CRISPRimmunity

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Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP046761	Vibrio parahaemolyticus strain AM46865 chromosome 1, complete sequence	0 crisprs	DEDDh,DinG,csx1,cas3,csa3	0	0	4	0
NZ_CP046762	Vibrio parahaemolyticus strain AM46865 chromosome 2, complete sequence	1 crisprs	cas3,DEDDh,csa3,WYL	0	0	2	0

Results visualization

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CRISPR-Cas detection and classification

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

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

365664 : 382847

uncultured_Mediterranean_phage(20.0%)

tRNA

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

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_005455581.1\|365664_367305_+	CTP synthase	A0A1J0FA14	Only_Syngen_Nebraska_virus	4.2e-155	52.4
WP_005455579.1\|367383_368685_+	phosphopyruvate hydratase	A0A1X9I5Z8	Streptococcus_phage	4.2e-134	59.2
WP_005455577.1\|369098_369380_+	cell division protein FtsB	NA	NA	NA	NA
WP_005487195.1\|369381_370086_+	2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase	A0A2H4UTB4	Bodo_saltans_virus	2.6e-05	23.6
WP_005380896.1\|370103_370580_+	2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase	NA	NA	NA	NA
WP_158113708.1\|370626_371670_+\|tRNA	tRNA pseudouridine(13) synthase TruD	NA	NA	NA	NA
WP_005478553.1\|371669_372446_+	5'/3'-nucleotidase SurE	A0A1B1ITZ2	uncultured_Mediterranean_phage	5.0e-66	52.4
WP_005455562.1\|372445_373072_+	protein-L-isoaspartate(D-aspartate) O-methyltransferase	A0A1B1IU40	uncultured_Mediterranean_phage	1.3e-35	52.1
WP_005455560.1\|373086_374010_+	peptidoglycan DD-metalloendopeptidase family protein	D7RWE0	Brochothrix_phage	4.1e-06	35.2
WP_158113711.1\|375158_377720_-	DNA mismatch repair protein MutS	A0A1V0SC35	Catovirus	1.3e-33	23.7
WP_025795578.1\|377804_378287_+	nicotinamide-nucleotide amidase	B5TK85	Pseudomonas_phage	2.9e-27	48.7
WP_023623298.1\|378487_379531_+	recombinase RecA	A0A2D1GPX2	Mycobacterium_phage	8.1e-112	60.7
WP_005455548.1\|379654_380122_+	recombination regulator RecX	NA	NA	NA	NA
WP_140095445.1\|380264_382847_+\|tRNA	alanine--tRNA ligase	A0A1V0SK38	Klosneuvirus	1.0e-78	37.9

DBSCAN-SWA_2

1392235 : 1401105

Vibrio_phage(100.0%)

coat

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_140347371.1\|1392235_1393378_-	assembly protein	O88128	Vibrio_phage	1.1e-213	98.9
WP_158113909.1\|1393374_1393689_-	DUF2523 domain-containing protein	O88125	Vibrio_phage	1.8e-46	99.0
WP_158113912.1\|1393690_1395166_-	methyl-accepting chemotaxis protein	O88107	Vibrio_phage	2.3e-221	99.2
WP_015975175.1\|1395299_1395533_-\|coat	major coat protein	O88142	Vibrio_phage	1.0e-30	100.0
WP_015975174.1\|1395543_1395789_-	hypothetical protein	A0A1W6UH23	Vibrio_phage	1.2e-37	100.0
WP_158113915.1\|1395800_1396154_-	DUF1293 domain-containing protein	O88148	Vibrio_phage	1.9e-60	98.3
WP_158113918.1\|1396157_1397366_-	phage replication protein	Q7DKP2	Vibrio_phage	1.2e-244	99.8
WP_025526117.1\|1397289_1397505_-	hypothetical protein	A0A1W6UGD1	Vibrio_phage	4.5e-33	97.2
WP_158113921.1\|1397507_1397780_-	hypothetical protein	NA	NA	NA	NA
WP_158113923.1\|1397903_1398272_+	hypothetical protein	Q9MCC3	Vibrio_phage	1.2e-54	89.8
WP_021448543.1\|1398280_1398547_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_021448542.1\|1398689_1398881_+	hypothetical protein	NA	NA	NA	NA
WP_140070698.1\|1398877_1399252_+	hypothetical protein	NA	NA	NA	NA
WP_158113925.1\|1399248_1401105_+	hypothetical protein	A0A2I7RNF8	Vibrio_phage	7.7e-113	43.0

DBSCAN-SWA_3

1657222 : 1671139

Vibrio_phage(40.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_005495398.1\|1657222_1659448_-	ribonuclease R	Q0GXV6	Lactococcus_phage	8.2e-61	31.7
WP_005483265.1\|1659742_1659955_-	cold-shock protein	A0A1W6JNX5	Morganella_phage	2.9e-16	61.2
WP_005483162.1\|1660861_1661065_+	hypothetical protein	NA	NA	NA	NA
WP_005495402.1\|1661287_1661695_-	APSE-2 prophage; Q protein	NA	NA	NA	NA
WP_005495404.1\|1661731_1662133_-	NinG recombination protein/bacteriophage lambda NinG family protein	A0A2I7S3K0	Vibrio_phage	3.7e-20	45.0
WP_005495406.1\|1662122_1662305_-	hypothetical protein	NA	NA	NA	NA
WP_065766468.1\|1662301_1662952_-	DUF1367 family protein	K7PKS6	Enterobacteria_phage	7.0e-21	36.5
WP_065766470.1\|1662944_1663325_-	hypothetical protein	NA	NA	NA	NA
WP_071161315.1\|1663321_1664275_-	helix-turn-helix domain-containing protein	A0A1V0E831	Vibrio_phage	2.2e-39	35.7
WP_005495414.1\|1664340_1664559_-	hypothetical protein	NA	NA	NA	NA
WP_005495415.1\|1664555_1665020_-	hypothetical protein	K7PJS5	Enterobacterial_phage	3.0e-18	48.0
WP_021486590.1\|1665039_1665261_-	helix-turn-helix transcriptional regulator	A0A1P8DTF8	Proteus_phage	2.8e-06	40.6
WP_071161314.1\|1665369_1666038_+	helix-turn-helix domain-containing protein	A0A1V0E8B5	Vibrio_phage	1.9e-66	57.1
WP_127463331.1\|1666749_1666929_+	hypothetical protein	NA	NA	NA	NA
WP_080524852.1\|1666941_1670106_+	hypothetical protein	I3PUZ3	Vibrio_phage	1.1e-23	33.6
WP_021453095.1\|1670098_1670626_+	siphovirus Gp157 family protein	NA	NA	NA	NA
WP_021453797.1\|1670950_1671139_+	hypothetical protein	F6LQB8	Bdellovibrio_phage	8.8e-09	52.8

DBSCAN-SWA_4

2393955 : 2400657

Staphylococcus_phage(50.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_005440184.1\|2393955_2394426_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	1.7e-32	49.3
WP_020840184.1\|2394595_2395705_-	bifunctional 3,4-dihydroxy-2-butanone-4-phosphate synthase/GTP cyclohydrolase II	A0A2H4PQS2	Staphylococcus_phage	2.0e-63	39.6
WP_005483039.1\|2395874_2396528_-	riboflavin synthase	A0A2H4PQS5	Staphylococcus_phage	1.6e-33	37.5
WP_069506310.1\|2396540_2397665_-	bifunctional diaminohydroxyphosphoribosylaminopyrimidine deaminase/5-amino-6-(5-phosphoribosylamino)uracil reductase RibD	A0A1V0SE20	Indivirus	6.9e-48	36.0
WP_005482986.1\|2397672_2398122_-	transcriptional regulator NrdR	NA	NA	NA	NA
WP_025508739.1\|2398249_2399500_-	glutamate-5-semialdehyde dehydrogenase	A0A1X9I5D4	Streptococcus_phage	3.6e-98	47.9
WP_100662159.1\|2399517_2400657_-	glutamate 5-kinase	A0A1X9I5D0	Streptococcus_phage	1.0e-62	41.7

Anti-CRISPR protein detection

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

2. NZ_CP046762

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP046762_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP046762_1

1324979-1325076

Orphan

Consensus_repeat	Method
TATTTTTAAAATGCCTTTTCAAAAA	CRISPRCasFinder

1 spacers

DEDDh

The CRISPR arrays of NZ_CP046762_1

>merge|NZ_CP046762|1|1324979-1325076|CRISPRCasFinder
TATTTTTAAAATGCCTTTTCAAAAATTTGAAACCGCGCAATTAAAGAATTCAGAAAAACAAGATCGCAATCAATATTTTTAAAACGCCTTTTCAAAAA

>NZ_CP046762|1|1|1324979-1325076|CRISPRCasFinder
TATTTTTAAAATGCCTTTTCAAAAA	TTTGAAACCGCGCAATTAAAGAATTCAGAAAAACAAGATCGCAATCAA
TATTTTTAAAACGCCTTTTCAAAAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP046762.1\|WP_005464959.1\|1315374_1316466_-\|GGDEF-domain-containing-protein	unknown	unknown	gnl\|CDD\|143635
NZ_CP046762.1\|WP_140093641.1\|1314960_1315365_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP046762.1\|WP_025501292.1\|1319715_1320522_+\|arylamine-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366312
NZ_CP046762.1\|WP_005460834.1\|1329512_1330136_+\|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	unknown	unknown	gnl\|CDD\|235577
NZ_CP046762.1\|WP_025508929.1\|1321472_1322183_-\|DNA-polymerase-III-subunit-epsilon	DEDDh	cd06127_DEDDh_CAS-I	gnl\|CDD\|236392
NZ_CP046762.1\|WP_005464962.1\|1318273_1319422_-\|S-(hydroxymethyl)glutathione-dehydrogenase/class-III-alcohol-dehydrogenase	unknown	unknown	gnl\|CDD\|176260
NZ_CP046762.1\|WP_025550686.1\|1328571_1329501_+\|sugar-kinase	unknown	unknown	gnl\|CDD\|238571
NZ_CP046762.1\|WP_005482916.1\|1325175_1325937_+\|2-dehydro-3-deoxy-D-gluconate-5-dehydrogenase-KduD	unknown	unknown	gnl\|CDD\|181605
NZ_CP046762.1\|WP_140093637.1\|1322185_1324054_-\|CBS-domain-containing-protein	unknown	unknown	gnl\|CDD\|225457
NZ_CP046762.1\|WP_005464972.1\|1320602_1321472_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176159
NZ_CP046762.1\|WP_158114217.1\|1332883_1335112_+\|exopolygalacturonate-lyase	unknown	unknown	unknown
NZ_CP046762.1\|WP_140093630.1\|1330321_1332061_-\|transporter	unknown	unknown	gnl\|CDD\|271371
NZ_CP046762.1\|WP_140093635.1\|1325955_1326480_+\|YgjV-family-protein	unknown	unknown	gnl\|CDD\|378474
NZ_CP046762.1\|WP_005482833.1\|1316465_1316927_-\|oxidoreductase	unknown	unknown	gnl\|CDD\|226429
NZ_CP046762.1\|WP_140093632.1\|1327561_1328473_+\|alpha/beta-hydrolase-fold-domain-containing-protein	unknown	unknown	gnl\|CDD\|223730
NZ_CP046762.1\|WP_005467181.1\|1326487_1326808_+\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380366
NZ_CP046762.1\|WP_005482845.1\|1332190_1332868_+\|porin	unknown	unknown	gnl\|CDD\|368776
NZ_CP046762.1\|WP_005460779.1\|1326848_1327484_+\|RpiB/LacA/LacB-family-sugar-phosphate-isomerase	unknown	unknown	gnl\|CDD\|181746
NZ_CP046762.1\|WP_005497702.1\|1324137_1324935_-\|DNA-binding-transcriptional-regulator-KdgR	unknown	unknown	gnl\|CDD\|185046
NZ_CP046762.1\|WP_158114215.1\|1317372_1318212_-\|S-formylglutathione-hydrolase	unknown	unknown	gnl\|CDD\|178061

Protein	Function_ID	Function_description	E-value
NZ_CP046762.1\|WP_005464959.1\|1315374_1316466_-\|GGDEF-domain-containing-protein	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	5.06677e-44
NZ_CP046762.1\|WP_025550686.1\|1328571_1329501_+\|sugar-kinase	gnl\|CDD\|238571	cd01166, KdgK, 2-keto-3-deoxygluconate kinase (KdgK) phosphorylates 2-keto-3-deoxygluconate (KDG) to form 2-keto-3-deoxy-6-phosphogluconate (KDGP). KDG is the common intermediate product, that allows organisms to channel D-glucuronate and/or D-galacturinate into the glycolysis and therefore use polymers, like pectin and xylan as carbon sources.	1.39478e-102
NZ_CP046762.1\|WP_025501292.1\|1319715_1320522_+\|arylamine-N-acetyltransferase	gnl\|CDD\|366312	pfam00797, Acetyltransf_2, N-acetyltransferase. Arylamine N-acetyltransferase (NAT) is a cytosolic enzyme of approximately 30kDa. It facilitates the transfer of an acetyl group from Acetyl Coenzyme A on to a wide range of arylamine, N-hydroxyarylamines and hydrazines. Acetylation of these compounds generally results in inactivation. NAT is found in many species from Mycobacteria (M. tuberculosis, M. smegmatis etc) to man. It was the first enzyme to be observed to have polymorphic activity amongst human individuals. NAT is responsible for the inactivation of Isoniazid (a drug used to treat Tuberculosis) in humans. The NAT protein has also been shown to be involved in the breakdown of folic acid.	1.53608e-97
NZ_CP046762.1\|WP_005460834.1\|1329512_1330136_+\|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	gnl\|CDD\|235577	PRK05718, PRK05718, keto-hydroxyglutarate-aldolase/keto-deoxy-phosphogluconate aldolase; Provisional.	4.28455e-121
NZ_CP046762.1\|WP_025508929.1\|1321472_1322183_-\|DNA-polymerase-III-subunit-epsilon	gnl\|CDD\|236392	PRK09146, PRK09146, DNA polymerase III subunit epsilon; Validated.	4.25942e-39
NZ_CP046762.1\|WP_005464962.1\|1318273_1319422_-\|S-(hydroxymethyl)glutathione-dehydrogenase/class-III-alcohol-dehydrogenase	gnl\|CDD\|176260	cd08300, alcohol_DH_class_III, class III alcohol dehydrogenases. Members identified as glutathione-dependent formaldehyde dehydrogenase(FDH), a member of the zinc dependent/medium chain alcohol dehydrogenase family. FDH converts formaldehyde and NAD(P) to formate and NAD(P)H. The initial step in this process the spontaneous formation of a S-(hydroxymethyl)glutathione adduct from formaldehyde and glutathione, followed by FDH-mediated oxidation (and detoxification) of the adduct to S-formylglutathione. MDH family uses NAD(H) as a cofactor in the interconversion of alcohols and aldehydes or ketones. Like many zinc-dependent alcohol dehydrogenases (ADH) of the medium chain alcohol dehydrogenase/reductase family (MDR), these FDHs form dimers, with 4 zinc ions per dimer. The medium chain alcohol dehydrogenase family (MDR) have a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The N-terminal region typically has an all-beta catalytic domain. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which have a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site and a structural zinc in a lobe of the catalytic domain. NAD(H) binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding.	0
NZ_CP046762.1\|WP_005482916.1\|1325175_1325937_+\|2-dehydro-3-deoxy-D-gluconate-5-dehydrogenase-KduD	gnl\|CDD\|181605	PRK08993, PRK08993, 2-dehydro-3-deoxy-D-gluconate 5-dehydrogenase KduD.	0
NZ_CP046762.1\|WP_140093637.1\|1322185_1324054_-\|CBS-domain-containing-protein	gnl\|CDD\|225457	COG2905, COG2905, Predicted signal-transduction protein containing cAMP-binding and CBS domains [Signal transduction mechanisms].	5.03134e-139
NZ_CP046762.1\|WP_005464972.1\|1320602_1321472_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|176159	cd08470, PBP2_CrgA_like_1, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator CrgA-like, contains the type 2 periplasmic binding domain. This CD represents the substrate binding domain of an uncharacterized LysR-type transcriptional regulator (LTTR) CrgA-like 1. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.14139e-108
NZ_CP046762.1\|WP_140093630.1\|1330321_1332061_-\|transporter	gnl\|CDD\|271371	cd11477, SLC5sbd_u1, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	1.41438e-108
NZ_CP046762.1\|WP_140093635.1\|1325955_1326480_+\|YgjV-family-protein	gnl\|CDD\|378474	pfam10688, Imp-YgjV, Bacterial inner membrane protein. This is a family of inner membrane proteins. Many of the members are YgjV protein.	3.47724e-49
NZ_CP046762.1\|WP_005482833.1\|1316465_1316927_-\|oxidoreductase	gnl\|CDD\|226429	COG3915, COG3915, Uncharacterized protein conserved in bacteria [Function unknown].	3.9997e-40
NZ_CP046762.1\|WP_140093632.1\|1327561_1328473_+\|alpha/beta-hydrolase-fold-domain-containing-protein	gnl\|CDD\|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	2.96251e-18
NZ_CP046762.1\|WP_005467181.1\|1326487_1326808_+\|cupin-domain-containing-protein	gnl\|CDD\|380366	cd02238, cupin_KdgF, pectin degradation protein KdgF and related proteins, cupin domain. This family includes bacterial and archaeal pectin degradation protein KdgF that catalyzes the linearization of unsaturated uronates from both pectin and alginate, which are polysaccharides found in the cell walls of plants and brown algae, respectively, and represent an important source of carbon. These polysaccharides, mostly consisting of chains of uronates, can be metabolized by bacteria through a pathway of enzymatic steps to the key metabolite 2-keto-3-deoxygluconate (KDG). Pectin degradation is used by many plant-pathogenic bacteria during infection, and also, pectin and alginate can both represent abundant sources of carbohydrate for the production of biofuels. These proteins belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	1.13072e-54
NZ_CP046762.1\|WP_005482845.1\|1332190_1332868_+\|porin	gnl\|CDD\|368776	pfam06178, KdgM, Oligogalacturonate-specific porin protein (KdgM). This family consists of several bacterial proteins which are homologous to the oligogalacturonate-specific porin protein KdgM from Erwinia chrysanthemi. The phytopathogenic Gram-negative bacteria Erwinia chrysanthemi secretes pectinases, which are able to degrade the pectic polymers of plant cell walls, and uses the degradation products as a carbon source for growth. KdgM is a major outer membrane protein, whose synthesis is strongly induced in the presence of pectic derivatives. KdgM behaves like a voltage-dependent porin that is slightly selective for anions and that exhibits fast block in the presence of trigalacturonate. In contrast to most porins, KdgM seems to be monomeric.	3.08357e-24
NZ_CP046762.1\|WP_005460779.1\|1326848_1327484_+\|RpiB/LacA/LacB-family-sugar-phosphate-isomerase	gnl\|CDD\|181746	PRK09273, PRK09273, hypothetical protein; Provisional.	2.15977e-144
NZ_CP046762.1\|WP_005497702.1\|1324137_1324935_-\|DNA-binding-transcriptional-regulator-KdgR	gnl\|CDD\|185046	PRK15090, PRK15090, DNA-binding transcriptional regulator KdgR; Provisional.	0
NZ_CP046762.1\|WP_158114215.1\|1317372_1318212_-\|S-formylglutathione-hydrolase	gnl\|CDD\|178061	PLN02442, PLN02442, S-formylglutathione hydrolase.	2.15636e-142

>NZ_CP046762.1|WP_005497702.1|1324137_1324935_-|DNA-binding-transcriptional-regulator-KdgR
MKGATMEKSTQPEAVSSVLKVFHILQALGEQKAIGVSELSQRLMMSKATTYRFLQTMKSLGYVSQEGEADKYSLTLKLFELGAKSLEYVDLIELADKEMRHISEQTNEALHLGALDENAIIYIHKIDSGYNLRMQSRIGRRNPLYSTAIGKVLLSERDESFVRDVLSDVEFIKHTEKTLENTDQVLEELAKVRDFHYAEDNEEQEPGLRCIAAPIYDRFGQIIAGLSISFPTIRFDEERMEYYVGLLHQAGKNISEQLGYHDYPA
>NZ_CP046762.1|WP_140093637.1|1322185_1324054_-|CBS-domain-containing-protein
MGTSVTPNIFDFLIKIDPFDKLPEPVVESIANSVKVKYLVRGETIGFSALCDQRYLYIIRTGAIEQRTPNGELRARLGQDDQFGFTFLDPLENAEDGYQAEAIEDSLLYLIPHSELKLVSEEHPEFADYFAAQANVRLSSAVKYVCRKEEKGLFFRTVGEIASENIAIVDVNDSIRNVAQTMCGKQRSSCAVVMKDGETIGLVTDRDMTKSVVAQDMDTNQPIADVMTPNPVLIEDDAKVIQAISLMLQYNIRCLPVVHGKQVKGLLTTTHLVHNHRTQSLFLIEKIKYASSLNALAALKEERQTIFQALVESGVSAEIQGRVMSMIMDAFTRRIIQLNEELLGPPPCDYAWLVAGSHARNEVHMLSDQDSAIVLSDDATEEHKLYFTHLAMRVCNGLAACGYPLCDGKYMAASPKWCQPIRRWKEYYQKWVASPEYNKLLSISVFLEVRAIHGNREFVDQIQQHLHDCIQKSPSFIPALVRDAIDTQPPLGIFNNLVLEKGGENSNTLNIKKYALNLIIDLARIFSLAAGGSLTGTEERFRYAAQHGTLSKDSVENIIGAYRFITQVRFRHQLNAILAGTTPDNHIAPDDFSSFERKHLKDAFKIISELQDVAKLKFLKGA
>NZ_CP046762.1|WP_025508929.1|1321472_1322183_-|DNA-polymerase-III-subunit-epsilon
MIKRWFKRWETPLSPEQKRQAIHVIDDWPMVLKDYLQQPLVDDSTTLKNLSFVALDFETTGVDAQGDKILSIGVVDLTLDGIDIASSKEWYICHGQFIKPETAKINGLTPQDLAKGLPLDEGMNRLLERITGKVVLAHGCCIEKAFIHAYFSSRYQVEDFPAYFIDTLQIEKQFSYAGKSGAHSSYQLDDLRRYYHLPGYLSHSAASDALACAELFLVQSKKLTALPDVTLRQLMR
>NZ_CP046762.1|WP_005464972.1|1320602_1321472_+|LysR-family-transcriptional-regulator
MANWEGVSEFVAVAETNSFTGAAAKLKTSVAQISRRVSALEERLAVKLLHRTTRKVSLSEAGQLYYQQCKHLVEGLELAELAVTQMQTEPRGLLRVTAPVTYGEMNLAPLLHQFLEKYPRVDLDLVLTNQKLDLIEQGVDVAIRLGRLQDSSMIAKRLSSRQTYVCASPMYLERFGEPHTLSELGRHQCLVGSVDYWHFKENKRDKSLRVSGRIKCNSGFALVDAAKRGLGLVQLPDYYVQEALDSGELVEVLTDYRDDREGIWALYPQSRNLSPKVRLLIDFLAQELA
>NZ_CP046762.1|WP_025501292.1|1319715_1320522_+|arylamine-N-acetyltransferase
MNKTDLNAYLTKLGLPSELPADLESLHKIHVAQHRCLPFENFDISLQRGISVEIEDIIQKTVYHSRGGYCFELNGLMLDVLKTLGFEARSLLGRVHVMGTPTGRSHQITLVTLDEQAWIVDVGFGSNTPRAPLPFILNQVIQTDLQTFRFVEDAQFGYFLQVLSTDGTDTWNNLYSFDLEFVFAGDIACGNFFTSTSPHSRFTSARVAAKATESGLVTLLNYTLKYTSEGEQTELELEPGQAYLDALKEYFGIELDAQYGDLRPLPDA
>NZ_CP046762.1|WP_005464962.1|1318273_1319422_-|S-(hydroxymethyl)glutathione-dehydrogenase/class-III-alcohol-dehydrogenase
MTLEIKPGQTHIKSKAMVAWAAGEPLKMEEVDVQLPKAGEVLVRIVATGVCHTDAFTLSGDDPEGIFPSILGHEGGGIVEMVGEGVTSVEVGDHVIPLYTAECGECKFCKSGKTNLCQAVRETQGKGLMPDGTSRFSINGETIFHYMGCSTFSEYTVLPEISLAKVNKQAPLEEVCLLGCGVTTGMGAVLNTAKVEKGDTVAIFGLGGIGLSAIIGARMAGASRIIGIDINESKFDLAKQLGATDVINPQKFDKPIQEVIVEMTDGGVDYSFECIGNVNVMRQALECCHKGWGESVIIGVAGAGQEISTRPFQLVTGRVWRGSAFGGVKGRSELPEIVNRYMAGEFGLQEFITHTMGLEDVNKAFDLMHEGKSIRTVIHMDK
>NZ_CP046762.1|WP_158114215.1|1317372_1318212_-|S-formylglutathione-hydrolase
MTIENVSQTKVFGGWHKQYTHDSKALNCTMRFAIFLPPNATKCNPVPALYWLSGLTCTDENFMQKAGAFRMAAELGIAIIAPDTSPRGEGVADDASYDLGQGAGFYLNATQAPWSLHYHMYDYVTQELPAIIEANFPISDVKSISGHSMGGHGALTIGLKNPTLYRSISAFSPISNPMQCPWGQKAFTAYLGTDIESWKQYDASELLKKEKSPLPILVDQGDADGFLSEQLKPEVLLAAAKQHGSELNLRMQSGYDHSYYFISSFIDNHLNFHAKYLFA
>NZ_CP046762.1|WP_005482833.1|1316465_1316927_-|oxidoreductase
MKKIVSLSLLLFAPFLSANSITFSSPQQPSVTLKLEELQSLPTTSYTTDLPWIQQSSEFLGVKLSTLLTHVYGSIPEQVDIGSLNNYHSTLSRKDIVRYQPILAYQQDHHYIKVRNKGPYWVIYPLSQYPELDHNEYHAQMVWQVNEMKIKQK
>NZ_CP046762.1|WP_005464959.1|1315374_1316466_-|GGDEF-domain-containing-protein
MKLSEAYPIKQKNYSTTSKMLLLVFATSLLLANVILLQQTRVLAQSFTDEQKQATWFLFQLSKELSELVSEARRLDENVLKIEGAELQYELAWSRFDLLINSKDVYTFFSRNHIQQYFLQLFNEFKELEPLLVEAKTGDSQAAAQFYRATQTLYLNLVEFVNQNFRLTSQVYETQKDESQRLMKAQYMLFATFVLSILSLTYFFYRESHFHRKLALSDPLTGLGNRNALFVTLRNNTRNRTAFSLCLLDLNGFKNVNDTYGHQAGDTVLCEIAKRLKDMNIDSFSTYRMGGDEFAVVIESSDVDAEEAKKHIHSVFDTPVLNANNVSSLSTSIGVAHYPSDSDNVDFLISIADKRMYKMKFQR
>NZ_CP046762.1|WP_140093641.1|1314960_1315365_-|hypothetical-protein
MMRKFMQILLLLAIIAAGVLAWVFIPSHETIGQKTLEQALNDDYSLVGHRIYSTDPDAGNRFGYFVLATGQSIEEQEPFLVTSDQFIRMEQTGDNTLSVTVNGCIYQYHNDLWVPKSDGKLQHFLVSATANYVR
>NZ_CP046762.1|WP_005482916.1|1325175_1325937_+|2-dehydro-3-deoxy-D-gluconate-5-dehydrogenase-KduD
MILDSFNLEGKVAIVTGCDTGLGQGMALGLAKAGCDIVGVNISEPTETIEKVEAEGRKFVDIRANLMKLDDIPTIVDRAVTELGRIDILVNNAGIIRRNDAIEFSEQDWDDVMNINVKSVFFMSQAVAKQFIAQGEGGKIINIASMLSFQGGIRVPSYTASKSGVMGVTRLMANEWASHGINVNAIAPGYMATNNTAALRADEQRNKEIVDRIPAARWGTPEDLAGPCVFLASKAADYINGYTIAVDGGWLAR
>NZ_CP046762.1|WP_140093635.1|1325955_1326480_+|YgjV-family-protein
MVDTTILAQALGFISFGLGFSVFYQKNDRHLKILMLIFNLNHLLHFLLLGSMVSALSALLSALRTTTAIFVSSKRVAAVFIVISLVSGFWVAEQWRDLWPIIGTVIGTYSVFCLSGIRMRIGFLLGASCWLTNNILVGSIGGTLLEMTMIVMNLLTIYRLHRQQSESMINQSSY
>NZ_CP046762.1|WP_005467181.1|1326487_1326808_+|cupin-domain-containing-protein
MFVFNQDIPMEDLGEGISRKVLAHSDNMMSVEVHFEEGAIGAMHSHPHEQLTYVLSGEFEFTIGDEKKIVKTGDTMYKEPNIEHGCVCLKAGVLIDTFTPMRKDFV
>NZ_CP046762.1|WP_005460779.1|1326848_1327484_+|RpiB/LacA/LacB-family-sugar-phosphate-isomerase
MKIALMMENSQAAKNAMVAGELNSVAGGLGHDVFNVGMTDENDHHLTYIHLGIMASILLNSKAVDFVVTGCGTGQGALMSCNLHPGVVCGYCLEPSDAFLFNQINNGNAISLAFAKGFGWAGELNVRYIFEKAFTGKRGEGYPIERAAPQQANAAILNNVKSAVAKDVVEGLRAIDQELVKTAVGSTQFQECFFAHCQVPEIAEYVKSLLD
>NZ_CP046762.1|WP_140093632.1|1327561_1328473_+|alpha/beta-hydrolase-fold-domain-containing-protein
MHVAPITSLQTWFPEHPVLPLWSEPQIPSHLVQSYQERNPNELLPDRAVFDITYPEIVVFEPEQSNGMGILLMPGGGYQRVSVDKEGADSARVLNQAGFTVFVMTYRMPNEGHEFGSWTPLADAQRAMRLVRQLPLASHLSSIGVLGFSAGGHVAASLATSHALDIYPLQDEADRVSAKPDFCALMYPVISMNTDIAHMGSRAELLANLERESDLLRFSLEKQVTSDMPPCFLLHASDDTAVSVENSLVFWQALRQHEIATEMHLFEQGKHGFGIRDAQGLPVAAWPQLLSAWLQNLTEKARR
>NZ_CP046762.1|WP_025550686.1|1328571_1329501_+|sugar-kinase
MNPISRVAIIGECMVELKKHDGVLQQGFGGDTLNTAVYLSRLTKQHGVETSYVTGLGHDPFSREMLAAWREEGINTDMVYLSEDKLPGIYAIETAEDGERSFFYWRNDAAAKYWLRERALLSLVKDLCQHQMIYLSGISLAIISDDCRQMLIELLTMCRKEGVKIAFDNNFRPKLWPNIEQARDFYSKILSVTDMAFLTFDDEVMLWGDKHEDEAISRTKNFGVKEIIVKRGADDCFVVTQDQQHTVAALKVDAVVDTTAAGDSFSAGYLAKRILGGDVAESALAGHKVAGTVIQHRGAIIPSQAMPTI
>NZ_CP046762.1|WP_005460834.1|1329512_1330136_+|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase
MKDLNQQLSEIKVVPVIAIKDAGKAVKLAQVLIENGLPCAEVTFRTEDAALAIKNMREAYPEMLIGAGTVLTSAQVDEAIDAGVDFIVSPGFNPTTVKYCQQRNVTIVPGVNNPSLVEQAMEMGLRTLKFFPAEPSGGVAMLKALSAVYPVKFMPTGGVSPSNVKDYLSISSVLACGGTWMVPGDLIDNEQWDELAKLVREVAGIIE
>NZ_CP046762.1|WP_140093630.1|1330321_1332061_-|transporter
MTLLDSMIVMIYLLFIGIAAWLFRRFSTSSNDFLQGGGTMMWWMAGATAFMTQFSAWTFTGAAAKAYEDGISVMFIFWGNALGFFVAAAFFARRYRRLRVETAMEVIRVRFGHTSEQLFTWLSFPLTLIACAIWMNGLASFFSAVFAIEMSITILAMGVVVTLIAVSGGAWTVSVTNVIQLILLIAITLVIGYTALQHFDSPSEVFAYTTPIYGEQIRMPSLFVMWAIAMLLQQTMSNNHTLSCYRFLTTANDKDATKAAFVAGVLFVFAPVLWFMPAWFVAAQNIDLLAIYPALEQSANNAAYLYYIQHYMPQGLLGLVMVALVAATIAPLSSAHNRNAGIVVKSLYQVWFNPNATSRQQLMVGKIATIVSGVLATVTALLLASVESYSLFDMMIVFAAFIQMPINIPSLLALVSLKTPNWSGWATVMVGCAVSLFMMFIFDVQWLSSSPLTPRESKDLSVVATLAVHLLVTGGFFLFTRVFYAKEPPSIQQSRTALAIQLATPISDEELSPINHKQGLYVGSITALAGMLLILAGVVLAGSSQSIFVAIGCIVLLFSLFLLQPTLHSKRAWQKQKTK
>NZ_CP046762.1|WP_005482845.1|1332190_1332868_+|porin
MKVRYLTSALLLAMTSGLAAAASVDIRHEYVPDRDGDEHRDRIYVSHRFDNQIGFSVEAKWNYKDGHMGNAGHETGVSYRWKATDNFSLTPGINIDASPSGASVFKYNLTGAYKINDEWDVAARIRHGYKNTDDSRYNQLNLYANRKFEWGKLGVEAEYKDIHGGEGGWKDKGHDQLIDFKGEYTKLESGVIPFFAIAAITHKGDGSEFKDEYVPRFRVGLKYNF
>NZ_CP046762.1|WP_158114217.1|1332883_1335112_+|exopolygalacturonate-lyase
MKKHTLALCLAAILAPAAHAAEIKVEDLTWKAITFGQSTDMNFGSTILPEKVGVNQVTFNGEAVAAGKLASTFTIESRGGKLANSHEGLTFYYTELPTDVNFTLSADVVLEQLGPETGATPNRQEGAGLMVRDILGVERLVPQPEGHEEFPSASNMVMNLMRSHTRTNDGMTNINASFREGVYQPWGTPGNRLSRVDYVEGVPYGTAETYRMTLTRTNDGFKVSYRNGEKFVEQAVKGANANIVEMQNSDSQYVGFFASRNAKMTVSNVDLQLAAADTVDAPKYAAKQGELVFQIASSPRSATKEYPVQARANYSGEFEVLHNGKVVAKQTVTAGELFSQWLTLDSGANQMEVRFTAIDGPNKETQAHRYSVDVVSLPDPMTLYVAPNGSDKGNGSQAQPLDFATAVELLPAGGTIILKDGDYQGMEIPLTASGSADKLKHLRAEGDNVRFVSELRHEANYWHYQGIEVAGAQFIVHGSHNTFEKMVTHGAPDTGFVITSPENIGRALWASYNQVIESESYNNMDPSQINADGFAAKMRIGDGNTFIRCLSHHNIDDGWDLFNKVEDGANGAVTILDSISFSNGRTLDVANKGGTIGNGFKLGGEGIPVPHVVKNSLSFNNNMDGFTDNFNPGALVLSDNVSIDNKRFNYLFRKSPYSGEIEQGTFTNNRSYRFHVSSKYDDVINSAKSTGNALVENGTTYTSDGKAVDSKTLAPLKQASVIDTQQAIPGKQEAMQLKQLIH

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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

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

399168 : 409940

Vibrio_phage(75.0%)

coat

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_158114160.1\|399168_399537_-	hypothetical protein	Q858Q3	Vibrio_phage	3.1e-42	72.0
WP_005389161.1\|399721_400024_+	hypothetical protein	NA	NA	NA	NA
WP_031778509.1\|400023_402054_+	replication endonuclease	A0A0F6YPA7	Vibrio_phage	1.4e-197	53.2
WP_005389159.1\|402137_402443_+	hypothetical protein	Q2PZB5	Vibrio_virus	1.1e-19	51.0
WP_025506202.1\|402713_402977_+	hypothetical protein	R9TI50	Vibrio_phage	1.5e-06	41.7
WP_024701224.1\|404679_405039_+\|coat	minor coat protein	R9TIT8	Vibrio_phage	4.6e-22	45.6
WP_029830241.1\|405038_406112_+	hypothetical protein	O80263	Vibrio_phage	2.1e-126	63.1
WP_025522920.1\|406129_407482_+	type II secretory pathway protein	R9TEZ5	Vibrio_phage	3.0e-122	57.2
WP_031777856.1\|407521_408160_-	DUF2726 domain-containing protein	NA	NA	NA	NA
WP_031777857.1\|408356_409940_+	hypothetical protein	A0A1S5SA14	Streptococcus_phage	4.1e-30	29.0

DBSCAN-SWA_2

685220 : 704224

Vibrio_phage(76.19%)

head,capsid,tail,portal,terminase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_053048186.1\|685220_685484_-	hypothetical protein	A0A2I7RNJ9	Vibrio_phage	2.0e-30	78.3
WP_025558379.1\|685480_685717_-	hypothetical protein	A0A1D9C9R8	Salinivibrio_phage	1.0e-09	42.7
WP_025558380.1\|685719_685950_-	hypothetical protein	NA	NA	NA	NA
WP_025558381.1\|685949_686459_-	hypothetical protein	A0A2I7S7C4	Vibrio_phage	1.9e-21	41.7
WP_025558382.1\|686455_686665_-	molecular chaperone DnaK	A0A2I7RNJ6	Vibrio_phage	2.0e-17	70.6
WP_025558383.1\|686692_687148_-	DUF2597 family protein	A0A2I7RNI0	Vibrio_phage	8.3e-77	94.0
WP_069484948.1\|687151_688282_-	DUF2586 family protein	A0A2I7RNI8	Vibrio_phage	2.6e-188	86.7
WP_069484947.1\|688297_688954_-	virion morphogenesis protein	A0A2I7RNI6	Vibrio_phage	1.0e-104	87.6
WP_053048192.1\|688937_689432_-\|tail	phage tail protein	A0A2I7RNH2	Vibrio_phage	2.4e-82	93.2
WP_025558387.1\|689428_689848_-\|head	head protein	A0A2I7RNH7	Vibrio_phage	9.4e-43	61.2
WP_025558388.1\|689969_690680_-\|terminase	terminase	A0A2I7RNJ0	Vibrio_phage	4.7e-71	55.8
WP_025558389.1\|690683_691688_-\|capsid	phage major capsid protein, P2 family	R9TPZ5	Vibrio_phage	5.8e-99	59.3
WP_069484946.1\|691687_692569_-\|capsid	phage capsid protein	A0A2I7RNH1	Vibrio_phage	4.5e-87	63.1
WP_069484945.1\|694528_695536_+\|portal	phage portal protein	A0A1D9C9P9	Salinivibrio_phage	4.5e-115	60.4
WP_025558391.1\|696054_697155_+	hypothetical protein	NA	NA	NA	NA
WP_071936904.1\|697212_697464_+	ogr/Delta-like zinc finger family protein	R9TNQ2	Vibrio_phage	1.7e-28	73.5
WP_025558392.1\|697414_698398_-	hypothetical protein	NA	NA	NA	NA
WP_025558393.1\|698406_698625_-	hypothetical protein	Q8HA64	Vibrio_phage	1.1e-13	58.3
WP_140093959.1\|698752_700582_-	replication endonuclease	A0A2P1CKY6	Pseudoalteromonas_phage	5.3e-66	37.5
WP_025558395.1\|700583_700850_-	hypothetical protein	NA	NA	NA	NA
WP_053048196.1\|700924_701413_-	hypothetical protein	NA	NA	NA	NA
WP_025558397.1\|701420_701651_-	hypothetical protein	A0A2I7RNG5	Vibrio_phage	2.3e-19	59.2
WP_140093957.1\|701755_702037_-	hypothetical protein	NA	NA	NA	NA
WP_069484942.1\|702047_702587_-	transcriptional regulator	A0A2I7RNI1	Vibrio_phage	2.9e-52	58.1
WP_045607456.1\|702701_702914_-	hypothetical protein	U3PFJ1	Vibrio_phage	3.0e-13	52.9
WP_069484941.1\|703004_703613_+	phage repressor protein CI	A0A1D9C9M6	Salinivibrio_phage	4.2e-36	39.4
WP_140093955.1\|703640_703940_+	hypothetical protein	NA	NA	NA	NA
WP_069485024.1\|704014_704224_+	hypothetical protein	A0A0H5AWA7	Pseudomonas_phage	3.8e-05	84.6

Anti-CRISPR protein detection

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

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP046761

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CRISPR-Cas detection and classification

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection

2. NZ_CP046762

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CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection