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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：Q8N4I3 New Search
2PDB entries
2Biological assembly
7chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q8N4I3 2ux0 CALCIUM-CALMODULIN DEPENDENT PROTEIN KINASE (CAM KINASE) II GAMMA Author chain A Reference sequence 387–527 1 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q8N4I3 2ux0 CALCIUM-CALMODULIN DEPENDENT PROTEIN KINASE (CAM KINASE) II GAMMA Author chain B Reference sequence 387–527 1 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q8N4I3 2ux0 CALCIUM-CALMODULIN DEPENDENT PROTEIN KINASE (CAM KINASE) II GAMMA Author chain C Reference sequence 387–527 1 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q8N4I3 2ux0 CALCIUM-CALMODULIN DEPENDENT PROTEIN KINASE (CAM KINASE) II GAMMA Author chain D Reference sequence 387–527 1 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q8N4I3 2ux0 CALCIUM-CALMODULIN DEPENDENT PROTEIN KINASE (CAM KINASE) II GAMMA Author chain E Reference sequence 387–527 1 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q8N4I3 2ux0 CALCIUM-CALMODULIN DEPENDENT PROTEIN KINASE (CAM KINASE) II GAMMA Author chain F Reference sequence 387–527 1 Protein homooligomer Homooligomer Protein 12 dodecameric （12） Consistent with protein count
Q8N4I3 2v7o CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE TYPE II GAMMA CHAIN Author chain A Reference sequence 5–315 1 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.