Species | ||||||||||||
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Lineage | Bacteria; Firmicutes_A; Clostridia; UMGS1810; UMGS1810; ; | |||||||||||
CAZyme ID | MGYG000004439_00705 | |||||||||||
CAZy Family | GT28 | |||||||||||
CAZyme Description | Processive diacylglycerol beta-glucosyltransferase | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 27265; End: 28380 Strand: - |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT28 | 204 | 353 | 5.3e-27 | 0.9808917197452229 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
cd17507 | GT28_Beta-DGS-like | 2.08e-91 | 3 | 365 | 1 | 361 | 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 | 5.49e-56 | 2 | 365 | 6 | 367 | diacylglycerol glucosyltransferase; Provisional |
PLN02605 | PLN02605 | 1.95e-40 | 3 | 315 | 1 | 326 | monogalactosyldiacylglycerol synthase |
COG0707 | MurG | 1.00e-36 | 2 | 365 | 1 | 353 | UDP-N-acetylglucosamine:LPS N-acetylglucosamine transferase [Cell wall/membrane/envelope biogenesis]. |
PRK13608 | PRK13608 | 2.73e-33 | 2 | 359 | 7 | 361 | diacylglycerol glucosyltransferase; Provisional |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
QGT51146.1 | 4.35e-118 | 1 | 365 | 1 | 365 |
CDZ24104.1 | 1.01e-110 | 1 | 370 | 1 | 373 |
ADU27709.1 | 4.08e-110 | 1 | 364 | 1 | 367 |
AYF42976.1 | 4.08e-110 | 1 | 364 | 1 | 367 |
AYF40136.1 | 4.08e-110 | 1 | 364 | 1 | 367 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
4WYI_A | 1.43e-29 | 2 | 353 | 7 | 370 | 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 |
---|---|---|---|---|---|---|
A8FED1 | 6.73e-46 | 2 | 366 | 6 | 368 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus pumilus (strain SAFR-032) OX=315750 GN=ugtP PE=3 SV=1 |
A0R9F0 | 1.05e-45 | 2 | 366 | 6 | 368 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus thuringiensis (strain Al Hakam) OX=412694 GN=ugtP PE=3 SV=1 |
B7HU46 | 1.47e-45 | 2 | 364 | 6 | 366 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus cereus (strain AH187) OX=405534 GN=ugtP PE=3 SV=1 |
B9J2U2 | 1.47e-45 | 2 | 364 | 6 | 366 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus cereus (strain Q1) OX=361100 GN=ugtP PE=3 SV=1 |
Q73DZ5 | 4.02e-45 | 2 | 364 | 6 | 366 | Processive diacylglycerol beta-glucosyltransferase OS=Bacillus cereus (strain ATCC 10987 / NRS 248) OX=222523 GN=ugtP PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000038 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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