GapMind for catabolism of small carbon sources

 

Protein WP_085545426.1 in Dethiosulfovibrio salsuginis USBA 82

Annotation: NCBI__GCF_900177735.1:WP_085545426.1

Length: 321 amino acids

Source: GCF_900177735.1 in NCBI

Candidate for 7 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
putrescine catabolism potA med PotG aka B0855, component of Putrescine porter (characterized) 42% 82% 244.6 CP4-6 prophage; ABC transporter ATP-binding protein AfuC 48% 249.6
L-arabinose catabolism xacJ med Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) 43% 71% 220.3 CP4-6 prophage; ABC transporter ATP-binding protein AfuC 48% 249.6
L-histidine catabolism hutV lo HutV aka HISV aka R02702 aka SMC00670, component of Uptake system for hisitidine, proline, proline-betaine and glycine-betaine (characterized) 37% 88% 170.2 CP4-6 prophage; ABC transporter ATP-binding protein AfuC 48% 249.6
L-proline catabolism hutV lo HutV aka HISV aka R02702 aka SMC00670, component of Uptake system for hisitidine, proline, proline-betaine and glycine-betaine (characterized) 37% 88% 170.2 CP4-6 prophage; ABC transporter ATP-binding protein AfuC 48% 249.6
D-glucosamine (chitosamine) catabolism AO353_21725 lo ABC transporter for D-glucosamine, ATPase component (characterized) 35% 92% 152.5 CP4-6 prophage; ABC transporter ATP-binding protein AfuC 48% 249.6
L-serine catabolism Ac3H11_1692 lo ABC transporter ATP-binding protein (characterized, see rationale) 34% 97% 117.5 CP4-6 prophage; ABC transporter ATP-binding protein AfuC 48% 249.6
L-tyrosine catabolism Ac3H11_1692 lo ABC transporter ATP-binding protein (characterized, see rationale) 34% 97% 117.5 CP4-6 prophage; ABC transporter ATP-binding protein AfuC 48% 249.6

Sequence Analysis Tools

View WP_085545426.1 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

MYLELRGLNKSFQGSRAVKDLSLTVEQGEMISLLGPSGCGKTTTLKMIGGFCLPDSGNIV
LEGEDITSMAPEGRPTATVFQSYALFPHMSVMGNVTYGLKFKGIHKDRRTSMGREMLEKV
GLPGSGNKGIHQLSGGEQQRVALARSLMIQPKVLLLDEPLSNLDAKLRVKMRAEIRRIQR
ELGITAVYVTHDQEEAMALSDRIAVMEKGSIVQIGTPREVYGEPSTPFVADFIGRSNVIL
SPEGYISVHPEDVVISDEKGDMEGIITDRQYKGAMTTYFIVVGELELEADLPSRSNQTWE
KGSMVRVSFIGPHTLRRESNG

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