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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：Q96P70 New Search
7PDB entries
8Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q96P70 10sm Importin-9 Author chain D Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q96P70 6n1z Importin-9 Author chain A Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96P70 6n1z Importin-9 Author chain D Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96P70 6n1z Importin-9 Author chain A Reference sequence 1–1041 2 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96P70 6n1z Importin-9 Author chain D Reference sequence 1–1041 2 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96P70 8f7a Importin-9 Author chain A Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q96P70 9qno Importin-9 Author chain A Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q96P70 9qon Importin-9 Author chain A Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 11 11-meric （11） Consistent with protein count
Q96P70 9qoo Importin-9 Author chain A Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 12 12-meric （12） Consistent with protein count
Q96P70 9qop Importin-9 Author chain A Reference sequence 1–1041 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） 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.