Protein WP_028321963.1 in Desulfatiglans anilini DSM 4660
Annotation: NCBI__GCF_000422285.1:WP_028321963.1
Length: 218 amino acids
Source: GCF_000422285.1 in NCBI
Candidate for 18 steps in catabolism of small carbon sources
| Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
|---|
| L-arginine catabolism | artP | lo | Arginine transport ATP-binding protein ArtM (characterized) | 39% | 90% | 159.1 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-asparagine catabolism | glnQ | lo | Glutamine ABC transporter ATP-binding protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized) | 39% | 88% | 157.5 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-glutamate catabolism | gltL | lo | Glutamine ABC transporter ATP-binding protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized) | 39% | 88% | 157.5 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-asparagine catabolism | aatP | lo | Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) | 36% | 90% | 146 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-aspartate catabolism | aatP | lo | Glutamate/aspartate transport ATP-binding protein GltL aka B0652, component of Glutamate/aspartate porter (characterized) | 36% | 90% | 146 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-arabinose catabolism | xacJ | lo | Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) | 41% | 54% | 142.5 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-asparagine catabolism | bztD | lo | BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) | 35% | 82% | 139 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-aspartate catabolism | bztD | lo | BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) | 35% | 82% | 139 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-asparagine catabolism | peb1C | lo | PEB1C, component of Uptake system for glutamate and aspartate (characterized) | 35% | 90% | 137.9 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-aspartate catabolism | peb1C | lo | PEB1C, component of Uptake system for glutamate and aspartate (characterized) | 35% | 90% | 137.9 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-lysine catabolism | hisP | lo | ABC transporter for L-Lysine, ATPase component (characterized) | 36% | 87% | 137.5 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| D-maltose catabolism | thuK | lo | ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) | 41% | 61% | 137.1 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| sucrose catabolism | thuK | lo | ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) | 41% | 61% | 137.1 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| trehalose catabolism | thuK | lo | ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) | 41% | 61% | 137.1 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-asparagine catabolism | bgtA | lo | ATPase (characterized, see rationale) | 38% | 77% | 136.3 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-aspartate catabolism | bgtA | lo | ATPase (characterized, see rationale) | 38% | 77% | 136.3 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| L-histidine catabolism | hisP | lo | histidine transport ATP-binding protein hisP (characterized) | 35% | 89% | 134.8 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
| glycerol catabolism | glpS | lo | GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized) | 34% | 59% | 116.7 | Cell division ATP-binding protein FtsE | 50% | 212.6 |
Sequence Analysis Tools
View WP_028321963.1 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
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Sequence
MIQLFRLSKSFGACVALKDVNLTLNTGEFIFLTGPSGAGKTTLLRLIFGSEKPTSGGILI
HGINLSRISRSNLDLLRRKIGFVFQDFKLLPGKTVFENVALALEVCGERPGVIRKKTHQT
LRSLGLADKESMFPLELSGGEQQRVAIARAIVKDPLILLADEPTGNLDWDLTLEIMHVLR
KIQAKGTTVIIATHNRELLEEMGHRRIRLDRGAVLDDP
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