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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：P82889 New Search
3PDB entries
9Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P82889 1hgv PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 1 Protein homooligomer Homooligomer Protein 35 helical （35） Consistent with protein count
P82889 1hgv PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P82889 1hgv PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 3 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P82889 1hgz PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 1 Protein homooligomer Homooligomer Protein 35 helical （35） Consistent with protein count
P82889 1hgz PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P82889 1hgz PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 3 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P82889 1hh0 PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 1 Protein homooligomer Homooligomer Protein 35 helical （35） Consistent with protein count
P82889 1hh0 PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P82889 1hh0 PH75 INOVIRUS MAJOR COAT PROTEIN Author chain A Reference sequence 1–46 3 Protein monomer Monomer Protein 1 monomeric （1） 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.