Protein WP_041937000.1 in Rhizobium leguminosarum 3841
Annotation: NCBI__GCF_000009265.1:WP_041937000.1
Length: 247 amino acids
Source: GCF_000009265.1 in NCBI
Candidate for 14 steps in catabolism of small carbon sources
| Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
|---|
| L-alanine catabolism | braG | hi | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 41% | 99% | 188 | ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM | 37% | 166.8 |
| L-isoleucine catabolism | natE | hi | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 41% | 99% | 188 | High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine | 40% | 169.5 |
| L-leucine catabolism | natE | hi | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 41% | 99% | 188 | High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine | 40% | 169.5 |
| L-proline catabolism | natE | hi | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 41% | 99% | 188 | High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine | 40% | 169.5 |
| L-serine catabolism | braG | hi | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 41% | 99% | 188 | ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM | 37% | 166.8 |
| L-threonine catabolism | braG | hi | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 41% | 99% | 188 | ABC transporter ATP-binding protein-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM | 37% | 166.8 |
| L-valine catabolism | natE | hi | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized) | 41% | 99% | 188 | High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine | 40% | 169.5 |
| L-isoleucine catabolism | livF | med | ABC transporter ATP-binding protein (characterized, see rationale) | 40% | 95% | 184.5 | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) | 41% | 188.0 |
| L-leucine catabolism | livF | med | ABC transporter ATP-binding protein (characterized, see rationale) | 40% | 95% | 184.5 | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) | 41% | 188.0 |
| L-phenylalanine catabolism | livF | med | ABC transporter ATP-binding protein (characterized, see rationale) | 40% | 95% | 184.5 | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) | 41% | 188.0 |
| L-proline catabolism | HSERO_RS00900 | med | ABC transporter ATP-binding protein (characterized, see rationale) | 40% | 95% | 184.5 | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) | 41% | 188.0 |
| L-serine catabolism | Ac3H11_1692 | med | ABC transporter ATP-binding protein (characterized, see rationale) | 40% | 95% | 184.5 | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) | 41% | 188.0 |
| L-tyrosine catabolism | Ac3H11_1692 | med | ABC transporter ATP-binding protein (characterized, see rationale) | 40% | 95% | 184.5 | NatE, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) | 41% | 188.0 |
| L-histidine catabolism | natE | med | NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 41% | 96% | 176 | High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine | 40% | 169.5 |
Sequence Analysis Tools
View WP_041937000.1 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
MEGNSQLLIRDLRAGYGNLDILNGVDLDVPAGQFVALMGPNGAGKSTLLKTLYGMTTIKQ
GSIDWRGKNIAGSKSRSILGEGISFVPQGRCNFPVMSVDENLQMAAYTLRDAKVKADRDY
VYDLFPILKNRRATLAGNMSGGEQQLLEVAMAVLQRPKVLLVDEPSVGLSPAAIGIVFDE
LLRLHADGMTILLVEQNTKKAMEVAERAVILRLGKVIWDGLPKDITHDELGELFLTGKMR
GETEAVH
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