Species | Collinsella sp900759335 | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Actinobacteriota; Coriobacteriia; Coriobacteriales; Coriobacteriaceae; Collinsella; Collinsella sp900759335 | |||||||||||
CAZyme ID | MGYG000001173_00964 | |||||||||||
CAZy Family | GT28 | |||||||||||
CAZyme Description | Processive diacylglycerol beta-glucosyltransferase | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 1058; End: 1909 Strand: - |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT28 | 102 | 242 | 2.3e-25 | 0.8853503184713376 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
cd17507 | GT28_Beta-DGS-like | 2.58e-42 | 4 | 255 | 120 | 363 | beta-diglucosyldiacylglycerol synthase and similar proteins. beta-diglucosyldiacylglycerol synthase (processive diacylglycerol beta-glucosyltransferase EC 2.4.1.315) is involved in the biosynthesis of both the bilayer- and non-bilayer-forming membrane glucolipids. This family of glycosyltransferases also contains plant major galactolipid synthase (chloroplastic monogalactosyldiacylglycerol synthase 1 EC 2.4.1.46). 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. The structures of the formed glycoconjugates are extremely diverse, reflecting a wide range of biological functions. The members of this family share a common 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. |
PRK13609 | PRK13609 | 7.61e-32 | 3 | 259 | 124 | 373 | diacylglycerol glucosyltransferase; Provisional |
PRK13608 | PRK13608 | 6.03e-29 | 8 | 255 | 129 | 369 | diacylglycerol glucosyltransferase; Provisional |
COG0707 | MurG | 5.54e-21 | 7 | 257 | 115 | 357 | UDP-N-acetylglucosamine:LPS N-acetylglucosamine transferase [Cell wall/membrane/envelope biogenesis]. |
PLN02605 | PLN02605 | 6.43e-16 | 2 | 257 | 125 | 381 | monogalactosyldiacylglycerol synthase |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
BCS57039.1 | 3.48e-202 | 1 | 283 | 128 | 410 |
BAN76837.1 | 1.04e-201 | 1 | 283 | 198 | 480 |
BCA88843.1 | 1.16e-201 | 1 | 283 | 201 | 483 |
QOS69492.1 | 1.18e-127 | 1 | 283 | 195 | 478 |
ACV55211.1 | 8.90e-126 | 1 | 283 | 233 | 516 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
B9DQ98 | 1.61e-26 | 5 | 229 | 126 | 344 | Processive diacylglycerol beta-glucosyltransferase OS=Staphylococcus carnosus (strain TM300) OX=396513 GN=ugtP PE=3 SV=1 |
Q49WE6 | 1.07e-24 | 5 | 241 | 126 | 355 | Processive diacylglycerol beta-glucosyltransferase OS=Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) OX=342451 GN=ugtP PE=3 SV=1 |
P54166 | 6.61e-24 | 3 | 247 | 124 | 361 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus subtilis (strain 168) OX=224308 GN=ugtP PE=1 SV=1 |
Q65IA4 | 1.27e-23 | 4 | 247 | 125 | 361 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / CCUG 7422 / NBRC 12200 / NCIMB 9375 / NCTC 10341 / NRRL NRS-1264 / Gibson 46) OX=279010 GN=ugtP PE=3 SV=1 |
Q4L524 | 9.43e-23 | 6 | 231 | 127 | 345 | Processive diacylglycerol beta-glucosyltransferase OS=Staphylococcus haemolyticus (strain JCSC1435) OX=279808 GN=ugtP PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000035 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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