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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：Q96RI0 New Search
3PDB entries
5Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q96RI0 2zpk Proteinase-activated receptor 4 Author chain P Reference sequence 46–53 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 2zpk Proteinase-activated receptor 4 Author chain Q Reference sequence 46–53 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 2zpk Proteinase-activated receptor 4 Author chain P Reference sequence 46–53 2 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 2zpk Proteinase-activated receptor 4 Author chain Q Reference sequence 46–53 2 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 3qdz Proteinase-activated receptor 4 Author chain E Reference sequence 39–47 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 3qdz Proteinase-activated receptor 4 Author chain F Reference sequence 39–47 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 3qdz Proteinase-activated receptor 4 Author chain E Reference sequence 39–47 2 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 3qdz Proteinase-activated receptor 4 Author chain F Reference sequence 39–47 2 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96RI0 8yrq Proteinase-activated receptor 4,Maltose/maltodextrin-binding periplasmic protein Author chain R Reference sequence 48–385 1 Insufficient information Heteromer Protein 5 pentameric （5） 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.