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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：Q63K37 New Search
4PDB entries
6Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q63K37 2ixr MEMBRANE ANTIGEN Author chain A Reference sequence 10–310 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2izp PUTATIVE MEMBRANE ANTIGEN Author chain A Reference sequence 8–310 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2izp PUTATIVE MEMBRANE ANTIGEN Author chain B Reference sequence 8–310 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2izp PUTATIVE MEMBRANE ANTIGEN Author chain A Reference sequence 8–310 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2izp PUTATIVE MEMBRANE ANTIGEN Author chain B Reference sequence 8–310 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2j9t MEMBRANE ANTIGEN Author chain A Reference sequence 10–310 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2j9t MEMBRANE ANTIGEN Author chain B Reference sequence 10–310 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2j9t MEMBRANE ANTIGEN Author chain A Reference sequence 10–310 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 2j9t MEMBRANE ANTIGEN Author chain B Reference sequence 10–310 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q63K37 3nft Translocator protein bipD Author chain A Reference sequence 8–310 1 Protein homooligomer 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.