Species | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Actinobacteriota; Coriobacteriia; Coriobacteriales; Coriobacteriaceae; Collinsella; | |||||||||||
CAZyme ID | MGYG000004305_01349 | |||||||||||
CAZy Family | GT28 | |||||||||||
CAZyme Description | Processive diacylglycerol beta-glucosyltransferase | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 16; End: 507 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT28 | 4 | 119 | 2.6e-20 | 0.7388535031847133 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
cd17507 | GT28_Beta-DGS-like | 6.71e-16 | 24 | 133 | 247 | 356 | 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 | 1.60e-15 | 25 | 142 | 233 | 357 | UDP-N-acetylglucosamine:LPS N-acetylglucosamine transferase [Cell wall/membrane/envelope biogenesis]. |
PRK13608 | PRK13608 | 2.11e-14 | 3 | 141 | 234 | 370 | diacylglycerol glucosyltransferase; Provisional |
PRK00726 | murG | 7.94e-13 | 28 | 142 | 236 | 357 | undecaprenyldiphospho-muramoylpentapeptide beta-N- acetylglucosaminyltransferase; Provisional |
PRK13609 | PRK13609 | 2.17e-12 | 8 | 150 | 238 | 379 | diacylglycerol glucosyltransferase; Provisional |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
ATP53616.1 | 3.61e-112 | 1 | 163 | 271 | 433 |
AZH69564.1 | 5.12e-112 | 1 | 163 | 271 | 433 |
QIA34715.1 | 1.12e-110 | 1 | 163 | 258 | 420 |
AEB07075.1 | 7.07e-79 | 1 | 163 | 276 | 438 |
QWT17007.1 | 7.55e-74 | 1 | 163 | 256 | 418 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q7U336 | 7.09e-10 | 17 | 139 | 224 | 353 | UDP-N-acetylglucosamine--N-acetylmuramyl-(pentapeptide) pyrophosphoryl-undecaprenol N-acetylglucosamine transferase OS=Haemophilus ducreyi (strain 35000HP / ATCC 700724) OX=233412 GN=murG PE=3 SV=1 |
Q1D0T0 | 1.60e-08 | 1 | 140 | 215 | 358 | UDP-N-acetylglucosamine--N-acetylmuramyl-(pentapeptide) pyrophosphoryl-undecaprenol N-acetylglucosamine transferase OS=Myxococcus xanthus (strain DK1622) OX=246197 GN=murG PE=3 SV=1 |
P54166 | 4.64e-07 | 15 | 147 | 241 | 379 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus subtilis (strain 168) OX=224308 GN=ugtP PE=1 SV=1 |
Q49WE6 | 6.35e-07 | 4 | 140 | 235 | 369 | 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 |
A8FED1 | 8.55e-07 | 4 | 132 | 234 | 361 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus pumilus (strain SAFR-032) OX=315750 GN=ugtP PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000060 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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