Species | Collinsella sp900760215 | |||||||||||
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Lineage | Bacteria; Actinobacteriota; Coriobacteriia; Coriobacteriales; Coriobacteriaceae; Collinsella; Collinsella sp900760215 | |||||||||||
CAZyme ID | MGYG000003209_01498 | |||||||||||
CAZy Family | GT28 | |||||||||||
CAZyme Description | Processive diacylglycerol beta-glucosyltransferase | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 8884; End: 10185 Strand: + |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT28 | 256 | 388 | 1.5e-20 | 0.8343949044585988 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
cd17507 | GT28_Beta-DGS-like | 9.32e-47 | 33 | 403 | 1 | 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. |
PRK13609 | PRK13609 | 5.28e-33 | 158 | 420 | 124 | 379 | diacylglycerol glucosyltransferase; Provisional |
PRK13608 | PRK13608 | 1.16e-25 | 160 | 411 | 126 | 370 | diacylglycerol glucosyltransferase; Provisional |
COG0707 | MurG | 2.44e-23 | 136 | 412 | 91 | 357 | UDP-N-acetylglucosamine:LPS N-acetylglucosamine transferase [Cell wall/membrane/envelope biogenesis]. |
cd03785 | GT28_MurG | 6.65e-17 | 198 | 403 | 146 | 348 | undecaprenyldiphospho-muramoylpentapeptide beta-N-acetylglucosaminyltransferase. MurG (EC 2.4.1.227) is an N-acetylglucosaminyltransferase, the last enzyme involved in the intracellular phase of peptidoglycan biosynthesis. It transfers N-acetyl-D-glucosamine (GlcNAc) from UDP-GlcNAc to the C4 hydroxyl of a lipid-linked N-acetylmuramoyl pentapeptide (NAM). The resulting disaccharide is then transported across the cell membrane, where it is polymerized into NAG-NAM cell-wall repeat structure. MurG belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic 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. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
ATP53616.1 | 7.58e-304 | 1 | 433 | 1 | 433 |
QIA34715.1 | 1.04e-300 | 14 | 433 | 1 | 420 |
AZH69564.1 | 1.20e-300 | 1 | 433 | 1 | 433 |
QWT17007.1 | 4.07e-212 | 28 | 433 | 13 | 418 |
AEB07075.1 | 1.38e-210 | 30 | 433 | 35 | 438 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
4WYI_A | 2.66e-09 | 33 | 421 | 8 | 395 | 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 |
---|---|---|---|---|---|---|
Q65IA4 | 1.43e-22 | 163 | 408 | 129 | 367 | 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 |
A8FED1 | 3.05e-21 | 158 | 402 | 124 | 361 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus pumilus (strain SAFR-032) OX=315750 GN=ugtP PE=3 SV=1 |
P54166 | 5.56e-21 | 158 | 417 | 124 | 379 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus subtilis (strain 168) OX=224308 GN=ugtP PE=1 SV=1 |
A0R9F0 | 7.45e-19 | 158 | 408 | 124 | 367 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus thuringiensis (strain Al Hakam) OX=412694 GN=ugtP PE=3 SV=1 |
Q49WE6 | 7.65e-19 | 160 | 410 | 126 | 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 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000052 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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