CG14662 is a 550-residue leucine-rich-repeat protein with two predicted hydrophobic membrane-spanning segments. It is a plausible membrane interaction protein, while ligand recognition, membrane topology, and physiological function remain unresolved.
Exact input: Q9VN74, 550 residues. The accession was fetched explicitly with the gene-directory alias; no canonical-sequence substitution is made.
Raw emitted predictions: CG14662-predictions-source.json. Source features: CG14662-uniprot.txt, with an exact extraction in CG14662-sequence-evidence.json.
These are sequence/domain observations or explicitly named feature predictions, not measurements of biological function. ARBA assertions and ProtNLM-derived UniProt names are not counted as validation.
DR InterPro; IPR032675; LRR_dom_sf.
FT TRANSMEM 29..50
FT /note="Helical"
FT /evidence="ECO:0000256|SAM:Phobius"
FT TRANSMEM 421..447
FT /note="Helical"
FT /evidence="ECO:0000256|SAM:Phobius"
The snapshot emits names and location/keyword statements, with no GO or EC prediction for this target. Each actual statement is assessed below; no GO term has been substituted for it. Categories follow the function-prediction rubric, with nonspecific “uncharacterized” names marked UNC because they contain no testable function. CNN records an independently supported existing annotation; it does not assert a particular training-set composition.
| Kind | Verbatim emitted statement | Assessment | Evidence and limitation |
|---|---|---|---|
| Name | Uncharacterized protein | UNC | Uncharacterized protein supplies no testable activity claim. The LRR fold suggests an interaction scaffold without specifying ligands. |
| Location | Membrane (SL-0162) | COR | Two independently called Phobius transmembrane segments support the broad membrane hypothesis. The result remains a sequence-based localization inference; it does not identify topology or organelle residence. |
No target-specific primary finding is used to establish a molecular activity here. The current assessment is bounded by exact-record architecture and the explicitly identified curated inferences.
Genuine external literature research is requested through the repository Falcon wrapper, with perplexity-lite configured as fallback. Provider output is retained separately as CG14662-deep-research-<provider>.md; its source leads are checked against the underlying publications and exact sequence record.