Species | Veillonella sp900757715 | |||||||||||
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Lineage | Bacteria; Firmicutes_C; Negativicutes; Veillonellales; Veillonellaceae; Veillonella; Veillonella sp900757715 | |||||||||||
CAZyme ID | MGYG000002640_01210 | |||||||||||
CAZy Family | GT28 | |||||||||||
CAZyme Description | Processive diacylglycerol beta-glucosyltransferase | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 14652; End: 15806 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT28 | 205 | 353 | 1.8e-30 | 0.9617834394904459 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
cd17507 | GT28_Beta-DGS-like | 9.85e-83 | 9 | 369 | 1 | 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 | 7.49e-63 | 1 | 373 | 1 | 374 | diacylglycerol glucosyltransferase; Provisional |
COG0707 | MurG | 1.41e-52 | 8 | 367 | 1 | 354 | UDP-N-acetylglucosamine:LPS N-acetylglucosamine transferase [Cell wall/membrane/envelope biogenesis]. |
PRK13608 | PRK13608 | 3.36e-50 | 6 | 377 | 5 | 378 | diacylglycerol glucosyltransferase; Provisional |
PLN02605 | PLN02605 | 8.40e-32 | 9 | 364 | 1 | 375 | monogalactosyldiacylglycerol synthase |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
QQB17499.1 | 7.12e-275 | 1 | 384 | 1 | 384 |
SNU99964.1 | 7.12e-275 | 1 | 384 | 1 | 384 |
ACZ25036.1 | 7.12e-275 | 1 | 384 | 1 | 384 |
CAB1274854.1 | 1.68e-273 | 1 | 384 | 1 | 384 |
VEG93043.1 | 1.84e-261 | 1 | 384 | 1 | 384 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
4WYI_A | 3.94e-24 | 7 | 332 | 6 | 346 | Thecrystal structure of Arabidopsis thaliana galactolipid synthase, MGD1 (apo-form) [Arabidopsis thaliana],4X1T_A The crystal structure of Arabidopsis thaliana galactolipid synthase MGD1 in complex with UDP [Arabidopsis thaliana] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
A0R9F0 | 9.99e-47 | 8 | 366 | 6 | 367 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus thuringiensis (strain Al Hakam) OX=412694 GN=ugtP PE=3 SV=1 |
A9VSQ8 | 1.40e-46 | 8 | 365 | 6 | 366 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus mycoides (strain KBAB4) OX=315730 GN=ugtP PE=3 SV=1 |
B9J2U2 | 1.40e-46 | 8 | 365 | 6 | 366 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus cereus (strain Q1) OX=361100 GN=ugtP PE=3 SV=1 |
B7HU46 | 1.40e-46 | 8 | 365 | 6 | 366 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus cereus (strain AH187) OX=405534 GN=ugtP PE=3 SV=1 |
Q6HNU4 | 3.82e-46 | 8 | 365 | 6 | 366 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus thuringiensis subsp. konkukian (strain 97-27) OX=281309 GN=ugtP PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000042 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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