De novo GDP-fucose biosynthesis in Drosophila melanogaster
GDP-L-fucose is the donor substrate for fucosyltransferases, including the O-fucosyltransferase that modifies Notch EGF repeats and the Golgi fucosyltransferases that fucosylate N-glycans. Drosophila makes it de novo from GDP-mannose in the cytosol: GDP-mannose 4,6-dehydratase (Gmd) forms GDP-4-keto-6-deoxymannose, and GDP-L-fucose synthase (Gmer) epimerizes and reduces this intermediate to GDP-L-fucose. GDP-fucose is then carried into the secretory pathway by two transporters, the Golgi GDP-fucose transporter (Gfr) and the endoplasmic reticulum transporter Efr. Loss of Gmd or of both transporters impairs Notch O-fucosylation and Notch signaling.
Boundary. The module covers the four FlyBase members. GDP-mannose supply is modelled in the GDP-mannose biosynthesis module; the fucosyltransferases that consume GDP-fucose (for example O-fut1 and FucT6) are downstream and not parts. Drosophila is reported to lack the fucose salvage pathway, so the de novo route is its source of GDP-fucose. FlyBase groups realized by this module: GDPFUC (FBgg0002026). Participants were generated from the FlyBase gene-group membership and mapped to UniProtKB by projects/FLYBASE_GENE_GROUPS/generate_modules.py from module_specs/dmel_gdp_fucose_biosynthesis.yaml. Member genes with a gene review in this repository: Efr, Gfr, Gmd, Gmer.
Derived QC
Recommended-field compliance
All recommended fields populated.
Module deep research
✗ none found
No MODULE:dmel_gdp_fucose_biosynthesis deep-research report alongside the module YAML.
Leaf nodes lacking representative members
✓ every leaf node grounds to a representative protein.
Template conformance
✓ every declared conforms_to bundle matches its template motif.
Reaction chaining (advisory)
✓ every PRECEDES step chains, or its break is acknowledged via chaining_status.
- gdp_mannose_dehydration → gdp_fucose_synthesis [NOT_CHECKED]
- gdp_fucose_synthesis → gdp_fucose_transport [NOT_CHECKED]
Function consistency and core coverage
3 gene-function check(s) reflected in core functions · 0 conflict(s) · 0 evidence or coverage gap(s) (3 comparison(s))
Retained noncore functions are reported separately; they do not require promotion to core functions. Support from representative genes does not establish conservation across the whole family. Missing reviews or identifiers leave a claim unverified.
| Annoton | Participant | Function | Assessment |
|---|---|---|---|
| gdp_mannose_dehydration_gmd | Gmd UniProtKB:Q9VMW9 Gene |
GDP-mannose 4,6-dehydratase activity GO:0008446 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| gdp_fucose_synthesis_gmer | Gmer UniProtKB:Q9W1X8 Gene |
GDP-L-fucose synthase activity GO:0050577 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| gdp_fucose_transport_gfr | Gfr UniProtKB:Q9VHT4 Gene |
GDP-fucose transmembrane transporter activity GO:0005457 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
Gene-review completeness (4/4 grounded genes reviewed)
4 complete review(s) · 4 with deep research · 0 missing review · 0 reviewed but lacking deep research
| Gene | Review | Complete | Deep research |
|---|---|---|---|
| Efr Q9W429 | ✓ | ✓ | ✓ |
| Gfr Q9VHT4 | ✓ | ✓ | ✓ |
| Gmd Q9VMW9 | ✓ | ✓ | ✓ |
| Gmer Q9W1X8 | ✓ | ✓ | ✓ |
Details
Gmd and Gmer convert GDP-mannose to GDP-fucose, which Gfr and Efr import into the Golgi and endoplasmic reticulum.
Connections
Annotons
Annotons
Function
Gfr imports GDP-fucose into the Golgi; Efr acts in the endoplasmic reticulum and also transports other nucleotide sugars.
Annotons
Function
Golgi GDP-fucose transporter
endoplasmic reticulum nucleotide-sugar transporter