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
AP018040	Petrimonas sp. IBARAKI DNA, complete genome	3 crisprs	cas7,cas5,cas3,cas6,cas1,cas2,cas4,DEDDh,PD-DExK,RT,csa3,cas8b6	0	11	0	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: AP018040_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

AP018040_1

704690-707352

TypeI-B

Consensus_repeat	Method
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	PILER-CR
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CRISPRCasFinder
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CRT

36 spacers

cas4,cas2,cas1,cas6,cas3,cas5,cas7,cas8b1

The CRISPR arrays of AP018040_1

>merge|AP018040|1|704690-707352|PILER-CR,CRISPRCasFinder,CRT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAACCTCCCTTTCCTTTCCATCCAATACCAACCCTGTATCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTAAGGATGCTATTAACGCAGCAACAAGCGGGACACACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTTCCTTTTTGGTGTCCAGTAACCATTGTCACTCCGCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACACTTTTCCCCGTCTGGTGCCAGCTTCAACGATTCGGCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTTTTTCATTCCAAACACTCCTTAACTTTTTTCTCGAACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTTAACAATATCCCTTATTTCTTCTGCTTTTTGACAGACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTCTCACTTCTCGTCAGTCGCATTGCGTTTTTGTACGCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACCGTCGAGACTTTCCGTTCATCTCGATGATGTTGAACACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACAACAAATTAGGGTTGCCTCCTCCTTTTTTTCCTGCCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACCGGTCGCCCGTCTTGGTCGTCTAAATTCCTCGTCGCACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACCATTCGATTGAGACGAATTCCCTGCATGTACGCAACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTCCTCGACAGAGAGGGTGAAAATGGCGAGGCTCACTTCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACAAATGAACCGTTCGTTTTTCTCGAGCCGTGAGGAAAACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACAACTTCGAGCAAAACGAGCGAGAAACCATGGCGGGACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACAAATCAATAAAATCTTCTTTGTCTTTTTCAATTAATTCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACAAAAACAAACAAAATGAAAACAAAATCGGCTTTAATCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTCGGGTTATGTATACTTATACCTTACCGATTCAGTCCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACACTCGTCTATTTTTTTAAGGTATTCCCTTTTCGTACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTATGCAAAAGTTATCGACAATTAAAAACAATTTAAACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTAATGATAACCCGCAATGAGGTTAGCCTTGTCTAGCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTATGTTCTACAACATATTTTGCGATTTTAACATAATGACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTTAACAGTCAATGCTTGGAGTGGTAGCCGGGTTTCTTCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTTCTCCAAATCAACGTCAATCGAGTGGTCGCACCTCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACCAGGCTTTCAGCATCTTAGTATATTTTTCGTTGTCACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTGACGCGTGCATCTTCCGGACTGTGCTCCTGAGCTACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTTCTTTGAGCGGTAGATATCGAACAATCAAAAAGTTCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTGTTGTTCTACGTTATATCTTTGCATCAACAACAAACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTCAAATTCTGTTTTAGGTCTATTCAGCAACGGTAACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTGCCCCGGGACTTATGCTCCCGAATGCAAGCGTAGCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACATGGACATATAATTAGTAAAAGTGTATGGAACAAAACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACAAAGATTATAGAATATTTCTGCCTTTTCAATTGTCCCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACACATAATAAAAAACCGGGAATTTCTCCCCGGCTTACTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTCCAAATCACCCATTCCTTAACCGTTCGCCATACTCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTCTCCGGAACATTCCTGTTTTTTCTTGAATTACCGGCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACAAACGATATTCCTTTTTTCTTTGAACGGAACATAGTCTTCCAGAACTACATCCAGCACAACAAGGATTGAAACTAAGGACTTTCTCTCTTATAAGGACGATATCAACGCTTCCAGAACTACATCCAGCATAATAAGGCATAAGGC

>AP018040|1|1|704690-707280|PILER-CR
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CTCCCTTTCCTTTCCATCCAATACCAACCCTGTAT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAAGGATGCTATTAACGCAGCAACAAGCGGGACACA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCCTTTTTGGTGTCCAGTAACCATTGTCACTCCG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACTTTTCCCCGTCTGGTGCCAGCTTCAACGATTCGG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTTTTCATTCCAAACACTCCTTAACTTTTTTCTCGAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTAACAATATCCCTTATTTCTTCTGCTTTTTGACAGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCTCACTTCTCGTCAGTCGCATTGCGTTTTTGTACG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CGTCGAGACTTTCCGTTCATCTCGATGATGTTGAACA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AACAAATTAGGGTTGCCTCCTCCTTTTTTTCCTGC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CGGTCGCCCGTCTTGGTCGTCTAAATTCCTCGTCGCA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CATTCGATTGAGACGAATTCCCTGCATGTACGCAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCCTCGACAGAGAGGGTGAAAATGGCGAGGCTCACTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAATGAACCGTTCGTTTTTCTCGAGCCGTGAGGAAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AACTTCGAGCAAAACGAGCGAGAAACCATGGCGGGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAATCAATAAAATCTTCTTTGTCTTTTTCAATTAATT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAAAACAAACAAAATGAAAACAAAATCGGCTTTAAT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCGGGTTATGTATACTTATACCTTACCGATTCAGTC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACTCGTCTATTTTTTTAAGGTATTCCCTTTTCGTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TATGCAAAAGTTATCGACAATTAAAAACAATTTAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAATGATAACCCGCAATGAGGTTAGCCTTGTCTAG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TATGTTCTACAACATATTTTGCGATTTTAACATAATGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTAACAGTCAATGCTTGGAGTGGTAGCCGGGTTTCTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCTCCAAATCAACGTCAATCGAGTGGTCGCACCT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CAGGCTTTCAGCATCTTAGTATATTTTTCGTTGTCA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGACGCGTGCATCTTCCGGACTGTGCTCCTGAGCTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCTTTGAGCGGTAGATATCGAACAATCAAAAAGTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGTTGTTCTACGTTATATCTTTGCATCAACAACAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCAAATTCTGTTTTAGGTCTATTCAGCAACGGTAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGCCCCGGGACTTATGCTCCCGAATGCAAGCGTAG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ATGGACATATAATTAGTAAAAGTGTATGGAACAAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAAGATTATAGAATATTTCTGCCTTTTCAATTGTCC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACATAATAAAAAACCGGGAATTTCTCCCCGGCTTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCCAAATCACCCATTCCTTAACCGTTCGCCATACT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCTCCGGAACATTCCTGTTTTTTCTTGAATTACCGG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAACGATATTCCTTTTTTCTTTGAACGGAACATAGT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC

>AP018040|1|1|704690-707352|CRISPRCasFinder
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CTCCCTTTCCTTTCCATCCAATACCAACCCTGTAT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAAGGATGCTATTAACGCAGCAACAAGCGGGACACA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCCTTTTTGGTGTCCAGTAACCATTGTCACTCCG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACTTTTCCCCGTCTGGTGCCAGCTTCAACGATTCGG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTTTTCATTCCAAACACTCCTTAACTTTTTTCTCGAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTAACAATATCCCTTATTTCTTCTGCTTTTTGACAGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCTCACTTCTCGTCAGTCGCATTGCGTTTTTGTACG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CGTCGAGACTTTCCGTTCATCTCGATGATGTTGAACA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AACAAATTAGGGTTGCCTCCTCCTTTTTTTCCTGC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CGGTCGCCCGTCTTGGTCGTCTAAATTCCTCGTCGCA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CATTCGATTGAGACGAATTCCCTGCATGTACGCAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCCTCGACAGAGAGGGTGAAAATGGCGAGGCTCACTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAATGAACCGTTCGTTTTTCTCGAGCCGTGAGGAAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AACTTCGAGCAAAACGAGCGAGAAACCATGGCGGGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAATCAATAAAATCTTCTTTGTCTTTTTCAATTAATT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAAAACAAACAAAATGAAAACAAAATCGGCTTTAAT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCGGGTTATGTATACTTATACCTTACCGATTCAGTC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACTCGTCTATTTTTTTAAGGTATTCCCTTTTCGTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TATGCAAAAGTTATCGACAATTAAAAACAATTTAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAATGATAACCCGCAATGAGGTTAGCCTTGTCTAG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TATGTTCTACAACATATTTTGCGATTTTAACATAATGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTAACAGTCAATGCTTGGAGTGGTAGCCGGGTTTCTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCTCCAAATCAACGTCAATCGAGTGGTCGCACCT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CAGGCTTTCAGCATCTTAGTATATTTTTCGTTGTCA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGACGCGTGCATCTTCCGGACTGTGCTCCTGAGCTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCTTTGAGCGGTAGATATCGAACAATCAAAAAGTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGTTGTTCTACGTTATATCTTTGCATCAACAACAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCAAATTCTGTTTTAGGTCTATTCAGCAACGGTAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGCCCCGGGACTTATGCTCCCGAATGCAAGCGTAG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ATGGACATATAATTAGTAAAAGTGTATGGAACAAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAAGATTATAGAATATTTCTGCCTTTTCAATTGTCC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACATAATAAAAAACCGGGAATTTCTCCCCGGCTTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCCAAATCACCCATTCCTTAACCGTTCGCCATACT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCTCCGGAACATTCCTGTTTTTTCTTGAATTACCGG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAACGATATTCCTTTTTTCTTTGAACGGAACATAGT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAAGGACTTTCTCTCTTATAAGGACGATATCAACG
CTTCCAGAACTACATCCAGCATAATAAGGCATAAGGC

>AP018040|1|1|704690-707352|CRT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CTCCCTTTCCTTTCCATCCAATACCAACCCTGTAT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAAGGATGCTATTAACGCAGCAACAAGCGGGACACA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCCTTTTTGGTGTCCAGTAACCATTGTCACTCCG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACTTTTCCCCGTCTGGTGCCAGCTTCAACGATTCGG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTTTTCATTCCAAACACTCCTTAACTTTTTTCTCGAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTAACAATATCCCTTATTTCTTCTGCTTTTTGACAGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCTCACTTCTCGTCAGTCGCATTGCGTTTTTGTACG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CGTCGAGACTTTCCGTTCATCTCGATGATGTTGAACA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AACAAATTAGGGTTGCCTCCTCCTTTTTTTCCTGC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CGGTCGCCCGTCTTGGTCGTCTAAATTCCTCGTCGCA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CATTCGATTGAGACGAATTCCCTGCATGTACGCAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCCTCGACAGAGAGGGTGAAAATGGCGAGGCTCACTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAATGAACCGTTCGTTTTTCTCGAGCCGTGAGGAAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AACTTCGAGCAAAACGAGCGAGAAACCATGGCGGGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAATCAATAAAATCTTCTTTGTCTTTTTCAATTAATT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAAAACAAACAAAATGAAAACAAAATCGGCTTTAAT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCGGGTTATGTATACTTATACCTTACCGATTCAGTC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACTCGTCTATTTTTTTAAGGTATTCCCTTTTCGTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TATGCAAAAGTTATCGACAATTAAAAACAATTTAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAATGATAACCCGCAATGAGGTTAGCCTTGTCTAG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TATGTTCTACAACATATTTTGCGATTTTAACATAATGA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTAACAGTCAATGCTTGGAGTGGTAGCCGGGTTTCTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCTCCAAATCAACGTCAATCGAGTGGTCGCACCT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	CAGGCTTTCAGCATCTTAGTATATTTTTCGTTGTCA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGACGCGTGCATCTTCCGGACTGTGCTCCTGAGCTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TTCTTTGAGCGGTAGATATCGAACAATCAAAAAGTT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGTTGTTCTACGTTATATCTTTGCATCAACAACAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCAAATTCTGTTTTAGGTCTATTCAGCAACGGTAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TGCCCCGGGACTTATGCTCCCGAATGCAAGCGTAG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ATGGACATATAATTAGTAAAAGTGTATGGAACAAAA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAAGATTATAGAATATTTCTGCCTTTTCAATTGTCC
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	ACATAATAAAAAACCGGGAATTTCTCCCCGGCTTA
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCCAAATCACCCATTCCTTAACCGTTCGCCATACT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TCTCCGGAACATTCCTGTTTTTTCTTGAATTACCGG
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	AAACGATATTCCTTTTTTCTTTGAACGGAACATAGT
CTTCCAGAACTACATCCAGCACAACAAGGATTGAAAC	TAAGGACTTTCTCTCTTATAAGGACGATATCAACG
CTTCCAGAACTACATCCAGCATAATAAGGCATAAGGC

Protein	Signature genes	Signature genes Name	Protein_function
AP018040.2\|BBD44578.1\|720700_724267_+\|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase	unknown	unknown	gnl\|CDD\|131231
AP018040.2\|BBD44574.1\|714221_715262_+\|L-asparaginase-I	unknown	unknown	gnl\|CDD\|214873
AP018040.2\|BBD44559.1\|695354_695579_+\|Hypothetical-protein	unknown	unknown	unknown
AP018040.2\|BBD44564.1\|701972_702629_+\|Hypothetical-protein	cas6	cls000004_cas6_CAS-I:CAS-III	gnl\|CDD\|379957
AP018040.2\|BBD44573.1\|713610_714030_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|224679
AP018040.2\|BBD44571.1\|710866_712036_-\|membrane-protein	unknown	unknown	gnl\|CDD\|367882
AP018040.2\|BBD44572.1\|712240_713500_-\|phosphoglycerate-kinase	unknown	unknown	gnl\|CDD\|234613
AP018040.2\|BBD44563.1\|699532_701965_+\|Cas3:-CRISPR-associated-helicase-Cas3	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|350688
AP018040.2\|BBD44577.1\|718193_720362_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|184712
AP018040.2\|BBD44570.1\|708185_710648_-\|phenylalanyl-tRNA-synthetase-subunit-beta	unknown	unknown	gnl\|CDD\|234804
AP018040.2\|BBD44576.1\|717080_718169_-\|Membrane-protein	unknown	unknown	gnl\|CDD\|366370
AP018040.2\|BBD44560.1\|695929_697807_+\|Crispr-associated-protein,-Csh1-family	cas8b1	cd09730_cas8b1_CAS-I-B	gnl\|CDD\|378190
AP018040.2\|BBD44562.1\|698734_699490_+\|Crispr-associated-protein-Cas5,-hmari-subtype	cas5	cls001430_cas5_CAS-I-B	gnl\|CDD\|131641
AP018040.2\|BBD44565.1\|702642_703635_+\|CRISPR-associated-endonuclease-Cas1	cas1	pfam01867_cas1_CAS-I:CAS-II:CAS-III	gnl\|CDD\|187766
AP018040.2\|BBD44561.1\|697830_698745_+\|Crispr-associated-protein,-Csh2-family	cas7	cd09690_cas7_CAS-I-B	gnl\|CDD\|274217
AP018040.2\|BBD44569.1\|707444_708155_-\|YebC/PmpR-family-DNA-binding-regulatory-protein	unknown	unknown	gnl\|CDD\|237084
AP018040.2\|BBD44566.1\|703631_703922_+\|CRISPR-associated-protein-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
AP018040.2\|BBD44567.1\|703921_704494_+\|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl\|CDD\|273040
AP018040.2\|BBD44575.1\|715300_717094_+\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|225922
AP018040.2\|BBD44558.1\|692749_693844_+\|arginine/ornithine-transport-system-ATPase	unknown	unknown	gnl\|CDD\|236515

Protein	Function_ID	Function_description	E-value
AP018040.2\|BBD44574.1\|714221_715262_+\|L-asparaginase-I	gnl\|CDD\|214873	smart00870, Asparaginase, Asparaginase, found in various plant, animal and bacterial cells. Asparaginase catalyses the deamination of asparagine to yield aspartic acid and an ammonium ion, resulting in a depletion of free circulatory asparagine in plasma. The enzyme is effective in the treatment of human malignant lymphomas, which have a diminished capacity to produce asparagine synthetase: in order to survive, such cells absorb asparagine from blood plasma..- if Asn levels have been depleted by injection of asparaginase, the lymphoma cells die.	1.43657e-126
AP018040.2\|BBD44560.1\|695929_697807_+\|Crispr-associated-protein,-Csh1-family	gnl\|CDD\|378190	pfam09484, Cas_TM1802, CRISPR-associated protein TM1802 (cas_TM1802). Clusters of short DNA repeats with non-homologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This minor cas protein is found in at least five prokaryotic genomes: Methanosarcina mazei, Sulfurihydrogenibium azorense, Thermotoga maritima, Carboxydothermus hydrogenoformans, and Dictyoglomus thermophilum, the first of which is archaeal while the rest are bacterial.	1.78785e-72
AP018040.2\|BBD44564.1\|701972_702629_+\|Hypothetical-protein	gnl\|CDD\|379957	pfam17262, DUF5328, Family of unknown function (DUF5328). This family of unknown function can be found in Bacteria and Archaea. Some of the proteins in this family are annotated in UniProt as putative DNA repair proteins.	3.25319e-41
AP018040.2\|BBD44573.1\|713610_714030_-\|Hypothetical-protein	gnl\|CDD\|224679	COG1765, COG1765, Predicted redox protein, regulator of disulfide bond formation [Posttranslational modification, protein turnover, chaperones].	5.09354e-30
AP018040.2\|BBD44578.1\|720700_724267_+\|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase	gnl\|CDD\|131231	TIGR02176, pyruvate_flavodoxin/ferrodoxin_oxidoreductase, pyruvate:ferredoxin (flavodoxin) oxidoreductase, homodimeric. This model represents a single chain form of pyruvate:ferredoxin (or flavodoxin) oxidoreductase. This enzyme may transfer electrons to nitrogenase in nitrogen-fixing species. Portions of this protein are homologous to gamma subunit of the four subunit pyruvate:ferredoxin (flavodoxin) oxidoreductase.	0
AP018040.2\|BBD44572.1\|712240_713500_-\|phosphoglycerate-kinase	gnl\|CDD\|234613	PRK00073, pgk, phosphoglycerate kinase; Provisional.	0
AP018040.2\|BBD44563.1\|699532_701965_+\|Cas3:-CRISPR-associated-helicase-Cas3	gnl\|CDD\|350688	cd17930, DEXHc_cas3, DEXH/Q-box helicase domain of Cas3. CRISPR-associated (Cas) 3 is a nuclease-helicase responsible for degradation of dsDNA. The two enzymatic units of Cas3, a histidine-aspartate (HD) nuclease and a Superfamily 2 (SF2) helicase, may be expressed from separate genes as Cas3' (SF2 helicase) and Cas3'' (HD nuclease) or may be fused as a single HD-SF2 polypeptide. The nucleolytic activity of most Cas3 enzymes is transition metal ion-dependent. Cas3 is a member of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	1.67204e-37
AP018040.2\|BBD44577.1\|718193_720362_-\|Hypothetical-protein	gnl\|CDD\|184712	PRK14501, PRK14501, putative bifunctional trehalose-6-phosphate synthase/HAD hydrolase subfamily IIB; Provisional.	0
AP018040.2\|BBD44570.1\|708185_710648_-\|phenylalanyl-tRNA-synthetase-subunit-beta	gnl\|CDD\|234804	PRK00629, pheT, phenylalanyl-tRNA synthetase subunit beta; Reviewed.	0
AP018040.2\|BBD44576.1\|717080_718169_-\|Membrane-protein	gnl\|CDD\|366370	pfam00924, MS_channel, Mechanosensitive ion channel. Two members of this protein family of M. jannaschii have been functionally characterized. Both proteins form mechanosensitive (MS) ion channels upon reconstitution into liposomes and functional examination by the patch-clamp technique. Therefore this family are likely to also be MS channel proteins.	1.27815e-17
AP018040.2\|BBD44571.1\|710866_712036_-\|membrane-protein	gnl\|CDD\|367882	pfam04235, DUF418, Protein of unknown function (DUF418). Probable integral membrane protein.	1.29019e-40
AP018040.2\|BBD44562.1\|698734_699490_+\|Crispr-associated-protein-Cas5,-hmari-subtype	gnl\|CDD\|131641	TIGR02592, hypothetical_protein_CTC_01466, CRISPR-associated protein Cas5, subtype I-B/HMARI. This is a CRISPR-associated protein unique to the hmari subtype of cas genes and CRISPR repeat, which is the only subtype present in Haloarcula marismortui ATCC 43049. The hmari type, though uncommon, is also found in the Aquificae, Thermotogae, Firmicutes, and Dictyoglomi.	6.30752e-36
AP018040.2\|BBD44565.1\|702642_703635_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|187766	cd09634, Cas1_I-II-III, CRISPR/Cas system-associated protein Cas1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas1 is the most universal CRISPR system protein thought to be involved in spacer integration; Cas1 is metal-dependent deoxyribonuclease, also binds RNA; Shown to possess a unique fold consisting of a N-terminal beta-strand domain and a C-terminal alpha-helical domain.	1.84861e-83
AP018040.2\|BBD44561.1\|697830_698745_+\|Crispr-associated-protein,-Csh2-family	gnl\|CDD\|274217	TIGR02590, hypothetical_protein_MM_0563, CRISPR-associated protein Cas7/Csh2, subtype I-B/HMARI. This model represents one of two closely related CRISPR-associated proteins that belong to the larger family of TIGR01595. Members are the Csh2 protein of the Hmari subtype of CRISPR/cas system. CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats. The related model is TIGR02589, the Csd3 protein of the Dvulg CRISPR subtype.	3.10317e-73
AP018040.2\|BBD44569.1\|707444_708155_-\|YebC/PmpR-family-DNA-binding-regulatory-protein	gnl\|CDD\|237084	PRK12378, PRK12378, YebC/PmpR family DNA-binding transcriptional regulator.	4.57343e-129
AP018040.2\|BBD44566.1\|703631_703922_+\|CRISPR-associated-protein-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	2.85563e-20
AP018040.2\|BBD44567.1\|703921_704494_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	1.55705e-22
AP018040.2\|BBD44575.1\|715300_717094_+\|Hypothetical-protein	gnl\|CDD\|225922	COG3387, SGA1, Glucoamylase and related glycosyl hydrolases [Carbohydrate transport and metabolism].	2.73321e-115
AP018040.2\|BBD44558.1\|692749_693844_+\|arginine/ornithine-transport-system-ATPase	gnl\|CDD\|236515	PRK09435, PRK09435, methylmalonyl Co-A mutase-associated GTPase MeaB.	0

>AP018040.2|BBD44567.1|703921_704494_+|CRISPR-associated-protein-Cas4
MSITPSHIIEYLYCPRFTYYEHVLCIPQFEERHYKVEKGRNLHDLKLERNRDYLRKRIGAVDKYLDQYLTNELLRGVVDEILVLKDGTMAPLDYKFAKFEERIYNTYQTQLECYAVLIEDNFHRRVDKGFLVYTRSANKLVEIVISETAKQEIRNICEQVNEIIFNNFFPKATKSKKRCIGCTYRNICIK
>AP018040.2|BBD44566.1|703631_703922_+|CRISPR-associated-protein-Cas2
MICWVIYDIKKDKPRTKISKICKKVGLYRVQKSVFLGSLDENDKDTLELSVTELIDEETDSLYIFPMSKNELRQTVLLGQAFDKKLVTDDVKALFF
>AP018040.2|BBD44565.1|702642_703635_+|CRISPR-associated-endonuclease-Cas1
MQLIINTYGTYVHVKDDLFEVSLTKDGEKQKHHFASQKVTSILMSKGAALSTDAIILAMKNNIDIIVFEYDGMPIGRFWHSKPGSTSKIRKQQLDASLNEIGVHWTKSWLTKKIENQIEFLKRLKSHRLTSAEQIQEKIEIIKGISLKINGLKGSKIEDIDSTLRGLEGTSGRVYFRVLSSLLAERYQFEGRSFRPAADPFNAFLNYAYGVLYSRVEKVLVIAGLDPYVGFMHRDDYNMKSMVFDFIEPYRTYAEEVVFKLFSAKKINDSHTSKITNGYSLNAEGKNLLMQSLLSFLEEDTIRYNGRNQTRVNAMQMDAHQFANQLIKKT
>AP018040.2|BBD44564.1|701972_702629_+|Hypothetical-protein
MQITQTIIQFPDIRLKTRDAHKLRGYFGNLFKEHSPLLHNHYQDGTSRYAYPLVQYKVIRNVPMLIGFEEGADLLISLFLKIRELDIEGEYYPISAKNIHQTRCELTVNQQLYNYAFETLWMALNQDNHRKYILLDTKQKKEFLNRQLQNNILSFYKGVSFRVSENIMGVVQLEEKQTKFKDQQMLAFSGRFTTNAYLPEWVGIGKAVSRGFGAVSQI
>AP018040.2|BBD44563.1|699532_701965_+|Cas3:-CRISPR-associated-helicase-Cas3
MEELQIDKEGLLSHPKKLLIDHLSVVAVIARATVEEKGYRFVVRETEITNRQLSDLVWIAAISHDIAKATGYFQNYIRNPEEIHSNLKNHSLLSSVFAYFVASRYCEREFKDKLLQEFLPILVLIAVKRHHGNIQNLQKEILFSNEDIEYLSEQIKSIHAPSVELILSSLCDHGPIKITWRAFTEYWELASFQQRLKDFRLYFKLNYPKLDEKTQVELFNLFQVIYSALMYSDKNDVILKDVNTTNTTTDITGCLNRYREKNGFNIPVSEINRIKNEAYFGTLEHLERVFTRDQHLYSITLPTGLGKTLTAFSVADKIRSLTGNINAKVTIVIPYTSIIDQNFEVYREVLETDSSEFLLKHHHLSEPRYKDSSEKVYEENQSQFLIETWQSETIVTTFVQFLETILSMDKTKLMKLVNLRNAVILLDEIQTIPYELWETVRKTFLSLGETLNIYFILISATQPLIFAPRVDIVELVPDHRKYFKVFNRTRLVYHKDKISFEDFIDIISDYIYNEPKKDVLIILNTKKAARRCFEELTKQEQEILDNVQYFFLSTLITPHERKEIIQKIKKRSHKRKIIVSTQLIEAGVDISVDTIFRQLSPIDSIIQSAGRANRYNEKEQVSDIFLYDIDDEHGKATSRIYGSDLMLKTRNTLSDIEVMEERDYLDLIDRYYEEVRKQSDETSSDLLDAIRDLRFMEIDLKLIQERKTESVFIQLNEEAKYVWERYVSLYDEELTPWERKTKFASFKSLFYDYVINVPVPYGETKINFDSEQVHGFYLSSLEQPSAFYSYSANDTRENIGYNTNKTSITI
>AP018040.2|BBD44562.1|698734_699490_+|Crispr-associated-protein-Cas5,-hmari-subtype
MKYKELLIFDIMGEYGHFRKYNTTTSPLTYSIPTRTAIAGMLGAILGMERETSDGHYAEGIEPVQEFFSKERSGIAVQVMQPVKKENIGFNLINTKISFYDLTRARHTQTEFELVKDPHYRIYLAMDDTAKFEELSERIQHRRHHFTPYLGLAQFTARVDFVQRATARVVTSNSEIVEIITAVNLSKVVGEPPIDFQKEWFYSANNMPVAMNREREVLEYSEILIEKNGNPLHARVPEYLTLDGIGNILFL
>AP018040.2|BBD44561.1|697830_698745_+|Crispr-associated-protein,-Csh2-family
MSEIIDSRSELLFLYDIENANPNGDPLNENRPRFDTESSVALVSDVRLKRTIRDYWYEYKEFNGLDDRQDIFVRETTYDEGDKKYVKDGKRRARDFQEQADIILAKCIDIRVFGGVIPLAKDSITYIGPVQFQMGKSLNKTEIIEEQGTGAFASAEKKIQATFRTEYKIPYAVIGFNGIINEKAARYSRMTTEDKSLLLEGIWEGTKNLISRSKFGQSPLFLLEVEYKEPFYIGNLRQRLKLDYGEMNELQIRGTNDYKLDISELLEALKENKEKIAKIHLKLDSRLTMISNGKLITNISKDEI
>AP018040.2|BBD44560.1|695929_697807_+|Crispr-associated-protein,-Csh1-family
MNDRSISEIGHWQLEQKSFLDPVDLYIENLFPGKDYQVLLMVFEIIDNKGELQCQYRGIDIEKVRKDSSSYRKYAYRKGSARGGDVTFTTKLGNPPDKKLNNIKEAQFKKLTHGKHLEAQLFKLVEAEFLLNEQRIAWQIADYFNNATQEERTTTGISLRIHREKELYLYDFETVRTTILNSGSEKKYEHNGTISRTADVVCSVTGEKADEVYGFAAPFKYSTPDKPGFISGFFNKEKFWRNYPVSSKEALALEYGEKYIRQHLTGYFYGYEFLFVPHTVLQNDREKLETIVELLKSAFADARIKKESSEERADSEEHVQKIIAQQNNFFYVDMLFFSEDKMSKAISIKMMLEEVLPSRFNELFSRVPNAVNRIPLFRNATIKGKEQQDLKFSFGIIKEFFDDKFLEVVQNIFLGRPISKDFMFEKIMNVIRKNYNEAHTREKTTKSTRRSILEAIMLINYLQELKIIQNNINYNFMNKMDTVKDEQKTNRFNLDEFNRFVTNNRSFLDSDIKIGIFAVGILVRFVFDAQYRKLSSTPFESKLRGYNLNSEHLMQIYLEALDKIQKHLKNNVYPELREIINNYFTIKKQDMVSMSNNELSFYFVAGLEMGSRFKREKSEENTESE
>AP018040.2|BBD44559.1|695354_695579_+|Hypothetical-protein
MKSHTAQENDQVNEVCLNATGSYAVYTLNAAQRSDGSASFEMPGGWKPASSHFGMFLTSYDLQFNSNNLYIVFQ
>AP018040.2|BBD44558.1|692749_693844_+|arginine/ornithine-transport-system-ATPase
MHHPENDPKYLGLNVNKGVVQPPSINPYLHLRKKQQRKEYSVKEFAEGILAGNITVLSQAVTLVESSKPEHQAMAQAIIEKCLPYSGNAIRVGITGVPGAGKSTSIDAFGMYLVEKGHKLAVLAIDPSSERTKGSILGDKTRMERLSVQENAFIRPSPSAGSLGGVARKTRETIVLCEAAGFDYIFVETVGVGQSETAVHSMVDFFLLIQLAGTGDELQGIKRGIMEMADGIVINKADGDNVEKAKMAQSQLRNALHLFPLPESEWSPEVLTYSGYYALGIEEVWDMIHRYIEFVKDSGYFDVRRNKQSKFWMYETINERLRNDFYQNAEIEQLMPLLESEVLSARKSSFVAAKEALDRYYLKK
>AP018040.2|BBD44569.1|707444_708155_-|YebC/PmpR-family-DNA-binding-regulatory-protein
MGRAFEYRKATKLKRWGNMARVFTKLGKQITIATRDGGPDPENNPRLRVLIQQAKKENMPKENVERAIKKATDKDVSDYKEMVYEGYGPYGVAIVVETATDNPTRTVANVRSYFNKHGGSLGTSGSLEFLFDHKCVFKISPKEGVSLEDLELELIDYGVDEVEEDEGDIILYGEFKSYSDIQSYLEENDFEIHSAEFERIPHDTKSLSDEQRTQIEKLLEKFEEDDDVQNVFHNME
>AP018040.2|BBD44570.1|708185_710648_-|phenylalanyl-tRNA-synthetase-subunit-beta
MNISYNWLKDYLQFDLSPQETAAALTSIGLETGSVEEIQTVKGGLEGLVIGEVLTCTHHPNSDHLHLTTVNIGNGEEPLKIVCGAPNVAAGQKVVVATVGTKIYFGDEPVTIKRSKIRGEESFGMICAEDEIGIGTSHEGIIVLPDDAEVGMLAKDYYNVKSDFVLEVDITPNRIDAASHYGVARDLAAYLKQSGKPFSLTKPSVDGFKTDKSEGGIDVVVENSAACPRYSGLTVRGVTVKESPDWLKNKLLVIGLRPINNIVDITNFILHETGHPMHAFDVNYIEGNTVVVRTLPGKSKFLTLDEQERELNENDLMICNTKEGMCIAGVFGGLKSGVTESTTDVFLESAYFNPTWVRKTARRHGLNTDSSFRFERGADPGNTVYVLKRAAMLIKEIAGGEIEGEIRDIYPVKINNAQVVLPFRKVNSLIGKEIPKETIKNILQSLDIETENESEEALTLSIPTYRVDVTRDVDVIEEILRIYGYNNVDFSDSLRANLSYQTPTDRKHKLQTLISEQLTASGFSEIMNNSLTRKSYYEDNTTFPGENGVKLLNPLSNDLGVMRQTLLYGGLESIAYNRNRKHYDLHFYEFGNCYFFDTDRKQEGNILSGYSEETHLGLWICGDSNPKNWAAPQTETSVFQLKAHIENILNRLGFTQNQVTFESTQSGIYASGMNIRTFNRQIGSFGIISGNILKKFDIDTDVFFAEMSWDALLKETSASEVHFSEISRFPSVSRDLALLVDKSVTFAAIEQTAKKAERKLLQELSLFDVYEGKNLPEGKKSYAVNFVLQDKEKTLNDKQIDAVMQKIQQNLEKELGALLR
>AP018040.2|BBD44571.1|710866_712036_-|membrane-protein
MEISTGKTSRIEVVDSLRGFAIMAILLVHNVDHFFFPEFPTHSPHWLTILDQLSVKIIFTLFSGKTYAIFTMLFGFTFYIQHNNQKKKGKDFGYRFLWRMALLAVFAVLNAAFFPAGDVLMLFVYVSLVLFICRNWPDRAVLVFIIVLLLQPVEWIHFILSRFNPAYQLPDFGAVSLHQQVVENTKNGSFLDFIRVNVTLGQKVSLMWALGSGRFLQAAGLFLLGFYIGRKQFFINTPDNLRFWKRVLIISSVSFILFNIIKKLLLQSDPMAQQTVGLIFDIWYKLALTFVLIASFVLLYEKRFFRKRLSGLRFYGKMSLTNYVSQSIFGALIYFPIGLYLAPYCGRTFSLVIGIAVFSLQMMFSRFWLGKHKQGPLEGIWHKWTWINS
>AP018040.2|BBD44572.1|712240_713500_-|phosphoglycerate-kinase
MQTIDTFNFAGKKAFIRVDFNVPLDENFKITDDTRIRAAIPTLKKILKEGGSVIIGSHLGRPKGPTEKYSLKHILPRVSELLGVDVHFANDCIGEETEAKAAALRPGEALLLENLRFYAEEEGKPRLPEGATEEETAAAKKAVKESQKEFTKKLASYADVYVNDAFGTAHRAHASTALIADYFDAGNKMFGYLMQNEVNAVEKVMSDTERPFTAIMGGSKVSTKIELIKNLLDKVDNLILAGGMTYTFAKAGGGKIGDSIVENDKLDLANEIVDLAKEKGVNLVLATDAKLADSFSNDAKTDFGSVKEIPDGWEGLDIGPETEKVFAEVIKNSKTILWNGPVGVFEFDNFDKGSRAVADAIVEATQKGAFSLIGGGDSVACINKFGLADDVSYVSTGGGALLEMIEGKVLPGIKAIRGY
>AP018040.2|BBD44573.1|713610_714030_-|Hypothetical-protein
MTHSIKTIWKDNNIFETDVDGHNVVIDLAEDAGGNDAGPRPKKLLLVAAAGCTGLDVVEILKKMRIDIKGFNVQIESGMTDEYPKQYTDLKVVYEFEGKDLPKDKLERACQLSFDKYCGVLAMYKKAVPVSYEVKITDV
>AP018040.2|BBD44574.1|714221_715262_+|L-asparaginase-I
MIDKNARVLLIYTGGTIGMVENLETGALEAFNFSHLKSNVPEMKRLNFNVDTYLFDPPIDSSEVSPQNWQDMATVVEDNYNDYDGFVILHGTDTMSYTASVLSLMFENLTKPVIFTGSQLPIGKLRTDGKENLITALEIAADKDKSGRPVVPELCIYMQNLLMRGNRTTKVNSENFSAFNSPNYPYLAEVGVDIRYHDKFILQPDYDKPVIFNFRLDHNVAILKLFPGIQESVVRSILSVPALRGVVLETYGSGNAPTDQWFIDALQEAIDQGIVIVNVTQCLYGNVEMHRYETGQHLEKLGVVSGHDITTEAALAKLMILQGNGKTPDQVRRLMSVSLRGELTER
>AP018040.2|BBD44575.1|715300_717094_+|Hypothetical-protein
MKNLDYGVIGNCRTAALVSKEGSIDWLCLPDFDSPSVFTRLLDEEKGGSFAFLVSGEYVVTQTYLGNTNILSTRFEAPEGAFTVLDYMPRYRTSEKSHYLPPEVHRYLRVLHGKPKMRILYNPKMNYAGEEAVHTVFPNYIRTSSAVDAEDKIYLYSSVNFDVILSGEEFTLTDHQFFLLSYNQKLVAIDENRVLLDYERTKVYWLNWINRSREYRQYGDMVNRSMLVLKLMSYQHSGAMLAAVTTSLPESIGETRNWDYRFCWLRDASMSIDTLLHMKHQGTAERFIGFIKRILKSREDTFQIMYGIRGERELTEEILSHLAGYENSYPVRIGNAAYNQLQNDSLGYLMDVIYKYYLYFPGTLDEVEEIWEVVRNMVRMVLKSWRSPDQSIWEFRTRELNFVFSKVMSWVALDRASLIAELLHKDNYAELWRKEANGIKEEIHEKGWNEELQCFTQAYENTDHDSSLLLMQFYDFIDARDERYVKTVKAIKENLFHNGLMYRYKAEDDFGKPTSSFTICTFWLIEALFVIGETDQAREIFESMITYSNHVGLYSEDLDFETKRQLGNFPQAYSHLAFINTATLLSEEKKLSRFIRP
>AP018040.2|BBD44576.1|717080_718169_-|Membrane-protein
MNDITDLITENKWRHIFVSLIFIILFILLTLASNFIFKKLRNRALRSQSLIDDFIVRLFKVPSAWIIFSILLNIFSSLLDKNTRVYDIIQKTGQVLLILSIGWLIVQAVRALFRYFQNKLDVNQSDNLTARRRLTQLNMIEKVLIVTVVIVFTGIASMTFETVKGLGMSLLASAGVLGIVVGLAAQRSVGQILSGVQIAITQPIRLDDVVVIQGEWGRIEEINITYAVVKIWDERRLIVPIDYFLNNPVQNWTRTSSNILGTVFLYVSYGLPVAPLRKKLAGLVKNDPNWDGRVQNIQVTDSKQWYKEIRVLVSSEDSSKNWDLRVSVREKLIDFINENYPGSFARISTTGEEKQRHTATDG
>AP018040.2|BBD44577.1|718193_720362_-|Hypothetical-protein
MKILIIANRLPVKIERTEDSFVVKRSEGGLATGLGSLETDAEMHWVGWPGVHVDDENEKQEITEKLNELNYHPVFLSGEQIENYYEGYSNSTIWPLCHYFFAYIQYKAEYWEAYRQVNTLFCEEALPFIEDDDIVWIQDYQLMLLPKKIRDKKPKVNIGYFHHIPFPSYELFRVLPEREQVLEGLLGADLIGFHTHDYMRHFISAIYRVLDLNCNLDEISLKDRIVHVDAFPMGINYEQYHRAPSLPEVKKISKRLIEELGNQTIVLSVDRLDYSKGILHRLNGFANFLENHPEYHKKVSLAMIVVPSRDAVDRYADLKTRIDQYIGKINGMYSTLGWTPVYYFYQSFPFNELVALYDIADIAMVTPLRDGMNLVAKEYLATKRGKPGVLILSEMAGAAIELTDAIIINPNDTQEIEAAILQALTMPKKEQRIRLNNMQKRISTQTVKKWANDFVKELLYISKQNNEIFQKIVGKRQLSQIKKEYDQAYTRLILLDYDGTLSPFVKNPEDAVPSKELLNLLKKMTADKKNKVVINSGRNRQVLDKWFKGIDLDFAAEHGAFFKENHKWHKNVQEKITWDDEILRIIEHTIDKTPRSRMEIKDSSLVWHYRNVDVWLAELRQKQLINALMGPASRLNLQIVPGNKIVEIKSPDFNKGSEVKRLLGKNNYDFILAIGDDTTDEDMFHALPPGGVSIKVGHFSPAAKYRIPVQSSVIPFFENLIK
>AP018040.2|BBD44578.1|720700_724267_+|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase
MTKKKNYLTCDGNQAAAHIAYMFSEVAAIYPITPSSTMAEYIDEWAAAGRKNIFGQPVLVQEMQSEAGAAGAVHGSLQAGALTSTFTASQGLLLMLPNMYKIAGELLPGVFHVSARAIAAQALSIFGDHQDVMAARPTGFASFATGSVQEVMDLAAVAHLAAIESRVPFLHFFDGFRTSHEIQKIEALTNDDLAPLINQEALAGFRQRALSPDAPVTRGTAQNDDIYFQSREAANPFYNAVPGIVEKYLEKLAAVTGRKYGLFDYYGDPEAERVIIAMGSVTEAIREVVDHKNANGEKVGMVAVHLYRPFKAEAFLSVIPKTARRIAVLDRTKEPGATGQPLYLDVKDSFYGKENAPVIVGGIYGLSSKDTTPGQIISVYDNLAMNMPKNDFTIGIVDDVTFKSLPKVEEVSMDETTYEAKFYGLGSDGTVGANKNSIKIIGDNTDKYVQAYFAYDSKKSGGFTCSHLRFGDNRIRSTYLVNTPNFVACHVPAYLHLYDVTAGLKKGGTFLLNSLWSKEEVGNHLPDNVKKYLAKNNIKLYIINATNIADEIGLGNRTNTILQSAFFKISNVIPYELAVEQMKKFIVKSYGRKGEEIIKMNYAAVDRGGEVEEVEVLREWADLNVDMVQKDDAPEFIQKVVRPVNAQRGYDLPVSVFVGREDGTWEHGTATYEKRGVAASVPVWNPDNCIQCNQCAYVCPHATIRPFVLDEKEQKGLGEEVALLKTQGKQFEGTAFRIQVDVLDCLGCGNCVDVCPGKKGQSALEMVPITTQYDNQKNWDYMVQHVSSKAHLVDTKLNVKNSQFAKPLFEFSGACSGCGETPYIKLITQLYGDRMMIANATGCSSIYGASAPSTPYTKNEEGKGPSWANSLFEDNAEFGFGFVIAQASMRNRVGDLMQKARKSADFSDSQKELFVQWIENKDNGEAVKEISAQIVGVLTGMENEIAKEILSLEKYLTKKSIWVFGGDGWAYDIGFGGLDHVLAMGQDINVLVLDTEVYSNTGGQSSKSTPTAAVAKFAAAGKRIRKKDLGMIAATYGYVYVAQVAMGANQAHYLKALKEAEEYNGPSLIIAYSPCISHGLRSGMGMAQTEQKKAVECGYWSLWRYNPKLEEEGKNPFVLDSKEPDWSKFRDFLMGEVRYTQLVKSFPHEADELFEAAKENAQWRYRSYQRMANAHFGSVDAETAKAEG

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Crispr_ID: AP018040_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

AP018040_2

1434124-1434196

Orphan

Consensus_repeat	Method
AATCCTATAGGTTTAGTAGGATA	CRISPRCasFinder

1 spacers

The CRISPR arrays of AP018040_2

>merge|AP018040|2|1434124-1434196|CRISPRCasFinder
AATCCTATAGGTTTAGTAGGATAATGCGTGAAAAAATGCAATATCAATCCAATCCTATAGGTTTAGTGGGATA

>AP018040|2|2|1434124-1434196|CRISPRCasFinder
AATCCTATAGGTTTAGTAGGATA	ATGCGTGAAAAAATGCAATATCAATCC
AATCCTATAGGTTTAGTGGGATA

Protein	Signature genes	Signature genes Name	Protein_function
AP018040.2\|BBD45172.1\|1427328_1427976_-\|phosphate-transport-regulator	unknown	unknown	gnl\|CDD\|224310
AP018040.2\|BBD45184.1\|1441163_1441832_+\|Peptidase-S54,-rhomboid-domain-protein	unknown	unknown	gnl\|CDD\|366759
AP018040.2\|BBD45179.1\|1434209_1434602_-\|transcriptional-regulator,-badm/rrf2-family	unknown	unknown	gnl\|CDD\|273242
AP018040.2\|BBD45181.1\|1436362_1437691_-\|glycoside-hydrolase,-family-57	unknown	unknown	gnl\|CDD\|212107
AP018040.2\|BBD45174.1\|1429561_1430797_+\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|224688
AP018040.2\|BBD45177.1\|1431961_1433308_-\|Hypothetical-protein-(Precursor)	unknown	unknown	unknown
AP018040.2\|BBD45187.1\|1444023_1444923_+\|Prolipoprotein-diacylglyceryl-transferase	unknown	unknown	gnl\|CDD\|234599
AP018040.2\|BBD45176.1\|1431260_1431899_-\|YceI-family-protein-(Precursor)	unknown	unknown	gnl\|CDD\|214870
AP018040.2\|BBD45185.1\|1441839_1442841_-\|Inosine/uridine-preferring-nucleoside-hydrolase	unknown	unknown	gnl\|CDD\|239118
AP018040.2\|BBD45188.1\|1444885_1446214_+\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|223503
AP018040.2\|BBD45171.1\|1426239_1427271_-\|phosphate-transporter	unknown	unknown	gnl\|CDD\|376541
AP018040.2\|BBD45183.1\|1439056_1440997_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|283786
AP018040.2\|BBD45173.1\|1428373_1429486_+\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|273213
AP018040.2\|BBD45175.1\|1430705_1431251_+\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|379474
AP018040.2\|BBD45169.1\|1423891_1425214_+\|RIP-metalloprotease-RseP	unknown	unknown	gnl\|CDD\|272878
AP018040.2\|BBD45182.1\|1437730_1438987_-\|glycosyl-transferase-family-protein	unknown	unknown	gnl\|CDD\|340831
AP018040.2\|BBD45178.1\|1433352_1433943_-\|YceI-family-protein-(Precursor)	unknown	unknown	gnl\|CDD\|214870
AP018040.2\|BBD45186.1\|1443038_1443992_+\|meso-diaminopimelate-D-dehydrogenase	unknown	unknown	gnl\|CDD\|273877
AP018040.2\|BBD45180.1\|1434797_1436228_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|215071
AP018040.2\|BBD45170.1\|1425284_1426235_+\|methylenetetrahydrofolate-reductase-(NAD(P)H)	unknown	unknown	gnl\|CDD\|273212

Protein	Function_ID	Function_description	E-value
AP018040.2\|BBD45172.1\|1427328_1427976_-\|phosphate-transport-regulator	gnl\|CDD\|224310	COG1392, COG1392, Phosphate transport regulator (distant homolog of PhoU) [Inorganic ion transport and metabolism].	5.91072e-31
AP018040.2\|BBD45187.1\|1444023_1444923_+\|Prolipoprotein-diacylglyceryl-transferase	gnl\|CDD\|234599	PRK00052, PRK00052, prolipoprotein diacylglyceryl transferase; Reviewed.	1.08121e-83
AP018040.2\|BBD45179.1\|1434209_1434602_-\|transcriptional-regulator,-badm/rrf2-family	gnl\|CDD\|273242	TIGR00738, Putative_HTH-type_transcriptional_regulator, Rrf2 family protein. This model represents a superfamily of probable transcriptional regulators. One member, RRF2 of Desulfovibrio vulgaris is an apparent regulatory protein experimentally (MEDLINE:97293189). The N-terminal region appears related to the DNA-binding biotin repressor region of the BirA bifunctional according to results after three rounds of PSI-BLAST with a fairly high stringency. [Unknown function, General].	3.3975e-21
AP018040.2\|BBD45170.1\|1425284_1426235_+\|methylenetetrahydrofolate-reductase-(NAD(P)H)	gnl\|CDD\|273212	TIGR00676, 510-methylenetetrahydrofolate_reductase., 5,10-methylenetetrahydrofolate reductase, prokaryotic form. The enzyme activities methylenetetrahydrofolate reductase (EC 1.5.1.20) and 5,10-methylenetetrahydrofolate reductase (FADH) (EC 1.7.99.5) differ in that 1.5.1.20 (assigned in many eukaryotes) is defined to use NADP+ as an acceptor, while 1.7.99.5 (assigned in many bacteria) is flexible with respect to the acceptor; both convert 5-methyltetrahydrofolate to 5,10-methylenetetrahydrofolate. From a larger set of proteins assigned as 1.5.1.20 and 1.7.99.5, this model describes the subset of proteins found in bacteria, and currently designated 1.7.99.5. This protein is an FAD-containing flavoprotein. [Amino acid biosynthesis, Aspartate family].	1.84762e-94
AP018040.2\|BBD45174.1\|1429561_1430797_+\|Hypothetical-protein	gnl\|CDD\|224688	COG1774, COG1774, Uncharacterized homolog of PSP1 [Function unknown].	1.33534e-42
AP018040.2\|BBD45181.1\|1436362_1437691_-\|glycoside-hydrolase,-family-57	gnl\|CDD\|212107	cd10795, GH57N_MJA1_like, N-terminal catalytic domain of a thermoactive alpha-amylase from Methanococcus jannaschii and similar proteins; glycoside hydrolase family 57 (GH57). The subfamily is represented by a thermostable alpha-amylase (MJA1, EC 3.2.1.1) encoded from the hyperthermophilic archaeon Methanococcus jannaschii locus, M J1611. MJA1 has a broad pH optimum 5.0-8.0. It exhibits extremely thermophilic alpha-amylase activity that catalyzes the hydrolysis of large sugar polymers with alpha-l,6 and alpha-l,4 linkages, and yields products including glucose polymers of 1-7 units. MJ1611 also encodes another alpha-amylase with catalytic features distinct from MJA1, which belongs to glycoside hydrolase family 13 (GH-13), and is not included here. This subfamily also includes many uncharacterized proteins found in bacteria and archaea.	1.06011e-167
AP018040.2\|BBD45176.1\|1431260_1431899_-\|YceI-family-protein-(Precursor)	gnl\|CDD\|214870	smart00867, YceI, YceI-like domain. E. coli YceI is a base-induced periplasmic protein. The recent structure of a member of this family shows that it binds to polyisoprenoid. The structure consists of an extended, eight-stranded, antiparallel beta-barrel that resembles the lipocalin fold.	0.000628
AP018040.2\|BBD45185.1\|1441839_1442841_-\|Inosine/uridine-preferring-nucleoside-hydrolase	gnl\|CDD\|239118	cd02652, nuc_hydro_2, NH_2: A subgroup of nucleoside hydrolases. This group contains eukaryotic and bacterial proteins similar to nucleoside hydrolases. Nucleoside hydrolases cleave the N-glycosidic bond in nucleosides generating ribose and the respective base. These enzymes vary in their substrate specificity. .	1.08091e-55
AP018040.2\|BBD45188.1\|1444885_1446214_+\|Hypothetical-protein	gnl\|CDD\|223503	COG0426, FpaA, Uncharacterized flavoproteins [Energy production and conversion].	1.994e-119
AP018040.2\|BBD45171.1\|1426239_1427271_-\|phosphate-transporter	gnl\|CDD\|376541	pfam01384, PHO4, Phosphate transporter family. This family includes PHO-4 from Neurospora crassa which is a is a Na(+)-phosphate symporter. This family also contains the leukaemia virus receptor.	4.80625e-92
AP018040.2\|BBD45184.1\|1441163_1441832_+\|Peptidase-S54,-rhomboid-domain-protein	gnl\|CDD\|366759	pfam01694, Rhomboid, Rhomboid family. This family contains integral membrane proteins that are related to Drosophila rhomboid protein. Members of this family are found in bacteria and eukaryotes. Rhomboid promotes the cleavage of the membrane-anchored TGF-alpha-like growth factor Spitz, allowing it to activate the Drosophila EGF receptor. Analysis has shown that Rhomboid-1 is an intramembrane serine protease (EC:3.4.21.105). Parasite-encoded rhomboid enzymes are also important for invasion of host cells by Toxoplasma and the malaria parasite.	1.87388e-14
AP018040.2\|BBD45173.1\|1428373_1429486_+\|Hypothetical-protein	gnl\|CDD\|273213	TIGR00678, DNA_polymerase_III_subunit_delta', DNA polymerase III, delta' subunit. This model describes the N-terminal half of the delta' subunit of DNA polymerase III. Delta' is homologous to the gamma and tau subunits, which form an outgroup for phylogenetic comparison. The gamma/tau branch of the tree is much more tighly conserved than the delta' branch, and some members of that branch score more highly against this model than some proteins classisified as delta'. The noise cutoff is set to detect weakly scoring delta' subunits rather than to exclude gamma/tau subunits. At position 126-127 of the seed alignment, this family lacks the HM motif of gamma/tau; at 132 it has a near-invariant A vs. an invariant F in gamma/tau. [DNA metabolism, DNA replication, recombination, and repair].	7.76756e-56
AP018040.2\|BBD45175.1\|1430705_1431251_+\|Hypothetical-protein	gnl\|CDD\|379474	pfam14109, GldH_lipo, GldH lipoprotein. Members of this protein family are predicted lipoproteins, exclusive to the Bacteroidetes phylum. Proteins in this family are typically between 155 and 167 amino acids in length. Members include GldH, a protein linked to a type of rapid surface gliding motility found in certain Bacteroidetes, such as Flavobacterium johnsoniae and Cytophaga hutchinsonii. Gliding motility appears closely linked to chitin utilization in the model species Flavobacterium johnsoniae. Not all Bacteroidetes with members of this protein family may have gliding motility.	3.15758e-43
AP018040.2\|BBD45169.1\|1423891_1425214_+\|RIP-metalloprotease-RseP	gnl\|CDD\|272878	TIGR00054, Putative_zinc_metalloprotease_slr1821, RIP metalloprotease RseP. Members of this nearly universal bacterial protein family are regulated intramembrane proteolysis (RIP) proteases. Older and synonymous gene symbols include yaeL in E. coli, mmpA in Caulobacter crescentus, etc. This family includes a region that hits the PDZ domain, found in a number of proteins targeted to the membrane by binding to a peptide ligand. The N-terminal region of this family contains a perfectly conserved motif HEXGH as found in a number of metalloproteinases, where the Glu is the active site and the His residues coordinate the metal cation. Membership in this family is determined by a match to the full length of the seed alignment; the model also detects fragments as well matches a number of members of the PEPTIDASE FAMILY S2C. The region of match appears not to overlap the active site domain. [Protein fate, Degradation of proteins, peptides, and glycopeptides].	1.42815e-48
AP018040.2\|BBD45182.1\|1437730_1438987_-\|glycosyl-transferase-family-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in certain bacteria and archaea.	2.52457e-51
AP018040.2\|BBD45178.1\|1433352_1433943_-\|YceI-family-protein-(Precursor)	gnl\|CDD\|214870	smart00867, YceI, YceI-like domain. E. coli YceI is a base-induced periplasmic protein. The recent structure of a member of this family shows that it binds to polyisoprenoid. The structure consists of an extended, eight-stranded, antiparallel beta-barrel that resembles the lipocalin fold.	3.96436e-14
AP018040.2\|BBD45186.1\|1443038_1443992_+\|meso-diaminopimelate-D-dehydrogenase	gnl\|CDD\|273877	TIGR01921, Meso-diaminopimelate_D-dehydrogenase, diaminopimelate dehydrogenase. This model represents the diaminopimelate dehydrogenase enzyme which provides an alternate (shortcut) route of lysine buiosynthesis in Corynebacterium, Bacterioides, Porphyromonas and scattered other species. The enzyme from Corynebacterium glutamicum has been crystallized and characterized.	1.36398e-126
AP018040.2\|BBD45183.1\|1439056_1440997_-\|Hypothetical-protein	gnl\|CDD\|283786	pfam06202, GDE_C, Amylo-alpha-1,6-glucosidase. This family includes human glycogen branching enzyme AGL. This enzyme contains a number of distinct catalytic activities. It has been shown for the yeast homolog GDB1 that mutations in this region disrupt the enzymes Amylo-alpha-1,6-glucosidase (EC:3.2.1.33).	2.65746e-76
AP018040.2\|BBD45180.1\|1434797_1436228_-\|Hypothetical-protein	gnl\|CDD\|215071	PLN00137, PLN00137, NHAD transporter family protein; Provisional.	3.41937e-135

>AP018040.2|BBD45178.1|1433352_1433943_-|YceI-family-protein-(Precursor)
MKSNFLFKFPTVLIAFIFVLTGTTVKAQTLKIKSSTITISGTTNVHPYTTTSTQASGELTVSNNKATVLNVNVPVKSIINGEKLMDKKTHETFNEPKNPFINFKMSEVKSITTNGSDISVVIGGTLAMAGTSKTVTLEANGKEIKPGTYTFEGSLPLKMSDYNMKAPTAMLGVMKVGDQVTVKYNVTFEGPAVQFN
>AP018040.2|BBD45177.1|1431961_1433308_-|Hypothetical-protein-(Precursor)
MKMKQRGLLLAATLLASGMMFAQLRPTNKDGINVFETPKTETEFEGFNVQLGGALTLPFSMLDHSNTVTRESGYNYDYANPAANSLVPLTSGFGLPQANLYIKSNLSDGIYLNFELYLASRHHNETWVKGGFLQFEKMEFLPWDFVDEIMKYTTIKVGQFDVNYGDAHFRRSDGGLTFYNPFMENHIMDEFATEIGAEVDVHVGDFILVGAVTNGKLNNDLTKIDTTRAQTKYSNGVHNPAWIGKLAYDKQINSQFRLRASASGYYTAGSVRNTLFGGDRTGSNYYGVMYNAPISNANFTNGRFNPGFGDKVAAVMGNLFLKFSPVQGFSLESFTTLENAGGRGANEPDVRKSNQFVTDLVVRFGADEDFYVGARYNTMKADMGAAQGEPNHYEVDINRVAIAAGWYMTKNVMAKIEYVNQKYNGFPARSIQDGAEFNGLTLQGSIAF
>AP018040.2|BBD45176.1|1431260_1431899_-|YceI-family-protein-(Precursor)
MKALFALLLIGILTTGAVVAQTSSAVVAVDVNKNSSLSINGSSNIVNFTLTQSSENFIQKNMIITASQNDKKLYLSENRLIVPVKRFTSSNKMALRDFYKLLKSDKYPTMDIQLNHIDLPENPKLATGVAVVDVTITGVTKKYQFPIKTEKNGTRYIFDIEKHINIRDFGLEPPVQMMGMLKVDEMININLKMICNIQPAESAQLNLSGSSE
>AP018040.2|BBD45175.1|1430705_1431251_+|Hypothetical-protein
MEVLLKGENQGGVDRTTETGKENRLNKMRSKLFVGFLVVFACLSSCDEGEVYYRFHPIKNSSWSKQATANFLIDSLSVDPDKRYDIVLEIVNNNRYPYQNIWLLVQQNITDTTFVGDTVEITLADPQGKWLGKGTAGLYQLSVPYKTSVALDSARAYLIRIRQVMKDNPIKGIEKVGVLVK
>AP018040.2|BBD45174.1|1429561_1430797_+|Hypothetical-protein
MPLDNINVYIMDREKLSDRLADIVPERITTVRNSGSCKGCPKHSTKLHVYDWLHDFPEMQELTNMVEVQFKNTRKGYYINSNNIDLKKGDVVAVEASPGHDIGTVTLTGKLVEAQMRKNNYREDGNSGPRRVYRLVRPADMEKYELAKAKEQPTMIRSRELAESLGLNMKIGDVEYQGDGSKAIFYYIADERVDFRQLIKDFAAEFRVKIEMKQIGARQEAGRIGGVGPCGRELCCSSWMSSFVSVSTSAARYQDISFNPQKLAGQCGKLKCCMNYEVDAYVEASRRLPSREIVLQTKDSDYFHFKTDILSGQITYSTDKNNPINLETISKERVFQIIEWNKKGKKPSKLVSETESGETKEETIQNDLLGDQSITRFDKKDDGSTSKRRKPRRGRQDNRNRKGKPPKQNEE
>AP018040.2|BBD45173.1|1428373_1429486_+|Hypothetical-protein
MYFRNIIGLHDVKKHLTDSVQRGFIPHARLFHGPEGVGKLPLAIAYARYLNCEDRTLEDSCGKCASCHKFDKLMHPDLHFVFPVVKSKVSDEYLPEWREFLSGQTYFNLNDWLNFINAENAQGIIYSKESDEIIRKLSLKVYEALYKIMIVWLPEKMHDACANKLLKMIEEPPEKTVFLLVSEDLDHVLPTIQSRCQPLNIRAVEPDEMVASIRSVYGLQEEEAKYVTHIANGSFSKAVSIIQSADDNKYFFSLFKEMMRSSVSRNIKAIKSVAGEMASMGREMQKSYLLYSLRLFREFFISNFNEPDMIYLSEEEKEFGERFAPFINEGNIQSFNDEFQLAYRQIEQNGNAKIIFLDLCLKGTMLLKNK
>AP018040.2|BBD45172.1|1427328_1427976_-|phosphate-transport-regulator
MNNSFFSKFTPKEPKFFPLLKGIVEVIKSASYLMLEFVEKGNHANAADYYKKIKEEERKGDTLSNKIFDELNATFITPFDREDIHNLATKMDDVTDYINSAAKKVFLYNPKEMPAAAKDMVELIIEASAQIEKAVNELDVLKKSRKRVSDYCRELHLIENRADDVYEHFLIDLFENQKESIELIKKKEIMFELEKATDAAEGVGKIIKTIIVKYA
>AP018040.2|BBD45171.1|1426239_1427271_-|phosphate-transporter
MTLLIVIISLALIFDFINGFHDAANSIATIVSTKVLTPFQAVLWAAMFNFVAFFIAKYLIGGFGIADTVSKTVIAEFITLPIIFSGLVAAITWNLLTWWLGIPSSSSHTLIGGFAGAAIAKWASFSVIKVSVIVKIASFIFIAPLVGMLVAMILTIVLQWSVKRANPHKANTWFKHFQLVSSALFSIGHGLNDSQKVMGIIAAALIATHIQHPEIGFGIESISDLPNWVAFSCFFAISLGTMSGGWKIVKTMGTRITKVTPFEGVVAETAGAFTLYLTEFLKIPVSTTHTITGAIIGVGSVKRLSAVRWGVTRKLLVAWILTIPVSALIAATVYFTAGKFLYF
>AP018040.2|BBD45170.1|1425284_1426235_+|methylenetetrahydrofolate-reductase-(NAD(P)H)
MKISDLIHQTSKPVFSFELLPPLKGNSIKQVFNTIDRLKEFGPKYINITTHHSENTYKEDENGIIRKVNVRKRPGSVAIAAAIQNKYGIRAVPHIISQGFSKEETEYALIDLSFLGVTDLLLLRGDTKKLDADQRKMDCHSYATGLQEQVNNFNNGIALDGSTFPAPETPFTYGMACYPEKHEESPNMESEIYYTKMKAQNGADYLVTQMFFDNQKYFDFVDRCRAEGITIPIVPGIKPIHLKNQLNVLPKIFRTEIPEDLEHELRKCKTDADAVEVGVEWCLLQSRELVQRGVPGIHFYALGATESIYRVAREVY
>AP018040.2|BBD45169.1|1423891_1425214_+|RIP-metalloprotease-RseP
METFLIKALQLILSLSILVVIHEFGHFIFARVFKIRVEKFYLFFDPWFALFRYKPRNSETEYGVGWLPLGGYVKISGMIDESMDKEQMAQPVQPWEFRAKSTWQRLLVMIGGVLFNIILAFFIYSMIVFRWGDSYIPMSKVKSGMEFSETAERAGFRDGDVLLYADGKEIIDRAGIVDNFAAQVIDAQTVTVLRSGQEINIPMPADFVQQLMRDKKGFAGYKDDVPTVVEKVQKGSEAEKIGLMKGDSLVGVNSVLTPTFQDFRSELQKNKGLRISIDFYREGVLQTASAQLDTTAVLGFNIASYLVTDHYTFFASFPAGVKYGIRTLKGYVSQFKHIFTKEGASSLGGFGTIGNLFPAKWNWYSFWMMTAFLSVILAFMNILPIPGLDGGHVLFLLVEAISGRKPSDKFLEYAQIAGMFLLIGLVLYANGMDIVRAIFK
>AP018040.2|BBD45179.1|1434209_1434602_-|transcriptional-regulator,-badm/rrf2-family
MIEIACCKEPTGILQKDIAKNQNISVKYLDYIISALKLKGLISNTKGRGSGYMLARPADKITMLDIYTAFEQIVIIECVKNRSFCERATHQCTANNYWKQFRHQIIEILSAKTLEQIIKETKYDCPEICE
>AP018040.2|BBD45180.1|1434797_1436228_-|Hypothetical-protein
MIYAMILLFIAGYFFIAMEHTIKVNKASVALLIGTLLWVIYVYLAPSTVLSVSPDAFNHYIHSHPELQHHAFGIQVRHFVIDHQILESIGDISEMLFFLLAAMTIVELIDVHGGFTYITEKITTRKKRRLLWLISFITFFMSAVLDNLTTTIVMIMLTRRIIREPRERWLFGSIIVIAANSGGAWSPIGDVTTIMLWVKGNITASIIPQLFFPSLVSMIAPVFVAQFLLKGNIQEEEISQTEEKENSELLLHMQKKDRLGILIFGVSILVLSPVFKGVTHLPPFIGLLLGVSLLWIYTEILYNQKNQLNENLKLRVSKVLGRIDFSTLMFFLGILLAVDALQSAGILQQSSAFMAQHLPNVYAQAYAIGLLSAIVDNVPLVAAAIGMYPVLDPAALSTMADPVFMQNFVEDGVFWHFLAYCAGVGGSILIIGSAAGVVFMGLEKVPFGWYLKRISLIALIGYTFGAGAYILQQAIF
>AP018040.2|BBD45181.1|1436362_1437691_-|glycoside-hydrolase,-family-57
MKTICFYFQIHQPYRLKRYRFFNIGRDHYYYDDYSNEDIMQQIAARSFIPANRMLLDLINTYKGKFKFAISVSGVALDQMEVYAPEVIDGLKELSRTGAVEFLAETYSHSLSSLIDPVEFQSQVQQQTQKIKLLFDQKPKVLRNTEMIFSDDIAEMAYNMGYTKMVSEGAKLILSWRSPNYVYKSENQPNMKLLLRNSQFSDDISLRFSDYTWKEYPLTAEKYISWIAATSPQEEVFNIFMNYETFGNLQPAHSGIFEFMKALPKFAFDKGIEFSTPSQIMDTHKPVGTVSVPLAISWSDEERDLSRWLGNKLQKSAFNTLYEISERIRLANDRRLKKDWQYLQSSDHFYYMSTKHFYDGSMHSKFSPYQSPYDAFNNYMNVLSDFIDRVKAQFPDSVDNEELNSLLTTIHNQEREIKKLQSELKKVLTENEEKLVEKTPVK
>AP018040.2|BBD45182.1|1437730_1438987_-|glycosyl-transferase-family-protein
MKALMLGWEFPPHILGGLGTASYGLTKGMAKQEDMEILFVIPKPWGDEDQSFLKIIGCNNTPVVWRDVSWETAKARLEKYMNPEEYFWMRDNIYANFNYMNTNDLGCLEFSGRYPNNILEETNNYSIVTGVIARTYEYDIIHAHDWLTYSSGLHAKSVSGKPLVIHVHATEFDRSRGKPNPTVYGIEKNGMDHCDHIICVSNLTRKTVIENYHQPEWKVSTVHNAVEPLSPEIEAIERISGVKEKVITFLGRITMQKGPEFFVDAATQVLRRTKHIRFVMAGSGDMMNQMIRLVADRGIADRFHFTGFLRGEQVYEMLKSSDVYVMPSVSEPFGISPLEAMQCGVPSIISYQSGCAEILNNVIKTDYWDVDAMADAMYSICTYPGMAEFLKEEGKREVDSIVWEDAGKKIRAIYDSLV
>AP018040.2|BBD45183.1|1439056_1440997_-|Hypothetical-protein
MSYLKFDKDLMINLEYSLYRNILRTNRKGAYQNTSISGCNTSKYQGLLVMPVPFLDDDNHLILSSIDETVIQHGAQFNLGIHKYNDDNYSPKGHKYIREYNIDSVPKTIYRVGGVILSKEIMFSSKENRLMIRYKLMDAHSPTTMRFKPCMAFRNISQLTRQNDQVDRSYREVENGISTSMYYGYPEFFMQFNKRVDFMYQPYWNQGVEYIQDMQNGDTFKEDLYVPGYFEMPIAKGEEVIFSAGDILVNTSALTDEFNAELKKRTPRSSFYNCLKNSAHQFYYIPKTDEMYLLAGYPWFKVRARDQFVSLPGCTLSVGRPDDFTKIMDSAIPHIQDFLNDKPRKNIIKQIDDPDVLLWVTWALQQYWKENKPVFKEKYVDFLFSIINFILSNKHPNLTVDPENGLVSTYGRDVAVSWMNAVQNGKPVTPRSGYLVEFNALWHNALKFAEEVAAATNKEVLATTYEEKALKAQQSFIETFLNDAGYLYDYVDGTYADRNVRPNMIFAVSMDYSPLDRRQKKLVIDFVTKELLTPVGIRSLSPKGYNYRPRYAGTSEEKEYAYFNGCAFPWLIGAYIEAYLKVFSMSGLSLADRVMIELEDQMQNDCIGTLSEFYDSSPPFYAHGGYSFAMSVSETLRAKRLIRSFG
>AP018040.2|BBD45184.1|1441163_1441832_+|Peptidase-S54,-rhomboid-domain-protein
MDNATIHTERWQKKRIRLATIPALVICVLVWLTFLIDYARIFRFNFSLLGIYPRQLNGLAGIVFSPFIHGSLSHLVSNTFPMLVLFSLLFYFYNQIAFKSLTLLWLLSGFFTWLIGRNSYHVGASGLIFALVFFLFFSGLFRKYIPLVAVSMVVAFVYGSTVWSIFPITEYIDVNLSWEAHLSGAAAGLIVAFVFRSRGPQKPEVLWEEDGEDDNDETVITG
>AP018040.2|BBD45185.1|1441839_1442841_-|Inosine/uridine-preferring-nucleoside-hydrolase
MKALFVYLLIPLLVFFSCNSNPQEGAVASPEKIIFDTDMGPDYDDVGAIAILHALADLGECEILATLASDGHPSIAPTIEMFNRYYGKGGIPVGIPDNGVANFTASNNWNDSLLVRFAPDLKSKTDYPKASEIYRKVLASQPDKSVTIVTVGFTTNLAELLKTGNDDYSPLSGVELVKKKVKKWVAMAGRFPEGREFNVFIDSVSSSYVLERWPTPILFSGFEIGERIFTGSKVAEKNDQNNPVSWAYKYNLATYENKPVKNRMSWDQTAVLCAIRDPERYFYVCGPGKIIVNSSGYNNWDPDSTKDHYFLVHKYPYQDISDTLEGLMMYQPK
>AP018040.2|BBD45186.1|1443038_1443992_+|meso-diaminopimelate-D-dehydrogenase
MSRQKSAFFTIFVHQNYKKMKKIRAAVIGYGNIGKYVMESLIDAPDFEITGVVRRDATNVPAELKGFEVVNSISQLKNTDVALLCTPTRSVEKFAKECLALGINTVDSYDIHGGIVDLRHSLNDVAKQHNAVSIVSAGWDPGSDSVVRTLMEAMAPKGITYTNFGPGMSMGHTVAVKAIEGVKAALSMTIPTGTGVHRRMVYIELNDGYDFDQVAKAIQSDDYFAHDETHVFRVENVEALKDMGHGVLMERKGVSGNTQNQLFRFDMRINNPALTAQVMVGCARAAVKQKPGAYTLIEIPVVDLLPGDREKWIKKLV
>AP018040.2|BBD45187.1|1444023_1444923_+|Prolipoprotein-diacylglyceryl-transferase
MNTLLTVTWNVDPTIFTVLSREIRWYGLLWVIGLIVAVYIVQRIYKSEKLPEKWFDSLFVYMMLGIILGARLGHCLFYEPEYYLANPVEMLKIWEGGLASHGGVIGIIIAVWLYSKRVTKKSMLWTFDRVMVPTGFTAAMIRFGNLMNHEIYGGPTDLPWGFRFIDNVGLWMRGAEPVYTEPSHPTQIYEALIYLLVFGITMYMYWKTNAKNRQGLILGVGIALIFIARFFIEFVKNVQVDSEIAMRENTGLILGQWLSIPFIIWGLWLIWRSMKRKAELPVQKEKINADYSQNVKPKK
>AP018040.2|BBD45188.1|1444885_1446214_+|Hypothetical-protein
MQITAKTLNRRNRVKSEGNEDVKLLNCKLYTVMYKPFEIKENLFYVGVNDRTKHLFENLWPLPKGVSYNSYIINDEKIALIDTVDICYADVFFNKIRSVLGDKQIDYLIVNHMEPDHSGSVELLKTRYPQIKIVGNSRTAEMLKGYYGITDNVVVIEDKEELNLGKNNLQFYLTPMVHWPETMMTYVKESKTLFSADAFGTFGTLDGGVTDIQLNPERYWDEMIRYYSNIVGKFGSPVQAALKKLSGMGIETICSTHGPVWTQPDTLGKVVSLYDRLSRYESENGLVIAYGSMYGNTEQLAEIIAAAAAENGARNIIMHNVSKSHESEVLRDIFKYRGLIIGSPTYNNKLYPAVESLLSALQNRNVKNKFFSFFSGHTWADGAKRELKAFAEGMEFETICESVEMKQSLNRNVMENAYALGKAMAERLHSGDAVIPHKTTCH

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Crispr_ID: AP018040_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

AP018040_3

2376836-2381247

Unclear

I-A,II-B,III-A

Consensus_repeat	Method
CTTTTAATCGTACTATCGTAGAATTGAAAT	PILER-CR
CTTTTAATCGTACTATCGTAGAATTGAAAT	CRISPRCasFinder
CTTTTAATCGTACTATCGTAGAATTGAAAT	CRT

67 spacers

cas2,cas1,cas4,cas7,cas8b6,cas3,cas5,cas6

The CRISPR arrays of AP018040_3

>merge|AP018040|3|2376836-2381247|PILER-CR,CRISPRCasFinder,CRT
CTTTTAATCGTACTATCGTAGAATTGAAATGGGGCCGCAAAACTTAACGACATGATGGTCCTGTCTTTTAATCGTACTATCGTAGAATTGAAATACGATATACAAGCCGAGGAAGAACAGTAGTTCCCGGACTTTTAATCGTACTATCGTAGAATTGAAATAAATAATAAAAGACTTTATTTTTTTCATCTCATAATTCTTTTAATCGTACTATCGTAGAATTGAAATGATAATGCTCCGATACTTTTCATGTTTTCAAAGCCTTTTAATCGTACTATCGTAGAATTGAAATTTAAGCCCGGCACATACCCACAAGTCGGCGTTGTCTTTTAATCGTACTATCGTAGAATTGAAATGATGTAACCTAGATCATGTGTTGATCTTTCATAATTCTTTTAATCGTACTATCGTAGAATTGAAATTCTCGTCGTATGTTACAGGAACACCCAATATATTAGCTTTTAATCGTACTATCGTAGAATTGAAATATATATAGGTGCAACGTTAAAAACTTCAACTATTAACTTTTAATCGTACTATCGTAGAATTGAAATTTCACATTAGTGAAAATAAGCGAAAAATGGCAAATACTTTTAATCGTACTATCGTAGAATTGAAATTTCGCAGGAGCGATGGTTACAGGACTTGCCGAAGCTTTTAATCGTACTATCGTAGAATTGAAATTCCGTCGATGCAGGCAAAACGTCCGCCTCGTTGCTCACTTTTAATCGTACTATCGTAGAATTGAAATTCAAAAAAATCGACGAGTTGTACGACGTATCACCCGCTTTTAATCGTACTATCGTAGAATTGAAATCCTCGTAACCATCTGTACCGCATTCGCCTCCTGAACTTTTAATCGTACTATCGTAGAATTGAAATTTATATGGAACTACTGACGTGGAAACAAACTATCTTTCTTTTAATCGTACTATCGTAGAATTGAAATCCTCGTAACCATCTGTACCGCATTCGCCTCCTGAACTTTTAATCGTACTATCGTAGAATTGAAATCTGTTTTACACGGCGTGCGGGTGGCCACGGAACGGCTTTTAATCGTACTATCGTAGAATTGAAATCTCGATATTCAGTGCCGGGAAATTATTAGAGATTCTTTTAATCGTACTATCGTAGAATTGAAATTTCCTTGCTTATTGTCGCTTGCTATTCCTCCGGAACTTTTAATCGTACTATCGTAGAATTGAAATTCATGGGATGAAATTTATAATATAATCCATCGGAGCTTTTAATCGTACTATCGTAGAATTGAAATTCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAGCTTTTAATCGTACTATCGTAGAATTGAAATTCCTCAAACGAGGCGGCATTGGCGACTGGGCGCAAACTTTTAATCGTACTATCGTAGAATTGAAATACGGTTTTGATTTGTCTAATTTGAAATCAGTTCTACTTTTAATCGTACTATCGTAGAATTGAAATGCACGTCAGAGTTTGTTAACCTGATTGCTTCAGGTCTTTTAATCGTACTATCGTAGAATTGAAATGGATACGGTGCTTGATCAGATCAAGGCGGTCAAGCTTTTAATCGTACTATCGTAGAATTGAAATTGAGGATGCGCTGTATGATGCGCTGCCTGGTGCGGTCTTTTAATCGTACTATCGTAGAATTGAAATCTTAGCCACATATTGGATAAAGTCTCCCGTATGTCTTTTAATCGTACTATCGTAGAATTGAAATAAAGTATTAGAAGGTAATTATGATAACAGAAGTAAACTTTTAATCGTACTATCGTAGAATTGAAATTTAAGAATCTCATACAACGACGTTCTACTTTTCACTTTTAATCGTACTATCGTAGAATTGAAATTTATTACGTTGATCGCTTGTAGTTGTGCGATGGCTTCTTTTAATCGTACTATCGTAGAATTGAAATTAAAGTAAATGAATGTTTGGAATGAAACAGTTTACTTTTAATCGTACTATCGTAGAATTGAAATCTCTGACAAGTCCCTTTTTTACAAGGCTTGAAATACTTTTAATCGTACTATCGTAGAATTGAAATACGTGGAAAACACGTAAAAGCGGGTAAAGGTACTCTCTTTTAATCGTACTATCGTAGAATTGAAATGAAGTCTCAAAATAAGGAACAGGCGATGGGAGACGCTTTTAATCGTACTATCGTAGAATTGAAATCATACGAACGGCGAGATTGATCACCTGACCATTCAAACTTTTAATCGTACTATCGTAGAATTGAAATTGTTTTATTTCTTTAATTTTAGAATTGATTCCATTCTTTTAATCGTACTATCGTAGAATTGAAATCTACGCCAAAACGCAGGTAAAGTTGTACGCATTCTCTTTTAATCGTACTATCGTAGAATTGAAATCAATGTGATCACACCCAGATGCTATACCGTAAGCTCTTTTAATCGTACTATCGTAGAATTGAAATATATATTACAGAAATAAAATATATTCCGACGATGACTTTTAATCGTACTATCGTAGAATTGAAATTAAGAAAAAGTTCATACACATAAGTTACTCAATCCTTTTAATCGTACTATCGTAGAATTGAAATTATATATCCCAGATCATGTGTTGATCTTTCATAATTGCTTTTAATCGTACTATCGTAGAATTGAAATAACTAAATCTACAAGCCATAAGGGTAGCCGAGAGACCTTTTAATCGTACTATCGTAGAATTGAAATTCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAGCTTTTAATCGTACTATCGTAGAATTGAAATATTCCTGGCGTTGGTTCCAATACATTTCGCACTCCTTTTAATCGTACTATCGTAGAATTGAAATACGCGTATATTTCCGACAATGTAACAAAAACTGGGGCTTTTAATCGTACTATCGTAGAATTGAAATATCATATACAGGACTGTAGCGCTCAGCTTCGTGTTCCTTTTAATCGTACTATCGTAGAATTGAAATTCGTATTATTCCCTTTCCCTTCATCATCGAAAAACTTTTAATCGTACTATCGTAGAATTGAAATTCGCTTTCAGCATAACGAAGTAAATATCGCCTGCTTCTTTTAATCGTACTATCGTAGAATTGAAATATAAATGGACCTGCTGATTTTCAGAACATATCTAACTTTTAATCGTACTATCGTAGAATTGAAATTTCTTGATATGGGTAAGATTGGAATCAAGGTTCAAACTTTTAATCGTACTATCGTAGAATTGAAATTTATGAGTAAAATGAATTTCGCCATAGCCCTACGGACTTTTAATCGTACTATCGTAGAATTGAAATATCAATATTTAACCCAAATCTATCTTTTAGAATAGCTTTTAATCGTACTATCGTAGAATTGAAATGGAGAACCGCTCCGTCGAGTTGCTTGTGCGCCAGCTGCTTTTAATCGTACTATCGTAGAATTGAAATGCTTCAAACAATTCTTTTAGAGAATCATCAGACAACTTTTAATCGTACTATCGTAGAATTGAAATTGCAGACAATTCATTTGCTTTTGTGCAACCGGTTTCTTTTAATCGTACTATCGTAGAATTGAAATGTCGCAACCTTGAAGCTCTTACAACGCTCCAAAAGCCTTTTAATCGTACTATCGTAGAATTGAAATTCCTTCACAAATCCGACATTCAAACCTGGATCAATCCTTTTAATCGTACTATCGTAGAATTGAAATCCGGAAGCATCACGTGCTAATTGATTGTACTCGTTCTTTTAATCGTACTATCGTAGAATTGAAATCCATTTCAAAAGTAGATGCCTATACAAAGGACGTTTCTTTTAATCGTACTATCGTAGAATTGAAATGGATATTTTCTTCCCCCTCCATGCTCGTGATACACTTTTAATCGTACTATCGTAGAATTGAAATCTCTCAATCCTTTCTTAAGATAATACTTTATCACCTTTTAATCGTACTATCGTAGAATTGAAATCCGGGAAAACGCGCGACGCCGCAAATCGAATTTGCCTTTTAATCGTACTATCGTAGAATTGAAATACAAGCAGGAAATTCAACAGCGTTTGCGTCAGAATGCTTTTAATCGTACTATCGTAGAATTGAAATATTTTGAAACTAAAGAAATGAAAACATGGAAGAATGTCTTTTAATCGTACTATCGTAGAATTGAAATTTGATTATTATGCCCTCCATTACATTCATCTCATCCTTTTAATCGTACTATCGTAGAATTGAAATCTTTTGGCGTTTCCGAAAACGGATCGAACGCGGGCAATCTTTTAATCGTACTATCGAGGAATTGAAATCGCTGTTCGTCTTCGCGGCATGATATTCGTCCAGGACTTTTAATCGTACTATCGTAGAATTGAAATTTTTGCTTTTCGTTTTTGACTACATTTCCGTTTGCTTTTAATCGTACTATCGTAGAATTGAAAT

>AP018040|3|2|2376836-2381247|PILER-CR
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGGGCCGCAAAACTTAACGACATGATGGTCCTGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGATATACAAGCCGAGGAAGAACAGTAGTTCCCGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	AAATAATAAAAGACTTTATTTTTTTCATCTCATAATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GATAATGCTCCGATACTTTTCATGTTTTCAAAGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTAAGCCCGGCACATACCCACAAGTCGGCGTTGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GATGTAACCTAGATCATGTGTTGATCTTTCATAATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCTCGTCGTATGTTACAGGAACACCCAATATATTAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATATATAGGTGCAACGTTAAAAACTTCAACTATTAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCACATTAGTGAAAATAAGCGAAAAATGGCAAATA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCGCAGGAGCGATGGTTACAGGACTTGCCGAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCGTCGATGCAGGCAAAACGTCCGCCTCGTTGCTCA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCAAAAAAATCGACGAGTTGTACGACGTATCACCCG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCTCGTAACCATCTGTACCGCATTCGCCTCCTGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATATGGAACTACTGACGTGGAAACAAACTATCTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCTCGTAACCATCTGTACCGCATTCGCCTCCTGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTGTTTTACACGGCGTGCGGGTGGCCACGGAACGG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCGATATTCAGTGCCGGGAAATTATTAGAGATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCCTTGCTTATTGTCGCTTGCTATTCCTCCGGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCATGGGATGAAATTTATAATATAATCCATCGGAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCTCAAACGAGGCGGCATTGGCGACTGGGCGCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGGTTTTGATTTGTCTAATTTGAAATCAGTTCTA
CTTTTAATCGTACTATCGTAGAATTGAAAT	GCACGTCAGAGTTTGTTAACCTGATTGCTTCAGGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGATACGGTGCTTGATCAGATCAAGGCGGTCAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGAGGATGCGCTGTATGATGCGCTGCCTGGTGCGGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTTAGCCACATATTGGATAAAGTCTCCCGTATGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	AAAGTATTAGAAGGTAATTATGATAACAGAAGTAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTAAGAATCTCATACAACGACGTTCTACTTTTCA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATTACGTTGATCGCTTGTAGTTGTGCGATGGCTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TAAAGTAAATGAATGTTTGGAATGAAACAGTTTA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCTGACAAGTCCCTTTTTTACAAGGCTTGAAATA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGTGGAAAACACGTAAAAGCGGGTAAAGGTACTCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GAAGTCTCAAAATAAGGAACAGGCGATGGGAGACG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CATACGAACGGCGAGATTGATCACCTGACCATTCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGTTTTATTTCTTTAATTTTAGAATTGATTCCATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTACGCCAAAACGCAGGTAAAGTTGTACGCATTCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CAATGTGATCACACCCAGATGCTATACCGTAAGCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATATATTACAGAAATAAAATATATTCCGACGATGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TAAGAAAAAGTTCATACACATAAGTTACTCAATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TATATATCCCAGATCATGTGTTGATCTTTCATAATTG
CTTTTAATCGTACTATCGTAGAATTGAAAT	AACTAAATCTACAAGCCATAAGGGTAGCCGAGAGAC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATTCCTGGCGTTGGTTCCAATACATTTCGCACTC
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGCGTATATTTCCGACAATGTAACAAAAACTGGGG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATCATATACAGGACTGTAGCGCTCAGCTTCGTGTTC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGTATTATTCCCTTTCCCTTCATCATCGAAAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGCTTTCAGCATAACGAAGTAAATATCGCCTGCTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATAAATGGACCTGCTGATTTTCAGAACATATCTAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCTTGATATGGGTAAGATTGGAATCAAGGTTCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATGAGTAAAATGAATTTCGCCATAGCCCTACGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATCAATATTTAACCCAAATCTATCTTTTAGAATAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGAGAACCGCTCCGTCGAGTTGCTTGTGCGCCAGCTG
CTTTTAATCGTACTATCGTAGAATTGAAAT	GCTTCAAACAATTCTTTTAGAGAATCATCAGACAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGCAGACAATTCATTTGCTTTTGTGCAACCGGTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GTCGCAACCTTGAAGCTCTTACAACGCTCCAAAAGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCTTCACAAATCCGACATTCAAACCTGGATCAATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCGGAAGCATCACGTGCTAATTGATTGTACTCGTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCATTTCAAAAGTAGATGCCTATACAAAGGACGTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGATATTTTCTTCCCCCTCCATGCTCGTGATACA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCTCAATCCTTTCTTAAGATAATACTTTATCAC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCGGGAAAACGCGCGACGCCGCAAATCGAATTTGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACAAGCAGGAAATTCAACAGCGTTTGCGTCAGAATG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATTTTGAAACTAAAGAAATGAAAACATGGAAGAATGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTGATTATTATGCCCTCCATTACATTCATCTCATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTTTTGGCGTTTCCGAAAACGGATCGAACGCGGGCAAT
CTTTTAATCGTACTATCGAGGAATTGAAAT	CGCTGTTCGTCTTCGCGGCATGATATTCGTCCAGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTTTGCTTTTCGTTTTTGACTACATTTCCGTTTG
CTTTTAATCGTACTATCGTAGAATTGAAAT

>AP018040|3|3|2376836-2381247|CRISPRCasFinder
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGGGCCGCAAAACTTAACGACATGATGGTCCTGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGATATACAAGCCGAGGAAGAACAGTAGTTCCCGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	AAATAATAAAAGACTTTATTTTTTTCATCTCATAATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GATAATGCTCCGATACTTTTCATGTTTTCAAAGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTAAGCCCGGCACATACCCACAAGTCGGCGTTGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GATGTAACCTAGATCATGTGTTGATCTTTCATAATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCTCGTCGTATGTTACAGGAACACCCAATATATTAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATATATAGGTGCAACGTTAAAAACTTCAACTATTAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCACATTAGTGAAAATAAGCGAAAAATGGCAAATA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCGCAGGAGCGATGGTTACAGGACTTGCCGAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCGTCGATGCAGGCAAAACGTCCGCCTCGTTGCTCA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCAAAAAAATCGACGAGTTGTACGACGTATCACCCG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCTCGTAACCATCTGTACCGCATTCGCCTCCTGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATATGGAACTACTGACGTGGAAACAAACTATCTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCTCGTAACCATCTGTACCGCATTCGCCTCCTGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTGTTTTACACGGCGTGCGGGTGGCCACGGAACGG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCGATATTCAGTGCCGGGAAATTATTAGAGATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCCTTGCTTATTGTCGCTTGCTATTCCTCCGGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCATGGGATGAAATTTATAATATAATCCATCGGAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCTCAAACGAGGCGGCATTGGCGACTGGGCGCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGGTTTTGATTTGTCTAATTTGAAATCAGTTCTA
CTTTTAATCGTACTATCGTAGAATTGAAAT	GCACGTCAGAGTTTGTTAACCTGATTGCTTCAGGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGATACGGTGCTTGATCAGATCAAGGCGGTCAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGAGGATGCGCTGTATGATGCGCTGCCTGGTGCGGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTTAGCCACATATTGGATAAAGTCTCCCGTATGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	AAAGTATTAGAAGGTAATTATGATAACAGAAGTAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTAAGAATCTCATACAACGACGTTCTACTTTTCA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATTACGTTGATCGCTTGTAGTTGTGCGATGGCTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TAAAGTAAATGAATGTTTGGAATGAAACAGTTTA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCTGACAAGTCCCTTTTTTACAAGGCTTGAAATA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGTGGAAAACACGTAAAAGCGGGTAAAGGTACTCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GAAGTCTCAAAATAAGGAACAGGCGATGGGAGACG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CATACGAACGGCGAGATTGATCACCTGACCATTCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGTTTTATTTCTTTAATTTTAGAATTGATTCCATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTACGCCAAAACGCAGGTAAAGTTGTACGCATTCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CAATGTGATCACACCCAGATGCTATACCGTAAGCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATATATTACAGAAATAAAATATATTCCGACGATGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TAAGAAAAAGTTCATACACATAAGTTACTCAATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TATATATCCCAGATCATGTGTTGATCTTTCATAATTG
CTTTTAATCGTACTATCGTAGAATTGAAAT	AACTAAATCTACAAGCCATAAGGGTAGCCGAGAGAC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATTCCTGGCGTTGGTTCCAATACATTTCGCACTC
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGCGTATATTTCCGACAATGTAACAAAAACTGGGG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATCATATACAGGACTGTAGCGCTCAGCTTCGTGTTC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGTATTATTCCCTTTCCCTTCATCATCGAAAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGCTTTCAGCATAACGAAGTAAATATCGCCTGCTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATAAATGGACCTGCTGATTTTCAGAACATATCTAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCTTGATATGGGTAAGATTGGAATCAAGGTTCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATGAGTAAAATGAATTTCGCCATAGCCCTACGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATCAATATTTAACCCAAATCTATCTTTTAGAATAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGAGAACCGCTCCGTCGAGTTGCTTGTGCGCCAGCTG
CTTTTAATCGTACTATCGTAGAATTGAAAT	GCTTCAAACAATTCTTTTAGAGAATCATCAGACAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGCAGACAATTCATTTGCTTTTGTGCAACCGGTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GTCGCAACCTTGAAGCTCTTACAACGCTCCAAAAGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCTTCACAAATCCGACATTCAAACCTGGATCAATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCGGAAGCATCACGTGCTAATTGATTGTACTCGTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCATTTCAAAAGTAGATGCCTATACAAAGGACGTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGATATTTTCTTCCCCCTCCATGCTCGTGATACA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCTCAATCCTTTCTTAAGATAATACTTTATCAC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCGGGAAAACGCGCGACGCCGCAAATCGAATTTGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACAAGCAGGAAATTCAACAGCGTTTGCGTCAGAATG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATTTTGAAACTAAAGAAATGAAAACATGGAAGAATGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTGATTATTATGCCCTCCATTACATTCATCTCATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTTTTGGCGTTTCCGAAAACGGATCGAACGCGGGCAAT
CTTTTAATCGTACTATCGAGGAATTGAAAT	CGCTGTTCGTCTTCGCGGCATGATATTCGTCCAGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTTTGCTTTTCGTTTTTGACTACATTTCCGTTTG
CTTTTAATCGTACTATCGTAGAATTGAAAT

>AP018040|3|2|2376836-2381247|CRT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGGGCCGCAAAACTTAACGACATGATGGTCCTGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGATATACAAGCCGAGGAAGAACAGTAGTTCCCGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	AAATAATAAAAGACTTTATTTTTTTCATCTCATAATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GATAATGCTCCGATACTTTTCATGTTTTCAAAGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTAAGCCCGGCACATACCCACAAGTCGGCGTTGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GATGTAACCTAGATCATGTGTTGATCTTTCATAATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCTCGTCGTATGTTACAGGAACACCCAATATATTAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATATATAGGTGCAACGTTAAAAACTTCAACTATTAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCACATTAGTGAAAATAAGCGAAAAATGGCAAATA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCGCAGGAGCGATGGTTACAGGACTTGCCGAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCGTCGATGCAGGCAAAACGTCCGCCTCGTTGCTCA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCAAAAAAATCGACGAGTTGTACGACGTATCACCCG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCTCGTAACCATCTGTACCGCATTCGCCTCCTGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATATGGAACTACTGACGTGGAAACAAACTATCTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCTCGTAACCATCTGTACCGCATTCGCCTCCTGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTGTTTTACACGGCGTGCGGGTGGCCACGGAACGG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCGATATTCAGTGCCGGGAAATTATTAGAGATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCCTTGCTTATTGTCGCTTGCTATTCCTCCGGAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCATGGGATGAAATTTATAATATAATCCATCGGAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCTCAAACGAGGCGGCATTGGCGACTGGGCGCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGGTTTTGATTTGTCTAATTTGAAATCAGTTCTA
CTTTTAATCGTACTATCGTAGAATTGAAAT	GCACGTCAGAGTTTGTTAACCTGATTGCTTCAGGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGATACGGTGCTTGATCAGATCAAGGCGGTCAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGAGGATGCGCTGTATGATGCGCTGCCTGGTGCGGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTTAGCCACATATTGGATAAAGTCTCCCGTATGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	AAAGTATTAGAAGGTAATTATGATAACAGAAGTAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTAAGAATCTCATACAACGACGTTCTACTTTTCA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATTACGTTGATCGCTTGTAGTTGTGCGATGGCTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TAAAGTAAATGAATGTTTGGAATGAAACAGTTTA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCTGACAAGTCCCTTTTTTACAAGGCTTGAAATA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGTGGAAAACACGTAAAAGCGGGTAAAGGTACTCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GAAGTCTCAAAATAAGGAACAGGCGATGGGAGACG
CTTTTAATCGTACTATCGTAGAATTGAAAT	CATACGAACGGCGAGATTGATCACCTGACCATTCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGTTTTATTTCTTTAATTTTAGAATTGATTCCATT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTACGCCAAAACGCAGGTAAAGTTGTACGCATTCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CAATGTGATCACACCCAGATGCTATACCGTAAGCT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATATATTACAGAAATAAAATATATTCCGACGATGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TAAGAAAAAGTTCATACACATAAGTTACTCAATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TATATATCCCAGATCATGTGTTGATCTTTCATAATTG
CTTTTAATCGTACTATCGTAGAATTGAAAT	AACTAAATCTACAAGCCATAAGGGTAGCCGAGAGAC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGACACTTCCTCTAAAATGGGCGGTGCGTGGAAAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATTCCTGGCGTTGGTTCCAATACATTTCGCACTC
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACGCGTATATTTCCGACAATGTAACAAAAACTGGGG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATCATATACAGGACTGTAGCGCTCAGCTTCGTGTTC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGTATTATTCCCTTTCCCTTCATCATCGAAAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCGCTTTCAGCATAACGAAGTAAATATCGCCTGCTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATAAATGGACCTGCTGATTTTCAGAACATATCTAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTCTTGATATGGGTAAGATTGGAATCAAGGTTCAAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTATGAGTAAAATGAATTTCGCCATAGCCCTACGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATCAATATTTAACCCAAATCTATCTTTTAGAATAG
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGAGAACCGCTCCGTCGAGTTGCTTGTGCGCCAGCTG
CTTTTAATCGTACTATCGTAGAATTGAAAT	GCTTCAAACAATTCTTTTAGAGAATCATCAGACAA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TGCAGACAATTCATTTGCTTTTGTGCAACCGGTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GTCGCAACCTTGAAGCTCTTACAACGCTCCAAAAGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	TCCTTCACAAATCCGACATTCAAACCTGGATCAATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCGGAAGCATCACGTGCTAATTGATTGTACTCGTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCATTTCAAAAGTAGATGCCTATACAAAGGACGTTT
CTTTTAATCGTACTATCGTAGAATTGAAAT	GGATATTTTCTTCCCCCTCCATGCTCGTGATACA
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTCTCAATCCTTTCTTAAGATAATACTTTATCAC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CCGGGAAAACGCGCGACGCCGCAAATCGAATTTGC
CTTTTAATCGTACTATCGTAGAATTGAAAT	ACAAGCAGGAAATTCAACAGCGTTTGCGTCAGAATG
CTTTTAATCGTACTATCGTAGAATTGAAAT	ATTTTGAAACTAAAGAAATGAAAACATGGAAGAATGT
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTGATTATTATGCCCTCCATTACATTCATCTCATC
CTTTTAATCGTACTATCGTAGAATTGAAAT	CTTTTGGCGTTTCCGAAAACGGATCGAACGCGGGCAAT
CTTTTAATCGTACTATCGAGGAATTGAAAT	CGCTGTTCGTCTTCGCGGCATGATATTCGTCCAGGA
CTTTTAATCGTACTATCGTAGAATTGAAAT	TTTTGCTTTTCGTTTTTGACTACATTTCCGTTTG
CTTTTAATCGTACTATCGTAGAATTGAAAT

Protein	Signature genes	Signature genes Name	Protein_function
AP018040.2\|BBD45981.1\|2376361_2376625_+\|CRISPR-associated-protein-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
AP018040.2\|BBD45989.1\|2389381_2390164_-\|Hypothetical-protein	unknown	unknown	unknown
AP018040.2\|BBD45992.1\|2395493_2397233_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|379121
AP018040.2\|BBD45986.1\|2382953_2384111_-\|PHP-family-phosphohydrolase,-histidinol-phosphatase	unknown	unknown	gnl\|CDD\|213996
AP018040.2\|BBD45978.1\|2373656_2374709_+\|hypothetical-protein	cas7	mkCas0088_cas7_CAS-I-B	gnl\|CDD\|274215
AP018040.2\|BBD45984.1\|2381480_2381813_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|376874
AP018040.2\|BBD45973.1\|2367997_2368786_+\|CRISPR-associated-endoribonuclease	cas6	cd09759_cas6_CAS-I-A	gnl\|CDD\|187889
AP018040.2\|BBD45974.1\|2368921_2369581_+\|DNA-binding-protein	cas6	cd09652_cas6_CAS-I:CAS-III	gnl\|CDD\|187783
AP018040.2\|BBD45991.1\|2392075_2395288_-\|SusC/RagA-family-TonB-linked-outer-membraneprotein	unknown	unknown	gnl\|CDD\|274948
AP018040.2\|BBD45993.1\|2397267_2399043_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|369630
AP018040.2\|BBD45990.1\|2390294_2392064_-\|RagB/SusD-family-protein	unknown	unknown	gnl\|CDD\|369630
AP018040.2\|BBD45975.1\|2369587_2370175_+\|hypothetical-protein	cas5	mkCas0069_cas5_CAS-I-B	unknown
AP018040.2\|BBD45977.1\|2372312_2373632_+\|Hypothetical-protein	cas8b6	mkCas0111_cas8b6_CAS-I-B	unknown
AP018040.2\|BBD45979.1\|2374746_2375277_+\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|366863
AP018040.2\|BBD45972.1\|2364934_2366278_-\|adenylosuccinate-lyase	unknown	unknown	gnl\|CDD\|236452
AP018040.2\|BBD45987.1\|2384122_2385871_-\|RagB/SusD-family-protein	unknown	unknown	gnl\|CDD\|369630
AP018040.2\|BBD45988.1\|2385885_2389122_-\|SusC/RagA-family-TonB-linked-outer-membraneprotein	unknown	unknown	gnl\|CDD\|274948
AP018040.2\|BBD45985.1\|2381937_2382846_-\|Hypothetical-protein	unknown	unknown	gnl\|CDD\|378342
AP018040.2\|BBD45976.1\|2370174_2372316_+\|metal-dependent-phosphohydrolase	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|224124
AP018040.2\|BBD45980.1\|2375343_2376360_+\|CRISPR-associated-endonuclease-Cas1,-HMARI/TNEAPsubtype	cas1	cd09722_cas1_CAS-I-B	gnl\|CDD\|187853

Protein	Function_ID	Function_description	E-value
AP018040.2\|BBD45981.1\|2376361_2376625_+\|CRISPR-associated-protein-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	1.35686e-29
AP018040.2\|BBD45973.1\|2367997_2368786_+\|CRISPR-associated-endoribonuclease	gnl\|CDD\|187889	cd09759, Cas6_I-A, CRISPR/Cas system-associated RAMP superfamily protein Cas6. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas6 is an endoribonuclease that generates crRNAs, predicted subunit of Cascade complex; RAMP superfamily protein; Possesses double RRM/ferredoxin fold.	6.58702e-40
AP018040.2\|BBD45992.1\|2395493_2397233_-\|Hypothetical-protein	gnl\|CDD\|379121	pfam13320, DUF4091, Domain of unknown function (DUF4091). This presumed domain is functionally uncharacterized. This domain family is found in bacteria, archaea and eukaryotes, and is approximately 70 amino acids in length. There is a single completely conserved residue G that may be functionally important.	9.56229e-20
AP018040.2\|BBD45986.1\|2382953_2384111_-\|PHP-family-phosphohydrolase,-histidinol-phosphatase	gnl\|CDD\|213996	cd12112, PHP_HisPPase_Chlorobi_like, Polymerase and Histidinol Phosphatase domain of Chlorobi like. The PHP (also called histidinol phosphatase-2/HIS2) domain is associated with several types of DNA polymerases, such as PolIIIA and family X DNA polymerases, stand alone histidinol phosphate phosphatases (HisPPases), and a number of uncharacterized protein families. Chlorobi PHP is uncharacterized protein. HisPPase catalyzes the eighth step of histidine biosynthesis, in which L-histidinol phosphate undergoes dephosphorylation to produce histidinol. The HisPPase can be classified into two types: the bifunctional Hisppase found in proteobacteria that belongs to the DDDD superfamily and the monofunctional Bacillus subtilis type that is a member of the PHP family. The PHP domain has four conserved sequence motifs and contains an invariant histidine that is involved in metal ion coordination. The PHP domain of HisPPase is structurally homologous to other members of the PHP family that have a distorted (beta/alpha)7 barrel fold with a trinuclear metal site on the C-terminal side of the barrel.	4.11546e-89
AP018040.2\|BBD45978.1\|2373656_2374709_+\|hypothetical-protein	gnl\|CDD\|274215	TIGR02585, conserved_protein, CRISPR-associated protein Cas7/Cst2/DevR, subtype I-B/TNEAP. CRISPR is a term for Clustered Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This clade is a member of the DevR family (TIGR01875) and includes the DevR protein of Myxococcus xanthus, a protein whose expression appears to be regulated through a number of means, including both location and autorepression; DevR mutants are incapable of fruiting body development.	0.00380478
AP018040.2\|BBD45984.1\|2381480_2381813_-\|Hypothetical-protein	gnl\|CDD\|376874	pfam02635, DrsE, DsrE/DsrF-like family. DsrE is a small soluble protein involved in intracellular sulfur reduction. This family also includes DsrF.	9.62514e-11
AP018040.2\|BBD45979.1\|2374746_2375277_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	4.54449e-56
AP018040.2\|BBD45974.1\|2368921_2369581_+\|DNA-binding-protein	gnl\|CDD\|187783	cd09652, Cas6-I-III, CRISPR/Cas system-associated RAMP superfamily protein Cas6. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas6 is an endoribonuclease that generates crRNAs, predicted subunit of Cascade complex; RAMP superfamily protein; Possesses double RRM/ferredoxin fold.	6.58869e-15
AP018040.2\|BBD45991.1\|2392075_2395288_-\|SusC/RagA-family-TonB-linked-outer-membraneprotein	gnl\|CDD\|274948	TIGR04056, OMP_RagA_SusC, TonB-linked outer membrane protein, SusC/RagA family. This model describes a distinctive clade among the TonB-linked outer membrane proteins (OMP). Members of this family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 alone. Published descriptions of members of this family are available for RagA from Porphyromonas gingivalis, SusC from Bacteroides thetaiotaomicron, and OmpW from Bacteroides caccae. Members form pairs with members of the SusD/RagB family (pfam07980). Transporter complexes including these outer membrane proteins are likely to import large degradation products of proteins (e.g. RagA) or carbohydrates (e.g. SusC) as nutrients, rather than siderophores. [Transport and binding proteins, Unknown substrate].	0
AP018040.2\|BBD45993.1\|2397267_2399043_-\|Hypothetical-protein	gnl\|CDD\|369630	pfam07980, SusD_RagB, SusD family. This domain is found in bacterial cell surface proteins such SusD and SusD-like proteins, as as well RagB, outer membrane surface receptor antigen. Bacteroidetes, one of the two dominant bacterial phyla in the human gut, are Gram-negative saccharolytic microorganisms that utilize a diverse array of glycans. Hence, they express starch-utilization system (Sus) for glycan uptake. SusD has 551 amino acids, and is almost entirely alpha-helical, with 22 alpha-helices, eight of which form 4 tetra-trico peptide repeats (TPRs: helix-turn-helix motifs involved in protein-protein interactions). The four TPRs pack together to create a right-handed super-helix. This is predicted to mediate the formation of SusD and SusC porin complex at the cell surface. The interaction between SusC and TPR1/TPR2 region of SusD is predicted to be of functional importance since it allows SusD to be in position for oligosaccharide capture from other Sus lipoproteins and delivery of these glycans to the SusC porin. The non-TPR containing portion of SusD is where starch binding occurs. The binding site is a shallow surface cavity located on top of TPR1. SusD homologs such as SusD-like proteins have a critical role in carbohydrate acquisition. Both SusD and its homologs, contain about 15-20 residues at the N-terminus that might be a flexible linker region, anchoring the protein to the membrane and the glycan-binding domain. Other homologs to SusD have been examined in Porphyromonas gingivalis such as RagB, an immunodominant outer-membrane surface receptor antigen. Structural characterization of RagB shows substantial similarity with Bacteroides thetaiotaomicron SusD (i.e alpha-helices and TPR regions). Based on this structural similarity, functional studies suggest that, RagB binding of glycans occurs at pockets on the molecular surface that are distinct from those of SusD.	4.2056e-44
AP018040.2\|BBD45990.1\|2390294_2392064_-\|RagB/SusD-family-protein	gnl\|CDD\|369630	pfam07980, SusD_RagB, SusD family. This domain is found in bacterial cell surface proteins such SusD and SusD-like proteins, as as well RagB, outer membrane surface receptor antigen. Bacteroidetes, one of the two dominant bacterial phyla in the human gut, are Gram-negative saccharolytic microorganisms that utilize a diverse array of glycans. Hence, they express starch-utilization system (Sus) for glycan uptake. SusD has 551 amino acids, and is almost entirely alpha-helical, with 22 alpha-helices, eight of which form 4 tetra-trico peptide repeats (TPRs: helix-turn-helix motifs involved in protein-protein interactions). The four TPRs pack together to create a right-handed super-helix. This is predicted to mediate the formation of SusD and SusC porin complex at the cell surface. The interaction between SusC and TPR1/TPR2 region of SusD is predicted to be of functional importance since it allows SusD to be in position for oligosaccharide capture from other Sus lipoproteins and delivery of these glycans to the SusC porin. The non-TPR containing portion of SusD is where starch binding occurs. The binding site is a shallow surface cavity located on top of TPR1. SusD homologs such as SusD-like proteins have a critical role in carbohydrate acquisition. Both SusD and its homologs, contain about 15-20 residues at the N-terminus that might be a flexible linker region, anchoring the protein to the membrane and the glycan-binding domain. Other homologs to SusD have been examined in Porphyromonas gingivalis such as RagB, an immunodominant outer-membrane surface receptor antigen. Structural characterization of RagB shows substantial similarity with Bacteroides thetaiotaomicron SusD (i.e alpha-helices and TPR regions). Based on this structural similarity, functional studies suggest that, RagB binding of glycans occurs at pockets on the molecular surface that are distinct from those of SusD.	6.29507e-41
AP018040.2\|BBD45972.1\|2364934_2366278_-\|adenylosuccinate-lyase	gnl\|CDD\|236452	PRK09285, PRK09285, adenylosuccinate lyase; Provisional.	0
AP018040.2\|BBD45987.1\|2384122_2385871_-\|RagB/SusD-family-protein	gnl\|CDD\|369630	pfam07980, SusD_RagB, SusD family. This domain is found in bacterial cell surface proteins such SusD and SusD-like proteins, as as well RagB, outer membrane surface receptor antigen. Bacteroidetes, one of the two dominant bacterial phyla in the human gut, are Gram-negative saccharolytic microorganisms that utilize a diverse array of glycans. Hence, they express starch-utilization system (Sus) for glycan uptake. SusD has 551 amino acids, and is almost entirely alpha-helical, with 22 alpha-helices, eight of which form 4 tetra-trico peptide repeats (TPRs: helix-turn-helix motifs involved in protein-protein interactions). The four TPRs pack together to create a right-handed super-helix. This is predicted to mediate the formation of SusD and SusC porin complex at the cell surface. The interaction between SusC and TPR1/TPR2 region of SusD is predicted to be of functional importance since it allows SusD to be in position for oligosaccharide capture from other Sus lipoproteins and delivery of these glycans to the SusC porin. The non-TPR containing portion of SusD is where starch binding occurs. The binding site is a shallow surface cavity located on top of TPR1. SusD homologs such as SusD-like proteins have a critical role in carbohydrate acquisition. Both SusD and its homologs, contain about 15-20 residues at the N-terminus that might be a flexible linker region, anchoring the protein to the membrane and the glycan-binding domain. Other homologs to SusD have been examined in Porphyromonas gingivalis such as RagB, an immunodominant outer-membrane surface receptor antigen. Structural characterization of RagB shows substantial similarity with Bacteroides thetaiotaomicron SusD (i.e alpha-helices and TPR regions). Based on this structural similarity, functional studies suggest that, RagB binding of glycans occurs at pockets on the molecular surface that are distinct from those of SusD.	5.38044e-43
AP018040.2\|BBD45988.1\|2385885_2389122_-\|SusC/RagA-family-TonB-linked-outer-membraneprotein	gnl\|CDD\|274948	TIGR04056, OMP_RagA_SusC, TonB-linked outer membrane protein, SusC/RagA family. This model describes a distinctive clade among the TonB-linked outer membrane proteins (OMP). Members of this family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 alone. Published descriptions of members of this family are available for RagA from Porphyromonas gingivalis, SusC from Bacteroides thetaiotaomicron, and OmpW from Bacteroides caccae. Members form pairs with members of the SusD/RagB family (pfam07980). Transporter complexes including these outer membrane proteins are likely to import large degradation products of proteins (e.g. RagA) or carbohydrates (e.g. SusC) as nutrients, rather than siderophores. [Transport and binding proteins, Unknown substrate].	0
AP018040.2\|BBD45985.1\|2381937_2382846_-\|Hypothetical-protein	gnl\|CDD\|378342	pfam09992, NAGPA, Phosphodiester glycosidase. This is a family conserved from bacteria to humans. The structure of a member from Bacteroides has been crystallized and modelled onto the luminal region of the human member of the family, the transmembrane glycoprotein N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase. There is some conservation of potentially functional residues, implying that in the bacterial members this family acts in some way as a phosphodiester glycosidase. The human protein is also present, so the eukaryotic members are likely to be catalyzing the second step in the formation of the mannose 6-phosphate targeting signal on lysosomal enzyme oligosaccharides.	6.18312e-46
AP018040.2\|BBD45976.1\|2370174_2372316_+\|metal-dependent-phosphohydrolase	gnl\|CDD\|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	2.27127e-54
AP018040.2\|BBD45980.1\|2375343_2376360_+\|CRISPR-associated-endonuclease-Cas1,-HMARI/TNEAPsubtype	gnl\|CDD\|187853	cd09722, Cas1_I-B, CRISPR/Cas system-associated protein Cas1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas1 is the most universal CRISPR system protein thought to be involved in spacer integration; Cas1 is metal-dependent deoxyribonuclease, also binds RNA; Shown to possess a unique fold consisting of a N-terminal beta-strand domain and a C-terminal alpha-helical domain.	8.60915e-168

>AP018040.2|BBD45981.1|2376361_2376625_+|CRISPR-associated-protein-Cas2
MYVILVYDCGEKRVGKMLKLCRKYLTWIQNSVFEGEITEVKLKELTLKAEKIMDSEVDSLIIFSSRQEKWLEKQIIGKERSRTNNFL
>AP018040.2|BBD45980.1|2375343_2376360_+|CRISPR-associated-endonuclease-Cas1,-HMARI/TNEAPsubtype
MKKTYYLFNPGRLSRKDNTLKFVPMEEDGNGIPCEGQPRYIPVETVDQFYVFGSLDANSSLYNFLGQNDIALHFFDYYENYTGSFMPRDSLLAGRMILAQTKAFQNKKKRMEIARQFIYGASFNMQKNLQYYNRRGKDMEGTMELIAVHSANIEKATAPHELMGIEGNIRQVYYDAFNLILNDFEMGNRTKQPPRNEVNALISFGNMMCYSECLRAIHQTQLNPTISYLHTPGERRYSLALDIAEIFKPIIVDRVIFKLLNKKEIQERHFDKRLNSCLLNSAGKKIFVKAVEERFNETIKHRSLNRNVSYKYLIKLECYKLAKCLLGMETYQPFKMYW
>AP018040.2|BBD45979.1|2374746_2375277_+|CRISPR-associated-protein-Cas4
MNLTATHINYYQICKRKLWLFANGINMEHTSDMVYDGKLLHETSYPQRAERYEEMLISAEYEGVSLFGQIDYFDARINIVHETKRSDKVEEAHARQLKFYLWLLEINGVEGATGLLEYPKLRKTDGIFLEDTDREQLKKSVLEIKTLIERDTCPPVINAKICKSCSYFDFCYSSEP
>AP018040.2|BBD45978.1|2373656_2374709_+|hypothetical-protein
MSTIYVRTLKRAEHTVFCVADGQKTYYDVQFDRYIPFSSGQQVKRSIVDAISNALNEVPSPTTFLFDVTKQKELKEGEVYGTCDPSYADQLFGGWMKAAKGGKDRTLKRRSPLSISAMRALHPLLAGVSRENISFDRSDRPNNEVIVRNADGEIMTEEEISAFLEGKDRSLSRKWIPNNSRATGLFVFDIAIDLRRLFCVSTSQLEPEITEETIVKLRENGWIDTKNAFGECLLAPLALREKWAKALAYAIVNWKITSNQSRTFSLMDTLAIAISDNANLIGGSIRAKLSEENSEKAQPIIEEDMKNVDTFISLQAGGFIQTKGEKIDALEKAEQKLIDLMMAFDYGNQL
>AP018040.2|BBD45977.1|2372312_2373632_+|Hypothetical-protein
MITTIIGKTFLKVYNELFGKDYSAKEFFVKEYFELFFNHPKYMQWVTNSPFVQMKKGQKPELLSTDERLEKLMNLHEKVSEEVADASFAIGYPASESGDFASTSGLVSDIITTADEEDIYFSWIGSGLGIGVAGGYNLLIDDATILMEIYEGWRHYRKYLNDPTLDKLRGNQINTWNGQWLTFKLGNDFVKDFDFTRLHTQQIFSITDKVMEINTVNWSNLFFSLSNLYPNGNVTAYVYSFGQTNKTVGFIPFYFRSGSRLKDIWRQLYGNPERFNDKEFQSLFGMHIKRACEIGSIGLHALRPEGLKKYMDEAKNISFKKEEDTIIYQSYKTWLIAMMSRNKEEITDFTENLAELILRFRKGASGTDRKNLIEQRLFGGKTTKKVFLDALTEMAAGVEGEDLERLKELRNDIHLMTNEEFGYFNTLLKFDYAYLEKNS
>AP018040.2|BBD45976.1|2370174_2372316_+|metal-dependent-phosphohydrolase
MNIYAKSGPEWTPLVEHLKYVCTAVEKVAIHLGMDTEVARNGAILHDIGKSHPVFQKRLRDKHQVYVDVFRHEIASLFFLSAFPREQWNELIEMVVSHHKSVRNDVNKLGLLDLEQLCDYEEFHLGNWDKWSEDAWKILLELGVSYKLITVREARENLLYCVKYCAQKNKRRGFSEWKGLMMVGDHLASALIDKTAENSTKLFTKPDLSFYNRTHSLYPLSQIKADSPGKHTIVVACTGAGKTDYLFRRCKGRVFYTLPFQASINAMFKRVGKDLEKDNPDLDIRVLHSTSKIIKRKNTDEEVVLQSQIGASVKILTPHQLSALAFGMKGYEALILDLKGCDVILDEVHTYTRVSQAIVLKLVEVLKRIGCKIHIGTATMPIILYKKIKELLGNDVLEIKLSPAELDKFDRHIIHKISSFHDSEALIKKAISKKEKVLIVLNKVKTAQDIFDYIKSKKEFENIPTMLLHSRFKRGDRNQKEKNLIGLDEDGKSLNVYNTSSDGCIVISTQILEVSLDISFDIMITECAPLDALIQRFGRVNRVRNLQTIGKYKPVYVISPPDDEKNARPYDLEVLKKSYAQLDDGQVLHERDLQNKIDNVFTQIDFMSIEEHSVFKSNGEISIDCLSHNGKAILFDLLEIDSVACVTESDLYKYENSSFEQRLNLEIPTYYYTVSKKRQSDKGNRPFIIPDYAYCTEKGLLADKINSSTGVIL
>AP018040.2|BBD45975.1|2369587_2370175_+|hypothetical-protein
MKNKLFVVKYSGPFGFIKPWTAVRDSETFSQQFLTPSIVEGIEKKLFPELLGIVGIRKIVGHRLSYDQISQQQEVIQTRGWNSKRKGTQIHFERPTAIIVRGLLLNPVLFLAFENEDDADVAFNQHICLCRNEDILLPIETFKIDVEDFDNEDTFSGFELMFEKNDKSFPVGIDRNTGHQMFGWLKIIGTPVKEF
>AP018040.2|BBD45974.1|2368921_2369581_+|DNA-binding-protein
MRLHIKTSKSNQEIDFNYQPLLAGCIHKWLGVNNLEHGKMSLYSFSWLQNIDTSKKGIKLKNGSYFTLNFYDIQLVKTVVKNILEKPEMFAGSRVLDIRIEFTPQFSEKEHFFLASPVLVKRYNEDKETHYTYLDDEANNFMTETLKAKAKIAGLNTEKLKVYFDRSYHSPKTKIISYKGIQNKVNICPVIIEGLPEMIAFAWDVGLGNSTGIGFGALK
>AP018040.2|BBD45973.1|2367997_2368786_+|CRISPR-associated-endoribonuclease
MRFKLSLHIDKSVFGDKLPLNYTYELSSVVYKIFSKSDKEFAVWLHENGFSSGNKKFKLFTFSRLHVPLFRIEGEFMHILSDTVEWQISFLPERSTLEFISGVFQNQTFELGTRQANVRFNVYEISVMPPPIFTETMEFETLSPICISLRRENEKVDYLSPDNPEALPIIRQNLLNKYFAFHGKEYDSKFDFNFEVLSKPKSVLVTIKSNTPQQTRVRGFMCRFRMTAPLELMKVAYDAGVGEKGSTGFGMVKSRQELKAYS
>AP018040.2|BBD45972.1|2364934_2366278_-|adenylosuccinate-lyase
MKLDELSAISPIDGRYRDKTRELALYFSEYALIKYRTQVEVEYFIALCELGISPLDKVEKPVFGVLRKMAEDFSEQDAQRIKEIEKITNHDVKAVEYFLKEKFDELHLDAFKEFIHFGLTSQDINNTATPMMWKEALQNTYIPQLEELTALIGKFAEEWKEVPMLARTHGQPASPTRLGKEIQVFEYRLRNQTEVLKRIPAKAKFGGATGNFNAHRVAYPHIDWKEFANSFLSNKLGLVREEYTTQISNYDALAASCDALKRINTILIDFTRDVWQYVSMEYFKQRIREGEVGSSAMPHKVNPIDFENAEGNLGIANAWLEHLAAKLPISRLQRDLTDSTVIRNIGMPLAHGLIAIKSTTKGLHKLLLNEEAIERDLENNWAVVAEGIQTILRREGYPKPYEALKALTRTNRHITKESISDFIDTLEVNEEIKKELKAISPKNYTGI
>AP018040.2|BBD45984.1|2381480_2381813_-|Hypothetical-protein
MQQIMKIGIILETKEFEKAWNAFRFAVTARKQGHEVKVFLMGEAVECEGLTHEKYNVDEQLKAFVNVGGEILACGTCLTSRQLNSTEACPISTMVDCVNLVVWADKTVTF
>AP018040.2|BBD45985.1|2381937_2382846_-|Hypothetical-protein
MRNIFYVCFTVLGLVIFQLGVYGQKTAGQLTKSPASQSEELSPDYKTIKATAWNDSTLATGVVWKHYHFSNLFASNQFVNVLDVNLSVAEIAIDIPHVTEGFIKTSQAALDNGATAAINGSYFNTTAGGSTVFFRKNGIIVKNTEEGFTHYRENGAFAITRENSPAIIKRPSSGWESADSETILSSGPLLIYGNEIIEQEQTAFNLNRHPRTAIGITANNHIIAVVVDGRNAQSQGMNIEELSILMKALGCVEALNMDGGGSSTMWINNKGVVNHPSDNKLFDNEGERGVATIITFKGNYHK
>AP018040.2|BBD45986.1|2382953_2384111_-|PHP-family-phosphohydrolase,-histidinol-phosphatase
MMKLNSVSALLLTALLFAVSNISAQQTVNIPDIPGYKTLKCDFHLHTVFSDGSVWPNLRVNEAIRDGLDVIAMTDHIDYEGFPELIARDYNKPYEIALQAVKDKGLIVINGGEISPRVSPYHNNAIFLKDVNKLPIDYMQETKKKFVMKENIRKEELMAPFLEAQSQGAFVFYNHPGYSWWDKKDTAIFTQFHRELFDKGILRGVEVVNGRYNIIAHRMAEKYNLTMLGNSDAHGDIFYTYRNSHRPMTLVFAKEKSEAAVKEALINRRTAVYTDDNIIARLPEADALFKASLNISKESRDRNGEPIWIVSITNESSVPYRIRIRSEHNIENYPLGQLVLEPNQPRQVIIKELWNHPEQVKLQVDVFNIAISPDNHLETSIIINK
>AP018040.2|BBD45987.1|2384122_2385871_-|RagB/SusD-family-protein
MKKFNILTTVLFIIISLSSCEDFLNSEPVDKLVPSTFFQTEKDLELYTNSFYQRGLPDGLALVQSDEMGDYTSKIQSPKFIAGSYDSGDAPAWNWSDLRNINYFLMNFNNNAIPQEARNHYEGIARFWRAHFYFEKVKTYGDVPWYSKALATDDKDLYKPRDPRAAVMDSVLADLNFACENIRDTKDNTSSLITRQVALAFKSRVCLFEGTFRKYHPEFNLQSSANKFLEEAVDASTKVINSKKYSIYNTGNPETDYRTLFISENPVNTEVMLAVIYNNALRRWHNITWKFNSATYGSRWGLNKQFVNTYLMTDGSRFTDKTNYDMLLFTEEMKDRDYRLAQTIRSLGYKRSDGSAAPPNFGYTYTGYHILKFSLDDKRLDGTSEAYNSISIIRYAEVLLNHAEALAELNRFDETTWNQTIALLRKRAGVNAKAPDAADTYLQEVYFPEISDKYLLEIRRERGIELCYEGFRYDDLLRWKKGHLLEMSWKGIYIPAMDYPMDLDGNGTPDVSFVAKAPAKGTTGIFYFVIDNKASRLSEGDKGHILWREDEVRKFEDKKYLYPISETDITLNSALTQNPGWN
>AP018040.2|BBD45988.1|2385885_2389122_-|SusC/RagA-family-TonB-linked-outer-membraneprotein
MVKVNLSNTFICLIVLFFALSIRVSGQNSTLKGVVKDVDGIPLIGVNVVEKGTTNGTVTDIDGNFSINVKTHSTVIFTYIGFAEQELVWDGNSVMNVVLREDSELLDEVVVVGYGTQRKVNLTGAVSQVSNEVLENRPAPNLTRLLQGTLPNLNIRMSDGSPTRTADYNIRGITSIGAGGSALVLIDGVEGDPNLLNPNDIESVSILKDASSAAIYGSRAAFGVVLIITRSAQEGKPKVNLNISQSFNKRTIDPGLVTNGYQWAKNFDDAFYAWYDYITHPISVNSIFPFSLEYLDRLKEHDENPDLPEVVFNEQLNRYEYFGNTDWFDVLYKDVMPATDVALNVAGGTRNTNFYISGRYYHQDGIFNNSSDNYDRFNVRAKGEVKANDWLTFQDNFDISTYTYSYPLLPNGDAGIWRYFAVQGFPMTVLKNPDGTYTHNTAYTMASFVEGNSKSEQRNFYVRNTAAVIAEPIKDLLQLKADITFSKKWDKDKRWNNFINYSNAPGEINRYGNSRLRQFNDETTYWVSNLTANVNKTFKESHTVNMLAGLNIEKNRLEKLNTDRDVLLVESKPDYNLLDGLNYRITGGGNDWAYVGLFYRLNYNYLNKYLIELNGRYDGSSKFPITQQWGFFPSVSAGWNVTEETFMKNIQHGLDYLKLRASYGSLGNGNVAPYRFLETMSVSKTGVILGGVQPGYTSMPSVIPDGLTWERATTFDVGADVILLDNRLSLTYDWYNRKTTDMFTAGPPLPNVFGATVPYGNYADLSTKGWEFTLSWKDQFMLGGKPFRYGFTGSLWDSKSFITKFNSPLDESGNPIKLINSHYVGKQMGEIWGFETLGLFTSEEEVAKHADQSYLRNSNSNKWLPGDLKFADLNNDDVINQGNNTLDNPGDRKIIGNDSPRYQFGFTLSGNWNGFGVSAFFQGIGKRDWYFAPEADLFYGPYNRPYGFQPVKLYEDMWSEDNPNGYFPRYRGYTALGTNRSLGAPQTRYLQDASYIRLKNLMVDYTLPKQLVDNMKISSAQVFISGQNILTFSGIFKHTDSFDPEVIENPLGEMTNSHGQGDAYPMLKTWTIGLNLTF
>AP018040.2|BBD45989.1|2389381_2390164_-|Hypothetical-protein
MILDFDNSADSVKKVNWYLKTSEVMNMPDTMIRHMRTVDDHKSVDNHTKILICSSSGGTLLVDRATRKCLFYAITPNAHSVEYLPGNRIAVALSTADKGNRLEIYDAGRSNIVLFSDSLYSGHGVTWMAGRNLLYALGYDELRAYSLVDWDTPNPGLQLEEKWTLPETGGHDLYASSENQLLITTSKKVWKFDLNSNAFEPFAPLANEPDVKSVYYDEKADHLIYTKGEISWWTHNIYSINPTKKITIPEIDVYKVRVIK
>AP018040.2|BBD45990.1|2390294_2392064_-|RagB/SusD-family-protein
MKTIKYLHLTVIITAIIFLYSCNDDFLELKPLTKLAESEAFWENESSIETFSNSFYNYIDRGDILADFTSDNCEHKTSPPALRRGVYSMPTALGSGGWNWSQLRNINYFIHNVNNSKLDPSVKNKHIALGKFFRAWFYYKKVQQFGDVPWYSQPLATSDEDLIFKPRDPRTLIVDSIRKDVDFAIRYLPVEKTKNRISKWMGLALKSRILLYEGTYSKYHGLRDANACKVLLQEAVDASKELMESGMYTIYSTGDPHRDYFNLFQPKDAYTEEVILARSTQNQYFYYTPNFTSTSNGNYGATYSLISDYLMSNGETFQKRYPDESKRRALPYMDEFKDRDPRLWQTLVFPGYVRVGTSAEALTDFNQNTTGYMIHKRVGPPIEDQGGGLRDVIMIRYAEVLLNYAEAKAELGILTQEDLDISVNLIRKRVNLPPLSINSPLDPYLDDYYKNTSDPMILEIRRERRVELAFEGFRTEDLKRWKEGQLFRDRYQGMYIKEFNTYIDLNNDGSPDLYVLKNNQTPPSDRIAGVQYFRLADVAALSEGEYGRIIPYSRELPEFKDWEYLNPIPTEELTLNKMLKQNPGWDNLN
>AP018040.2|BBD45991.1|2392075_2395288_-|SusC/RagA-family-TonB-linked-outer-membraneprotein
MVRSKLSSVFISLIVLFWALSAGAVAQNSTLRGTVKDITGIPLIGVNVIQKGTTNGTVTDVDGNFSINVPANAAIVFTYIGFSAQEVVWDGASAMNVVMHEDAELLDEVVVVGYGTQKKVNLTGAVDNMSESRLASLHVNTMGEALQGQLPGVYVSTADGKPGRFSSFNIRGTTSINGGDPLIVIDGVPQSSNSLNNLSPNDIEDISILKDAASATIYGARASFGVILITTKTGKKGKSKVEYNNYFGFSKATIVPEIYDNPVDYIDINQNEFNKYIGQSYFTDAQVEYPYLYEKDPTLPQAKLEIIGGRSTLLLGGKVYNYYKEWLRKYTPQQNHQISVSGANDSFQYYLAGDYNYEEGNIKFKPEKIKRYTLLSNLRYNLNKNVSLFNNTTMVKRDEEHPNQYLYGFTSNVYRFIENSNAMMPEYVDIDGKMVPTDIGFYRRFLEKQSGIEKDVHDVKTTLGVDISLLNKDLEIRIDGTYQNENTDYLRWWDNVGPYLSNSFNNRNIVLDYYSDAGPAKIYRSNWKSVLTNINAYGTYSKLINDHDIKVMGGYNQEHYDYLYSYAEKLYPLPVDQHSLNLATGASNTRDDDNRNSSRSIFSRLNYNWKSRYLVEFNTSYFLSSRFEKQKRGHGYLSSSAAWRISEEAFFEPLKTIVPNLKLRFSYGSLGNANIGSYDYIPIMSVSQSGFSLDGNLVNLTSAPAPKSDNFTWETVESFNLGLDFSLFNSKFNTTLDVFRRDTKDMLANYRSLPSVFGASVPKENIASLRTKGWELNVNWNDSFTLLDDRFMYGVYFNVSDYMSQITDYYNPTNYLADYYVGQTIGEIWGLTTLGYFLTDEEAKKSAVLSSSSTSRVYASAGTIKFEDKNNDGVISWGDRTLDNPGDYRVIGNETPRYQFGLTLNGAWKGFDMNVFFNGVGKRDIYPGAEAVNFWGPYNRKYQVMTKHVIENRWTPENPNAYFPKPQGYIALGGNDLGQPQTKYMQNAAYIRLKNFSFGYSLPHDLVKKIKLNSLRFFVSGQNLWEYTKLHFSLDPEGLMKDPDANQGSVGLGTAYPIQRVYSFGAQIQF
>AP018040.2|BBD45992.1|2395493_2397233_-|Hypothetical-protein
MNMTLKNNTSYLSNSVKRTFLNAIILLFVICFSGFSCDSKEIQFEYVDPMEKILAESSFFPGSQEAISEVVRGEHASLQFVVRSPYTINNLRVTVTQASNKDKLLPASKVRFVGFVKVGRSIWDYSRDRINSPSGYFPDPLLEEDEIDVKFGNSQPIWITIPIPSDASPGLYSGKVIINGNIENKEFHIEKDYSVRVYPVTIDKTSLWVTNWFTIDAAQLKWMNRGEDFESFSPQHWEYIRKLAKMMAEYRQNSARISPLDLSDFAFINGKWQVDFGRFDKVVEIFIQEGVIGRLEGGHIGTRESNWDSQFVVRVPSVDRNAENRFEKLPLSNERAQQFYVDFFTSLKQHLKEKGWEGNYLQYIADEPTPTNVQSYVEIARFVKQVYPEIKIIEATHSKDLEDIVDIYVPQLDFMNKDYYFYNNINKNSEGKEAWFYTCLSPKGEYANRFIELPLLKTRYIHWLNFKYNIPGYLHWGLNHWRTDPWDEQTSINYEGGNILPGGDSWIIYPQGDKLLSSIRFEAMRDGIVDYELFKMLEKKDPEAARDIIDKVIYSFDRYDNNITAFREHRRRLMELLSE
>AP018040.2|BBD45993.1|2397267_2399043_-|Hypothetical-protein
MKKIIYLIVFSFTVLTSCDLDDYLNKTPLDSITDVDYWKSASDLQLYVNQFYTMLPQFPSWGGGYLWEDNNSDNMASRFYDNRLAGTNTITTNNGSWDYSRIRSINIMLNKYKEMSVSESEIAPYVGEAYFFRAFAYFNLVRQYGDVPYVSQVLTPDSEELFAARTPRKEVIDYILDDLSQAIEKLPPKAASTRNRINKESALLYKSRVALYEGTWEKYHQETVFGVKGSNGQEYLEIAASAAKQLMDMNTIELYSTGNPEVDYASLFNRDDLSGIGEVLLSRDYNISLNTVHNLQRYTTSGAGTGLTKSLIESYLCEDGKPISLSPLYRGDKSLEMVVENRDPRLRQMIYWKEGEPRRTQNGVLVPGYEFTRPYIDQGGEGGNTTGYMLKKGLDTESKGQPEQNASETSMPIFRYAEALLNYAEAKAELGTITQNDIDLTINKIRSRAAMPALSLHSMANDPDWQFPELSPIINEVRRERRVELACEGYRADDLLRWRAHHLIVGKRPLGYWFDKDFWTGVQDSEDNYVDGGPLLIPGKDIFVNEDGYLDPYQKNLPNGFGFKPDRDYLYPVPPAQISLNGELTQNPGWE

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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
AP018040_2	2.1\|1434147\|27\|AP018040\|CRISPRCasFinder	1434147-1434173	27	KR093640	Moraxella phage Mcat16, complete genome	10394-10420	5	0.815
AP018040_2	2.1\|1434147\|27\|AP018040\|CRISPRCasFinder	1434147-1434173	27	KR093642	Moraxella phage Mcat18, complete genome	9309-9335	5	0.815
AP018040_2	2.1\|1434147\|27\|AP018040\|CRISPRCasFinder	1434147-1434173	27	KR093641	Moraxella phage Mcat17, complete genome	1871-1897	5	0.815
AP018040_2	2.1\|1434147\|27\|AP018040\|CRISPRCasFinder	1434147-1434173	27	KR093643	Moraxella phage Mcat19, complete genome	5920-5946	5	0.815
AP018040_2	2.1\|1434147\|27\|AP018040\|CRISPRCasFinder	1434147-1434173	27	KR093639	Moraxella phage Mcat15, complete genome	9853-9879	5	0.815
AP018040_3	3.6\|2377192\|36\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377192-2377227	36	MH617335	Microviridae sp. isolate ctcb564, complete genome	64-99	5	0.861
AP018040_2	2.1\|1434147\|27\|AP018040\|CRISPRCasFinder	1434147-1434173	27	MF360958	Salicola phage SCTP-2, complete genome	263310-263336	6	0.778
AP018040_3	3.5\|2377128\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377128-2377161	34	MG945157	UNVERIFIED: Microviridae sp. isolate 369-1801, complete genome	2256-2289	7	0.794
AP018040_3	3.35\|2379088\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379088-2379122	35	NZ_HG813246	Staphylococcus epidermidis PM221 plasmid 1, complete sequence	42531-42565	7	0.8
AP018040_3	3.4\|2377064\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377064-2377097	34	NZ_AP017296	Nostoc sp. NIES-3756 plasmid pNOS3756_1, complete sequence	313375-313408	8	0.765
AP018040_3	3.5\|2377128\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377128-2377161	34	MG945136	UNVERIFIED: Microviridae sp. isolate 221-1801, complete genome	2408-2441	8	0.765
AP018040_3	3.16\|2377850\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377850-2377884	35	MH745368	Escherichia phage fp01, complete genome	4751-4785	8	0.771
AP018040_3	3.38\|2379283\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379283-2379317	35	NC_021325	Clostridium phage vB_CpeS-CP51, complete genome	35372-35406	8	0.771
AP018040_3	3.5\|2377128\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377128-2377161	34	MG945908	UNVERIFIED: Microviridae sp. isolate 5193-1602, partial genome	138-171	9	0.735
AP018040_3	3.24\|2378371\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2378371-2378404	34	NZ_CP023549	Rhodobacter sp. CZR27 plasmid unnamed1, complete sequence	58450-58483	9	0.735
AP018040_3	3.61\|2380787\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2380787-2380821	35	NC_009475	Bradyrhizobium sp. BTAi1 plasmid pBBta01, complete sequence	51173-51207	9	0.743
AP018040_3	3.17\|2377915\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377915-2377948	34	NZ_CP012500	Escherichia coli strain 09-00049 plasmid pCFSAN004180G, complete sequence	10132-10165	10	0.706
AP018040_3	3.17\|2377915\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377915-2377948	34	NZ_CP042296	Escherichia coli strain RM9088 plasmid p1RM9088, complete sequence	122751-122784	10	0.706
AP018040_3	3.17\|2377915\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377915-2377948	34	NZ_CP012499	Escherichia coli strain GB089 plasmid pCFSAN004181P, complete sequence	109856-109889	10	0.706
AP018040_3	3.17\|2377915\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2377915-2377948	34	NZ_CP012501	Escherichia coli strain 08-00022 plasmid pCFSAN004179G, complete sequence	30043-30076	10	0.706
AP018040_3	3.35\|2379088\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379088-2379122	35	MT375526	Pelagibacter phage Himinglaeva EXVC011P, complete genome	31585-31619	10	0.714
AP018040_3	3.35\|2379088\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379088-2379122	35	MH598807	Pelagibacter phage HTVC120P, complete genome	7115-7149	10	0.714
AP018040_3	3.35\|2379088\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379088-2379122	35	MT375531	Pelagibacter phage Unn EXVC019P, complete genome	13118-13152	10	0.714
AP018040_3	3.35\|2379088\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379088-2379122	35	MT375520	Pelagibacter phage Bylgja EXVC0, complete genome	31585-31619	10	0.714
AP018040_3	3.35\|2379088\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379088-2379122	35	AP013545	Uncultured phage_MedDCM-OCT-S46-C10 DNA, complete genome, group G8, isolate: uvMED-CGR-U-MedDCM-OCT-S46-C10	14194-14228	10	0.714
AP018040_3	3.35\|2379088\|35\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2379088-2379122	35	MT375527	Pelagibacter phage Hroenn EXVC0, complete genome	25003-25037	10	0.714
AP018040_3	3.59\|2380659\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2380659-2380692	34	NZ_CP021375	Rhizobium sp. ACO-34A plasmid pRACO34Aa, complete sequence	14941-14974	10	0.706
AP018040_3	3.24\|2378371\|34\|AP018040\|PILER-CR,CRISPRCasFinder,CRT	2378371-2378404	34	MG592399	Vibrio phage 1.015.O._10N.222.51.E5, partial genome	38974-39007	11	0.676

1. spacer 2.1|1434147|27|AP018040|CRISPRCasFinder matches to KR093640 (Moraxella phage Mcat16, complete genome) position: , mismatch: 5, identity: 0.815

atgcgtgaaaaaatgcaatatcaatcc	CRISPR spacer
atgcgtcaaaaaatgcaacatcatttg	Protospacer
****** ***********.**** *.

2. spacer 2.1|1434147|27|AP018040|CRISPRCasFinder matches to KR093642 (Moraxella phage Mcat18, complete genome) position: , mismatch: 5, identity: 0.815

atgcgtgaaaaaatgcaatatcaatcc	CRISPR spacer
atgcgtcaaaaaatgcaacatcatttg	Protospacer
****** ***********.**** *.

3. spacer 2.1|1434147|27|AP018040|CRISPRCasFinder matches to KR093641 (Moraxella phage Mcat17, complete genome) position: , mismatch: 5, identity: 0.815

atgcgtgaaaaaatgcaatatcaatcc	CRISPR spacer
atgcgtcaaaaaatgcaacatcatttg	Protospacer
****** ***********.**** *.

4. spacer 2.1|1434147|27|AP018040|CRISPRCasFinder matches to KR093643 (Moraxella phage Mcat19, complete genome) position: , mismatch: 5, identity: 0.815

atgcgtgaaaaaatgcaatatcaatcc	CRISPR spacer
atgcgtcaaaaaatgcaacatcatttg	Protospacer
****** ***********.**** *.

5. spacer 2.1|1434147|27|AP018040|CRISPRCasFinder matches to KR093639 (Moraxella phage Mcat15, complete genome) position: , mismatch: 5, identity: 0.815

atgcgtgaaaaaatgcaatatcaatcc	CRISPR spacer
atgcgtcaaaaaatgcaacatcatttg	Protospacer
****** ***********.**** *.

6. spacer 3.6|2377192|36|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MH617335 (Microviridae sp. isolate ctcb564, complete genome) position: , mismatch: 5, identity: 0.861

gatgtaacctagatcatgtgttgatctttcataatt	CRISPR spacer
tacataacctaggtcatgtgttgatctttcgtaatt	Protospacer
 *..********.*****************.*****

7. spacer 2.1|1434147|27|AP018040|CRISPRCasFinder matches to MF360958 (Salicola phage SCTP-2, complete genome) position: , mismatch: 6, identity: 0.778

atgcgtgaaaaaatgcaatatcaatcc	CRISPR spacer
gctaatgaaacaatgcaatatcaatcc	Protospacer
..  .***** ****************

8. spacer 3.5|2377128|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MG945157 (UNVERIFIED: Microviridae sp. isolate 369-1801, complete genome) position: , mismatch: 7, identity: 0.794

--ttaagcccggcacatacccacaagtcggcgttgt	CRISPR spacer
ggtttaccct--cacatacgcacatgtcggcgttgt	Protospacer
  ** * **.  ******* **** ***********

9. spacer 3.35|2379088|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_HG813246 (Staphylococcus epidermidis PM221 plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.8

tgttttatttctttaattttagaattgattccatt	CRISPR spacer
tgttttattgcttgaattttagaattgttatcaac	Protospacer
********* *** ************* * .** .

10. spacer 3.4|2377064|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP017296 (Nostoc sp. NIES-3756 plasmid pNOS3756_1, complete sequence) position: , mismatch: 8, identity: 0.765

gataatgctccgatacttttcatgttttcaaagc	CRISPR spacer
taaaattcttcgatacttttcatgtttttataaa	Protospacer
 * *** **.******************.* *.

11. spacer 3.5|2377128|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MG945136 (UNVERIFIED: Microviridae sp. isolate 221-1801, complete genome) position: , mismatch: 8, identity: 0.765

--ttaagcccggcacatacccacaagtcggcgttgt	CRISPR spacer
ggtttgccct--cacatacgcacatgtcggcgttgt	Protospacer
  ** . **.  ******* **** ***********

12. spacer 3.16|2377850|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MH745368 (Escherichia phage fp01, complete genome) position: , mismatch: 8, identity: 0.771

ctgttttacacggcgtgcgggtggccacggaacgg	CRISPR spacer
acgctgtagtcggcgtgcgggtggactcggaacgg	Protospacer
 .*.* **  ************** * ********

13. spacer 3.38|2379283|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NC_021325 (Clostridium phage vB_CpeS-CP51, complete genome) position: , mismatch: 8, identity: 0.771

atatattacagaaataaaatatattccgacgatga	CRISPR spacer
atatattacataaataaaaaatatttagaaaaagt	Protospacer
********** ******** *****. ** .* *

14. spacer 3.5|2377128|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MG945908 (UNVERIFIED: Microviridae sp. isolate 5193-1602, partial genome) position: , mismatch: 9, identity: 0.735

ttaagcccg---gcacatacccacaagtcggcgttgt	CRISPR spacer
---ggcttgccctcacatacgcacatgtcggcgttgt	Protospacer
   .**..*    ******* **** ***********

15. spacer 3.24|2378371|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP023549 (Rhodobacter sp. CZR27 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

ggatacggtgcttgatcagatcaaggcggtcaag	CRISPR spacer
cgccacgctgctggatcagatcaaggcgcaggag	Protospacer
 * .*** **** ***************   .**

16. spacer 3.61|2380787|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NC_009475 (Bradyrhizobium sp. BTAi1 plasmid pBBta01, complete sequence) position: , mismatch: 9, identity: 0.743

ccgggaaaacgcgcgacgccgcaaatcgaatttgc	CRISPR spacer
cggtgcaaacgcgcgccgccgcagatcgaatccag	Protospacer
* * * ********* *******.*******...

17. spacer 3.17|2377915|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012500 (Escherichia coli strain 09-00049 plasmid pCFSAN004180G, complete sequence) position: , mismatch: 10, identity: 0.706

ctcgatattcagtgccgggaaattattagagatt	CRISPR spacer
tctgatgttcagtgcagggaaattattaacccgt	Protospacer
...***.******** ************.    *

18. spacer 3.17|2377915|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP042296 (Escherichia coli strain RM9088 plasmid p1RM9088, complete sequence) position: , mismatch: 10, identity: 0.706

ctcgatattcagtgccgggaaattattagagatt	CRISPR spacer
tctgatgttcagtgcagggaaattattaacccgt	Protospacer
...***.******** ************.    *

19. spacer 3.17|2377915|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012499 (Escherichia coli strain GB089 plasmid pCFSAN004181P, complete sequence) position: , mismatch: 10, identity: 0.706

ctcgatattcagtgccgggaaattattagagatt	CRISPR spacer
tctgatgttcagtgcagggaaattattaacccgt	Protospacer
...***.******** ************.    *

20. spacer 3.17|2377915|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP012501 (Escherichia coli strain 08-00022 plasmid pCFSAN004179G, complete sequence) position: , mismatch: 10, identity: 0.706

ctcgatattcagtgccgggaaattattagagatt	CRISPR spacer
tctgatgttcagtgcagggaaattattaacccgt	Protospacer
...***.******** ************.    *

21. spacer 3.35|2379088|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MT375526 (Pelagibacter phage Himinglaeva EXVC011P, complete genome) position: , mismatch: 10, identity: 0.714

tgttttatttctttaattttagaattgattccatt	CRISPR spacer
tgttttatttctttacttttagacttctcttttgc	Protospacer
*************** ******* **  .*..  .

22. spacer 3.35|2379088|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MH598807 (Pelagibacter phage HTVC120P, complete genome) position: , mismatch: 10, identity: 0.714

tgttttatttctttaattttagaattgattccatt	CRISPR spacer
tgttttatttctttacttttagacttctcttttgc	Protospacer
*************** ******* **  .*..  .

23. spacer 3.35|2379088|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MT375531 (Pelagibacter phage Unn EXVC019P, complete genome) position: , mismatch: 10, identity: 0.714

tgttttatttctttaattttagaattgattccatt	CRISPR spacer
tgttttatttctttacttttagacttctcttttgc	Protospacer
*************** ******* **  .*..  .

24. spacer 3.35|2379088|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MT375520 (Pelagibacter phage Bylgja EXVC0, complete genome) position: , mismatch: 10, identity: 0.714

tgttttatttctttaattttagaattgattccatt	CRISPR spacer
tgttttatttctttacttttagacttctcttttgc	Protospacer
*************** ******* **  .*..  .

25. spacer 3.35|2379088|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to AP013545 (Uncultured phage_MedDCM-OCT-S46-C10 DNA, complete genome, group G8, isolate: uvMED-CGR-U-MedDCM-OCT-S46-C10) position: , mismatch: 10, identity: 0.714

tgttttatttctttaattttagaattgattccatt	CRISPR spacer
tgttttatttctttacttttagacttctcttttgc	Protospacer
*************** ******* **  .*..  .

26. spacer 3.35|2379088|35|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MT375527 (Pelagibacter phage Hroenn EXVC0, complete genome) position: , mismatch: 10, identity: 0.714

tgttttatttctttaattttagaattgattccatt	CRISPR spacer
tgttttatttctttacttttagacttctcttttgc	Protospacer
*************** ******* **  .*..  .

27. spacer 3.59|2380659|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021375 (Rhizobium sp. ACO-34A plasmid pRACO34Aa, complete sequence) position: , mismatch: 10, identity: 0.706

ggatattttcttccccctccatgctcgtgataca	CRISPR spacer
gatcattttttttcccctccatgctcgtatcgaa	Protospacer
*. .*****.**.***************. .. *

28. spacer 3.24|2378371|34|AP018040|PILER-CR,CRISPRCasFinder,CRT matches to MG592399 (Vibrio phage 1.015.O._10N.222.51.E5, partial genome) position: , mismatch: 11, identity: 0.676

ggatacggtgcttgatcagatcaaggcggtcaag	CRISPR spacer
taatacggtgcttgattatatcaagggcgcgtta	Protospacer
 .**************.* *******  *.   .

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site	Prophage annotation

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. AP018040

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection