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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：A0A1V3W1N5 New Search
8PDB entries
8Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
A0A1V3W1N5 7nyh NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 7 heptameric （7） Consistent with protein count
A0A1V3W1N5 7nyr NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
A0A1V3W1N5 7nyu NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
A0A1V3W1N5 7nyv NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
A0A1V3W1N5 7z80 NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
A0A1V3W1N5 7z83 NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
A0A1V3W1N5 7z84 NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
A0A1V3W1N5 7zc5 NADH-quinone oxidoreductase subunit L Author chain L Reference sequence 1–613 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） 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.