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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：Q08109 New Search
6PDB entries
6Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q08109 5v6p ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain A Reference sequence 1–407 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q08109 5v6p ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain B Reference sequence 1–407 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q08109 6vjy ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain B Reference sequence 1–430 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q08109 6vjz ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain B Reference sequence 1–480 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q08109 6vk0 ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain B Reference sequence 1–480 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q08109 6vk1 ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain B Reference sequence 1–480 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q08109 9z0e ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain B Reference sequence 1–326 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q08109 9z0e ERAD-associated E3 ubiquitin-protein ligase HRD1 Author chain C Reference sequence 1–326 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） 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.