GapMind for catabolism of small carbon sources

 

Protein WP_085544084.1 in Dethiosulfovibrio salsuginis USBA 82

Annotation: NCBI__GCF_900177735.1:WP_085544084.1

Length: 447 amino acids

Source: GCF_900177735.1 in NCBI

Candidate for 4 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-tryptophan catabolism tnaT lo High affinity tryptophan:Na+ symporter, TnaT, of 501 aas and 12 TMSs (Androutsellis-Theotokis et al., 2003). The Km for Tryptophan is 145 nM; tryptamine and serotonin weakly inhibited with Ki values of 200 and 440 μM, respectively. An evolutionarily conserved role of adjacent transmembrane segments 7 and 8 has been proposed (characterized) 31% 90% 219.5 Neurotransmitter:sodium symporter of 455 aas, MhsT 49% 424.5
L-tyrosine catabolism tyt1 lo The 11 TMS Na+-dependent tyrosine transporter, Tyt1 (characterized) 34% 99% 215.7 Neurotransmitter:sodium symporter of 455 aas, MhsT 49% 424.5
L-alanine catabolism metP lo Transporter, component of The methionine/alanine uptake porter, MetPS (Trotschel et al., 2008) (MetP is the transporter; MetS is an essential auxiliary subunit) (characterized) 34% 78% 213 Neurotransmitter:sodium symporter of 455 aas, MhsT 49% 424.5
L-leucine catabolism leuT lo The amino acid (leucine):2 Na+ symporter, LeuTAa (Yamashita et al., 2005). LeuT possesses two ion binding sites, NA1 and NA2, both highly specific for Na+ but with differing mechanisms of binding (Noskov and Roux, 2008). X-ray structures have been determined for LeuT in substrate-free outward-open and apo inward-open states (characterized) 32% 90% 196.8 Neurotransmitter:sodium symporter of 455 aas, MhsT 49% 424.5

Sequence Analysis Tools

View WP_085544084.1 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

MANQVGQEREQWGSKIGFILAAAGSAVGLGNIWKFPYVTGTNGGGAFVLIYVLMVACIGF
SVMLAELVIGRRAQLNAVGSFEKIKGGAWPMVGWLGLACGFLILSYYGVVGGWTIKYILH
SFTGLMEIAGAGNAGEAFGGFISNPVMVVLYQAIFMFSVIWVVYRGVGEGIERYCKILMP
ALFILMIILIGRSVTLEGAGAGIEFYLKPDFSKVTAGTVLAALGQAFFSLSLGMGCMITY
GSYLQKDISLPGAAAQVCFLDTLVALLAGLVVFPAVFAFGVEPGAGPGLTFITLPGIFSK
MPGGMMWSGLFFLLLFVAALTSAISLLEVACSYFIDKGWTRAKAAWTMGTLIFLLGIPSA
ISLGGGLKIGGKDFIDAAGFMTDQIMMPIGGLLICVFVGWVIKDIAKEELTNNGKLPLFA
GFDAWVMFVKFVAPLSILYIFITGLKW

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