Protein WP_008236514.1 in Imtechella halotolerans K1
Annotation: NCBI__GCF_000260835.1:WP_008236514.1
Length: 313 amino acids
Source: GCF_000260835.1 in NCBI
Candidate for 27 steps in catabolism of small carbon sources
Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
putrescine catabolism | potA | lo | PotG aka B0855, component of Putrescine porter (characterized) | 34% | 72% | 160.2 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-cellobiose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-galactose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-glucose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
lactose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-maltose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-mannose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
sucrose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
trehalose catabolism | glcV | lo | monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) | 33% | 95% | 154.8 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-maltose catabolism | malK_Bb | lo | ABC-type maltose transport, ATP binding protein (characterized, see rationale) | 35% | 71% | 150.6 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-proline catabolism | opuBA | lo | BilEA aka OpuBA protein, component of A proline/glycine betaine uptake system. Also reported to be a bile exclusion system that exports oxgall and other bile compounds, BilEA/EB or OpuBA/BB (required for normal virulence) (characterized) | 36% | 71% | 147.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-maltose catabolism | thuK | lo | Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized) | 31% | 70% | 145.2 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
trehalose catabolism | thuK | lo | Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized) | 31% | 70% | 145.2 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-arabinose catabolism | xacJ | lo | Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) | 32% | 63% | 144.1 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-maltose catabolism | musK | lo | ABC-type maltose transporter (EC 7.5.2.1) (characterized) | 32% | 63% | 140.2 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
sucrose catabolism | thuK | lo | ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) | 32% | 78% | 137.9 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-maltose catabolism | malK | lo | Maltose-transporting ATPase (EC 3.6.3.19) (characterized) | 32% | 65% | 136.3 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-cellobiose catabolism | SMc04256 | lo | ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) | 30% | 80% | 132.9 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-arabinose catabolism | xacK | lo | Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale) | 33% | 63% | 132.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
D-maltose catabolism | malK_Sm | lo | MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized) | 31% | 65% | 127.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
trehalose catabolism | malK | lo | MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized) | 31% | 65% | 127.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-alanine catabolism | braG | lo | NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 30% | 98% | 105.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-histidine catabolism | natE | lo | NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 30% | 98% | 105.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-leucine catabolism | natE | lo | NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 30% | 98% | 105.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-proline catabolism | natE | lo | NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 30% | 98% | 105.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-serine catabolism | braG | lo | NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 30% | 98% | 105.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
L-threonine catabolism | braG | lo | NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) | 30% | 98% | 105.5 | Fe(3+)-transporting ATPase; EC 3.6.3.30 | 32% | 166.0 |
Sequence Analysis Tools
View WP_008236514.1 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
MLSIQNISFSYNNTPVLNQLSLDIIPGEHLSIIGASGCGKSTLLKLIYGLLTPSDGNLYW
NEKKLLGPDFNIVPGEDDMKYLAQDFGLMPFITASENIGKYLSNFYPIKKKKRIFELLEM
VGMAEYANVKAQFLSGGQQQRIALAQVLAQEPKVLLLDEPFSHIDNFQKNTLRRDLFHHL
KSSKITCLVATHDATDALSFADNVLVLKDGKKIAYNTPKELYLNPGSTYTASLFGDVNTI
DAQLFFPDRKGFLWIYPHQLKVKEDSKLRVKVLDNYFSGNGYLIKGISKGKILFFLHHTS
IPSGSETGLCLNR
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