Audited the existing REMOVE decision for the NAS annotation GO:0006979 (response to
oxidative stress), sourced to PMID:26527276 PMID:26527276.
The cached record for PMID:26527276 is abstract-only (full_text_available: false), and
the abstract itself does not mention oxidative stress at all. The prior review pass used
this absence as grounds to REMOVE the annotation, reasoning that SER3's function
(serine biosynthesis) has no connection to oxidative stress.
That reasoning does not hold up under closer scrutiny of the underlying biology:
yeastgenome.org/complex/S000377910/go) lists "response to oxidative stress" among theGO:1902494 "catalytic complex" and GO:0040029 "epigenetic regulation of geneMARK_AS_OVER_ANNOTATED rather than REMOVEd).just fetch-pmid), but the candidate PMID resolved to an unrelated nursingConclusion: the annotation was not fabricated or spurious — the SESAME complex
genuinely has a documented link to oxidative-stress resistance — but neither is there
direct evidence tying Ser3p's own dehydrogenase activity to that phenotype. Per project
policy (never confidently REMOVE an annotation on the strength of an abstract that is
simply silent on the topic; use UNDECIDED when full text cannot be accessed), changed
the action from REMOVE to UNDECIDED and rewrote review.summary/review.reason to
reflect this. No other annotation in this review was altered.
Review feedback on PR #2943 pointed out that the decisive fact was already in the repo,
and it was not the one being cited. It is right, and it changes the call.
The provenance is ComplexPortal, not a primary assay. All three PMID:26527276 rows
in the GOA are ASSIGNED BY = ComplexPortal:
SER3-goa.tsv:14 involved_in GO:0006979 response to oxidative stress NAS ComplexPortal
SER3-goa.tsv:15 involved_in GO:0040029 epigenetic regulation of gene expr. NAS ComplexPortal
SER3-goa.tsv:16 part_of GO:1902494 catalytic complex NAS ComplexPortal
These are complex-level annotations on CPX-9181, propagated to every subunit.
SER3-uniprot.txt:99 confirms the membership: DR ComplexPortal; CPX-9181; SESAME
metabolic enzyme complex.
That reframes the question. It is not "did Li et al. assay Ser3p?" but "does a
complex-level BP term belong on a metabolic-enzyme subunit?" — and this review already
answers that twice, marking the two siblings with identical provenance (same
reference, same evidence code, same assigning body) MARK_AS_OVER_ANNOTATED. Singling
out the third for UNDECIDED was inconsistent.
Crucially, the reason had named full-text access as the blocker. That was the wrong
diagnosis: full text would not convert a complex-level propagation into a subunit-level
claim. The limitation is structural, not evidentiary.
Changed the action to MARK_AS_OVER_ANNOTATED for consistency with GO:0040029 and
GO:1902494, and rewrote summary/reason around the checkable CPX-9181 grounding.
Removed the uncited claims from the YAML. review.summary had asserted an SGD
complex-page listing (bare URL, no references entry) and the PYK1/H3T11 oxidative-stress
finding that the notes above themselves admit could not be sourced — the candidate PMID
resolved to an unrelated nursing tribute article. Notes are the right home for
unverifiable corroboration; review.summary/reason are machine-readable output that
other tooling will believe. Both are now confined to this file.
Also addressed: the positional cross-reference ("the GO:1902494 annotation below") is
gone, terms are named directly; the summary no longer narrates the review file's own edit
history; the supported_by quote and the citation at the top of these notes were moved
off the paper title onto the abstract sentence that actually evidences Ser3p's SESAME
membership.
The two sibling annotations still carry title-only supporting_text, which was left
alone to keep this diff scoped to the annotation under review.
GO_REF:0000033 / IBA rows, so there was noGO:0005515 protein-binding rows were converted fromMARK_AS_OVER_ANNOTATED to REMOVE. Six of them are IntAct annotations toSER3 hit (PMID:41796364) engineered serine biosynthesis