Reviewed all 18 existing rows and the core functions with the review and annotation-reviewer workflows. Preserved every machine-sourced term, evidence code, qualifier, source identifier, WITH/FROM entry and row order. No new annotations were added in this audit.
PMID:9428669 supports modest acetyl-CoA-dependent activity and overexpression rescue, not replacement of dedicated NAGS under all native conditions. Leaky deletion implies another ornithine-release route whose enzyme is not identified. PMID:10753950 explicitly reports processing BEFORE mitochondrial targeting and loss of maturation/activity after T215A despite correct targeting. The prior matrix-cleavage claim is corrected without editing UniProt. The cytosol row is now UNDECIDED: native transient processing complicates a categorical exclusion, while leader-deletion localization does not establish a normal cytosolic catalytic pool. PMID:17651682 adds target-specific coupled-assay/deletion-extract evidence.
Normal publication caching completed. Normal Falcon research with Perplexity-lite fallback was attempted for this gene; authentication/quota failures prevented a generated report. Manual review used the actual cached primary sources and curated UniProt, and no provider-named research file was fabricated. Per-gene attempts and validation logs are in .cache/module-audit-logs/arginine-yeast-ARG7-*. Abstract-only or bibliographic-only sources are distinguished from full text in reference reviews; unavailable source details are not treated as experimental refutations.
Actions: ACCEPT 9, KEEP_AS_NON_CORE 3, MODIFY 5, UNDECIDED 1. Record sections were backfilled; focused schema/reference validation passed on the initial complete panel. Final targeted checks and HTML rendering are recorded in the audit logs.
Restored supported GO:0005739 mitochondrion rows to ACCEPT under the explicit root-organelle policy; existing matrix rows remain separate. Reasons distinguish organelle screens, direct targeting, publication-linked curated evidence and unavailable full text. No original annotation payload changed. Cytosol decisions use target-specific fractionation/processing evidence rather than relationship qualifiers or generic precursor transit. For Aga1, matrix inference does not imply universal post-import autoproteolysis.