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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：Q9NPJ4 New Search
3PDB entries
4Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q9NPJ4 4b6h PROLINE-RICH NUCLEAR RECEPTOR COACTIVATOR 2 Author chain C Reference sequence 1–121 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NPJ4 4b6h PROLINE-RICH NUCLEAR RECEPTOR COACTIVATOR 2 Author chain D Reference sequence 1–121 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NPJ4 4b6h PROLINE-RICH NUCLEAR RECEPTOR COACTIVATOR 2 Author chain C Reference sequence 1–121 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NPJ4 4b6h PROLINE-RICH NUCLEAR RECEPTOR COACTIVATOR 2 Author chain D Reference sequence 1–121 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NPJ4 5kq1 Proline-rich nuclear receptor coactivator 2 Author chain C Reference sequence 72–102 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q9NPJ4 5kq1 Proline-rich nuclear receptor coactivator 2 Author chain F Reference sequence 72–102 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q9NPJ4 5kq4 Proline-rich nuclear receptor coactivator 2 Author chain C Reference sequence 72–102 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q9NPJ4 5kq4 Proline-rich nuclear receptor coactivator 2 Author chain F Reference sequence 72–102 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） 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.