Species | Robinsoniella sp900539655 | |||||||||||
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Lineage | Bacteria; Firmicutes_A; Clostridia; Lachnospirales; Lachnospiraceae; Robinsoniella; Robinsoniella sp900539655 | |||||||||||
CAZyme ID | MGYG000000287_05723 | |||||||||||
CAZy Family | GT0 | |||||||||||
CAZyme Description | hypothetical protein | |||||||||||
CAZyme Property |
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Genome Property |
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Gene Location | Start: 1296; End: 2735 Strand: - |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
TIGR03590 | PseG | 1.05e-43 | 3 | 264 | 1 | 275 | UDP-2,4-diacetamido-2,4,6-trideoxy-beta-L-altropyranose hydrolase. This protein is found in association with enzymes involved in the biosynthesis of pseudaminic acid, a component of polysaccharide in certain Pseudomonas strains as well as a modification of flagellin in Campylobacter and Hellicobacter. The role of this protein is unclear, although it may participate in N-acetylation in conjunction with, or in the absence of PseH (TIGR03585) as it often scores above the trusted cutoff to pfam00583 representing a family of acetyltransferases. |
COG3980 | SpsG | 3.85e-25 | 3 | 278 | 2 | 275 | Spore coat polysaccharide biosynthesis protein SpsG, predicted glycosyltransferase [Cell wall/membrane/envelope biogenesis]. |
pfam00534 | Glycos_transf_1 | 0.002 | 223 | 296 | 71 | 145 | Glycosyl transferases group 1. Mutations in this domain of PIGA lead to disease (Paroxysmal Nocturnal haemoglobinuria). Members of this family transfer activated sugars to a variety of substrates, including glycogen, Fructose-6-phosphate and lipopolysaccharides. Members of this family transfer UDP, ADP, GDP or CMP linked sugars. The eukaryotic glycogen synthases may be distant members of this family. |
COG1519 | KdtA | 0.009 | 244 | 279 | 337 | 372 | 3-deoxy-D-manno-octulosonic-acid transferase [Cell wall/membrane/envelope biogenesis]. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
QRM70471.1 | 3.80e-139 | 1 | 477 | 1 | 481 |
CBW24212.1 | 8.63e-118 | 2 | 472 | 4 | 464 |
QUU04548.1 | 8.63e-118 | 2 | 472 | 4 | 464 |
QUT36299.1 | 4.95e-107 | 1 | 466 | 1 | 455 |
QBJ19933.1 | 3.06e-106 | 1 | 317 | 9 | 325 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
3HBM_A | 1.58e-10 | 3 | 272 | 2 | 267 | ChainA, UDP-sugar hydrolase [Campylobacter jejuni subsp. jejuni NCTC 11168 = ATCC 700819],3HBN_A Chain A, UDP-sugar hydrolase [Campylobacter jejuni subsp. jejuni NCTC 11168 = ATCC 700819] |
4XPK_A | 6.78e-09 | 334 | 472 | 17 | 151 | Thecrystal structure of Campylobacter jejuni N-acetyltransferase PseH [Campylobacter jejuni subsp. jejuni PT14],4XPL_A The crystal structure of Campylobacter jejuni N-acetyltransferase PseH in complex with acetyl coenzyme A [Campylobacter jejuni subsp. jejuni PT14] |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
Q58462 | 1.85e-20 | 3 | 460 | 2 | 467 | Uncharacterized protein MJ1062 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) OX=243232 GN=MJ1062 PE=1 SV=1 |
A1W0U6 | 4.44e-10 | 3 | 272 | 2 | 267 | UDP-2,4-diacetamido-2,4,6-trideoxy-beta-L-altropyranose hydrolase OS=Campylobacter jejuni subsp. jejuni serotype O:23/36 (strain 81-176) OX=354242 GN=pseG PE=3 SV=1 |
Q0P8U5 | 8.01e-10 | 3 | 272 | 2 | 267 | UDP-2,4-diacetamido-2,4,6-trideoxy-beta-L-altropyranose hydrolase OS=Campylobacter jejuni subsp. jejuni serotype O:2 (strain ATCC 700819 / NCTC 11168) OX=192222 GN=pseG PE=1 SV=1 |
Q0P8U4 | 2.09e-09 | 330 | 472 | 2 | 145 | Acetyltransferase PseH OS=Campylobacter jejuni subsp. jejuni serotype O:2 (strain ATCC 700819 / NCTC 11168) OX=192222 GN=pseH PE=3 SV=1 |
A1W0U7 | 1.79e-08 | 334 | 472 | 11 | 145 | Acetyltransferase PseH OS=Campylobacter jejuni subsp. jejuni serotype O:23/36 (strain 81-176) OX=354242 GN=pseH PE=3 SV=1 |
Other | SP_Sec_SPI | LIPO_Sec_SPII | TAT_Tat_SPI | TATLIP_Sec_SPII | PILIN_Sec_SPIII |
---|---|---|---|---|---|
1.000061 | 0.000000 | 0.000000 | 0.000000 | 0.000000 | 0.000000 |
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