← Back to search

Protein Structures and Oligomeric States

Enter a protein name, UniProt accession or PDB ID. Name searches ask you to confirm the protein identity before related structures are queried.

Current Protein Identity：E7EX29 New Search
1PDB entries
1Biological assembly
6chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
E7EX29 8p1h Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta,Neuronal acetylcholine receptor subunit alpha-7 Author chain A Reference sequence 1–72 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
E7EX29 8p1h Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta,Neuronal acetylcholine receptor subunit alpha-7 Author chain A Reference sequence 76–164 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
E7EX29 8p1h Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta,Neuronal acetylcholine receptor subunit alpha-7 Author chain A Reference sequence 168–237 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
E7EX29 8p1h Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta,Neuronal acetylcholine receptor subunit alpha-7 Author chain B Reference sequence 1–72 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
E7EX29 8p1h Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta,Neuronal acetylcholine receptor subunit alpha-7 Author chain B Reference sequence 76–164 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count
E7EX29 8p1h Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta,Neuronal acetylcholine receptor subunit alpha-7 Author chain B Reference sequence 168–237 1 Insufficient information Homooligomer Protein 2 dimeric （2） Consistent with protein count

“Homomeric versus heteromeric classification follows protein identity; different constructs of the same UniProt entry still require comparison of reference-sequence ranges, mutations and missing segments. Assemblies marked for review remain visible but are not included in the highest-confidence candidate set.