All 15 existing rows, including the prior NEW epigenetic-process assertion, were reassessed and retained in payload. The newer PMID:38851185 full text supports LD as a Ref2/PNUTS-like bridge rather than a DNA-binding transcription factor. It explicitly leaves the phosphatase substrate unresolved; the prior question about whether any LD phosphatase-module role exists has been updated to this experimentally meaningful gap. The SUF4 interaction remains a specific TF-binding refinement, and the primary genetic/chromatin evidence supports flowering and transcriptional regulation. No catalytic MF was manufactured for LD.
All seeded rows were reviewed, with original term, evidence, source, supporting-entity and qualifier/NOT payloads preserved. The shared normal Falcon attempt and perplexity-lite fallback both failed; logs are retained under .cache/module-audit-logs/autonomous-flowering-fetch/ARATH-LD-provider.log. No provider report was fabricated. Manual primary-literature assessment and normal publication fetching supplied this review. Source access limits are stated per reference/claim. Generic protein binding follows the current informative-function policy; its removal does not reject the physical interactions. Nuclear localization does not by itself exclude additional compartments.