Notes for DANRE gmppb
2026-05-09 review notes
- Core function is mannose-1-phosphate guanylyltransferase activity producing GDP-mannose PMID:23768512.
- Glycoprotein biosynthesis is retained because GDP-mannose is required for protein glycosylation and zebrafish knockdown reduces DAG1/alpha-dystroglycan glycosylation PMID:23768512.
- Muscle and neuron development terms are kept non-core as downstream phenotypes of impaired glycosylation PMID:35006422.
Re-review 2026-09-29
Starting state: valid with 1 warning (3 PENDING rows); reasons were one-liners repeated across
rows and the same five quotes (including deep-research paraphrases) were attached to unrelated
terms.
Resolved the 3 PENDING rows:
- GO:0004475 (IBA, PTN000500861): ACCEPT. Single-activity family with yeast, Candida,
Arabidopsis, human and zebrafish donors; the target's presence in its own WITH/FROM marks
the EXP grounding rather than circularity.
- GO:0005737 cytoplasm (IBA, PTN000500804): ACCEPT. GDP-mannose synthesis is cytosolic; no
signal peptide or anchor in UniProt. Added as the locations entry of the core function,
which previously had none.
- GO:0005575 cellular_component (ND): ACCEPT. Accurate statement that no experimental
localization exists for zebrafish gmppb; not in conflict with the cytoplasm IBA inference.
Action changes and arguments:
- GO:0009101 glycoprotein biosynthetic process (IMP, PMID:23768512): ACCEPT ->
KEEP_AS_NON_CORE, matching the IBA row for the same term, which had been non-core. The
participation test decides it: gmppb makes the donor sugar, the mannosyltransferases do the
glycosylation. Hypoglycosylation on knockdown PMID:23768512
demonstrates necessity, which is what supplying a substrate means.
- GO:0016740 transferase activity kept MODIFY to GO:0004475; GO:0005525 GTP binding kept
non-core, now argued as substrate binding within the annotated catalytic activity rather than
a switch function.
- The four developmental IMP rows (skeletal muscle, muscle cell, neuron development) stay
KEEP_AS_NON_CORE, now with the rescue evidence quoted [PMID:35006422 "GMPPB V111G mutant with
decreased activity fails to rescue axonal phenotype in gmppb MO-injected zebrafish."; "Thus,
enzymatic activity of GMPPB might be a critical determinant for phenotypes of zebrafish."],
which shows the phenotypes track catalytic competence and so are downstream of the metabolic
step.
- GO:0004475 EXP (PMID:33986552): kept ACCEPT, with a note that the enzymology is on the human
GMPPA-GMPPB complex while the same paper's in vivo test is in zebrafish PMID:33986552. This is the
ECO:0000269 source behind the UniProt catalytic activity.
- Replaced the repeated boilerplate supporting_text with term-specific quotes throughout; kept
one deep-research quote (Mg2+/mannose-1-P dependence of the assay) because it adds assay
detail absent from UniProt.
- Added reference_review to all 3 PMIDs (PMID:23768512 and PMID:33986552 are abstract-only
caches, noted), rewrote the description (mechanism, GMPPA feedback, zebrafish expression
profile, phenotypes) and the core function, and filled the empty questions and experiments.
Validation after edits: zero errors, zero warnings.
Quote cleanup (2026-10-04)
- Removed stray UniProt
CC line prefixes from the 'Catalyzes the formation of GDP-mannose ...' UniProt quote, used in 3 supported_by entries (GO:0009101 x2, GO:0005737).
- No action, reason or term changed;
just validate DANRE gmppb passes with zero errors.