← Back to search

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：Q9HK51 New Search
4PDB entries
4Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q9HK51 2dtd Glucose 1-dehydrogenase related protein Author chain A Reference sequence 2–255 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q9HK51 2dtd Glucose 1-dehydrogenase related protein Author chain B Reference sequence 2–255 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q9HK51 2dte Glucose 1-dehydrogenase related protein Author chain A Reference sequence 2–255 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q9HK51 2dte Glucose 1-dehydrogenase related protein Author chain B Reference sequence 2–255 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q9HK51 2dtx Glucose 1-dehydrogenase related protein Author chain A Reference sequence 2–255 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q9HK51 2dtx Glucose 1-dehydrogenase related protein Author chain B Reference sequence 2–255 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q9HK51 2zk7 Glucose 1-dehydrogenase related protein Author chain A Reference sequence 1–249 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q9HK51 2zk7 Glucose 1-dehydrogenase related protein Author chain B Reference sequence 1–249 1 Protein homooligomer Homooligomer Protein 4 tetrameric （4） 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.