GapMind for catabolism of small carbon sources

 

Protein WP_023431323.1 in Lutibaculum baratangense AMV1

Annotation: NCBI__GCF_000496075.1:WP_023431323.1

Length: 257 amino acids

Source: GCF_000496075.1 in NCBI

Candidate for 34 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
4-hydroxybenzoate catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
L-arginine catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
L-citrulline catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
L-isoleucine catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
L-lysine catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
phenylacetate catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
L-phenylalanine catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
L-proline catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
L-valine catabolism ech hi trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 AcuK 56% 284.6
4-hydroxybenzoate catabolism paaF med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 Enoyl-CoA hydratase [valine degradation] (EC 4.2.1.17) 62% 322.0
phenylacetate catabolism paaF med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 Enoyl-CoA hydratase [valine degradation] (EC 4.2.1.17) 62% 322.0
L-phenylalanine catabolism paaF med trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) (characterized) 65% 100% 327.4 Enoyl-CoA hydratase [valine degradation] (EC 4.2.1.17) 62% 322.0
4-hydroxybenzoate catabolism badK med BadK (characterized) 53% 100% 255.8 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
phenylacetate catabolism badK med BadK (characterized) 53% 100% 255.8 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-phenylalanine catabolism badK med BadK (characterized) 53% 100% 255.8 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-isoleucine catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 46% 100% 214.2 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
propionate catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 46% 100% 214.2 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-threonine catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 46% 100% 214.2 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-valine catabolism hpcD med 3-hydroxypropionyl-CoA dehydratase (EC 4.2.1.116) (characterized) 46% 100% 214.2 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-leucine catabolism liuC med methylglutaconyl-CoA hydratase (EC 4.2.1.18) (characterized) 41% 80% 175.3 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
phenylacetate catabolism paaG lo 2-(1,2-epoxy-1,2-dihydrophenyl)acetyl-CoA isomerase (EC 5.3.3.18) (characterized) 35% 96% 141 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-phenylalanine catabolism paaG lo 2-(1,2-epoxy-1,2-dihydrophenyl)acetyl-CoA isomerase (EC 5.3.3.18) (characterized) 35% 96% 141 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
phenylacetate catabolism paaZ1 lo Enoyl-CoA hydratase; EC 4.2.1.17 (characterized, see rationale) 34% 100% 135.6 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-phenylalanine catabolism paaZ1 lo Enoyl-CoA hydratase; EC 4.2.1.17 (characterized, see rationale) 34% 100% 135.6 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
4-hydroxybenzoate catabolism dch lo cyclohexa-1,5-dienecarbonyl-CoA hydratase monomer (EC 4.2.1.100) (characterized) 31% 100% 127.9 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
phenylacetate catabolism dch lo cyclohexa-1,5-dienecarbonyl-CoA hydratase monomer (EC 4.2.1.100) (characterized) 31% 100% 127.9 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-phenylalanine catabolism dch lo cyclohexa-1,5-dienecarbonyl-CoA hydratase monomer (EC 4.2.1.100) (characterized) 31% 100% 127.9 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
4-hydroxybenzoate catabolism badI lo BadI (characterized) 33% 98% 115.9 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
phenylacetate catabolism badI lo BadI (characterized) 33% 98% 115.9 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-phenylalanine catabolism badI lo BadI (characterized) 33% 98% 115.9 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-valine catabolism bch lo 3-hydroxyisobutyryl-CoA hydrolase, mitochondrial; 3-hydroxyisobutyryl-coenzyme A hydrolase; HIB-CoA hydrolase; HIBYL-CoA-H; EC 3.1.2.4 (characterized) 31% 58% 96.7 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
4-hydroxybenzoate catabolism oah lo 6-oxocyclohex-1-ene-1-carbonyl-CoA hydrolase; 6-OCH-CoA hydrolase; 6-oxocyclohex-1-ene-1-carbonyl-CoA hydratase; EC 3.7.1.21 (characterized) 31% 50% 67 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
phenylacetate catabolism oah lo 6-oxocyclohex-1-ene-1-carbonyl-CoA hydrolase; 6-OCH-CoA hydrolase; 6-oxocyclohex-1-ene-1-carbonyl-CoA hydratase; EC 3.7.1.21 (characterized) 31% 50% 67 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4
L-phenylalanine catabolism oah lo 6-oxocyclohex-1-ene-1-carbonyl-CoA hydrolase; 6-OCH-CoA hydrolase; 6-oxocyclohex-1-ene-1-carbonyl-CoA hydratase; EC 3.7.1.21 (characterized) 31% 50% 67 trans-2,3-dehydroadipyl-CoA hydratase (EC 4.2.1.17) 65% 327.4

Sequence Analysis Tools

View WP_023431323.1 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

MAYECITAETRGTTGLIRLDRPKAMNALNARLISELNGAVDGFEEDPHVRCIVITGSEKA
FAAGADIKEMQGKTFVQAYREDFIAEWERLSRARKPVIAAVAGYALGGGCELAMMCDFII
AAENAKFGQPEITLGIIPGAGGTQRLIRAIGKAKAMDMILTGRVMDAREAERSGLVSRVV
PVGELVDTALEAAERIGDLSMPALMMAKEAVNSAHETTLSEGCRLERRLFHSLFATEDQK
EGMKAFAEKRTPQFRHR

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