GapMind for catabolism of small carbon sources

 

Protein WP_036258213.1 in Methylocapsa aurea KYG

Annotation: NCBI__GCF_000746085.1:WP_036258213.1

Length: 477 amino acids

Source: GCF_000746085.1 in NCBI

Candidate for 18 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine catabolism gabD lo succinate-semialdehyde dehydrogenase [NAD(P)+]; EC 1.2.1.16 (characterized) 38% 99% 304.3 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
L-citrulline catabolism gabD lo succinate-semialdehyde dehydrogenase [NAD(P)+]; EC 1.2.1.16 (characterized) 38% 99% 304.3 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
putrescine catabolism gabD lo succinate-semialdehyde dehydrogenase [NAD(P)+]; EC 1.2.1.16 (characterized) 38% 99% 304.3 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
4-hydroxybenzoate catabolism ald-dh-CoA lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
2'-deoxyinosine catabolism ald-dh-CoA lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
2-deoxy-D-ribose catabolism ald-dh-CoA lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
ethanol catabolism ald-dh-CoA lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
ethanol catabolism etoh-dh-nad lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
L-threonine catabolism ald-dh-CoA lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
thymidine catabolism ald-dh-CoA lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
L-tryptophan catabolism ald-dh-CoA lo alcohol dehydrogenase [NAD(P)+] (EC 1.1.1.71); acetaldehyde dehydrogenase (acetylating) (EC 1.2.1.10) (characterized) 38% 52% 291.6 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
4-hydroxybenzoate catabolism adh lo aldehyde-alcohol dehydrogenase; EC 1.1.1.1; EC 1.2.1.10 (characterized) 36% 51% 270.8 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
2'-deoxyinosine catabolism adh lo aldehyde-alcohol dehydrogenase; EC 1.1.1.1; EC 1.2.1.10 (characterized) 36% 51% 270.8 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
2-deoxy-D-ribose catabolism adh lo aldehyde-alcohol dehydrogenase; EC 1.1.1.1; EC 1.2.1.10 (characterized) 36% 51% 270.8 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
ethanol catabolism adh lo aldehyde-alcohol dehydrogenase; EC 1.1.1.1; EC 1.2.1.10 (characterized) 36% 51% 270.8 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
L-threonine catabolism adh lo aldehyde-alcohol dehydrogenase; EC 1.1.1.1; EC 1.2.1.10 (characterized) 36% 51% 270.8 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
thymidine catabolism adh lo aldehyde-alcohol dehydrogenase; EC 1.1.1.1; EC 1.2.1.10 (characterized) 36% 51% 270.8 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4
L-tryptophan catabolism adh lo aldehyde-alcohol dehydrogenase; EC 1.1.1.1; EC 1.2.1.10 (characterized) 36% 51% 270.8 2-hydroxyethyl-CoM 2-dehydrogenase 70% 649.4

Sequence Analysis Tools

View WP_036258213.1 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

METLTKAPAVVPAEDEARCEIEAMVGRARVAQAAIEHYAQEEADALVTAVGWQVYKSREA
LAKLAVEEGGFGNVQDKVAKFANRVMGTLTDMASIKTCGVVEEDPARGLIKIAKPVGVIA
ALIPTTGPDATPPVKALGALKARNAIIIAPHPRTRKTSAAVVEVMRKGCLQVGAPADLIQ
VIERPSIAKTELLMRMSDLIVATGGAGMVKAAYSSGTPAYGVGVGNAVHVVDETADLDDA
AQMIANAKTFDYATSCLADNSVAAHSSIYEALKRKLVERGGHVCAPAEKARLQAAMWPKG
EHIPSIEVVAKSAARIAELAGIELAPDRTFLMVEEDGVGEAHPFSGEKLSVVLALYRYSG
GIDGAVDLVNRITSYQGAGHTCGIHSSRDDHVRTLAFGTRTARVIVNQSLNEGAGSVRNG
LPYTLSLSCGTWGGNITTENVNVRHFVNLTWVSRPVAPRRVAPEEVFGVHWLKYGNE

This GapMind analysis is from Apr 09 2024. 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