Protein HSERO_RS11445 in Herbaspirillum seropedicae SmR1
Annotation: FitnessBrowser__HerbieS:HSERO_RS11445
Length: 221 amino acids
Source: HerbieS in FitnessBrowser
Candidate for 20 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_2554 | hi | ABC transporter for L-Histidine, permease component 1 (characterized) | 73% | 100% | 328.6 | Basic amino acid uptake transporter, BgtAB | 45% | 176.0 |
| L-arginine catabolism | artM | lo | Amino acid (Lysine/arginine/ornithine/histidine/octopine) ABC transporter membrane protein, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) | 36% | 99% | 137.5 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-histidine catabolism | hisM | lo | Amino acid (Lysine/arginine/ornithine/histidine/octopine) ABC transporter membrane protein, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) | 36% | 99% | 137.5 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-lysine catabolism | hisM | lo | Amino acid (Lysine/arginine/ornithine/histidine/octopine) ABC transporter membrane protein, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) | 36% | 99% | 137.5 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| D-glucosamine (chitosamine) catabolism | AO353_21720 | lo | ABC transporter for D-Glucosamine, permease component 1 (characterized) | 34% | 93% | 132.1 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-histidine catabolism | BPHYT_RS24005 | lo | Polar amino acid ABC transporter, inner membrane subunit; Flags: Precursor (characterized, see rationale) | 33% | 90% | 129.8 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-asparagine catabolism | aatQ | lo | Glutamate/aspartate import permease protein GltJ (characterized) | 32% | 88% | 126.7 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-aspartate catabolism | aatQ | lo | Glutamate/aspartate import permease protein GltJ (characterized) | 32% | 88% | 126.7 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-glutamate catabolism | gltJ | lo | Glutamate/aspartate import permease protein GltJ (characterized) | 32% | 88% | 126.7 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-histidine catabolism | BPHYT_RS24010 | lo | Polar amino acid ABC transporter, inner membrane subunit (characterized, see rationale) | 33% | 89% | 125.9 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-arginine catabolism | artQ | lo | arginine/ornithine transport protein (characterized) | 36% | 92% | 124.4 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-lysine catabolism | hisQ | lo | ABC transporter for L-Lysine, permease component 1 (characterized) | 34% | 95% | 124 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-asparagine catabolism | natG | lo | NatG, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized) | 32% | 74% | 122.9 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-aspartate catabolism | natG | lo | NatG, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized) | 32% | 74% | 122.9 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-asparagine catabolism | aatM | lo | ABC transporter for L-Asparagine and possibly other L-amino acids, permease component 2 (characterized) | 32% | 98% | 121.7 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-aspartate catabolism | aatM | lo | ABC transporter for L-Asparagine and possibly other L-amino acids, permease component 2 (characterized) | 32% | 98% | 121.7 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-asparagine catabolism | natH | lo | NatH, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized) | 37% | 55% | 117.9 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-aspartate catabolism | natH | lo | NatH, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized) | 37% | 55% | 117.9 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-citrulline catabolism | AO353_03050 | lo | ABC transporter for L-Arginine and L-Citrulline, permease component 1 (characterized) | 35% | 92% | 115.9 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
| L-histidine catabolism | hisQ | lo | Histidine transport system permease protein HisQ (characterized) | 33% | 95% | 111.7 | ABC transporter for L-Histidine, permease component 1 | 73% | 328.6 |
Sequence Analysis Tools
View HSERO_RS11445 at FitnessBrowser
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
MKLDFSGVWESWPSLVHGTLVTVEITAASLVVGCVLGLLVGLGRLSPQRRVIYGLCTIYL
TLVRGTPLLVQLFLWFFGLPHVGVILPAYVCGILGLGIYSGAYVSEIVRGAIQSIERGQM
EAARSLGLPYRMAMRRVILPQAFVRMIPPLGNEFIALIKNSALVSLLTIADLMHEGEKII
SVTYRSLETYLAIALIYLLLTSVTTLILRRVEKVLRSEGRV
This GapMind analysis is from Sep 17 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