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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：Q5XXZ6 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
Q5XXZ6 7ti4 Capsid protein Author chain A Reference sequence 1–726 1 Protein homooligomer Homooligomer Protein 60 60-meric （60） Consistent with protein count
Q5XXZ6 7ti4 Capsid protein Author chain A Reference sequence 1–726 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q5XXZ6 7ti4 Capsid protein Author chain A Reference sequence 1–726 3 Protein homooligomer Homooligomer Protein 5 pentameric （5） Consistent with protein count
Q5XXZ6 7ti4 Capsid protein Author chain A Reference sequence 1–726 4 Protein homooligomer Homooligomer Protein 6 hexameric （6） Consistent with protein count
Q5XXZ6 7ti4 Capsid protein Author chain A Reference sequence 1–726 5 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q5XXZ6 7ti5 Capsid protein Author chain A Reference sequence 1–726 1 Protein heterocomplex Heteromer Protein 120 120-meric （120） Consistent with protein count
Q5XXZ6 7ti5 Capsid protein Author chain A Reference sequence 1–726 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q5XXZ6 7ti5 Capsid protein Author chain A Reference sequence 1–726 3 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
Q5XXZ6 7ti5 Capsid protein Author chain A Reference sequence 1–726 4 Protein heterocomplex Heteromer Protein 12 dodecameric （12） Consistent with protein count
Q5XXZ6 7ti5 Capsid protein Author chain A Reference sequence 1–726 5 Protein heterocomplex Heteromer 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.