Species | UBA1409 sp900553675 | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Firmicutes_A; Clostridia; Oscillospirales; Ruminococcaceae; UBA1409; UBA1409 sp900553675 | |||||||||||
CAZyme ID | MGYG000004587_01491 | |||||||||||
CAZy Family | GT28 | |||||||||||
CAZyme Description | Processive diacylglycerol beta-glucosyltransferase | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 47233; End: 48381 Strand: - |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT28 | 205 | 353 | 9.1e-26 | 0.9490445859872612 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
cd17507 | GT28_Beta-DGS-like | 3.69e-45 | 4 | 366 | 2 | 358 | 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. |
COG0707 | MurG | 8.43e-25 | 4 | 373 | 3 | 357 | UDP-N-acetylglucosamine:LPS N-acetylglucosamine transferase [Cell wall/membrane/envelope biogenesis]. |
PRK13609 | PRK13609 | 6.08e-23 | 4 | 365 | 8 | 363 | diacylglycerol glucosyltransferase; Provisional |
PRK13608 | PRK13608 | 5.82e-18 | 151 | 347 | 151 | 345 | diacylglycerol glucosyltransferase; Provisional |
PLN02605 | PLN02605 | 5.92e-15 | 4 | 325 | 2 | 332 | monogalactosyldiacylglycerol synthase |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
ASM70065.1 | 2.53e-105 | 1 | 369 | 1 | 367 |
AWY97452.1 | 2.83e-95 | 1 | 368 | 1 | 366 |
AEN95364.1 | 3.66e-90 | 1 | 363 | 1 | 382 |
QNM04818.1 | 1.34e-88 | 1 | 368 | 1 | 366 |
ABX42261.1 | 8.55e-86 | 1 | 378 | 1 | 388 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
A8FED1 | 2.40e-28 | 4 | 374 | 8 | 376 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus pumilus (strain SAFR-032) OX=315750 GN=ugtP PE=3 SV=1 |
P54166 | 2.22e-27 | 4 | 347 | 8 | 345 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus subtilis (strain 168) OX=224308 GN=ugtP PE=1 SV=1 |
Q65IA4 | 3.10e-27 | 2 | 375 | 6 | 377 | 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 |
Q49WE6 | 2.66e-24 | 84 | 331 | 91 | 329 | 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 |
Q81IA1 | 1.31e-21 | 4 | 322 | 8 | 320 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) OX=226900 GN=ugtP PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000064 | 0.000002 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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