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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：A0A2I0BU46 New Search
5PDB entries
5Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
A0A2I0BU46 8g6e Proteasome subunit beta Author chain M Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
A0A2I0BU46 8g6e Proteasome subunit beta Author chain a Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
A0A2I0BU46 8g6f Proteasome subunit beta-6 Author chain M Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
A0A2I0BU46 8g6f Proteasome subunit beta-6 Author chain a Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
A0A2I0BU46 9y0k Proteasome subunit beta Author chain M Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
A0A2I0BU46 9y0k Proteasome subunit beta Author chain a Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
A0A2I0BU46 9y0l Proteasome subunit beta Author chain M Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 15 pentadecameric （15） Consistent with protein count
A0A2I0BU46 9y1o Proteasome subunit beta Author chain M Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
A0A2I0BU46 9y1o Proteasome subunit beta Author chain a Reference sequence 1–240 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） 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.