Protein WP_110804240.1 in Rhodobacter viridis JA737
Annotation: NCBI__GCF_003217355.1:WP_110804240.1
Length: 356 amino acids
Source: GCF_003217355.1 in NCBI
Candidate for 10 steps in catabolism of small carbon sources
| Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
|---|
| D-fructose catabolism | frcC | hi | Fructose import permease protein FrcC (characterized) | 73% | 97% | 503.8 | Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR | 35% | 182.2 |
| D-mannose catabolism | frcC | hi | Fructose import permease protein FrcC (characterized) | 73% | 97% | 503.8 | Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR | 35% | 182.2 |
| D-ribose catabolism | frcC | hi | Fructose import permease protein FrcC (characterized) | 73% | 97% | 503.8 | Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR | 35% | 182.2 |
| sucrose catabolism | frcC | hi | Fructose import permease protein FrcC (characterized) | 73% | 97% | 503.8 | Putative beta-xyloside ABC transporter, permease component, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR | 35% | 182.2 |
| L-fucose catabolism | HSERO_RS05255 | lo | ABC-type sugar transport system, permease component protein (characterized, see rationale) | 34% | 99% | 191 | Fructose import permease protein FrcC | 73% | 503.8 |
| xylitol catabolism | PS417_12060 | lo | ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale) | 34% | 99% | 191 | Fructose import permease protein FrcC | 73% | 503.8 |
| D-mannose catabolism | HSERO_RS03645 | lo | ABC-type sugar transport system, permease component protein (characterized, see rationale) | 36% | 92% | 182.2 | Fructose import permease protein FrcC | 73% | 503.8 |
| D-ribose catabolism | rbsC | lo | ABC-type transporter, integral membrane subunit, component of D-ribose porter (Nanavati et al., 2006). Induced by ribose (characterized) | 34% | 92% | 162.9 | Fructose import permease protein FrcC | 73% | 503.8 |
| myo-inositol catabolism | PS417_11895 | lo | m-Inositol ABC transporter, permease component (iatP) (characterized) | 32% | 97% | 161.8 | Fructose import permease protein FrcC | 73% | 503.8 |
| L-rhamnose catabolism | rhaP | lo | RhaP, component of Rhamnose porter (Richardson et al., 2004) (Transport activity is dependent on rhamnokinase (RhaK; AAQ92412) activity (Richardson and Oresnik, 2007) This could be an example of group translocation!) (characterized) | 30% | 89% | 137.5 | Fructose import permease protein FrcC | 73% | 503.8 |
Sequence Analysis Tools
View WP_110804240.1 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
MASETRGPQGFERVIEAAPAKVAEFAETKTPVQKLQYALHQTPALVPLIVLVASIIGFGL
LLGHKFFSAYALTLILQQVAITGIVGAAQTLVVMTAGIELSVGAITVLSSVIMGQFTFRY
GIPAPISVLCGLGVGTFIGFLNGTMVARMKLPPFIVTLGMWQIVLAANFIYSANETIRAQ
DIEEKAPILQFFGETIRIGGAVLNFGAILMIAIVAVLAYVLRHTAFGRHVYAVGDDPDAA
ELAGVKVKSILISVYTISGLICGLAGWALIGRLGSVSPTSAQLENINSITAVVIGGISLF
GGRGSILGMMFGALIVGVFTLGLRMYGTDPQWTFLLIGSLIIAAVAVDQWIRKAAA
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