Oliver, Sanchez and Blazquez 2002, PMID:12445642 (abstract only; no PMC).
- Cloned PAO1 mutT, mutM and mutY complement the mutator phenotype of the
corresponding E. coli mutants:
PMID:12445642
PMID:12445642
- The abstract describes heterologous complementation of mutation frequency.
Whether a direct 8-oxo-dGTPase assay was done cannot be seen. The "necessary
and sufficient" statement may come from complementation with truncations.
Later work (not cached here) links P. aeruginosa GO-system defects (mutT,
mutY) to hypermutability in cystic fibrosis isolates; not needed for the
annotation calls.
E. coli MutT (P08337) carries GO:0006281 DNA repair as EcoCyc EXP
(acts_upstream_of_or_within, PMID:7739614) and UniProt IC (PMID:10373420);
human NUDT1 carries DNA repair (IC) and DNA protection (GO:0042262). GO
practice is to annotate MutT-type 8-oxo-dGTPases, which prevent
incorporation of oxidised guanine, to DNA repair. The PseudoCAP term follows
that convention and is accepted.
Seeds from .cache/paint/IBD.gaf; P08337 annotations from QuickGO 2026-11-05.
| PTN node | node term | n_seeds | leaf IBAs | seed annotation (term, evidence, PMID) | verdict | rationale | other seeds | IBD stands without this seed? |
|---|---|---|---|---|---|---|---|---|
| PTN000755027 | GO:0006281 DNA repair | 2 | 27 (22 taxa) | GO:0006281, IDA, PMID:12445642 | SOUND | Complementation of the E. coli mutT mutator phenotype shows the antimutator (GO system) function; DNA repair is the GO convention for MutT. The evidence is heterologous complementation (IGI), not IDA: PSEUDOCAP WRONG_EVIDENCE_CODE, PROBABLE (abstract states the method). Term suits the MutT clade. | E. coli MutT P08337 (EXP PMID:7739614, EcoCyc; IC PMID:10373420, UniProt) | Yes |
The other IBDs at this node (8-oxo-dGTP, 8-oxo-GTP pyrophosphatase; 8-oxo-dGDP,
8-oxo-GDP phosphatase) rest on P08337 only, with direct IDA data; PA4400 is
not a seed. No GO_CENTRAL defect.