GapMind for catabolism of small carbon sources

 

Protein 350994 in Bacteroides thetaiotaomicron VPI-5482

Annotation: FitnessBrowser__Btheta:350994

Length: 238 amino acids

Source: Btheta in FitnessBrowser

Candidate for 16 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-asparagine catabolism bgtA med ATPase (characterized, see rationale) 41% 79% 146 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
L-aspartate catabolism bgtA med ATPase (characterized, see rationale) 41% 79% 146 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
D-maltose catabolism thuK lo ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) 42% 60% 144.8 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
sucrose catabolism thuK lo ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) 42% 60% 144.8 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
trehalose catabolism thuK lo ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) 42% 60% 144.8 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
D-maltose catabolism malK lo ABC-type maltose transporter (subunit 3/3) (EC 7.5.2.1) (characterized) 40% 57% 140.2 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
xylitol catabolism Dshi_0546 lo ABC transporter for Xylitol, ATPase component (characterized) 38% 64% 139 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
L-proline catabolism opuBA lo BusAA, component of Uptake system for glycine-betaine (high affinity) and proline (low affinity) (OpuAA-OpuABC) or BusAA-ABC of Lactococcus lactis). BusAA, the ATPase subunit, has a C-terminal tandem cystathionine β-synthase (CBS) domain which is the cytoplasmic K+ sensor for osmotic stress (osmotic strength)while the BusABC subunit has the membrane and receptor domains fused to each other (Biemans-Oldehinkel et al., 2006; Mahmood et al., 2006; Gul et al. 2012). An N-terminal amphipathic α-helix of OpuA is necessary for high activity but is not critical for biogenesis or the ionic regulation of transport (characterized) 36% 54% 136.3 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
N-acetyl-D-glucosamine catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 39% 62% 136 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
D-glucosamine (chitosamine) catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 39% 62% 136 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
L-arabinose catabolism xacJ lo Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) 37% 54% 132.9 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
glycerol catabolism glpT lo GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized) 34% 57% 119.4 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
L-histidine catabolism hutV lo ABC transporter for L-Histidine, ATPase component (characterized) 32% 86% 119 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
citrate catabolism fecE lo iron(III) dicitrate transport ATP-binding protein FecE (characterized) 31% 85% 115.9 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
D-mannose catabolism TM1749 lo TM1749, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized) 33% 73% 114.8 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1
glycerol catabolism glpS lo GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized) 34% 53% 104 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 46% 211.1

Sequence Analysis Tools

View 350994 at FitnessBrowser

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

Find the best match in UniProt

Compare to protein structures

Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

Find homologs in fast.genomics

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Sequence

MIKTEKLSMLFTTEEVQTKALNEVTLHVEQGEFVAIMGPSGCGKSTLLNILGTLDSPTSG
SYFFEGKQVDKMNENQLTALRKNNLGFIFQSFNLIDELTVYENVELPLVYMGIKTAQRKE
KVNKVLEKVNLLHRANHYPQQLSGGQQQRVAIARAVVTDCKLLLADEPTGNLDSVNGVEV
MELLSELNRQGTTIIIVTHSQRDATYAHRIIRLLDGQIVSENINRPLEKSTSSKNEAV

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory