GapMind for catabolism of small carbon sources

 

Protein WP_012585753.1 in Thauera aminoaromatica S2

Annotation: NCBI__GCF_000310185.1:WP_012585753.1

Length: 236 amino acids

Source: GCF_000310185.1 in NCBI

Candidate for 8 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
D-sorbitol (glucitol) catabolism sdh med L-iditol 2-dehydrogenase (EC 1.1.1.14) (characterized) 42% 94% 162.5 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6
ethanol catabolism etoh-dh-nad lo alcohol dehydrogenase (EC 1.1.1.1) (characterized) 37% 98% 133.7 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6
D-galactose catabolism galdh lo Probable galactose dehydrogenase GalD; EC 1.1.1.- (characterized) 34% 96% 128.3 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6
lactose catabolism galdh lo Probable galactose dehydrogenase GalD; EC 1.1.1.- (characterized) 34% 96% 128.3 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6
L-arabinose catabolism xacB lo L-arabinose 1-dehydrogenase (EC 1.1.1.46) (characterized) 30% 96% 122.5 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6
D-xylose catabolism xdh lo D-xylose 1-dehydrogenase (EC 1.1.1.175) (characterized) 34% 94% 117.5 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6
D-sorbitol (glucitol) catabolism srlD lo Sorbitol-6-phosphate 2-dehydrogenase; EC 1.1.1.140; Glucitol-6-phosphate dehydrogenase; Ketosephosphate reductase (uncharacterized) 31% 97% 106.3 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6
L-isoleucine catabolism ivdG lo 3-hydroxyacyl-CoA dehydrogenase type-2; 17-beta-hydroxysteroid dehydrogenase 10; 17-beta-HSD 10; 3-hydroxy-2-methylbutyryl-CoA dehydrogenase; 3-hydroxyacyl-CoA dehydrogenase type II; Mitochondrial ribonuclease P protein 2; Mitochondrial RNase P protein 2; Scully protein; Type II HADH; EC 1.1.1.35; EC 1.1.1.51; EC 1.1.1.178 (characterized) 31% 98% 103.2 Acetoacetyl-CoA reductase; EC 1.1.1.36 43% 182.6

Sequence Analysis Tools

View WP_012585753.1 at NCBI

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

MGFSGELAGKVAIVTGGARGIGRTITDALVASGARVHVFDMTDSNESAGVLHRVNVADAQ
SVADAVAQLPEPATLLVNNAGITRDRSLLKMSDEEWRSVLDVNLSGAFHMLRACAPGMIA
AGRGRVVNITSINGLRGKFGQANYTAAKAGMIGLTKTAARELGPKGITVNAVAPGMVMTE
MARALPAEVLERALQESVMRELATPDDIAAAVVFLLSDMARMITGEVIRVDAGQYV

This GapMind analysis is from Sep 24 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