Species | Pauljensenia sp000411415 | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Bacteria; Actinobacteriota; Actinomycetia; Actinomycetales; Actinomycetaceae; Pauljensenia; Pauljensenia sp000411415 | |||||||||||
CAZyme ID | MGYG000001441_01551 | |||||||||||
CAZy Family | GT1 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 559609; End: 560763 Strand: - |
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT1 | 49 | 382 | 1.6e-22 | 0.8769633507853403 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
COG1819 | YjiC | 2.13e-21 | 1 | 383 | 2 | 399 | UDP:flavonoid glycosyltransferase YjiC, YdhE family [Carbohydrate transport and metabolism]. |
cd03784 | GT1_Gtf-like | 6.01e-20 | 1 | 382 | 1 | 404 | UDP-glycosyltransferases and similar proteins. This family includes the Gtfs, a group of homologous glycosyltransferases involved in the final stages of the biosynthesis of antibiotics vancomycin and related chloroeremomycin. Gtfs transfer sugar moieties from an activated NDP-sugar donor to the oxidatively cross-linked heptapeptide core of vancomycin group antibiotics. The core structure is important for the bioactivity of the antibiotics. |
TIGR00661 | MJ1255 | 1.00e-05 | 115 | 331 | 89 | 294 | conserved hypothetical protein. This model represents nearly the full length of MJ1255 from Methanococcus jannaschii and of an unpublished protein from Vibrio cholerae, as well as the C-terminal half of a protein from Methanobacterium thermoautotrophicum. A small region (~50 amino acids) within the domain appears related to a family of sugar transferases. [Hypothetical proteins, Conserved] |
pfam13579 | Glyco_trans_4_4 | 0.002 | 15 | 191 | 1 | 143 | Glycosyl transferase 4-like domain. |
cd03801 | GT4_PimA-like | 0.003 | 2 | 383 | 1 | 365 | phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). 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. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the 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. The members of this family are found mainly in certain bacteria and archaea. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
QCT36430.1 | 2.01e-245 | 8 | 383 | 1 | 376 |
QGS11935.1 | 5.25e-241 | 8 | 384 | 1 | 377 |
AHF25143.1 | 3.01e-123 | 1 | 383 | 13 | 405 |
BAR06867.1 | 7.22e-92 | 1 | 384 | 1 | 384 |
BAR05900.1 | 2.34e-90 | 1 | 377 | 29 | 410 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
3OTG_A | 3.74e-10 | 109 | 377 | 120 | 401 | CrystalStructure of CalG1, Calicheamicin Glycostyltransferase, TDP bound form [Micromonospora echinospora],3OTH_A Crystal Structure of CalG1, Calicheamicin Glycostyltransferase, TDP and calicheamicin alpha3I bound form [Micromonospora echinospora],3OTH_B Crystal Structure of CalG1, Calicheamicin Glycostyltransferase, TDP and calicheamicin alpha3I bound form [Micromonospora echinospora] |
4RIG_A | 4.44e-08 | 24 | 383 | 20 | 373 | ChimericGlycosyltransferase LanGT2S8Ac [Streptomyces fradiae],4RIG_B Chimeric Glycosyltransferase LanGT2S8Ac [Streptomyces fradiae],4RIH_A Chimeric Glycosyltransferase LanGT2S8Ac, carbasugar substrate complex [Streptomyces cyanogenus],4RIH_B Chimeric Glycosyltransferase LanGT2S8Ac, carbasugar substrate complex [Streptomyces cyanogenus],4RII_A Chimeric Glycosyltransferase LanGT2S8Ac, TDP complex [Streptomyces cyanogenus],4RII_B Chimeric Glycosyltransferase LanGT2S8Ac, TDP complex [Streptomyces cyanogenus] |
4RIE_A | 1.39e-07 | 24 | 383 | 20 | 373 | LandomycinGlycosyltransferase LanGT2 [Streptomyces cyanogenus],4RIE_B Landomycin Glycosyltransferase LanGT2 [Streptomyces cyanogenus],4RIF_A Landomycin Glycosyltransferase LanGT2, carbasugar substrate complex [Streptomyces cyanogenus],4RIF_B Landomycin Glycosyltransferase LanGT2, carbasugar substrate complex [Streptomyces cyanogenus] |
6KQW_A | 3.34e-07 | 281 | 380 | 282 | 382 | ChainA, Uncharacterized UDP-glucosyltransferase YjiC [Bacillus subtilis subsp. subtilis str. 168] |
6KQX_A | 3.38e-07 | 281 | 380 | 282 | 382 | ChainA, Uncharacterized UDP-glucosyltransferase YjiC [Bacillus subtilis subsp. subtilis str. 168],7BOV_A Chain A, Uncharacterized UDP-glucosyltransferase YjiC [Bacillus subtilis subsp. subtilis str. 168] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
O34539 | 1.85e-06 | 281 | 380 | 282 | 382 | NDP-glycosyltransferase YjiC OS=Bacillus subtilis (strain 168) OX=224308 GN=yjiC PE=1 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000032 | 0.000006 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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