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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：P12302 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
P12302 2vu4 OXYGEN-EVOLVING ENHANCER PROTEIN 2 Author chain A Reference sequence 82–267 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P12302 3jcu Oxygen-evolving enhancer protein 2, chloroplastic Author chain P Reference sequence 1–267 1 Protein heterocomplex Heteromer Protein 50 50-meric （50） Consistent with protein count
P12302 3jcu Oxygen-evolving enhancer protein 2, chloroplastic Author chain p Reference sequence 1–267 1 Protein heterocomplex Heteromer Protein 50 50-meric （50） Consistent with protein count
P12302 4rti Oxygen-evolving enhancer protein 2, chloroplastic Author chain A Reference sequence 82–267 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P12302 8z9d Oxygen-evolving enhancer protein 2, chloroplastic Author chain P Reference sequence 1–267 1 Protein heterocomplex Heteromer Protein 112 112-meric （112） Consistent with protein count
P12302 8z9d Oxygen-evolving enhancer protein 2, chloroplastic Author chain PP Reference sequence 1–267 1 Protein heterocomplex Heteromer Protein 112 112-meric （112） Consistent with protein count
P12302 8z9d Oxygen-evolving enhancer protein 2, chloroplastic Author chain Pp Reference sequence 1–267 1 Protein heterocomplex Heteromer Protein 112 112-meric （112） Consistent with protein count
P12302 8z9d Oxygen-evolving enhancer protein 2, chloroplastic Author chain p Reference sequence 1–267 1 Protein heterocomplex Heteromer Protein 112 112-meric （112） 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.