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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：Q9Q1V2 New Search
1PDB entries
5Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain A Reference sequence 66–590 1 Protein homooligomer Homooligomer Protein 120 120-MERIC （120） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain B Reference sequence 66–590 1 Protein homooligomer Homooligomer Protein 120 120-MERIC （120） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain A Reference sequence 66–590 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain B Reference sequence 66–590 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain A Reference sequence 66–590 3 Protein homooligomer Homooligomer Protein 10 decameric （10） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain B Reference sequence 66–590 3 Protein homooligomer Homooligomer Protein 10 decameric （10） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain A Reference sequence 66–590 4 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain B Reference sequence 66–590 4 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain A Reference sequence 66–590 5 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q9Q1V2 2vf1 CAPSID PROTEIN Author chain B Reference sequence 66–590 5 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.