Species | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Actinobacteriota; Coriobacteriia; Coriobacteriales; Coriobacteriaceae; Collinsella; | |||||||||||
CAZyme ID | MGYG000003067_01343 | |||||||||||
CAZy Family | GT32 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 1222; End: 2055 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT32 | 29 | 102 | 7.4e-20 | 0.9111111111111111 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
COG3774 | OCH1 | 5.37e-15 | 9 | 154 | 81 | 217 | Mannosyltransferase OCH1 or related enzyme [Cell wall/membrane/envelope biogenesis]. |
pfam04488 | Gly_transf_sug | 1.60e-10 | 25 | 109 | 1 | 93 | Glycosyltransferase sugar-binding region containing DXD motif. The DXD motif is a short conserved motif found in many families of glycosyltransferases, which add a range of different sugars to other sugars, phosphates and proteins. DXD-containing glycosyltransferases all use nucleoside diphosphate sugars as donors and require divalent cations, usually manganese. The DXD motif is expected to play a carbohydrate binding role in sugar-nucleoside diphosphate and manganese dependent glycosyltransferases. |
pfam05704 | Caps_synth | 4.32e-07 | 10 | 120 | 46 | 161 | Capsular polysaccharide synthesis protein. This family consists of several capsular polysaccharide proteins. Capsular polysaccharide (CPS) is a major virulence factor in Streptococcus pneumoniae. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
AFQ45980.1 | 5.53e-85 | 10 | 262 | 2 | 257 |
QUT53709.1 | 1.39e-83 | 10 | 263 | 2 | 257 |
QWT54350.1 | 1.04e-82 | 9 | 240 | 10 | 236 |
QIA43512.1 | 1.06e-81 | 10 | 245 | 6 | 229 |
ATP00764.1 | 1.06e-81 | 10 | 245 | 6 | 229 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000056 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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