The review retains 47 incoming contexts and separately proposes translation-repressor and protein-macromolecule adaptor activities. Generic-binding removals preserve measured interactions; eight informative refinements have functional or interface evidence.
f202a024d791f401495d0a91d8aac5b410becac7b3ac032ae9007561d301a929.The exact existing machine contexts govern. Positive screening pairs are not silently converted into physiological mechanisms. Where informative binding is retained, the external page identifies the separate interface or functional evidence. Incoming partner suffixes remain literal, including the unresolved NEK6 product crosswalk. The new activities do not assert direct RNA binding or its absence. No new biological-process annotation is proposed.
Normal-cache full-text flags describe actual cached content, including the legacy content_type: full_text_xml record. External full/selected reading is stated separately. Actual PMID:12771153 remains abstract-only; PMID:39018414 has full XML. All native titles match, and its 10-word excerpt uses exact native line wrapping.
Default validation, strict matching of all 47 GOA contexts, computed-status audit, genuine EDIT history, private rendering and scoped whitespace passed. The computed review status is COMPLETE with zero annotation advisories. All 21 sources and the ontology cache remain unchanged after acquisition.
The adaptor proposal uses human recruitment and interface evidence and retains the original 47 decisions. The archive and native acquisition snapshot remain the initial published records. One additional 10-word excerpt brings the two PMID:39018414 excerpts to 20 words in total; the original three quotations are unchanged. Default validation, strict matching of all 47 original GOA contexts, computed-status audit, genuine EDIT history, private rendering and scoped whitespace passed. Computed status is COMPLETE with zero annotation advisories. All 21 normal sources, the historical archive and the ontology cache are unchanged.