GapMind for catabolism of small carbon sources

 

Protein WP_012537671.1 in Acidithiobacillus ferrooxidans ATCC 23270

Annotation: NCBI__GCF_000021485.1:WP_012537671.1

Length: 309 amino acids

Source: GCF_000021485.1 in NCBI

Candidate for 45 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-lysine catabolism hisP lo Amino-acid ABC transporter, ATP-binding protein (characterized, see rationale) 38% 85% 134 nodulation ATP-binding protein I 48% 285.0
putrescine catabolism potA lo spermidine/putrescine ABC transporter, ATP-binding protein PotA; EC 3.6.3.31 (characterized) 36% 59% 133.7 nodulation ATP-binding protein I 48% 285.0
L-fucose catabolism SM_b21106 lo ABC transporter for L-Fucose, ATPase component (characterized) 33% 89% 133.3 nodulation ATP-binding protein I 48% 285.0
lactose catabolism lacK lo ABC transporter for Lactose, ATPase component (characterized) 36% 61% 133.3 nodulation ATP-binding protein I 48% 285.0
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) 35% 90% 131.7 nodulation ATP-binding protein I 48% 285.0
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) 35% 90% 131.7 nodulation ATP-binding protein I 48% 285.0
L-proline catabolism HSERO_RS00895 lo ABC-type branched-chain amino acid transport system, ATPase component protein (characterized, see rationale) 33% 93% 130.2 nodulation ATP-binding protein I 48% 285.0
D-cellobiose catabolism msiK lo MsiK protein, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized) 36% 53% 124.8 nodulation ATP-binding protein I 48% 285.0
L-isoleucine catabolism livG lo ABC transporter ATP-binding protein (characterized, see rationale) 31% 91% 122.1 nodulation ATP-binding protein I 48% 285.0
L-leucine catabolism livG lo ABC transporter ATP-binding protein (characterized, see rationale) 31% 91% 122.1 nodulation ATP-binding protein I 48% 285.0
L-phenylalanine catabolism livG lo ABC transporter ATP-binding protein (characterized, see rationale) 31% 91% 122.1 nodulation ATP-binding protein I 48% 285.0
L-serine catabolism Ac3H11_1693 lo ABC transporter ATP-binding protein (characterized, see rationale) 31% 91% 122.1 nodulation ATP-binding protein I 48% 285.0
L-tyrosine catabolism Ac3H11_1693 lo ABC transporter ATP-binding protein (characterized, see rationale) 31% 91% 122.1 nodulation ATP-binding protein I 48% 285.0
L-alanine catabolism braG lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 35% 91% 118.6 nodulation ATP-binding protein I 48% 285.0
L-isoleucine catabolism livF lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 35% 91% 118.6 nodulation ATP-binding protein I 48% 285.0
L-leucine catabolism livF lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 35% 91% 118.6 nodulation ATP-binding protein I 48% 285.0
L-serine catabolism braG lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 35% 91% 118.6 nodulation ATP-binding protein I 48% 285.0
L-threonine catabolism braG lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 35% 91% 118.6 nodulation ATP-binding protein I 48% 285.0
L-valine catabolism livF lo High-affinity branched-chain amino acid transport ATP-binding protein BraG, component of Branched chain amino acid uptake transporter. Transports alanine (characterized) 35% 91% 118.6 nodulation ATP-binding protein I 48% 285.0
D-maltose catabolism malK_Bb lo ABC-type maltose transport, ATP binding protein (characterized, see rationale) 31% 73% 116.3 nodulation ATP-binding protein I 48% 285.0
L-histidine catabolism Ac3H11_2560 lo ABC transporter for L-Histidine, ATPase component (characterized) 37% 83% 114.8 nodulation ATP-binding protein I 48% 285.0
L-phenylalanine catabolism livF lo High-affinity branched-chain amino acid transport ATP-binding protein (characterized, see rationale) 33% 95% 114.4 nodulation ATP-binding protein I 48% 285.0
L-proline catabolism HSERO_RS00900 lo ABC transporter ATP-binding protein (characterized, see rationale) 33% 89% 114 nodulation ATP-binding protein I 48% 285.0
L-serine catabolism Ac3H11_1692 lo ABC transporter ATP-binding protein (characterized, see rationale) 33% 89% 114 nodulation ATP-binding protein I 48% 285.0
L-tyrosine catabolism Ac3H11_1692 lo ABC transporter ATP-binding protein (characterized, see rationale) 33% 89% 114 nodulation ATP-binding protein I 48% 285.0
L-isoleucine catabolism natE lo 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) 33% 85% 113.2 nodulation ATP-binding protein I 48% 285.0
L-leucine catabolism natE lo 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) 33% 85% 113.2 nodulation ATP-binding protein I 48% 285.0
L-proline catabolism natE lo 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) 33% 85% 113.2 nodulation ATP-binding protein I 48% 285.0
L-valine catabolism natE lo 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) 33% 85% 113.2 nodulation ATP-binding protein I 48% 285.0
D-alanine catabolism AZOBR_RS08250 lo Leucine//isoleucine/valine ABC transporter,ATPase component; EC 3.6.3.- (characterized, see rationale) 31% 100% 112.1 nodulation ATP-binding protein I 48% 285.0
L-proline catabolism AZOBR_RS08250 lo Leucine//isoleucine/valine ABC transporter,ATPase component; EC 3.6.3.- (characterized, see rationale) 31% 100% 112.1 nodulation ATP-binding protein I 48% 285.0
L-arabinose catabolism xylGsa lo Xylose/arabinose import ATP-binding protein XylG; EC 7.5.2.13 (characterized, see rationale) 30% 86% 109.8 nodulation ATP-binding protein I 48% 285.0
L-histidine catabolism natE lo NatE aka LivF aka SLR1881, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized) 32% 88% 107.8 nodulation ATP-binding protein I 48% 285.0
D-fructose catabolism frcA lo Fructose import ATP-binding protein FrcA; EC 7.5.2.- (characterized) 30% 89% 106.7 nodulation ATP-binding protein I 48% 285.0
D-mannose catabolism frcA lo Fructose import ATP-binding protein FrcA; EC 7.5.2.- (characterized) 30% 89% 106.7 nodulation ATP-binding protein I 48% 285.0
D-ribose catabolism frcA lo Fructose import ATP-binding protein FrcA; EC 7.5.2.- (characterized) 30% 89% 106.7 nodulation ATP-binding protein I 48% 285.0
sucrose catabolism frcA lo Fructose import ATP-binding protein FrcA; EC 7.5.2.- (characterized) 30% 89% 106.7 nodulation ATP-binding protein I 48% 285.0
D-lactate catabolism PGA1_c12640 lo D-lactate transporter, ATP-binding component (characterized) 30% 94% 102.4 nodulation ATP-binding protein I 48% 285.0
L-arginine catabolism braG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 34% 95% 101.7 nodulation ATP-binding protein I 48% 285.0
L-glutamate catabolism braG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 34% 95% 101.7 nodulation ATP-binding protein I 48% 285.0
L-histidine catabolism braG lo ATP-binding component of a broad range amino acid ABC transporter (characterized, see rationale) 34% 95% 101.7 nodulation ATP-binding protein I 48% 285.0
D-ribose catabolism rbsA lo Ribose ABC transporter ATPase; SubName: Full=Sugar ABC transporter ATP-binding protein; SubName: Full=Sugar ABC transporter ATPase (characterized, see rationale) 30% 58% 97.1 nodulation ATP-binding protein I 48% 285.0
D-alanine catabolism AZOBR_RS08245 lo Leucine/isoleucine/valine ABC transporter,ATPase component; EC 3.6.3.- (characterized, see rationale) 30% 83% 90.5 nodulation ATP-binding protein I 48% 285.0
L-proline catabolism AZOBR_RS08245 lo Leucine/isoleucine/valine ABC transporter,ATPase component; EC 3.6.3.- (characterized, see rationale) 30% 83% 90.5 nodulation ATP-binding protein I 48% 285.0
glycerol catabolism glpS lo GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized) 31% 59% 87.4 nodulation ATP-binding protein I 48% 285.0

Sequence Analysis Tools

View WP_012537671.1 at NCBI

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

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Compare to protein structures

Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

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Sequence

MNPAFLELRALHKRYGGREVLRGVDLAVAAGECFALVGPNGAGKSTTVRAIQGLTPTDGG
EVRIDGRTLAEMGRTARTGMGVVPQTDNLDPDFTVQENLWTYGRYFGLPKALIRQRSAEL
LEFMALSGYATQPIHALSGGMQRRLTIARALINAPKLLLLDEPTTGLDPQARHLIWQRLR
ELRRQGTTLLLTTHYMDEAERLADRVGIIDHGRILAEDSPRGLIATHIPGGVVELRRVDG
DLPDPQDLHRQWVSFSERVGDTLICYGTNLTPLLTHFGDDPAYRWIQRPASLEDVFLRLT
GRDLREETE

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:

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:

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:

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