GapMind for catabolism of small carbon sources

 

Protein WP_108401500.1 in Limnohabitans curvus MWH-C5

Annotation: NCBI__GCF_003063475.1:WP_108401500.1

Length: 258 amino acids

Source: GCF_003063475.1 in NCBI

Candidate for 28 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
4-hydroxybenzoate catabolism badK hi BadK (characterized) 74% 100% 382.5 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 63% 334.3
phenylacetate catabolism badK hi BadK (characterized) 74% 100% 382.5 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 63% 334.3
L-phenylalanine catabolism badK hi BadK (characterized) 74% 100% 382.5 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 63% 334.3
4-hydroxybenzoate catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
4-hydroxybenzoate catabolism paaF med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-arginine catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-citrulline catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-isoleucine catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-lysine catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
phenylacetate catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
phenylacetate catabolism paaF med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-phenylalanine catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-phenylalanine catabolism paaF med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-proline catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-valine catabolism ech med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 63% 100% 334.3 BadK 74% 382.5
L-isoleucine catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 43% 99% 198.4 BadK 74% 382.5
propionate catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 43% 99% 198.4 BadK 74% 382.5
L-threonine catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 43% 99% 198.4 BadK 74% 382.5
L-valine catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 43% 99% 198.4 BadK 74% 382.5
phenylacetate catabolism paaG med 2-(1,2-epoxy-1,2-dihydrophenyl)acetyl-CoA isomerase (EC 5.3.3.18) (characterized) 41% 99% 155.6 BadK 74% 382.5
L-phenylalanine catabolism paaG med 2-(1,2-epoxy-1,2-dihydrophenyl)acetyl-CoA isomerase (EC 5.3.3.18) (characterized) 41% 99% 155.6 BadK 74% 382.5
L-leucine catabolism liuC lo Methylglutaconyl-CoA hydratase, mitochondrial; AU-specific RNA-binding enoyl-CoA hydratase; AU-binding enoyl-CoA hydratase; muAUH; Itaconyl-CoA hydratase; EC 4.2.1.18; EC 4.2.1.56 (characterized) 39% 82% 151 BadK 74% 382.5
4-hydroxybenzoate catabolism badI lo BadI (characterized) 34% 98% 120.6 BadK 74% 382.5
phenylacetate catabolism badI lo BadI (characterized) 34% 98% 120.6 BadK 74% 382.5
L-phenylalanine catabolism badI lo BadI (characterized) 34% 98% 120.6 BadK 74% 382.5
phenylacetate catabolism paaZ1 lo Enoyl-CoA hydratase; EC 4.2.1.17 (characterized, see rationale) 32% 97% 118.2 BadK 74% 382.5
L-phenylalanine catabolism paaZ1 lo Enoyl-CoA hydratase; EC 4.2.1.17 (characterized, see rationale) 32% 97% 118.2 BadK 74% 382.5
L-valine catabolism bch lo 3-hydroxyisobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized) 32% 51% 90.5 BadK 74% 382.5

Sequence Analysis Tools

View WP_108401500.1 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

MSQPTVLSERQGRVGVLTLNRPEQLNALNDTLMDALGAALLALDADDGIGAIVITGSDKA
FAAGADIAAMADWGYMDVFSSAFITRNWETIRQVRKPVIAAVAGFAMGGGCELALACDLI
VAAESAKFALPEVKLAMLPGAGGTQRLPRAIGKAKAMDMCLSARMLSAEEADRYGLVSRV
VPSDALMAETLKLANTIAGFSLPALIAIKESVNRAWEGSLTEGVKFERHALYARFASADA
HEGMHAFLEKRKPTFQHC

This GapMind analysis is from Sep 24 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