Function
Locations
Transfer the Dol-PP glycan onto Asn sequons co-translationally.
The oligosaccharyltransferase (OST) complex is the endoplasmic-reticulum-membrane enzyme that performs the central, committed step of N-linked glycosylation: en-bloc transfer of the preassembled Glc3Man9GlcNAc2 glycan from dolichyl diphosphate (Dol-PP) onto the side-chain amide of asparagine residues within N-X-S/T sequons of nascent secretory and membrane proteins. Humans have two OST isoforms distinguished by their catalytic subunit. The STT3A complex (OST-A) is docked at the SEC61 translocon and glycosylates sequons co-translationally as the polypeptide enters the ER; its subunit OSTC (DC2) tethers it to the translocon. The STT3B complex (OST-B) acts post-translationally and translocon-independently, providing a proofreading second pass that glycosylates skipped, C-terminal and closely-spaced sequons; its thioredoxin-like oxidoreductase subunits MAGT1 and TUSC3 use a CXXC motif to transiently engage substrate cysteines, enabling glycosylation of cysteine-proximal sequons. Both isoforms share a set of non-catalytic scaffold subunits - ribophorin I (RPN1), ribophorin II (RPN2), OST48 (DDOST) and DAD1 - required for complex integrity and substrate presentation. Defects in individual subunits cause congenital disorders of glycosylation (STT3A-, STT3B-, DDOST-CDG), X-linked immunodeficiency with magnesium defect (MAGT1/XMEN) and autosomal-recessive intellectual disability (TUSC3).
All recommended fields populated.
✗ none found
No MODULE:oligosaccharyltransferase_complex deep-research report alongside the module YAML.
✓ every leaf node grounds to a representative protein.
✓ every declared conforms_to bundle matches its template motif.
✓ every PRECEDES step chains, or its break is acknowledged via chaining_status.
9 complete review(s) · 0 with deep research · 0 missing review · 9 reviewed but lacking deep research
| Gene | Review | Complete | Deep research |
|---|---|---|---|
| DAD1 P61803 | ✓ | ✓ | ✗ |
| DDOST P39656 | ✓ | ✓ | ✗ |
| MAGT1 Q9H0U3 | ✓ | ✓ | ✗ |
| OSTC Q9NRP0 | ✓ | ✓ | ✗ |
| RPN1 P04843 | ✓ | ✓ | ✗ |
| RPN2 P04844 | ✓ | ✓ | ✗ |
| STT3A P46977 | ✓ | ✓ | ✗ |
| STT3B Q8TCJ2 | ✓ | ✓ | ✗ |
| TUSC3 Q13454 | ✓ | ✓ | ✗ |
Oligosaccharyltransferase (OST) complex - the ER-membrane machine that transfers the Dol-PP-linked Glc3Man9GlcNAc2 glycan onto Asn sequons (GO:0004579 / GO:0006487) - grounded to nine completed human gene reviews. Two isoforms share four scaffold subunits: catalytic STT3A (P46977, PTHR13872) with the translocon adaptor OSTC/DC2 (Q9NRP0, PTHR13160, GO:0030674) form OST-A (GO:0160226) for co-translational glycosylation (GO:0180058); catalytic STT3B (Q8TCJ2, PTHR13872) with the thioredoxin-like oxidoreductases MAGT1 (Q9H0U3) and TUSC3 (Q13454) (both PTHR12692, GO:0015036/GO:0015035) form OST-B (GO:0160227) for post-translational proofreading (GO:0180057). Shared scaffold: RPN1 (P04843 PTHR21049), RPN2 (P04844 PTHR12640), DDOST/OST48 (P39656 PTHR10830), DAD1 (P61803 PTHR10705) - modelled as non-catalytic subunits (in_complex GO:0008250, contributes_to GO:0004579 in their gene reviews). Module node locations are the anatomical ER membrane (GO:0005789); the OST-complex CC terms live in the gene reviews' in_complex. Curation notes: MAGT1/TUSC3 historical magnesium-transporter annotations are contested/secondary to the OST oxidoreductase role (kept non-core/over-annotated in the reviews); DAD1's anti-apoptotic role is downstream of OST integrity (non-core). Diseases: STT3A/STT3B/DDOST-CDG, MAGT1/XMEN, TUSC3 AR intellectual disability. Consumes the Dol-PP-glycan from the LLO/ALG assembly (reviewed) built on dolichol from the dolichyl_phosphate_biosynthesis module. GO term ids/labels verified against the local go.db; module passes structural + term-label validation.
Transfer the Dol-PP glycan onto Asn sequons co-translationally.
Anchor the STT3A OST complex to the translocon.
Glycosylate skipped/C-terminal Asn sequons post-translationally.
Engage substrate cysteines to expose Cys-proximal sequons for STT3B.