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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：Q8DL32 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
Q8DL32 6hum NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 18 octadecameric （18） Consistent with protein count
Q8DL32 6khi NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 20 eicosameric （20） Consistent with protein count
Q8DL32 6khj NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 18 octadecameric （18） Consistent with protein count
Q8DL32 6l7o NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 20 eicosameric （20） Consistent with protein count
Q8DL32 6l7p NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 18 octadecameric （18） Consistent with protein count
Q8DL32 6nbx NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 18 octadecameric （18） Consistent with protein count
Q8DL32 6nby NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 18 octadecameric （18） Consistent with protein count
Q8DL32 6tjv NAD(P)H-quinone oxidoreductase subunit 1 Author chain A Reference sequence 1–372 1 Protein heterocomplex Heteromer Protein 18 octadecameric （18） 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.