Entner-Doudoroff Sub-pathway Obsoletion (GO:0009255, GO:0061679, GO:0061680, GO:0061681)
Overview
A GO obsoletion proposal will retire four sub-variant terms under the
Entner-Doudoroff pathway and consolidate annotations to the parent term
GO:0061678 Entner-Doudoroff pathway:
- GO:0009255 Entner-Doudoroff pathway through 6-phosphogluconate
- GO:0061679 Entner-Doudoroff pathway through gluconate
- GO:0061680 Entner-Doudoroff pathway through gluconate to D-glyceraldehyde
- GO:0061681 Entner-Doudoroff pathway through gluconate to D-glyceraldehyde-3-phosphate
The intent is to flatten the over-specified sub-pathway hierarchy and let
biology be captured by the single parent ED-pathway term plus the relevant
enzyme MFs. This project tracks impact on the AI Gene Review repo and queues
follow-up edits to existing reviews and candidate gene reviews for the canonical
ED enzymes.
Upstream tickets
- Annotation tracker: geneontology/go-annotation#6390
- Ontology ticket: geneontology/go-ontology#31916
Obsoletion plan (per upstream)
| Obsoleted term | ID | Replacement |
|---|---|---|
| Entner-Doudoroff pathway through 6-phosphogluconate | GO:0009255 | GO:0061678 Entner-Doudoroff pathway |
| Entner-Doudoroff pathway through gluconate | GO:0061679 | GO:0061678 Entner-Doudoroff pathway |
| Entner-Doudoroff pathway through gluconate to D-glyceraldehyde | GO:0061680 | GO:0061678 Entner-Doudoroff pathway |
| Entner-Doudoroff pathway through gluconate to D-glyceraldehyde-3-phosphate | GO:0061681 | GO:0061678 Entner-Doudoroff pathway |
Affected upstream groups (from issue body)
| Group | Annotations | Status |
|---|---|---|
| EcoCyc | 1 | pending |
| UniProt | 3 | pending |
External mappings flagged for review (per upstream)
| Source | Mapping |
|---|---|
| MetaCyc:PWY-8004 → metacyc2go | GO:0009255 |
| InterPro:IPR004786 (6-phosphogluconate dehydratase) → interpro2go | GO:0009255 |
| HAMAP:MF_02094 → hamap2go | GO:0009255 |
| UniRule:UR000683091 → unirule2go | GO:0009255 |
| UniRule:UR001995752 → unirule2go | GO:0009255 |
| MetaCyc:NPGLUCAT-PWY → metacyc2go | GO:0061680 |
| MetaCyc:PWY-2221 → metacyc2go | GO:0061681 |
Impact on this repo
The obsoletion directly affects existing reviews. Two PSEPK gene reviews
already use GO:0009255 in their existing_annotations and core_functions:
| Gene | File | Current usage |
|---|---|---|
| PSEPK edd | genes/PSEPK/edd/edd-ai-review.yaml |
IEA from GO_REF:0000120, accepted; also referenced under core_functions[].directly_involved_in |
| PSEPK eda | genes/PSEPK/eda/eda-ai-review.yaml |
action: NEW annotation proposal (not in GOA) keyed off the UniProt pathway statement; also referenced under core_functions[].directly_involved_in |
Both reviews will need a refresh once the obsoletion lands so that the
directly_involved_in references and the existing_annotations review
entries point to GO:0061678 instead of GO:0009255. The biology is
unchanged — Edd (phosphogluconate dehydratase) and Eda (KDPG aldolase) are
the canonical ED-pathway enzymes in P. putida KT2440.
Scope
- Organisms: bacteria (E. coli, Pseudomonas spp., other ED-using
organisms). The repo's existing PSEPK coverage is the primary in-scope set. - GO branch: BP (carbohydrate catabolism, glycolysis-alternative). The
obsoletion is purely terminological — no MF terms are affected. - Type of fix: lift annotations one level to the parent term GO:0061678.
No enzyme-MF changes required.
Candidate genes for initial review
The two existing PSEPK reviews are the immediate work items; a small set of
ortholog reviews would round out coverage of the canonical ED pathway.
Existing reviews to refresh (post-obsoletion)
- edd (PSEPK) —
genes/PSEPK/edd/edd-ai-review.yaml. Update
GO:0009255 → GO:0061678 in bothexisting_annotationsand the
core_functions[].directly_involved_inblock. - eda (PSEPK) —
genes/PSEPK/eda/eda-ai-review.yaml. Same edit pattern
as edd.
New ortholog reviews (proactive)
Verify each with just fetch-gene <organism> <gene> before starting; do not
add files without confirming the UniProt accession from the UniProt API.
- edd (E. coli K-12) — phosphogluconate dehydratase; the founding
organism for the ED pathway and likely the EcoCyc-affected entry upstream. - eda (E. coli K-12) — KDPG aldolase; companion to E. coli edd,
completes the two-enzyme ED core. - zwf (PSEPK) — glucose-6-phosphate 1-dehydrogenase, the entry step into
the ED pathway via 6-phosphogluconate. Already partially covered in the
PSEPK gene set perprojects/SPKW/SPKW-PSEPK.md; verify status before adding. - gnd / 6PGD homologs — the diversion point between ED and the pentose
phosphate pathway; a clean review here clarifies why annotations should
sit at GO:0061678 rather than a sub-variant.
Proposed approach
- Wait for the obsoletion to land in a public GO release. The
ontology ticket (#31916) has not yet been merged at the time of writing,
so refreshing the PSEPK reviews now would need to be redone if labels
change. - Once the obsoletion is in a release, update the two PSEPK reviews in
one PR — the change is mechanical (term ID swap + label update) and the
review.summarytext already justifies pathway-level annotation. The
action differs by gene: for edd the existing IEA isACCEPTed and
staysACCEPTon the lifted parent term; for eda the annotation is
a curator-proposedNEW(no GOA row) and staysNEWon the lifted
parent term. Thereview.summarytext in eda also references the old
label "Entner-Doudoroff pathway through 6-phosphogluconate" and should
be updated to "Entner-Doudoroff pathway (GO:0061678)" alongside the
term-ID swap. - Re-run
just validate PSEPK eddandjust validate PSEPK edaafter
the edits to confirm the schema accepts the new term IDs. - Defer new ortholog reviews (E. coli edd/eda, zwf, gnd) to a follow-up
batch — the obsoletion does not block them, and they are best done as a
coherent ED-pathway batch rather than ad hoc.
Priority
Low–Medium. The obsoletion is mechanical and only two existing reviews
are affected; both can be updated in a single small PR once the ontology
release ships. Higher value is in using the moment to add E. coli ED
reviews, but those are independent of the obsoletion itself.