There is a gene-specific paper, and it was not being used. The UniProt entry
lists three EMBL records; the third (MK561737 / QEQ43371.1, liver) carries
RX PubMed=31506780 — He et al. 2019, Adaptive Evolution of C-Type Lysozyme in
Vampire Bats. Fetched into the cache (abstract only; full_text_available:
false). Key points:
finding_review and turned into a knowledge gap rather than an annotation.The second salivary-gland EMBL record (JAA45151.1) traces to the Vampirome study
(PMID:23411029), which puts lysozyme in the accessory gland at both transcript
and protein level PMID:23411029 and detects it directly by LC-MS/MS PMID:23411029.
Reversed three annotation calls made by the previous version. All three were
in the direction of throwing information away:
GO:0050830 (Gram-positive) and GO:0050829 (Gram-negative) had been set toGO:0042742 defense response to bacterium. That generalises twoGO:0050830 is IDA (PMID:21093056), GO:0050829 is IBA — the same TreeGrafterGO:0031640 killing of cells of another organism had been markedFilled a missing GO aspect. The GOA record has no cellular component term at
all. Added GO:0005576 extracellular region as a NEW (ISS) annotation, supported
independently by the signal peptide (SIGNAL 1..18), by the human orthologue's
IDA annotation to the same term, and by proteomic detection in the bat gland.
gene_symbol changed from the accession to LYZ, matching both the UniProt
GN Name=LYZ line and the GOA SYMBOL column.