Protein H281DRAFT_04061 in Paraburkholderia bryophila 376MFSha3.1
Annotation: FitnessBrowser__Burk376:H281DRAFT_04061
Length: 389 amino acids
Source: Burk376 in FitnessBrowser
Candidate for 15 steps in catabolism of small carbon sources
Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
L-isoleucine catabolism | livM | hi | ABC transporter ATP-binding protein (characterized, see rationale) | 63% | 99% | 449.9 | ABC amino acid transporter, ATP-binding, component of Uptake transporter, CamABCD of cholate (steroid) metabolites, 1β(2'-propanoate)-3aα-H-4α(3"(R)-hydroxy-3"-propanoate)-7aβ-methylhexahydro-5-indanone and a desaturated analog | 32% | 114.8 |
L-leucine catabolism | livM | hi | ABC transporter ATP-binding protein (characterized, see rationale) | 63% | 99% | 449.9 | ABC amino acid transporter, ATP-binding, component of Uptake transporter, CamABCD of cholate (steroid) metabolites, 1β(2'-propanoate)-3aα-H-4α(3"(R)-hydroxy-3"-propanoate)-7aβ-methylhexahydro-5-indanone and a desaturated analog | 32% | 114.8 |
L-phenylalanine catabolism | livM | hi | ABC transporter ATP-binding protein (characterized, see rationale) | 63% | 99% | 449.9 | ABC transporter membrane-spanning permease-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM | 32% | 179.5 |
L-proline catabolism | HSERO_RS00890 | hi | ABC transporter ATP-binding protein (characterized, see rationale) | 63% | 99% | 449.9 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
L-serine catabolism | Ac3H11_1694 | hi | ABC transporter ATP-binding protein (characterized, see rationale) | 63% | 99% | 449.9 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
L-tyrosine catabolism | Ac3H11_1694 | hi | ABC transporter ATP-binding protein (characterized, see rationale) | 63% | 99% | 449.9 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
L-arginine catabolism | braE | med | Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale) | 44% | 71% | 252.7 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
L-glutamate catabolism | braE | med | Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale) | 44% | 71% | 252.7 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
L-histidine catabolism | braE | med | Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale) | 44% | 71% | 252.7 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
L-valine catabolism | livM | med | Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale) | 44% | 71% | 252.7 | ABC amino acid transporter, ATP-binding, component of Uptake transporter, CamABCD of cholate (steroid) metabolites, 1β(2'-propanoate)-3aα-H-4α(3"(R)-hydroxy-3"-propanoate)-7aβ-methylhexahydro-5-indanone and a desaturated analog | 32% | 114.8 |
L-alanine catabolism | braE | med | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) | 46% | 71% | 250 | High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M | 42% | 231.5 |
L-serine catabolism | braE | med | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) | 46% | 71% | 250 | High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M | 42% | 231.5 |
L-threonine catabolism | braE | med | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) | 46% | 71% | 250 | High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M | 42% | 231.5 |
D-alanine catabolism | AZOBR_RS08240 | lo | Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale) | 45% | 61% | 247.3 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
L-proline catabolism | AZOBR_RS08240 | lo | Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale) | 45% | 61% | 247.3 | High-affinity branched-chain amino acid transport system permease protein BraE, component of Branched chain amino acid uptake transporter. Transports alanine | 46% | 250.0 |
Sequence Analysis Tools
View H281DRAFT_04061 at FitnessBrowser
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Find functional residues: SitesBLAST
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Predict transmenbrane helices: Phobius
Predict protein localization: PSORTb
Find homologs in fast.genomics
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Sequence
MTSIQPIEPSTTLIPEKNLAKTLTVGIITAFFVIAAPMIIGTAGGNYWVRVLDFAMLYVM
LALGLNVVVGFAGLLDLGYIAFYAVGAYTAALLSSPHLTSQFEWIAHLAPNGLHVPFLII
VPCAMAVAAFFGVILGAPTLRLRGDYLAIVTLGFGEIVRIFLNNLDRPVNITNGPKGITG
IDSVHLGDFSLAQTHSLFGFQFPSVYSYYYLFVLAALLVIWVCTRLQHSRIGRAWAAIRE
DEIAAKAMGINTRNVKLLAFAMGASFGGLSGAMFGAFQGFVSPESFTLPESIVVLACVVL
GGMGHIPGVILGAVLLAVLPEFLRSTMGPLQHMLFGHEIVDTEVIRQLVYALAMVLIMLY
RSEGLWPSPKHEDKIAKLSKRSGKKPVRA
This GapMind analysis is from Apr 09 2024. 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