GapMind for catabolism of small carbon sources

 

Protein Ac3H11_2934 in Acidovorax sp. GW101-3H11

Annotation: FitnessBrowser__acidovorax_3H11:Ac3H11_2934

Length: 474 amino acids

Source: acidovorax_3H11 in FitnessBrowser

Candidate for 5 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-lysine catabolism ydiJ med D-2-hydroxyglutarate dehydrogenase (EC 1.1.99.39) (characterized) 38% 81% 308.5 Putative D-lactate dehydrogenase C713.03, mitochondrial; EC 1.1.2.4 35% 273.1
D-lactate catabolism D-LDH lo D-2-hydroxyglutarate--pyruvate transhydrogenase DLD2; D-2HG--pyruvate transhydrogenase DLD2; Actin-interacting protein 2; D-lactate dehydrogenase [cytochrome] 2, mitochondrial; D-lactate ferricytochrome C oxidoreductase; D-LCR; EC 1.1.99.40; EC 1.1.2.4 (characterized) 35% 88% 295.8 D-2-hydroxyglutarate dehydrogenase (EC 1.1.99.39) 38% 308.5
L-threonine catabolism D-LDH lo D-2-hydroxyglutarate--pyruvate transhydrogenase DLD2; D-2HG--pyruvate transhydrogenase DLD2; Actin-interacting protein 2; D-lactate dehydrogenase [cytochrome] 2, mitochondrial; D-lactate ferricytochrome C oxidoreductase; D-LCR; EC 1.1.99.40; EC 1.1.2.4 (characterized) 35% 88% 295.8 D-2-hydroxyglutarate dehydrogenase (EC 1.1.99.39) 38% 308.5
D-lactate catabolism glcD lo D-lactate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized) 31% 97% 193.7 D-2-hydroxyglutarate dehydrogenase (EC 1.1.99.39) 38% 308.5
L-threonine catabolism glcD lo D-lactate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized) 31% 97% 193.7 D-2-hydroxyglutarate dehydrogenase (EC 1.1.99.39) 38% 308.5

Sequence Analysis Tools

View Ac3H11_2934 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

Fitness BLAST: loading...

Sequence

MTTLLDTLRAIVGPTHVITEGDLTAWEQDWRRRVRGKALAVVRPANTQEVAAVVKACAAV
GTAIVPQGGNTGLAVGSTPDDSGTQIVLSLTRMNAVRSVDTDNLTMTVEAGCILQNLQDV
AQNAGVLFPLSLAAEGSCTIGGNLGTNAGGTQVVRYGNARDLCLGLEVVTAQGEVWDGLK
GLRKDNTGYDLRDLFIGSEGTLGIITAATMKLYPQPAANLTAWAAAPSMEHAVALLGLAH
KQLGAGLTGFEVMGQFALSLVGKHMPQLRVPFLGDDNAPWCVLLENSDSESEEHARARFE
SLLETAFEMGCVTDAVVAENLTQAHQLWHIRESIPLAQAEEGLNIKHDISIQISRIPAFV
AHTDAVLQREIPGVRLVNFGHLGDGNLHYNVQAPAAGDPKAFLREQEARVNHLVYEAVAE
FGGSFSAEHGIGELKADKLAKYQSPVALGMMRAIKQALDPQGVMNPGRVLGHPG

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

Links

Downloads

Related tools

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