminase	gnl\|CDD\|236420	PRK09229, PRK09229, N-formimino-L-glutamate deiminase; Validated.	0
NZ_CP045118.1\|WP_152226879.1\|5717982_5719395_-\|cytosine-permease	gnl\|CDD\|224374	COG1457, CodB, Purine-cytosine permease and related proteins [Nucleotide transport and metabolism].	6.82223e-94
NZ_CP045118.1\|WP_152226906.1\|5734436_5738168_-\|DUF2339-domain-containing-protein	gnl\|CDD\|227665	COG5373, COG5373, Predicted membrane protein [Function unknown].	9.86778e-102
NZ_CP045118.1\|WP_152226908.1\|5738371_5740189_-\|translational-GTPase-TypA	gnl\|CDD\|224138	COG1217, TypA, Predicted membrane GTPase involved in stress response [Signal transduction mechanisms].	0
NZ_CP045118.1\|WP_152226899.1\|5729244_5730258_-\|class-1-fructose-bisphosphatase	gnl\|CDD\|236458	PRK09293, PRK09293, class 1 fructose-bisphosphatase.	0
NZ_CP045118.1\|WP_152226877.1\|5716351_5717881_-\|histidine-ammonia-lyase	gnl\|CDD\|236484	PRK09367, PRK09367, histidine ammonia-lyase; Provisional.	0
NZ_CP045118.1\|WP_152226905.1\|5733072_5734440_-\|DUF3999-family-protein	gnl\|CDD\|372507	pfam13163, DUF3999, Protein of unknown function (DUF3999). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 440 and 470 amino acids in length. There is a single completely conserved residue D that may be functionally important.	2.96631e-147

>NZ_CP045118.1|WP_152226893.1|5726239_5727604_+|formimidoylglutamate-deiminase
MPALIAPCALLPEGWAYDVRLEVSASGILEKISVGGSSEGAERLRGPVLAGMPNLHSHAFQRAMAGLAEVAGNPNDSFWTWRDLMYRLVGRLSPEQVGVIARQLYIEMLKAGYTGVAEFHYVHHDADGKPYANPAELALRVSQAAADAGIGLTLLPVLYSHAGFGGQAPSEGQRRFINSTEGYLKLIDGLRSHLATQPQQSVGLCFHSLRAVTPQQIAEVLGADSTGCPVHIHIAEQQKEVDDCLAWSGRRPLQWLYENVDVNERWCLVHATHAEADEVTSMARSGAVAGLCLTTEANLGDGIFPAVDYLAQGGRYGIGSDSHVSLSVVEELRWLEYGQRLRDQRRNRLYGANQPMVGRTLFDGALAGGAQALGQPTGALTVGKRADLLVLDGGDPYLQTASGDAILNRWLFAGGDRQVRDVMVAGQWRVRDGRHALEEQSAREFTDVLHELLN
>NZ_CP045118.1|WP_152226891.1|5725390_5726161_-|histidine-utilization-repressor
MTRRITVIKTPSRSSSLAAQLSDTPAPLYAQVKQMIIQQIQSGAWPAHHRVPSESELVEELGFSRMTINRALRELTADGLLLRMQGVGTFVAEPKGRSALFAVNNIADEIAARGHRHHCKVIRLAEELPSAERALALDLHNGQRVFHSLIVHYENEVPVQLEDRYVNAAVAPDYLKQDFTILTPYAYLSRVAPLTEGEHVVEAVLAEAEECRLLQIERNEPCLLIRRRTWSGNQAVTSARLIHPGSRHRLEGRFSS
>NZ_CP045118.1|WP_152226889.1|5724803_5725394_-|HutD-family-protein
MTQIQHFKAAEYPRMPWKNGAGSTLEIARDAGAGLDGFGWRLSIADVGADGGFSAFTGYQRVITVLEGEGMQLTVDGEQSRSLHQLDAFAFSGDSEVDCRLLGGAIRDFNLIYSPLRYRARLQWLSLEQPQRFFSSAATVLLFSAAQGLELRQEGASLAQLGRYDCLRIEGDAQLAAYELQAEVGGACCLIELLPR
>NZ_CP045118.1|WP_152226887.1|5723660_5724395_+|ATP-binding-cassette-domain-containing-protein
MIEVRDLIKTFNARGQLVRAVDNVGTSVAKGEVLVVLGPSGSGKSTFLRCLNGLEELDSGSIIIDGVDLAHPKTDINAYRREVGMVFQHFNLFPHMTVLENLCLAQKVVRKRGKAEREEKAKALLAKVGIAQKANEYPSRLSGGQQQRVAIARALCMGPKVMLFDEPTSALDPEMVGEVLDVMKTLAQEGMTMVCVTHEMGFAREVADRVLFFDHGKLLEDAPPAQFFDRPRDPRAQAFLKQVL
>NZ_CP045118.1|WP_152226885.1|5722645_5723668_+|ABC-transporter-permease-subunit
MNTLIRRLLPGNALAGQPAAKSLRKPGQWPWHALTIFLLIALAYGLWYSTSLISYEWRWNRVPQYFAYQAEDTQRAAEQGTVTKIDDEGDHTRVTLTGEDGKEQVVLVARDSLQVSQGDDLSEGDPVGVTRHWSAGPLFWGLWTTLWISFVSGAVGLLIGLFTGLCRLSNNPTLRDLSTVYVELVRGTPLLVQIFIFYFFIGTVLNLSREFAGVAALALFTGAYVGEIARAGVQSIARGQNEAARSLGLNAAQSMRHVILPQAFKRVLPPLAGQFISLVKDTSLVSVIAITELTKSGREAITTSFSTFEIWFCVAALYLLINLPLSQIANKLERRLGKSD
>NZ_CP045118.1|WP_152226883.1|5721770_5722565_+|transporter-substrate-binding-domain-containing-protein
MRKLLSMLLLSTCALTGLTAHAGAIDDAVKRGTLRVGMDPTYMPFEMTNKRGEIIGFEVDLLKAMAKSMGVKLELVSTSYDGIIPALLTDKFDMIGSGMTLTQERNLRINFSEPFIVVGQTLLIRKDLEGTIKSYKDLNDPKYRITSKIGTTGEMVAKKLIGKAQYHGFDNEQEAVLDVVNGKSDAFIYDAPYNVVAVNKAGAGKLTFLENPFTYEPLAFGLKKNDYDSLNWINNYLRQAREDGSYERIHSKWFKDTDWLKEME
>NZ_CP045118.1|WP_152226881.1|5719519_5721196_-|urocanate-hydratase
MNKPNRFRDVEIRAPRGTQLNAKSWLTEAPLRMLMNNLDPEVAENPKELVVYGGIGRAARNWECYDKIVETLKELNDDETLLVQSGKPVGVFKTHANAPRVLIANSNLVPHWASWEHFNELDAKGLAMYGQMTAGSWIYIGSQGIVQGTYETFVEAGRQHYNGNLTGRWVLTAGLGGMGGAQPLAATLAGACSLNIECQQTSIDFRLRSRYVDEQAADLDDALARIAKYTSEGKAISIALLGNAAEILPELVRRGVRPDMVTDQTSAHDPLNGYLPIGWTWDQYRDRAKTDPAAVVKAAKQSMAVHVQAMLDFQKQGVPTFDYGNNIRQMAKEEGVANAFDFPGFVPAYIRPLFCRGIGPFRWAALSGDPQDIYKTDAKVKELIPDDAHLHRWLDMARERISFQGLPARICWVGLGLRAKLGLAFNEMVRSGELSAPIVIGRDHLDSGSVSSPNRETEAMKDGSDAVSDWPLLNALLNTAGGATWVSLHHGGGVGMGFSQHSGMVIVCDGTDEAAARIARVLTNDPGTGVMRHADAGYQIAIDCAKEQGLNLPMITGK
>NZ_CP045118.1|WP_152226879.1|5717982_5719395_-|cytosine-permease
MSQASDSSKPLIERRSINYIPEAERHGKLYSQFTLWLGANLQITAIVTGALAVVLGGDVFWSLIGLLIGQLLGGGVMALHAAQGPKLGLPQMISSRVQFGVLGASIPMVLVCLMYMGFTATGTVLSGQALGQLFGVSDSVGILMFAGVIVLVTVLGYRVIHVIGRIASVIGVIAFVYLFSRLMTQTDIGALLAIRHFSWGGFLLAVSLAASWQIAFGPYVADYSRYLPSKTSSVKTFLAVGAGSVVGAQVAMIFGVFAAAMANGQFAGHEVAYIVGLGGSGTIAALLYFSIAFGKITISTLNSYGSFMCIATIISGFRGHLEVTRLQRLVFVLLIVGTATLIALLGQHSFLGAFKSFILFLLAFFTPWSAVNLVDYYCISRERYDVPALADPNGRYGRWNIPGISVYVTGVLVQLPFISTKFYTGPLVDALGGVDISWIIGLVVPAALYYLVARRTSVRSSCAEHPARGA
>NZ_CP045118.1|WP_152226877.1|5716351_5717881_-|histidine-ammonia-lyase
MKLHLKPGFLTLAELRQVHLAPVHLTLDASADAPINASVACVEKIIAEDRTAYGINTGFGLLASTRIASHDLENLQRSLVLSHAAGIGAPLDDAMVRLIMVLKINSLSRGFSGIRRKVIDALIALVNAEVYPHIPLKGSVGASGDLAPLAHMSLVLLGEGKARYKGEWLPASEALAVAGLEPLTLAAKEGLALLNGTQASTAYALRGLFQAEDLFASAIACGSLTVEAALGSRSPFDARIHDARGQRGQIDTAACFRDLLGDSSEVSKSHQDCGKVQDPYSLRCQPQVMGACLTQLRQAAEVLAIESNAVSDNPLVFAAEGDVISGGNFHAEPVAMAADNIALAIAEIGSLSERRISLMMDKHMSQLPPFLVANGGVNSGFMIAQVTAAALASENKALSHPHSVDSLPTSANQEDHVSMAPAAGKRLWEMAENTRGVLAIEWLGACQGLDLREGLKTSAKLEQARQTLRREVAHYDRDRFFSPDIEAASALLAKGCLTGLLLAGVLPSL
>NZ_CP045118.1|WP_152226875.1|5714852_5716253_-|amino-acid-permease
MQEGLKRGLSARHIRFMALGSAIGTGLFYGSASAIQMAGPAVLLAYLIGGAAVFMVMRALGEMAVHNPVAGSFGHYASTYLGPMAGFVLGWTYAFEMVIVAIADITAFGIYMGFWFPDVPRWMWVMSIVFLIGGLNLCNVKVFGEMEFWLSLLKVGAIVAMIVAGFGIMIFGLGHHVSADAAMGVSNLVGHGGFMPNGIGGLIASFAVVMFAFGGIEIIGVTAGEAKDPQHVLPRAINAVPARILLFYVLTLFVLMCLYPWPQIGTQGSPFVQIFSNLGIGSAAAVLNVVVISAAISAINSDIFGAGRMMYGLAQQGQAPRSFGKVSRHGVPWLTVVVMGGALLVGVLLNYLIPENVFLLIASIATFATVWVWLMILVSQVAMRRSMSREEAAQLKFPVPFWPYGPALAIAFMVFIVGVLGYFPDTQTALIVGVIWVVFLVASYLIWCKPRAGKGEQVREQASLNR
>NZ_CP045118.1|WP_152226895.1|5728311_5728566_-|outer-membrane-protein-assembly-factor-BamE
MSFRRLALVAFCVVLAACSKINQENYSKIKTGMTKTEVESLLGKPTECSGALGVSSCTWGDEKTFISIQYAGDKVLLFSAQGLK
>NZ_CP045118.1|WP_152226897.1|5728639_5729245_-|DUF924-family-protein
MAATPWQPLLDWWFGSALDAVEVSAQRSALWFGKSACQDVDSENRFGGLVRQALDGGLQDWVDEPQGWLALILLLDQLPRMIFRDSPRAFAGDARAQRLVRQGLEAGFDRKLPRVERVFVYIVLEHAEDLASQDQAVRLYEALQAESSDSEKVLFAGYLAYARKHQAVIARFGRFPHRNAILGRPSTAEETQFLTEPGSRF
>NZ_CP045118.1|WP_152226899.1|5729244_5730258_-|class-1-fructose-bisphosphatase
MSRVTLSRYLIEQTRSHNTPADLRFLVEVVARACKEISHAVSKGALGGVLGSMGTENVQGEVQKKLDVISNEILLEANEWAGNLAGMASEEMDHPYQIPGKYPKGAYLLVFDPLDGSSNIDVNVSVGTIFSVLRCPTEYLSQNDSLREEAFLQPGTTQVAAGYAIYGPQTMLILTLGNGVKGFTLDRELGSFVLTHENITVPTSTAEFAINMSNERHWEAPVKRYVSELLAGNEGPLGKNYNMRWIASMVADVHRILTRGGVFMYPRDSREPEKPGKLRLMYEANPMSFIIEQAGGAATNGHQRILDIQPENLHQRVAVFLGSKEEVERATAYHKEG
>NZ_CP045118.1|WP_152226901.1|5730401_5730932_-|lactoylglutathione-lyase
MTFTTELQPGVCAEPEAVTQDYVFNHTMLRVKNPAPSLDFYTRVLGMRLLRRLDFEEGRFSLYFLAHTQGQAVPDDPGERQRYTFGRESVLELTHNWGTESDDSQYHNGNGEPRGFGHICFSVPDIQAACERFEALGVPFVKPLARGMKNVAFIADPDGYWVEIVQASLNGELGRG
>NZ_CP045118.1|WP_152226903.1|5731059_5732967_-|autotransporter-domain-containing-protein
MIRQALTPLAAACVLAIASQASAAPSPYSTMVVFGDSLSDSGQFPDAGGPAGGATRFTNRTGPTYLDGHGEAFGPTAPMILGGKLGIAAADLNPSTSLVAGTQDGNDWAVGGYRTDQIYDSITAPGGSVVSAGGDTRTRDGYLVGRMADPNALYYLTGGGNDFLQLRITNDPTARAAAGRLVDSVDALHNAGARYIMVWLLPDLGLAPATNGTPLQSFGTQLSGIFNEELVNQLAASNANVIPLNIPGLLKEVLADPGAYGLATGTNLVGTCFSGNNCPENPLYGRHSATPDPTKLIFNDGVHPTIAGQRLIADYAYSVLAAPWEATLLPEMALGTYNGFQDTLHSQWLADWGNWQGTGQWRGFISGGGQHLDYDDQDSAASGDGFGYNLTLGGSYRLDDAWRVGAAAGFYRQKLEAGAEDSDYKLNSYLGSLFAQFQQNRWWADAAVTGGYLDYDEANRKFTLVDRTLEEKGDTKGSLLALSGRLGYDIAQGGENWHLSPFVSADWARVKVDSYDENGGHSTSLAFDEQDRYSRRLGAGLQGKLDLSAETQLFGEVAVEREYADDTQNIGMNFTSLPANGFTLQGYTPQSHMERLSLGFSQKLTPELSLRGGYSAHHSSDDLQQGVNLALSLDF
>NZ_CP045118.1|WP_152226905.1|5733072_5734440_-|DUF3999-family-protein
MKLNTFCLIAGACLLVATAASAAPVPTDFANRVPLEVAGKGPWYRLQLPIDVLFAARHGDLRDVRIFNAEGEALPYSLRTGTASESRVGSEVQARIFPLRGQSGRAAADSVKVVRSTTGTILEITPSAPTQDAQQVLRGWLLETGSGDLPLDRLQLDWKAESDGFQRLRIEASDDLEHWRSFGEGQLARLDFNGQRIEQSAIALPGETARYLRLWWESPEQAAQLSGAILSGSRSSAGPIPMLWSAPLAAKADANGDFSWSLPLALPVERVRILLEQANTLAPVALSGRHDGNVQWTPLARGVLYRLPGEGGEITQEELELPGSAVSQLRLQLDARGGGLGGSTASLSIGVRATEVVFLARGGEPYQLAVGSASATDGGLPLSTLVPGFDAKRLSAMGEAHLKGSLQTQVAVAPGVEPKADGRWKRYGLWAVLLAGVGLLGLMALSLLRSSRPQN
>NZ_CP045118.1|WP_152226906.1|5734436_5738168_-|DUF2339-domain-containing-protein
MQWIFMLVGLVIGAAAGESITGAVLGAVVGLALGQAIALQTLQRRNAAMSRELSAFADRFEQGTQALYERLQKVERGAEQAPPSSVEYVAPDRPAAPVEPAPEAAPAVADSAAPDLEWDIELPVAEPSPAPAAATAAPVEPGIEWSELALEPLETPQPSVTESQVRAEASQPQTAPAAPPLPPEPPAPSLFDRAFGAARDWLLGGNTVLRVGVVLLFLGLAFLLRYATEGMTMPPQGPYIGTAAAALALLGLGWWLRQRRPAYALVLQGTGIAVLYLTVFAGIKLYPAMNHGEVLIDPQAGFMLLVAVTLFSAILAILQDALGLAAAAALGGFAAPILASTGGGNHVALFSYFALLNAGIFAIAWFKAWRMLNLIGFFGTFGIGLAWGLRAYKPELFATTEPFLILFFLTYVAIGLLFARRRLHEATGGPQDDSREALLRWSARQANYVDGTVLFGTPLVGFGLQYGVIQHLEFGAAFSALALGLFYMVLARLLAGRTAGRALLLVETCLALGVVFGTLAIPLGLDARWTSAAWAVEGAGIFWLGLRQQRPLARIFALLLQIGAALAFLADLRSDPLSLHLLEGAPLGALMLGVALLFSFWNLRKADPLTLRSWEPNVRPILATFGLGFLYLIAPLCLGADGTAMVWAVAGLATLFAGLRLRSRTFLACAFAVQLLGGAVFLLHLRGAEAGSGVLGSGWRGLVTASLIGLALIAGMLIAARDSLVRDDRRLMLGLSVVLLLGLAFINLAVLFVLPWRTAAAVWAGSGLLILWLSLQLQQRAAFVFGLVLQMIGAGAFLIGGPALFGDLPSEGLKPLAHMGFWTPAVLALAALVGAWRLHRASEHERDLALGGLGLEQLSQLLLIWGAGWWALTALWEIARFVPAEMREHVALLVAAVSVALWSLLARREQWRALALLCLALSPLAVVALASAWNLEYHPLAQLGWLGWLAVFAVHFFALRRLDAWLPRKAAQVAHVLGCWLILGVAALELRYLFFALAEHYNAWRWLGWALVPSCYLILMGGFPRLPWPVAAFEREYRAIAAVPVAVVLLGWFWLVNLFSDGSAEPLPYLPLLNPLELGMLIVLAAVFQWTRLGLPQLGFADSTLRLPVQAVLGASLFALLTMTVCRTAHHWGGVPFEFDFLSQSMLVQAGLSIVWALIALGLMIAGHLRGRRDFWLVGAVLLVVVVIKLFLVDRASGGSLERIISFIGVGVLMLIVGYFAPLPPRRPPPPSQEQPQQEQPSA
>NZ_CP045118.1|WP_152226908.1|5738371_5740189_-|translational-GTPase-TypA
MIEKLRNIAIIAHVDHGKTTLVDKLLRLSGTLDRKEAENERVMDSNDQEKERGITILAKNTALKWNDYSINIVDTPGHADFGGEVERVMSMVDSVLLVVDAQDGPMPQTRFVTQKAFKAGLRPIVVVNKIDRPGARPDWVIDQIFDLFDNLGATDEQLDFPIVYASALNGIAGMDHEKMDDNMDALFQAIIDHVPAPKVDVDGPFQMQISQLDYNSFLGVIGIGRIARGKVKTNTPVVAISDDGSKRNGRILKIMGHSGLQRVEVAEAEAGDIVCVSGMDELYISDTLCDPQNVEARPPLTVDQPTVSMTFQVNDSPFAGKEGKFVTSRNIKDRLDKELLHNVALRVEQGDSPEKFKVSGRGELHLSVLIETMRREGFELAVGRPEVVIIEKDGEKQEPYENVTIDIEEQHQGSVMEQMGLRKGDLTNMIPDGKGRVRLEYTIPARGLIGFRNNFLTLTSGTGILTSTFSHYGPIKAGEVTNRQNGVLVSMATGTALTYSLETLQSRGKLFLGPGDEIYEGQLAGINSRDNDLVINPTKGKKLDNMRASGKDEVIALVPPIRFTLEQALEFIADDELVEVTPKSIRLRKKLLDENDRKRYERSKV
>NZ_CP045118.1|WP_152226910.1|5740359_5741814_-|tRNA-4-thiouridine(8)-synthase-ThiI
MKLIVKVFQEITIKSRPVRKRFIRQLAKNIRTVLRDLDPELRVEGEWDNLDVETKVTDPKVLREMIERLTCTPGIGHFLEVHEYPLGDFDDILEKCKLHFADKLPGKIFSMRCKRAGKHPFTSIDVERYVGGGLRQHCGAAGVSLKNPEVQVRVEIRYDRLYVIHAQHEGLGGYPLGALEQVLVLMSGGFDSTVAAYQMMRRGMISHFVFFNLGGRAHELGVMEVAHYLWEKYGRSQRVLFVSVPFEEVVGEILTKVDDSYMGVTLKRMMLRAASRVAERLELNALVTGEAISQVSSQTLPNLSVIDRVTDTLVLRPLIVSHKQDIIDTATQIGTAEFAKHMPEYCGVISVNPTTQAKPYRVDHEETKFDMAVLDRALERSTQMTVDRVIDELGKDLPVEMVDEVLPGQIVVDIRHPDAQEDEPLALEGIEVLPMPFYAINSKFKELDPNRQYLLYCDKGVMSRLHAHHLVNEGHTNVRVYRPQ
>NZ_CP045118.1|WP_152226912.1|5742145_5743555_+|glutamate--ammonia-ligase
MSYKSQQLIKDHDVKWVDLRFTDTKGKQHHVTMPARDALDDDFFEAGKMFDGSSIAGWKGIEASDMILLPDDSTAVLDPFTEEPTLIIVCDIIEPSTMQGYERDPRNIAKRAEEYLKSTGIGDTVFVGPEPEFFIFDEVKFKSDTSGSMFKIFSEQASWNTDADIESGNKGHRPGLKGGYFPVPPVDHDHEIRTAMCNAMEEMGLVIEVHHHEVATAGQNEIGVKFNTLVAKADEVQTLKYCIHNVADAYGKTVTFMPKPLYGDNGSGMHVHMSISKDGKNTFSGEGYAGLSDTALYFIGGIIKHGKALNGFTNPATNSYKRLVPGFEAPVMLAYSARNRSASIRIPYVSSPKARRIEARFPDPAANPYLCFAALLMAGLDGIQNKIHPGDAADKNLYDLPPEEAKEIPQVCGSLKEALEELDKGRAFLTKGGVFTDEFIDAYIEIKSEEEIKVRTFVHPLEYDLYYSV

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Crispr_ID: NZ_CP045118_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP045118_5

5890709-5890822

Orphan

Consensus_repeat	Method
TCATACCTTGCCCTCCAGCTCTTTAGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP045118_5

>merge|NZ_CP045118|5|5890709-5890822|CRISPRCasFinder
TCATACCTTGCCCTCCAGCTCTTTAGCCACGATCTTGGGTGAAGAGTCTGTTGAAGGGGATGATGGGGGGATCACCTTGAAGGAAGTCATACCTTGCCCTCCAGCTCTTTAGCC

>NZ_CP045118|5|5|5890709-5890822|CRISPRCasFinder
TCATACCTTGCCCTCCAGCTCTTTAGCC	ACGATCTTGGGTGAAGAGTCTGTTGAAGGGGATGATGGGGGGATCACCTTGAAGGAAG
TCATACCTTGCCCTCCAGCTCTTTAGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP045118.1\|WP_152227143.1\|5883510_5884449_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|225176
NZ_CP045118.1\|WP_152227139.1\|5881907_5882531_-\|2OG-Fe(II)-oxygenase	unknown	unknown	gnl\|CDD\|226274
NZ_CP045118.1\|WP_152227141.1\|5882631_5883372_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP045118.1\|WP_152227149.1\|5885887_5886940_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378890
NZ_CP045118.1\|WP_152227157.1\|5894323_5895424_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270377
NZ_CP045118.1\|WP_152227151.1\|5887047_5889435_+\|penicillin-acylase-family-protein	unknown	unknown	gnl\|CDD\|376618
NZ_CP045118.1\|WP_152227161.1\|5896968_5898327_-\|glutamine-synthetase	unknown	unknown	gnl\|CDD\|223252
NZ_CP045118.1\|WP_152227137.1\|5881348_5881897_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP045118.1\|WP_152228333.1\|5893008_5894076_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270377
NZ_CP045118.1\|WP_152227163.1\|5898367_5899117_-\|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|224982
NZ_CP045118.1\|WP_152227147.1\|5885236_5885737_+\|transcriptional-regulator	unknown	unknown	unknown
NZ_CP045118.1\|WP_152227167.1\|5901016_5902078_+\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270377
NZ_CP045118.1\|WP_152227135.1\|5880600_5881095_-\|DUF523-domain-containing-protein	unknown	unknown	gnl\|CDD\|224597
NZ_CP045118.1\|WP_152227169.1\|5902133_5902769_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP045118.1\|WP_152227171.1\|5903044_5904154_+\|agmatine-deiminase	unknown	unknown	gnl\|CDD\|184135
NZ_CP045118.1\|WP_152227155.1\|5891702_5892857_-\|polyamine-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|183226
NZ_CP045118.1\|WP_152227165.1\|5899395_5900775_+\|glutamine-synthetase	unknown	unknown	gnl\|CDD\|223252
NZ_CP045118.1\|WP_152227145.1\|5884574_5885150_+\|thiol-disulfide-isomerase	unknown	unknown	gnl\|CDD\|239267
NZ_CP045118.1\|WP_152227133.1\|5880034_5880466_-\|DUF4399-domain-containing-protein	unknown	unknown	gnl\|CDD\|373020
NZ_CP045118.1\|WP_152227159.1\|5895541_5896906_-\|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|180994

Protein	Function_ID	Function_description	E-value
NZ_CP045118.1\|WP_152227143.1\|5883510_5884449_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|225176	COG2267, PldB, Lysophospholipase [Lipid metabolism].	4.56163e-47
NZ_CP045118.1\|WP_152227139.1\|5881907_5882531_-\|2OG-Fe(II)-oxygenase	gnl\|CDD\|226274	COG3751, EGL-9, Predicted proline hydroxylase [Posttranslational modification, protein turnover, chaperones].	1.2284e-44
NZ_CP045118.1\|WP_152227149.1\|5885887_5886940_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378890	pfam12625, Arabinose_bd, Arabinose-binding domain of AraC transcription regulator, N-term. AraC is a bacterial transcriptional regulatory protein with a DNA-binding domain at the C-terminus, HTH_AraC, pfam00165, and this dimerization domain which harbours the arabinose-binding pocket at the N-terminus. AraC positively and negatively regulates expression of the proteins required for the uptake and catabolism of the sugar L-arabinose 1,2,3].	1.78511e-28
NZ_CP045118.1\|WP_152227157.1\|5894323_5895424_-\|extracellular-solute-binding-protein	gnl\|CDD\|270377	cd13659, PBP2_PotF, The periplasmic substrate-binding component of an ABC putrescine transport system and related proteins; contains the type 2 periplasmic-binding fold. This group represents the periplasmic substrate-binding domain that serves as the primary polyamine receptor of ABC-type putrescine-preferential transporter from gram-negative bacteria. Polyamine transport plays an essential role in the regulation of intracellular polyamine levels which are known to be elevated in rapidly proliferating cells and tumors. Natural polyamines are putrescine, spermindine, and spermine. They are polycations that play multiple roles in cell growth, survival and proliferation, and plant stress and disease resistance. They can interact with negatively charged molecules, such as nucleic acids, to modulate their functions. Members of this family belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	0
NZ_CP045118.1\|WP_152227151.1\|5887047_5889435_+\|penicillin-acylase-family-protein	gnl\|CDD\|376618	pfam01804, Penicil_amidase, Penicillin amidase. Penicillin amidase or penicillin acylase EC:3.5.1.11 catalyzes the hydrolysis of benzylpenicillin to phenylacetic acid and 6-aminopenicillanic acid (6-APA) a key intermediate in the the synthesis of penicillins. Also in the family is cephalosporin acylase and aculeacin A acylase which are involved in the synthesis of related peptide antibiotics.	0
NZ_CP045118.1\|WP_152227161.1\|5896968_5898327_-\|glutamine-synthetase	gnl\|CDD\|223252	COG0174, GlnA, Glutamine synthetase [Amino acid transport and metabolism].	9.17632e-157
NZ_CP045118.1\|WP_152227135.1\|5880600_5881095_-\|DUF523-domain-containing-protein	gnl\|CDD\|224597	COG1683, COG1683, Uncharacterized conserved protein [Function unknown].	6.32978e-62
NZ_CP045118.1\|WP_152228333.1\|5893008_5894076_-\|extracellular-solute-binding-protein	gnl\|CDD\|270377	cd13659, PBP2_PotF, The periplasmic substrate-binding component of an ABC putrescine transport system and related proteins; contains the type 2 periplasmic-binding fold. This group represents the periplasmic substrate-binding domain that serves as the primary polyamine receptor of ABC-type putrescine-preferential transporter from gram-negative bacteria. Polyamine transport plays an essential role in the regulation of intracellular polyamine levels which are known to be elevated in rapidly proliferating cells and tumors. Natural polyamines are putrescine, spermindine, and spermine. They are polycations that play multiple roles in cell growth, survival and proliferation, and plant stress and disease resistance. They can interact with negatively charged molecules, such as nucleic acids, to modulate their functions. Members of this family belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	0
NZ_CP045118.1\|WP_152227163.1\|5898367_5899117_-\|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein	gnl\|CDD\|224982	COG2071, COG2071, Predicted glutamine amidotransferases [General function prediction only].	2.42832e-102
NZ_CP045118.1\|WP_152227167.1\|5901016_5902078_+\|extracellular-solute-binding-protein	gnl\|CDD\|270377	cd13659, PBP2_PotF, The periplasmic substrate-binding component of an ABC putrescine transport system and related proteins; contains the type 2 periplasmic-binding fold. This group represents the periplasmic substrate-binding domain that serves as the primary polyamine receptor of ABC-type putrescine-preferential transporter from gram-negative bacteria. Polyamine transport plays an essential role in the regulation of intracellular polyamine levels which are known to be elevated in rapidly proliferating cells and tumors. Natural polyamines are putrescine, spermindine, and spermine. They are polycations that play multiple roles in cell growth, survival and proliferation, and plant stress and disease resistance. They can interact with negatively charged molecules, such as nucleic acids, to modulate their functions. Members of this family belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.39939e-149
NZ_CP045118.1\|WP_152227155.1\|5891702_5892857_-\|polyamine-ABC-transporter-ATP-binding-protein	gnl\|CDD\|183226	PRK11607, potG, putrescine ABC transporter ATP-binding subunit PotG.	1.15375e-178
NZ_CP045118.1\|WP_152227169.1\|5902133_5902769_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	7.15691e-09
NZ_CP045118.1\|WP_152227171.1\|5903044_5904154_+\|agmatine-deiminase	gnl\|CDD\|184135	PRK13551, PRK13551, agmatine deiminase; Provisional.	0
NZ_CP045118.1\|WP_152227165.1\|5899395_5900775_+\|glutamine-synthetase	gnl\|CDD\|223252	COG0174, GlnA, Glutamine synthetase [Amino acid transport and metabolism].	4.46897e-155
NZ_CP045118.1\|WP_152227145.1\|5884574_5885150_+\|thiol-disulfide-isomerase	gnl\|CDD\|239267	cd02969, PRX_like1, Peroxiredoxin (PRX)-like 1 family; hypothetical proteins that show sequence similarity to PRXs. Members of this group contain a conserved cysteine that aligns to the first cysteine in the CXXC motif of TRX. This does not correspond to the peroxidatic cysteine found in PRXs, which aligns to the second cysteine in the CXXC motif of TRX. In addition, these proteins do not contain the other two conserved residues of the catalytic triad of PRX. PRXs confer a protective antioxidant role in cells through their peroxidase activity in which hydrogen peroxide, peroxynitrate, and organic hydroperoxides are reduced and detoxified using reducing equivalents derived from either thioredoxin, glutathione, trypanothione and AhpF.	0.00102006
NZ_CP045118.1\|WP_152227133.1\|5880034_5880466_-\|DUF4399-domain-containing-protein	gnl\|CDD\|373020	pfam14347, DUF4399, Domain of unknown function (DUF4399). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria, archaea and eukaryotes. Proteins in this family are typically between 135 and 1079 amino acids in length.	1.28545e-47
NZ_CP045118.1\|WP_152227159.1\|5895541_5896906_-\|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|180994	PRK07480, PRK07480, putative aminotransferase; Validated.	0

>NZ_CP045118.1|WP_152227151.1|5887047_5889435_+|penicillin-acylase-family-protein
MKRTLTVLAVVVAAAAAGTGWYLHGKQPQRDGQLPLAGLHGEVTVRYDERGVPHIKAGSEDDLYRAIGYVHAQDRLFQMEMLRRLSRGELAEVLGPKLLDTDRMFRSLRIRDKAADYVARQDKNSPAWKALVAYLDGVNQFQDSHPRPLEFDILGIPKRPFTPEDTVSVAGYMAYSFAAAFRTEPVLTYVRDELGADYLKVFDLDWHPEGVLKPSSLAAADWQDLNAIARISHAALEEAGLPQFEGSNAWAVAGSRTKSGKPLLAGDPHIRFAAPAVWYEIQASAPGFELYGHYQALNPFASLGHNEQFGWSLTMFQNDDVDLVAEKVNPDNPNQVWYHGQWVDLTNEEQSIAVKGQAPVKITLRRSPHGPLVNDALGTAAGKTPIAMWWAFLETQNPILDAFYQLDRADTLDKARAAASKIHSPGLNVVWANARGDIGWWASAQLPVRPDGVVPYFLLDGSTGQADKNGFYPFSENPQEENPARGYIVSANFQPVPANGRPIPGYYNLPDRGQRLNERLADTSVKWDLQNSQALQLDTATGYGPRVLKPLLPLLREAASTAEETTLVEHLAAWQGDHPVDSATATLFNQLLYQIADGAMRDEMGDAFFDNLLSTRVLDIALPRLVADDSSPWWDNRKTPQKETRADIVKAAWKASLAHLRATLAQDSAEWQWGKAHTLTHSHPLGQQKPLDRIFNVGPFAAPGGHETPNNLSHRVGPAPWQVVYGPSTRRLIDFADPTHSLGINPVGQSGVPFDKHYDDQAEAYVEGQYLPQHYEDAEVKANTHGLLKLVPASR
>NZ_CP045118.1|WP_152227149.1|5885887_5886940_-|helix-turn-helix-domain-containing-protein
MSAPELHFPSAPALTQSATLRRLLYESLADLGFDPTDIYRLALQKVRLPAPAQSGRLVHDDAPLFWSTLDEITGDRDIGLHLGEVMKPRLLDVVGYLLMASADLREALASFVRFQHILSGGFAAQMLEEGEQVRLILDLNYLGVPSLRQQMECLMLLFLKLLALITDGEFRADAIEFRHALPSRLTEHRRLYGTTPRFGQPHDAVLFDRALLSRPSRTANPDLHRLLSAHAREQLGTFDENDLLNRLRYLIAVRLGAAECSLRSCAGELGVRPGLLQRSLAARAQTFRDVREDVRRQRAAQMLDQGMAIREVARACGFAELSPFYRAFRRWYSAPPERYRQWLRGGGAES
>NZ_CP045118.1|WP_152227147.1|5885236_5885737_+|transcriptional-regulator
MRLHSALAFCAVLALPMVAHADDTPSSSQVMAQHKQAINNRLADIDYKRKRIVEANMKLNPQEGEKFWPIYNSYRTEADKLSKKTLAIIIDYAGAYNTGAVSDDDATKLQKQVLQLQDDKQDLKEKYVKRIAKEVSPTRALRFLQIEDQLDAMAMLEVTREIPLAD
>NZ_CP045118.1|WP_152227145.1|5884574_5885150_+|thiol-disulfide-isomerase
MSPRRKTLIGWLLAALCLAGLLSTYWWYEKRYIRPFSHQPQLFSGDHLMLPAELAGPGRIRLVHFWDPACPCNVGNQQHLAELIARFASQGVDFYAVQRPGSHGQLPDTLKAMRTLPTLPSAEQLPASPAVAIWDAQGNLAYVGPYSEGAVCTSSNSFIEPILDALVQGRHVQATHTLAVGCYCPWISTAK
>NZ_CP045118.1|WP_152227143.1|5883510_5884449_-|alpha/beta-fold-hydrolase
MPEAFQPDLLRPLLRPLTAATTEGGVALYQRFYGLDLAGRYPGLQSRLGTFEAGGYRIAAQLWRPVVARGTLLLMHGYYDHMGLYRHVIDWAVGMGFAVLACDLPGHGLSEGKAASIGDFSEYQAVLAGLLGQAQALDLPKPWHLCGQSTGGAILLDYLLTGEMRPELGRTILLAPLVRPRAWGWSKLSYQVLRPFVDSIPRRFTENSTDPEFLAFLRDRDPLQPRTLPTAWVGALARWIPRIEAASPGPQSLLVVQGDADETVDWRYNLRVLEDKFEKIECLLLTGARHHLANESEVLRQRYFEFLSERLG
>NZ_CP045118.1|WP_152227141.1|5882631_5883372_+|hypothetical-protein
MRVLLALTLLVLGMPALADNYQRLYQAAGWPEQRAHFNDALHAAQKRYQGNLPPALYQALVDNSNRRFAAADIDQRALASLRQNLPDNSSALNFFESPLGQKVATAETFATRSDQLLKYANGLPRQQASDARRQLVQRLGKVLPAREAGAEVSLALASVAADSLSQMLPGLLGGGQAQGMLEGQRQKLMGQIGADLDNTLLYVYRGLSDAELSQFTAFGESPAGRGYYRAALAALRAGLSVSSDGQ
>NZ_CP045118.1|WP_152227139.1|5881907_5882531_-|2OG-Fe(II)-oxygenase
MDLDADSPLLHSIVDDLAEKGWSVQDDVLPAPLIAALAAECRARDAAGKLAAAGIGRGDGLAVREGVRGDRIQWIEPAQSEACDRYLVSLDALRQLINRSLFLGLEDFEGHFALYPPGAFYQKHLDRFRDDDRRSVSAVFYLNPDWQADQGGALRMYLPDGQALDLAPLGGRLVVFLSGDFPHEVLPANQERLSLTGWFRRRGDSSF
>NZ_CP045118.1|WP_152227137.1|5881348_5881897_+|hypothetical-protein
MSRLFALSAATAALLHLSVGQAALQALDNESLGAVTGQDGISIRADVLAHIGSAAWNDDGGSVSLRNVSIDNGCANAGDCPDGRGGSLPYGAAQLGLSLPIFGIEQPTLQVDVVQNASGQQQLALTLPDLTTINQQLNSSGLPAQTIRMRVIGDLYVGDGRLGTLEIRDIQDISGTIKVWGH
>NZ_CP045118.1|WP_152227135.1|5880600_5881095_-|DUF523-domain-containing-protein
MQKVLVSRCLLGHRVRYDGGAHGPFDLLARWLAQGRVVALCPEVAGGLPTPRAPAEIPGGQGMAVLERVKPVVTVDGEDVSQAFLLGADAAVKLVQHHDIRLAVLKARSPSCGNLENYDGSFSGRKVAGEGVTAAALKRMGVLVFSEEQLDAAAVCLAGLEAGG
>NZ_CP045118.1|WP_152227133.1|5880034_5880466_-|DUF4399-domain-containing-protein
MRTMLPCLGLAALLAASSAIAADMPRTPAPEGAKVYFIEPADGATVGKTFTVKFGLKGMGVAPAGVDSPATGHHHLLIDLKEQPAMNMPLPMTDNIKHFGKGQTETEVTLPPGKHTLQLLVGDKNHVPLDPPVESQTITVNVK
>NZ_CP045118.1|WP_152227155.1|5891702_5892857_-|polyamine-ABC-transporter-ATP-binding-protein
MAIASGAYKKALSGDQKPKEVLVKIDRVSKQFDETLAVDSVSLDIKKGEIFALLGGSGSGKSTLLRMLAGFERPTEGRIFLDGQDITDLPPYERPINMMFQSYALFPHMSVAQNIAFGLKQDGLPKGEIDKIVDEMLKLVQMTQYAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRSQMQLELVEIIERVGVTCVMVTHDQEEAMTMAQRIAIMHLGCIEQIGSPMDIYETPASRLICEFIGNVNLFDGEIVQDLQDHAVIACPQLENPIYIGHGISTRAENKRITYALRPEKVMVSAQKPENLEHEGFNWAQGTVYDIAYLGGHSVYYIKLASGMIVQAFMANAERHVARPTWEQPVYISWYDDSGVVLQA
>NZ_CP045118.1|WP_152228333.1|5893008_5894076_-|extracellular-solute-binding-protein
MAAVSVFGLASLAQAGQTVHIYNWSDYIGETTLADFEKETGIKPVYDVFDSNETLEGKLLAGRTGYDVVVPSNHFLGRQIKAGAFQKLDKSQLPNWSNLDPHLMKQLEANDPGNQYGVPYLWGTNGIGYNVDKVKAVLGVDKIDSWAILFEPENMKKLSQCGVAFLDSGDEMMPAVLKYMGLDPNSANPDDYKKVEEKLMAVRPYVTYFHSSKYISDLANGNICVAAGFSGDVFQAANRAKEAGKGVKIAYAIPKEGANLWFDILAIPKDASNPKAAHAFINYLLKPEVIAKVSDYVGYANPNPKAGEFMDESVRNNPEVYPPQEVLDKLFVQHELPPKILRLMTRSWTKIKSGK
>NZ_CP045118.1|WP_152227157.1|5894323_5895424_-|extracellular-solute-binding-protein
MFNTLGKSLLAVTLAGAVAGMAQADDKVLHVYNWSDYIAPDTVDKFTKETGIKVVYDVYDSNEVLEAKLLAGKSGYDIVVPSNSFFAKQIKAGVYQPLDRSKLPNWKNLNPDIMKTMEVSDPGNKYGIPYMWGTIGIGYNPDKVKAALGDNAPVDSWDLVFKPENIQKLKGCGVSFLDSPTEMLPAALHYLGYKSDSQDPKELKEAEALFLKIRPYISYFHSSKYISDLANGNICVAIGYSGDVYQAKSRAAEAKNGVKVAYNIPKEGAGAFFDTVAIPKDAENPEAALKWVNFILEPQIMAEISDTVSYPNGNAAATPLVSEAIRNDPGIYPTDAVMKKLYAFPDLPAKTQRLMTRSWTTIKSGK
>NZ_CP045118.1|WP_152227159.1|5895541_5896906_-|aminotransferase-class-III-fold-pyridoxal-phosphate-dependent-enzyme
MTIQTSAKTQHWQALSREHHLAPFTDYKQLNEKGARIITKAEGVYLWDSEGNKILDGMAGLWCVNVGYGRKELAEVAYKQMQELPYYNLFFQTAHPPVLELAKAIADIAPEGMNHVFFTGSGSESNDTVLRMVRHYWTIKGKPQKKVVIGRWNGYHGSTVAGVSLGGMKALHEQGDLPIPGIVHIPQPYWYGEGGDMSPEEFGVWAAEQLEKKILEVGEDKVAAFIAEPIQGAGGVIVPPETYWPKIREILAKYEILFIADEVICGFGRTGEWFGSQYYGNAPDLMPIAKGLTSGYIPMGGVIVRDEIVHTLNEGGEFYHGFTYSGHPVAAAVALENIRILREEKIVERVKAETAPYLQKRWQELADHPLVGEARGVGLVAALELVKNKKTRERFEKGVGMVCREHCFRNGLIMRAVGDTMIISPPLVIEKSQIDDLITLARKCLDQTAAAVLS
>NZ_CP045118.1|WP_152227161.1|5896968_5898327_-|glutamine-synthetase
MTTKLDQLSSWLKERKITEVECMIADLTGIARGKIAPTAKFLNEKGMRLPESVLLQTVTGDYVEDDIYYDLLDPADIDMVCRPDENAVFLVPWAIEPTAMVIHDTYDKMGNPIELSPRNVLKRVLKLYADKGWKPIVAPEMEFYLTKRSDDPDYPLQAPVGRSGRQETGRQSFSIDAANEFDPLFEDMYDWCELQGLDLDTLIHEEGTAQMEINFRHGDALDLADQIVVFKRTMREAALKHNVAATFMAKPMTGEPGSAMHLHQSIVDIKTGKNIFSNADGSMSELFLHHIGGLQKFIPEALPLFAPNVNSFRRFLPDTSAPVNVEWGEENRTVGLRVPDSNPENRRVENRLAGADANPYLALAASLLCGYIGMVEGLKPSAQVKGRGYERRNLRLPLTIEAALERMEGSKTLESYLGDKFIRGYVAVKRAEHENFKRVISSWEREFLLLSV
>NZ_CP045118.1|WP_152227163.1|5898367_5899117_-|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein
MSRLPLIGVSACIKQIGSKPYHVTGDKYLRAVISGASGIPVIIPSLGDAIDQEAMLAALDGLLFTGSSSNVEPHHYSGSASEAGTLHDPARDSTTLPLIRRAVAAGIPVLGICRGFQEMNVAFGGSLHQKVHEVEGLMDHREPADQPLEVQYGLRHAVSVQPGGVFAGIGLPSQFQVNSIHGQGVERLAPGLRVEALAPDGLVEAFSVEGAAFAVGVQWHPEWQVETNPNYLAIFQAFGKACGKRAGSR
>NZ_CP045118.1|WP_152227165.1|5899395_5900775_+|glutamine-synthetase
MSVPQSAVSLEEASEFLKEHPEVQFVDLLIADMNGVVRGKRIERTSLPKVYEKGINLPASLFALDITGSTVESTGLGLDIGDADRVCFPIPNTLSMEPWQKRPTAQLLMTMHEMEERVPFFADPREVLRQVVQKFTDIGLTIVAAFELEFYLIDQENVNGRPQPPRSPISGKRPQSVQVYSIDDLDEYADCLQDIIDGARAQGIPADAIVKESAPAQFEVNLHHVDDALKACDYAVLLKRLIKNVAYDHEMDSTFMAKPYPGQAGNGLHVHVSLLDKDGKNIFTSEDPEQNAALRHAIGGVLETLPASMAFLCPNVNSYRRFGSAFFVPNAPSWGLDNRTVALRVPTGAAEAVRLEHRVAGADANPYLLLSAVLAGIHHGLTNQVDPGAPIEGNAYEQLEQSLPNNLRDALRELDDSDVMNKYISPEYIDIFVACKEHEMQEFEYSISDLEYNWYLHTV
>NZ_CP045118.1|WP_152227167.1|5901016_5902078_+|extracellular-solute-binding-protein
MPRLYALMLLLLCPLSGWADQVIRVYNWNDYIAPEVLKDFEKDTGVRVEYHTYSTDEELLKALDQGEHIDVAVPSHNDLPALIRKKLIQPLDFAKLPNRSHLDSQLLSKLAAVDLNNQHAVPYLWGAVGLAINEPAAEKAYGGKLPDSWSLLFDPQQSQRLKSCGMSMLDAPDEAFSVLMNYQGRNFARSAPSQIRRAGEVLTQLRPNLRYIDSERYIQDLNSGKLCVAMAWVGDALNAANAGQPVRFVVPQEGSVLFIDNLVIPTSAEQPDLAHKFIDYLMQPKVAAQITAATLYPNGNKDSAQFLDAALRDQPGLYPDQETKRRLFALETAPEKTAPVITEVWGKLRAGGS
>NZ_CP045118.1|WP_152227169.1|5902133_5902769_+|TetR-family-transcriptional-regulator
MPAPTRKPRASSQARIAVILDAARAQLAEGGAASLSIYAVAERAQIPPSSVYHFFPSVPTLLQGLTSDVHAAFRACLEQPVDHAALRDWRDLARLVEQRTLAVYAGDAAARQLILASHGLAEVTQADSQHDVQLGQAMRELFERHFELPPLPQDLEVFSLAIELGDRVYALSVQRHGQITERLAEEGMRVIDAYLSLYLPPCLPKRPAPQQ
>NZ_CP045118.1|WP_152227171.1|5903044_5904154_+|agmatine-deiminase
MTTLTSTPRADGFRMPAEWEPHTQTWMVWPERPDNWRLGGKPAQAAFSAVARAIARFEPVTIGVSAGQYENARAQLADASNIRVVEISNDDAWVRDTGPTFVTNNSGEVRGVDWTFNAWGGLEGGLYFPWHRDDQVASKILGTERCDGYRTEGFVLEGGSIHVDGEGTVITTEECLLNHNRNPHLSREEIEANLRDHLAIDTVIWLPDGLFNDETDGHVDNFCCYVRPGEVLLAWTDDVNDPNYARCQAAMRVLETARDAKGRQLTVHKIVIPGPIHATEAECEHIDLVIGTQPRDPSIRLAGSYVNFLIVNGGIIAPRFDDPADAEAEATLKRIFPEHEVVMVPGREILLGGGNIHCITQQQPAPQKR

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP045118_2	2.1\|209979\|31\|NZ_CP045118\|CRISPRCasFinder	209979-210009	31	NC_049489	Arthrobacter phage DrYang, complete genome	62808-62838	9	0.71
NZ_CP045118_2	2.1\|209979\|31\|NZ_CP045118\|CRISPRCasFinder	209979-210009	31	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1565036-1565066	9	0.71
NZ_CP045118_2	2.1\|209979\|31\|NZ_CP045118\|CRISPRCasFinder	209979-210009	31	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1486273-1486303	9	0.71
NZ_CP045118_2	2.1\|209979\|31\|NZ_CP045118\|CRISPRCasFinder	209979-210009	31	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	328445-328475	9	0.71
NZ_CP045118_2	2.1\|209979\|31\|NZ_CP045118\|CRISPRCasFinder	209979-210009	31	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	1493316-1493346	9	0.71
NZ_CP045118_2	2.1\|209979\|31\|NZ_CP045118\|CRISPRCasFinder	209979-210009	31	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	57563-57593	9	0.71

1. spacer 2.1|209979|31|NZ_CP045118|CRISPRCasFinder matches to NC_049489 (Arthrobacter phage DrYang, complete genome) position: , mismatch: 9, identity: 0.71

gaaacccaagccggtggaaagggccatcccc	CRISPR spacer
gaaacccaagcccgtggaaaggaaagaacag	Protospacer
************ *********.  .  *

2. spacer 2.1|209979|31|NZ_CP045118|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.71

gaaacccaagccggtggaaagggccatcccc	CRISPR spacer
ccacaccatgccggtggaaaaggccatcgag	Protospacer
  *  *** ***********.*******

3. spacer 2.1|209979|31|NZ_CP045118|CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 9, identity: 0.71

gaaacccaagccggtggaaagggccatcccc	CRISPR spacer
ccacaccatgccggtggaaaaggccatcgag	Protospacer
  *  *** ***********.*******

4. spacer 2.1|209979|31|NZ_CP045118|CRISPRCasFinder matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.71

gaaacccaagccggtggaaagggccatcccc	CRISPR spacer
ccacaccatgccggtggaaaaggccatcgag	Protospacer
  *  *** ***********.*******

5. spacer 2.1|209979|31|NZ_CP045118|CRISPRCasFinder matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.71

gaaacccaagccggtggaaagggccatcccc	CRISPR spacer
ccacaccatgccggtggaaaaggccatcgag	Protospacer
  *  *** ***********.*******

6. spacer 2.1|209979|31|NZ_CP045118|CRISPRCasFinder matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 9, identity: 0.71

gaaacccaagccggtggaaagggccatcccc	CRISPR spacer
ccacaccatgccggtggaaaaggccatcgag	Protospacer
  *  *** ***********.*******

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

562113 : 602662

Pseudomonas_phage(72.22%)

capsid,head,terminase,portal,tRNA,tail,integrase

attL 560871:560920|attR 593139:593188

The bacterium proteins that are colored denote the protein is present at specific phage-related keywords (such as 'capsid', 'head', 'integrase', 'plate', 'tail', 'fiber', 'coat', 'transposase', 'portal', 'terminase', 'protease' or 'lysin' and 'tRNA')

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
560871:560920	attL	NA	NA	NA	NA
WP_152219708.1\|562113_564447_-	hypothetical protein	B5TAB2	Burkholderia_phage	7.4e-129	43.3
WP_152219709.1\|564463_565417_-	hypothetical protein	A0A0U4IBV2	Pseudomonas_phage	2.0e-101	58.9
WP_152219711.1\|565404_566094_-	hypothetical protein	A0A2I7RNK1	Vibrio_phage	7.9e-39	37.2
WP_152219713.1\|566090_566636_-	DNA-binding protein	A0A0U4J942	Pseudomonas_phage	7.9e-50	63.5
WP_152219715.1\|566632_567553_-	hypothetical protein	NA	NA	NA	NA
WP_152219718.1\|567549_568260_-\|tail	phage tail protein	A0A0U4JEJ6	Pseudomonas_phage	9.9e-53	44.3
WP_152219720.1\|568269_569880_-\|tail	phage tail protein	A0A0U4K5K2	Pseudomonas_phage	1.1e-139	51.8
WP_152219722.1\|569888_570470_-\|tail	phage tail protein	A0A0U4JVX3	Pseudomonas_phage	8.4e-74	77.0
WP_152219724.1\|570462_571635_-	hypothetical protein	A0A0U4JJ14	Pseudomonas_phage	1.2e-159	71.9
WP_152219726.1\|571631_571949_-	DUF2590 family protein	A0A0U4B0N5	Pseudomonas_phage	2.0e-37	78.8
WP_152219728.1\|571945_573850_-\|tail	phage tail tape measure protein	A0A0U4IJ81	Pseudomonas_phage	4.5e-193	54.7
WP_152219731.1\|574026_574314_-	hypothetical protein	A0A0U4B0P2	Pseudomonas_phage	6.2e-30	76.7
WP_152219733.1\|574310_574571_-	hypothetical protein	NA	NA	NA	NA
WP_152219734.1\|574570_574933_-	DUF1353 domain-containing protein	M1PQ58	Synechococcus_phage	4.0e-34	58.9
WP_152219736.1\|574922_575138_-	hypothetical protein	NA	NA	NA	NA
WP_152219738.1\|575138_575531_-	peptidase M15	A0A1D9C9S9	Salinivibrio_phage	2.7e-28	47.6
WP_152219740.1\|575527_575740_-	TraR/DksA family transcriptional regulator	NA	NA	NA	NA
WP_152219742.1\|575739_576189_-	DUF2597 family protein	A0A0U3TH58	Pseudomonas_phage	1.3e-63	79.9
WP_152219744.1\|576193_577309_-	DUF2586 family protein	A0A0U4KLE6	Pseudomonas_phage	6.0e-145	69.8
WP_152219746.1\|577320_577977_-	virion morphogenesis protein	A0A0U4ISN1	Pseudomonas_phage	4.6e-36	43.5
WP_152219748.1\|577957_578413_-\|tail	phage tail protein	A0A0U4IBS7	Pseudomonas_phage	7.8e-51	68.0
WP_152219750.1\|578409_578871_-\|head	head protein	A0A0U4J933	Pseudomonas_phage	9.6e-57	71.9
WP_152219752.1\|578969_579737_-\|terminase	terminase	A0A0U4JEJ1	Pseudomonas_phage	6.3e-77	66.3
WP_152219754.1\|579739_580762_-\|capsid	phage major capsid protein, P2 family	A0A0U4K5I9	Pseudomonas_phage	4.2e-121	66.7
WP_152219756.1\|580763_581696_-\|capsid	capsid scaffolding protein	A0A0U4JVV6	Pseudomonas_phage	2.5e-67	49.8
WP_152219758.1\|581855_583928_+\|terminase	terminase	A0A0U4JIZ9	Pseudomonas_phage	6.9e-296	77.9
WP_152219760.1\|583767_584685_+\|portal	phage portal protein	A0A0U4B0L9	Pseudomonas_phage	1.7e-108	81.5
WP_152219762.1\|584739_584994_+	transcriptional regulator	U3PB63	Vibrio_phage	8.2e-18	50.6
WP_152219764.1\|584972_585200_-	hypothetical protein	NA	NA	NA	NA
WP_152219766.1\|585691_585952_-	hypothetical protein	A0A0U4B0R1	Pseudomonas_phage	1.1e-17	56.9
WP_152219768.1\|585944_586148_-	hypothetical protein	NA	NA	NA	NA
WP_152219771.1\|586308_586557_-	hypothetical protein	NA	NA	NA	NA
WP_152219773.1\|586632_586827_-	carbon storage regulator CsrA	J7I430	Pseudomonas_phage	2.0e-11	64.7
WP_152219774.1\|586840_587104_-	hypothetical protein	NA	NA	NA	NA
WP_152219776.1\|587097_587454_-	hypothetical protein	A0A0U4JP55	Pseudomonas_phage	2.4e-39	69.0
WP_152219778.1\|587469_588000_-	hypothetical protein	NA	NA	NA	NA
WP_152219780.1\|587999_590654_-	hypothetical protein	A0A0U3TH43	Pseudomonas_phage	8.0e-297	55.5
WP_152219782.1\|590663_590882_-	hypothetical protein	A0A0U4KLD7	Pseudomonas_phage	1.1e-18	66.2
WP_152219784.1\|590974_591214_+	helix-turn-helix domain-containing protein	Q1JS21	Enterobacteria_phage	8.0e-15	46.8
WP_152227863.1\|591213_591453_+	helix-turn-helix domain-containing protein	A0A0U4ISL7	Pseudomonas_phage	3.3e-16	50.6
WP_152219786.1\|591456_592506_+\|integrase	tyrosine-type recombinase/integrase	A0A0U4IBS1	Pseudomonas_phage	5.3e-135	70.5
WP_152219788.1\|592506_593034_+	hypothetical protein	NA	NA	NA	NA
WP_152219790.1\|593236_596971_-	EAL domain-containing protein	A0A127AWB9	Bacillus_phage	1.6e-13	33.8
593139:593188	attR	NA	NA	NA	NA
WP_152219792.1\|597075_598932_-	RNA polymerase sigma factor RpoD	A0A2I7SAT0	Vibrio_phage	2.0e-36	33.1
WP_152219794.1\|599011_601018_-	DNA primase	A0A0K1LMQ9	Caulobacter_phage	4.9e-73	39.4
WP_003085057.1\|601220_601436_-	30S ribosomal protein S21	NA	NA	NA	NA
WP_152219796.1\|601636_602662_+\|tRNA	tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex transferase subunit TsaD	A0A0R6PI74	Moraxella_phage	5.6e-105	55.8

DBSCAN-SWA_2

2430735 : 2438617

uncultured_Caudovirales_phage(70.0%)

protease,tail

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152222779.1\|2430735_2431734_-	glycosyl transferase family protein	A0A2H4JBY5	uncultured_Caudovirales_phage	2.7e-141	73.0
WP_152222781.1\|2431730_2432066_-	TusE/DsrC/DsvC family sulfur relay protein	A0A2H4J8B6	uncultured_Caudovirales_phage	3.5e-40	73.9
WP_152222783.1\|2432062_2432368_-	sulfurtransferase complex subunit TusB	A0A2H4JG28	uncultured_Caudovirales_phage	1.4e-24	60.0
WP_152222785.1\|2432364_2432724_-	sulfurtransferase complex subunit TusC	A0A2H4J8C0	uncultured_Caudovirales_phage	5.2e-34	62.5
WP_152222787.1\|2432723_2433116_-	sulfurtransferase complex subunit TusD	A0A2H4JA39	uncultured_Caudovirales_phage	2.2e-49	74.4
WP_152222789.1\|2433102_2433351_+\|tail	tail fiber assembly protein	A0A0A0YSY3	Erwinia_phage	2.4e-06	50.0
WP_152222791.1\|2433357_2434404_-	acyltransferase family protein	NA	NA	NA	NA
WP_152222793.1\|2434572_2435016_+	structural protein P5	A0A2H4J6R1	uncultured_Caudovirales_phage	2.3e-39	59.3
WP_152222794.1\|2435104_2435479_+	hypothetical protein	J7HXL1	Pseudomonas_phage	4.6e-25	59.3
WP_152222796.1\|2435475_2435745_+	hypothetical protein	A0A125RNP3	Pseudomonas_phage	4.5e-22	63.6
WP_152222798.1\|2435794_2436439_+	hypothetical protein	NA	NA	NA	NA
WP_152222800.1\|2436542_2437232_-	SOS response-associated peptidase	NA	NA	NA	NA
WP_152222802.1\|2437316_2437565_+	hypothetical protein	NA	NA	NA	NA
WP_152222804.1\|2437951_2438617_+\|protease	FtsH protease modulator YccA	A0A2H4JFM9	uncultured_Caudovirales_phage	2.1e-84	78.5

DBSCAN-SWA_3

2981781 : 3025651

uncultured_Caudovirales_phage(50.0%)

transposase,integrase,plate

attL 2984641:2984660|attR 3028050:3028069

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152228091.1\|2981781_2982951_-\|integrase	site-specific integrase	NA	NA	NA	NA
WP_152223616.1\|2983265_2983685_-	globin	NA	NA	NA	NA
WP_152223617.1\|2984052_2984520_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	4.3e-36	50.7
2984641:2984660	attL	NA	NA	NA	NA
WP_152223618.1\|2985053_2986193_+	hypothetical protein	NA	NA	NA	NA
WP_152228093.1\|2986432_2987902_+	SMEK domain-containing protein	NA	NA	NA	NA
WP_152223619.1\|2987891_2989307_+	hypothetical protein	NA	NA	NA	NA
WP_152223620.1\|2989992_2990286_-\|transposase	transposase	NA	NA	NA	NA
WP_152223621.1\|2990391_2991294_-	hypothetical protein	NA	NA	NA	NA
WP_152223622.1\|2991393_2991648_+	hypothetical protein	NA	NA	NA	NA
WP_152223623.1\|2992147_2993983_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	NA	NA	NA	NA
WP_152223624.1\|2993982_2994849_+	AAA family ATPase	NA	NA	NA	NA
WP_152223625.1\|2994845_2995964_+	hypothetical protein	NA	NA	NA	NA
WP_152223626.1\|2996442_2996889_-	hypothetical protein	A0A2H4J163	uncultured_Caudovirales_phage	2.8e-05	27.0
WP_152223627.1\|2996973_2997261_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_152223628.1\|2997818_2998181_+	transcriptional regulator	NA	NA	NA	NA
WP_152223629.1\|2999217_2999718_+	type VI secretion system contractile sheath small subunit	NA	NA	NA	NA
WP_152223630.1\|2999740_3001279_+	type VI secretion system contractile sheath large subunit	NA	NA	NA	NA
WP_152223631.1\|3001300_3002656_+\|plate	type VI secretion system baseplate subunit TssK	NA	NA	NA	NA
WP_152223632.1\|3002652_3003324_+	DotU family type IV/VI secretion system protein	NA	NA	NA	NA
WP_152223633.1\|3003326_3005078_+	OmpA family protein	NA	NA	NA	NA
WP_152223634.1\|3005090_3005582_+	type VI secretion system tube protein Hcp	NA	NA	NA	NA
WP_152223635.1\|3005698_3008332_+	type VI secretion system ATPase TssH	K4FB40	Cronobacter_phage	4.5e-90	31.5
WP_152223636.1\|3008334_3010728_+	type VI secretion system tip protein VgrG	A0A2H4JCD4	uncultured_Caudovirales_phage	5.2e-21	31.4
WP_152223637.1\|3010743_3011529_+	DUF4123 domain-containing protein	NA	NA	NA	NA
WP_152223638.1\|3011575_3012103_+	DUF3304 domain-containing protein	NA	NA	NA	NA
WP_152228095.1\|3012215_3012716_+	DUF3304 domain-containing protein	NA	NA	NA	NA
WP_152223639.1\|3012703_3015079_+	DUF2235 domain-containing protein	NA	NA	NA	NA
WP_152223640.1\|3015078_3015342_+	PAAR domain-containing protein	NA	NA	NA	NA
WP_152228097.1\|3015482_3016472_+	hypothetical protein	NA	NA	NA	NA
WP_152223641.1\|3016461_3019845_+	type VI secretion protein VasK	NA	NA	NA	NA
WP_152228099.1\|3020200_3020662_+	hypothetical protein	NA	NA	NA	NA
WP_152223642.1\|3021727_3022234_+	hypothetical protein	NA	NA	NA	NA
WP_152223643.1\|3022272_3023859_+	type VI secretion system protein TssA	NA	NA	NA	NA
WP_152223644.1\|3023881_3025651_+\|plate	type VI secretion system baseplate subunit TssF	NA	NA	NA	NA
3028050:3028069	attR	NA	NA	NA	NA

DBSCAN-SWA_4

4567767 : 4575561

Bacillus_phage(16.67%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152224972.1\|4567767_4568823_-	recombinase RecA	A0A0S2MVG1	Bacillus_phage	1.2e-113	62.2
WP_152224974.1\|4568908_4569421_-	nicotinamide-nucleotide amidohydrolase family protein	B5TK85	Pseudomonas_phage	2.9e-54	73.6
WP_152228225.1\|4569536_4572077_+	DNA mismatch repair protein MutS	A0A1V0SGG8	Hokovirus	1.2e-26	22.8
WP_152224976.1\|4572143_4572467_+	DUF3470 domain-containing protein	NA	NA	NA	NA
WP_152224978.1\|4572900_4573905_-	RNA polymerase sigma factor RpoS	G8CLC7	Synechococcus_phage	3.5e-35	36.5
WP_152224980.1\|4574000_4574849_-	peptidoglycan DD-metalloendopeptidase family protein	A0A292GJG6	Xanthomonas_phage	2.9e-14	46.9
WP_152224982.1\|4574925_4575561_-	protein-L-isoaspartate(D-aspartate) O-methyltransferase	A0A1B1IU40	uncultured_Mediterranean_phage	6.0e-41	52.9

DBSCAN-SWA_5

6232889 : 6281624

Brucella_phage(28.57%)

protease,holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_152227714.1\|6232889_6234068_-\|holin	choline ABC transporter ATP-binding protein	G3M9Y6	Bacillus_virus	5.9e-26	36.4
WP_152227716.1\|6234073_6234913_-\|holin	choline ABC transporter permease subunit	NA	NA	NA	NA
WP_152227718.1\|6234967_6235906_-\|holin	choline ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_152227720.1\|6236147_6237074_-\|holin	choline ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_152227722.1\|6237165_6237375_-	hypothetical protein	NA	NA	NA	NA
WP_152227724.1\|6237416_6238793_+	L-serine ammonia-lyase	NA	NA	NA	NA
WP_152227726.1\|6239166_6240273_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_152227727.1\|6240371_6240776_-	hypothetical protein	NA	NA	NA	NA
WP_152227729.1\|6241805_6242108_+	type II toxin-antitoxin system RelE/ParE family toxin	A0A141GEX6	Brucella_phage	5.0e-22	60.2
WP_152227731.1\|6242100_6242394_+	putative addiction module antidote protein	A0A141GEX5	Brucella_phage	4.4e-15	50.0
WP_152227733.1\|6242847_6243327_-	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_152227734.1\|6243323_6253892_-	filamentous hemagglutinin N-terminal domain-containing protein	A0A0R6PJK4	Moraxella_phage	3.4e-32	37.8
WP_152227736.1\|6253995_6255696_-	ShlB/FhaC/HecB family hemolysin secretion/activation protein	NA	NA	NA	NA
WP_152227738.1\|6255862_6256111_-	hypothetical protein	NA	NA	NA	NA
WP_152227740.1\|6256396_6257281_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_152227742.1\|6257572_6258805_+	molybdopterin-dependent oxidoreductase	NA	NA	NA	NA
WP_152227744.1\|6258821_6259451_+	cytochrome C552	NA	NA	NA	NA
WP_152227746.1\|6259447_6260380_-	alpha/beta hydrolase fold domain-containing protein	A0A2K9L3Q5	Tupanvirus	1.2e-08	22.7
WP_152227748.1\|6260386_6260860_-	thioesterase	NA	NA	NA	NA
WP_152227750.1\|6261026_6261992_-	L-carnitine dehydrogenase	NA	NA	NA	NA
WP_152227752.1\|6262259_6263144_-	3-keto-5-aminohexanoate cleavage protein	NA	NA	NA	NA
WP_152227754.1\|6263211_6264150_-\|holin	choline ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_152227756.1\|6264385_6265360_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_152227758.1\|6265656_6266127_+	DUF1348 family protein	NA	NA	NA	NA
WP_152227760.1\|6266306_6268703_+	carbohydrate-binding family V/XII	NA	NA	NA	NA
WP_152227762.1\|6268842_6269757_+	AEC family transporter	NA	NA	NA	NA
WP_152227764.1\|6270090_6271395_+	citrate transporter	NA	NA	NA	NA
WP_152227766.1\|6271410_6272172_+	TerC family protein	A0A0R6PEZ3	Moraxella_phage	4.8e-37	44.0
WP_152227767.1\|6272235_6272721_-	water stress/hypersensitive response domain-containing protein	NA	NA	NA	NA
WP_152227769.1\|6273089_6274802_+	Na/Pi cotransporter family protein	NA	NA	NA	NA
WP_152227771.1\|6274907_6275942_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_152227773.1\|6276028_6276985_-	NAD-dependent epimerase/dehydratase family protein	NA	NA	NA	NA
WP_152227775.1\|6277178_6278552_+	insulinase family protein	NA	NA	NA	NA
WP_152227777.1\|6278573_6279128_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_152227779.1\|6279251_6280544_-	MFS transporter	Q6JIH2	Burkholderia_virus	6.4e-74	38.4
WP_152227781.1\|6280967_6281624_+\|protease	serine protease	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP045118

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection