Species | Peptacetobacter hiranonis | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Firmicutes_A; Clostridia; Peptostreptococcales; Peptostreptococcaceae; Peptacetobacter; Peptacetobacter hiranonis | |||||||||||
CAZyme ID | MGYG000001320_00925 | |||||||||||
CAZy Family | GT32 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 373991; End: 374725 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT32 | 21 | 100 | 7.3e-22 | 0.9333333333333333 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
COG3774 | OCH1 | 1.68e-31 | 1 | 234 | 81 | 310 | Mannosyltransferase OCH1 or related enzyme [Cell wall/membrane/envelope biogenesis]. |
pfam04488 | Gly_transf_sug | 1.31e-11 | 16 | 104 | 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 | 4.47e-06 | 21 | 136 | 67 | 190 | Capsular polysaccharide synthesis protein. This family consists of several capsular polysaccharide proteins. Capsular polysaccharide (CPS) is a major virulence factor in Streptococcus pneumoniae. |
pfam12919 | TcdA_TcdB | 3.64e-04 | 4 | 42 | 1 | 39 | TcdA/TcdB catalytic glycosyltransferase domain. This domain represents the N-terminal glycosyltransferase from a set of toxins found in some bacteria. This domain in TcdB glycosylates the host RhoA protein. |
pfam04572 | Gb3_synth | 3.87e-04 | 124 | 210 | 1 | 101 | Alpha 1,4-glycosyltransferase conserved region. The glycosphingolipids (GSL) form part of eukaryotic cell membranes. They consist of a hydrophilic carbohydrate moiety linked to a hydrophobic ceramide tail embedded within the lipid bilayer of the membrane. Lactosylceramide, Gal1,4Glc1Cer (LacCer), is the common synthetic precursor to the majority of GSL found in vertebrates. Alpha 1.4-glycosyltransferases utilize UDP donors and transfer the sugar to a beta-linked acceptor. This region appears to be confined to higher eukaryotes. No function has been yet assigned to this region. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
QEK20258.1 | 1.58e-187 | 1 | 244 | 1 | 244 |
QQQ86116.1 | 1.63e-180 | 1 | 244 | 1 | 244 |
AXU83986.1 | 5.76e-139 | 1 | 239 | 1 | 240 |
AXU72845.1 | 1.16e-138 | 1 | 239 | 1 | 240 |
AXU47385.1 | 2.34e-138 | 1 | 239 | 1 | 240 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q5UQW4 | 1.86e-11 | 1 | 219 | 1 | 227 | Uncharacterized glycosyltransferase L373 OS=Acanthamoeba polyphaga mimivirus OX=212035 GN=MIMI_L373 PE=3 SV=1 |
Q9UNA3 | 5.46e-10 | 61 | 202 | 142 | 290 | Alpha-1,4-N-acetylglucosaminyltransferase OS=Homo sapiens OX=9606 GN=A4GNT PE=1 SV=1 |
Q5ZU30 | 2.81e-08 | 2 | 116 | 28 | 162 | Subversion of eukaryotic traffic protein A OS=Legionella pneumophila subsp. pneumophila (strain Philadelphia 1 / ATCC 33152 / DSM 7513) OX=272624 GN=setA PE=1 SV=1 |
Q14BT6 | 8.97e-08 | 61 | 154 | 143 | 233 | Alpha-1,4-N-acetylglucosaminyltransferase OS=Mus musculus OX=10090 GN=A4gnt PE=2 SV=1 |
Q9JI93 | 1.26e-07 | 63 | 204 | 177 | 326 | Lactosylceramide 4-alpha-galactosyltransferase OS=Rattus norvegicus OX=10116 GN=A4galt PE=1 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000048 | 0.000001 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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