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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：A0A286KB20 New Search
2PDB entries
10Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
A0A286KB20 9c8g VP2 Author chain B Reference sequence 70–317 1 Protein heterocomplex Heteromer Protein 240 240-meric （240） Consistent with protein count
A0A286KB20 9c8g VP2 Author chain B Reference sequence 70–317 2 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
A0A286KB20 9c8g VP2 Author chain B Reference sequence 70–317 3 Protein heterocomplex Heteromer Protein 20 eicosameric （20） Consistent with protein count
A0A286KB20 9c8g VP2 Author chain B Reference sequence 70–317 4 Protein heterocomplex Heteromer Protein 24 24-meric （24） Consistent with protein count
A0A286KB20 9c8g VP2 Author chain B Reference sequence 70–317 5 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
A0A286KB20 9c8h VP2 Author chain B Reference sequence 70–317 1 Protein heterocomplex Heteromer Protein 180 180-meric （180） Consistent with protein count
A0A286KB20 9c8h VP2 Author chain B Reference sequence 70–317 2 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
A0A286KB20 9c8h VP2 Author chain B Reference sequence 70–317 3 Protein heterocomplex Heteromer Protein 15 pentadecameric （15） Consistent with protein count
A0A286KB20 9c8h VP2 Author chain B Reference sequence 70–317 4 Protein heterocomplex Heteromer Protein 18 octadecameric （18） Consistent with protein count
A0A286KB20 9c8h VP2 Author chain B Reference sequence 70–317 5 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.