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"Pseudomonas aeruginosa methylcitrate synthase PrpC PA0795" found the Dolan et al. 2022
mBio paper (DOI 10.1128/mbio.02541-22 = PMID:36377867, PMC9765439, full text cached) and
PDB 6S6F/6S87 (PrpC apo and oxaloacetate-bound).
.cache/paint/pseudocap.tsv).Interpretation: CSII of the 1995 paper (dimer, ~37-41 kDa subunit) matches PrpC, and CSI
(hexamer) matches GltA, so PseudoCAP's attribution is very likely right in substance, but
the 1995 paper itself cannot tie either enzyme to a gene. PrpC's citrate synthase
activity is a genuine secondary activity: comparable kcat with acetyl-CoA, and enough
in vivo to keep a gltA mutant alive. Its main role is 2-methylcitrate synthesis in the
2-methylcitrate cycle (propionate catabolism).
| PTN node | node term | n_seeds | leaf IBAs | seed annotation (term, evidence, PMID) | verdict | rationale | other seeds | IBD stands without this seed? |
|---|---|---|---|---|---|---|---|---|
| PTN000201223 | GO:0036440 citrate synthase activity | 19 | 270 (123 taxa) | GO:0036440, IDA, PMID:7626013 (PseudoCAP) | SOUND (gene identity inferred) | Purified CSII matches PrpC (dimer, ~41-kDa subunit) and purified recombinant PrpC has CS activity (PMID:36377867, full text). The 1995 paper does not identify the gene, so a SUSPECTED CHECK defect asks PseudoCAP to add/repoint to PMID:36377867. | E. coli PrpC (P31660), S. typhimurium PrpC (Q56063), yeast CIT1/CIT2/CIT3, S. pombe cit1, human/mouse/rat CS, Arabidopsis CSY4, Drosophila kdn, Dictyostelium and others | Yes; dozens of experimentally characterised citrate synthases. No GO_CENTRAL defect. |
| PTN000201223 | GO:0006099 tricarboxylic acid cycle | 4 | 270 (123 taxa) | GO:0006099, IDA, PMID:7626013 (PseudoCAP) | SOUND in substance (gene identity inferred; participation conditional) | PrpC supplies citrate in vivo when GltA is absent (ΔgltA ΔprpC not obtainable), so it can take part in the TCA cycle, but GltA is the TCA-cycle enzyme in wild type. The same CHECK defect applies. | yeast CIT1 (S000005284), CIT3 (S000006205), S. pombe cit1 (SPAC6C3.04) | Yes, on the mitochondrial citrate synthases. The term is right for the eukaryotic CS members; for the bacterial PrpC subclade it is a backup role. Not filed as a GO_CENTRAL defect (raised as a question). |