SEC11C PN Consistency Notes
- Generated: 2026-06-18
- Project: PROTEOSTASIS
- Scope: PN consistency rereview against local AIGR review and available deep-research artifacts
- UniProt: Q9BY50
- AIGR review status: COMPLETE
- Review batch: proteostasis-batch-2026-06-11
- Batch change status: added
Source Files Checked
Deep Research Files
AIGR Review Snapshot
- Description: SEC11C (SPC21, SEC11L3; EC 3.4.21.89) is a single-pass type II endoplasmic reticulum membrane protein and one of the two catalytic serine-endopeptidase subunits of the human signal peptidase complex (SPC). As the proteolytic subunit of the SPC-C paralog (with accessory subunits SPCS1, SPCS2 and SPCS3), SEC11C catalyzes cleavage of N-terminal signal (leader) peptides from secretory and membrane pre-proteins as they are translocated into the ER lumen. It belongs to peptidase family S26B and uses a Ser/His/Asp-type charge-relay catalytic system (Ser-68 nucleophile). Its active site abuts the ER membrane, where the complex locally thins the lipid bilayer, conferring selectivity for signal peptides whose hydrophobic h-region is shorter than ~18-20 residues. SEC11C is the paralog of the more broadly expressed SEC11A; the two catalytic subunits form distinct but functionally analogous SPC paralogs.
- Existing/core annotation action counts: ACCEPT: 18; KEEP_AS_NON_CORE: 6
PN Consistency Summary
- Consistency: Strong agreement. Deep research, review YAML, and PN all identify SEC11C as the catalytic serine-endopeptidase subunit of the SPC-C paralog (Ser-68 triad, EC 3.4.21.89), the paralog of SEC11A. PN's "ER signal peptidase" node correctly captures complex membership. No contradictions.
- PN story / NEW pressure: Identical to SEC11A. PN asserts CC membership (GO:0005787) + broad transport (GO:0015031), both already in the review, which additionally carries the catalytic MF (GO:0009003/GO:0004252, EXP/IDA from PMID:34388369). PN under-specifies the catalytic MF rather than over-reaching. No NEW term. Conclude: already captured.
- Evidence alignment: PN row carries no titles; review evidence (PMID:34388369 structure/triad; Reactome signalase reactions; PMID:36454823 QC redundancy with SEC11A; PMID:28423309 cavinafungin) and falcon deep research (liaci2021) converge on the catalytic identity. Note PMID:26446786 names SEC11A (not SEC11C) — review correctly downgraded its relevance to SEC11C to LOW (background only).
- Verdict: CONSISTENT; PN captures CC membership but omits catalytic MF (already in review). No edit required.
Full Consistency Review
- UniProt: Q9BY50 (SPC21) · batch: proteostasis-batch-2026-06-11 · review status: COMPLETE
- PN placement:
ER proteostasis|Protein transport|ER signal peptidase; PN-node mapping: group mapped, ok_for_propagation_to_go, GO:0005787 (signal peptidase complex); class GO:0015031 (protein transport).
- Consistency: Strong agreement. Deep research, review YAML, and PN all identify SEC11C as the catalytic serine-endopeptidase subunit of the SPC-C paralog (Ser-68 triad, EC 3.4.21.89), the paralog of SEC11A. PN's "ER signal peptidase" node correctly captures complex membership. No contradictions.
- PN story / NEW pressure: Identical to SEC11A. PN asserts CC membership (GO:0005787) + broad transport (GO:0015031), both already in the review, which additionally carries the catalytic MF (GO:0009003/GO:0004252, EXP/IDA from PMID:34388369). PN under-specifies the catalytic MF rather than over-reaching. No NEW term. Conclude: already captured.
- Mapping strategy: Same as SEC11A: node maps the catalytic+accessory group to the CC GO:0005787, which is correct for membership but does not surface SEC11C's catalytic peptidase MF. Node need not change; a catalytic-vs-accessory distinction note belongs at the node. GO:0015031 acceptably broad; no over-reach.
- Evidence alignment: PN row carries no titles; review evidence (PMID:34388369 structure/triad; Reactome signalase reactions; PMID:36454823 QC redundancy with SEC11A; PMID:28423309 cavinafungin) and falcon deep research (liaci2021) converge on the catalytic identity. Note PMID:26446786 names SEC11A (not SEC11C) — review correctly downgraded its relevance to SEC11C to LOW (background only).
- Verdict: CONSISTENT; PN captures CC membership but omits catalytic MF (already in review). No edit required.
- Recommended edits: [MAP] Same node-level note as SEC11A: flag that catalytic subunits SEC11A/SEC11C project signal peptidase MF (GO:0009003 / GO:0004252) distinct from the non-catalytic SPCS subunits.
PN Dossier Context
- review_batch: proteostasis-batch-2026-06-11
- review_yaml: genes/human/SEC11C/SEC11C-ai-review.yaml
- PN workbook rows: 1
PN row 1: ER proteostasis | Protein transport | ER signal peptidase
- UniProt: Q9BY50
- In branches: ER
- PN-node mapping records (path + ancestors):
- [group] ER proteostasis|Protein transport|ER signal peptidase
status=mapped scope=ok_for_propagation_to_go GO=[GO:0005787 signal peptidase complex]
rationale: This PN group denotes ER signal peptidase complex components. The matching GO cellular-component term is the direct propagation target.
- [class] ER proteostasis|Protein transport
status=mapped scope=ok_for_propagation_to_go GO=[GO:0015031 protein transport]
rationale: The PN ER Protein transport class groups ER-targeting and ER-insertion pathways. GO protein transport is the appropriate propagation target, while the source class remains ER-specific and broader than any single GO transport subtype.
- [branch] ER proteostasis
status=no_mapping scope= GO=[]
rationale: Reviewed as a top-level PN branch. This is a systems/taxonomy umbrella, not a direct GO assertion; narrower child curations carry any propagating GO mappings.
Projected GO annotations (2)
- GO:0015031 protein transport | scope=ok_for_propagation_to_go | goa_status=new_to_goa | from=ER proteostasis|Protein transport
- GO:0005787 signal peptidase complex | scope=ok_for_propagation_to_go | goa_status=already_in_goa_exact | from=ER proteostasis|Protein transport|ER signal peptidase
Note
This file is generated from the current PROTEOSTASIS phase-1 dossier and local gene-review artifacts. Edit the source review, PN mapping, or dossier rather than this generated note when correcting the underlying curation.