Protein WP_017177453.1 in Actinomyces timonensis 7400942
Annotation: NCBI__GCF_000295095.1:WP_017177453.1
Length: 300 amino acids
Source: GCF_000295095.1 in NCBI
Candidate for 13 steps in catabolism of small carbon sources
Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
L-histidine catabolism | Ac3H11_2560 | med | ABC transporter for L-Histidine, ATPase component (characterized) | 42% | 90% | 186.8 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
D-sorbitol (glucitol) catabolism | mtlK | lo | ABC transporter for D-Sorbitol, ATPase component (characterized) | 40% | 68% | 153.3 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
N-acetyl-D-glucosamine catabolism | SMc02869 | lo | N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) | 39% | 68% | 151 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
D-glucosamine (chitosamine) catabolism | SMc02869 | lo | N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) | 39% | 68% | 151 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
D-maltose catabolism | thuK | lo | ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) | 40% | 63% | 150.2 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
sucrose catabolism | thuK | lo | ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) | 40% | 63% | 150.2 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
trehalose catabolism | malK | lo | MsmK aka SMU.882, component of The raffinose/stachyose transporter, MsmEFGK (MalK (3.A.1.1.27) can probably substitute for MsmK; Webb et al., 2008). This system may also transport melibiose, isomaltotriose and sucrose as well as isomaltosaccharides (characterized) | 39% | 60% | 148.7 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
D-maltose catabolism | aglK | lo | ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) | 40% | 59% | 147.9 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
sucrose catabolism | aglK | lo | ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) | 40% | 59% | 147.9 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
trehalose catabolism | aglK | lo | ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) | 40% | 59% | 147.9 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
L-arabinose catabolism | xacJ | lo | Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) | 40% | 52% | 147.5 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
L-arabinose catabolism | xacK | lo | Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale) | 38% | 52% | 140.2 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
trehalose catabolism | treV | lo | TreV, component of Trehalose porter (characterized) | 39% | 65% | 140.2 | Nitrate import ATP-binding protein NrtC; EC 7.3.2.4 | 46% | 206.8 |
Sequence Analysis Tools
View WP_017177453.1 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
MTKNATSAPAAPDPGSTTSTAERPRGAEVALTGVTHRYPLHHELDHGWVPWAIRQVSPAA
RARYEAEAAKGSSLHVLDDVTLTIPPGQFVAVVGQSGCGKSTILRLLAGLETPSQGSVVV
DGERITRPAPERAMAFQDATLLPWRTVRDNVALGPQARGRLAIDQRRIDAALEIVGLRDF
AGAYPSTLSGGMAQRAALARALVNRPRLFLLDEPFGKLDALTRLGLQDEFARLWSSQAFT
AILVTHDVDEALRLAERVVVLSERPAHVVADLEVPAALADAPASTEYQDLKARILALLGR
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:
- ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
- HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.
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:
- ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
- ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
- HMMer finds a hit (regardless of coverage or other bits).
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:
- our ignorance of proteins' functions,
- omissions in the gene models,
- frame-shift errors in the genome sequence, or
- the organism lacks the pathway.
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