Finding step aatQ for L-aspartate catabolism in Burkholderia phytofirmans PsJN
5 candidates for aatQ: aspartate/asparagine ABC transporter, permease component 1 (AatQ)
| Score | Gene | Description | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
|---|
| hi | BPHYT_RS16695 | glutamate/aspartate ABC transporter permease GltJ | Glutamate/aspartate import permease protein GltJ (characterized) | 64% | 100% | 331.3 | Glutamine ABC transporter permease and substrate binding protein 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 | 32% | 118.2 |
| hi | BPHYT_RS34465 | glutamate/aspartate ABC transporter permease GltJ | Glutamate/aspartate import permease protein GltJ (characterized) | 52% | 99% | 263.1 | NatG, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB | 31% | 111.3 |
| lo | BPHYT_RS34460 | glutamate/aspartate transporter permease GltK | PP1070, component of Acidic amino acid uptake porter, AatJMQP (characterized) | 31% | 95% | 124.8 | Glutamate/aspartate import permease protein GltK | 57% | 248.8 |
| lo | BPHYT_RS13585 | amino acid ABC transporter permease | ABC transporter for L-asparagine and L-glutamate, permease component 1 (characterized) | 33% | 87% | 121.3 | ABC transporter for L-Histidine, permease component 1 | 43% | 165.2 |
| lo | BPHYT_RS21915 | ABC transporter permease | PP1070, component of Acidic amino acid uptake porter, AatJMQP (characterized) | 34% | 88% | 121.3 | ABC transporter for L-Histidine, permease component 1 | 80% | 357.1 |
Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.
GapMind searches the predicted proteins for candidates by using ublast (a fast alternative to protein BLAST) to find similarities to characterized proteins or by using HMMer to find similarities to enzyme models (usually from TIGRFams). For alignments to characterized proteins (from ublast), scores of 44 bits correspond to an expectation value (E) of about 0.001.
Also see fitness data for the candidates
Definition of step aatQ
- Curated sequence Q88NY3: PP1070, component of Acidic amino acid uptake porter, AatJMQP
- Curated sequence AO353_16285: ABC transporter for L-aspartate, L-asparagine, L-glutamate, and L-glutamine, permease component 2
- Curated sequence Pf1N1B4_772: ABC transporter for L-asparagine and L-glutamate, permease component 1
- Curated sequence PfGW456L13_4771: ABC transporter for L-Asparagine and possibly other L-amino acids, permease component 1
- Ignore hits to Q9I403 when looking for 'other' hits (Amino acid ABC transporter membrane protein, component of Amino acid transporter, AatJMQP. Probably transports L-glutamic acid, D-glutamine acid, L-glutamine and N-acetyl L-glutamic acid (Johnson et al. 2008). Very similar to 3.A.1.3.19 of P. putida)
- Curated sequence P0AER3: Glutamate/aspartate import permease protein GltJ. Glutamate/aspartate transport system permease protein GltJ aka B0654, component of Glutamate/aspartate porter. glutamate/aspartate ABC transporter membrane subunit GltJ (EC 7.4.2.1). glutamate/aspartate ABC transporter membrane subunit GltJ (EC 7.4.2.1)
- Comment: aatQ = PP1070 or AO353_16285 or gltJ
Or cluster all characterized aatQ proteins
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