GapMind for catabolism of small carbon sources

 

Finding step acs for L-lactate catabolism in Azospirillum brasilense Sp245

5 candidates for acs: acetyl-CoA synthetase, AMP-forming

Score Gene Description Similar to Id. Cov. Bits Other hit Other id. Other bits
hi AZOBR_RS00270 acetyl-CoA synthetase Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized) 69% 100% 938.7
hi AZOBR_RS00270 acetyl-CoA synthetase acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188) 99% 1052.5
med AZOBR_RS06340 acyl-CoA synthetase propionate-CoA ligase (EC 6.2.1.17) (characterized) 53% 92% 709.9 Propionate--CoA ligase (EC 6.2.1.17) 68% 898.7
med AZOBR_RS06255 acyl-CoA synthetase Acetate/butyrate--CoA ligase AAE7, peroxisomal; AMP-binding protein 7; AtAMPBP7; Acetyl-CoA synthetase; Acyl-activating enzyme 7; Butyryl-CoA synthetase; Protein ACETATE NON-UTILIZING 1; EC 6.2.1.1; EC 6.2.1.2 (characterized) 54% 97% 616.3 3-(methylthio)propionyl-CoA ligase (EC 6.2.1.44) 67% 769.6
med AZOBR_RS19480 acyl-CoA synthetase Acetate/butyrate--CoA ligase AAE7, peroxisomal; AMP-binding protein 7; AtAMPBP7; Acetyl-CoA synthetase; Acyl-activating enzyme 7; Butyryl-CoA synthetase; Protein ACETATE NON-UTILIZING 1; EC 6.2.1.1; EC 6.2.1.2 (characterized) 53% 96% 579.3 short chain acyl-CoA synthetase (EC 6.2.1.2) 60% 648.7
med AZOBR_RS09405 acyl-CoA synthetase Acetate/butyrate--CoA ligase AAE7, peroxisomal; AMP-binding protein 7; AtAMPBP7; Acetyl-CoA synthetase; Acyl-activating enzyme 7; Butyryl-CoA synthetase; Protein ACETATE NON-UTILIZING 1; EC 6.2.1.1; EC 6.2.1.2 (characterized) 50% 97% 557.8 3-(methylthio)propionyl-CoA ligase (EC 6.2.1.44) 61% 667.2

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 acs

Or cluster all characterized acs proteins

This GapMind analysis is from Sep 17 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:

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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