GapMind for catabolism of small carbon sources

 

Protein WP_089136840.1 in Lactobacillus silagei IWT126

Annotation: NCBI__GCF_002217945.1:WP_089136840.1

Length: 256 amino acids

Source: GCF_002217945.1 in NCBI

Candidate for 15 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-alanine catabolism braF lo NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) 34% 89% 121.3 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-isoleucine catabolism natA lo NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) 34% 89% 121.3 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-leucine catabolism natA lo NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) 34% 89% 121.3 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-proline catabolism natA lo NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) 34% 89% 121.3 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-serine catabolism braF lo NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) 34% 89% 121.3 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-threonine catabolism braF lo NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) 34% 89% 121.3 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-valine catabolism natA lo NatA, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) 34% 89% 121.3 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-arginine catabolism braF lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 32% 82% 119 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-glutamate catabolism braF lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 32% 82% 119 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-histidine catabolism braF lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 32% 82% 119 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-isoleucine catabolism livG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 32% 82% 119 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-leucine catabolism livG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 32% 82% 119 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-valine catabolism livG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 32% 82% 119 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
D-alanine catabolism AZOBR_RS08245 lo Leucine/isoleucine/valine ABC transporter,ATPase component; EC 3.6.3.- (characterized, see rationale) 32% 87% 115.5 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7
L-proline catabolism AZOBR_RS08245 lo Leucine/isoleucine/valine ABC transporter,ATPase component; EC 3.6.3.- (characterized, see rationale) 32% 87% 115.5 Phosphonates import ATP-binding protein PhnC; EC 7.3.2.2 41% 198.7

Sequence Analysis Tools

View WP_089136840.1 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

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Sequence

MLTVNHLAKSYDGEKKSLTDVSFSVRSGEVTVIIGPSGAGKTTILRSINQLIRDDEGEIL
FDQIDMRQLNRVQLRRARSHIGMIFQSYNLIEPLTAIENVLHGCLGTKSNFAGIFSIYNN
REKEEALKLLQKVGLEEFAYQQCRNLSGGQKQRVGIARALMQHPKIILCDEPIASLDPKS
TITVMDILRGLAVNDGISVLINLHQVDIAREYADHVIGINNGQVVFDDRTQALSDAAITG
IYRKNANLEGSLVHES

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