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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：P0DP01 New Search
2PDB entries
2Biological assembly
5chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P0DP01 7czy ;Immunoglobulin heavy variable 1-8,Immunoglobulin heavy variable 1-8,chain H of P5A-2F11_2B,Epididymis luminal protein 214,Epididymis luminal protein 214 ; Author chain H Reference sequence 20–117 1 Insufficient information Heteromer Protein 7 其他 23 heptameric （7） Consistent with protein count
P0DP01 7czy ;Immunoglobulin heavy variable 1-8,Immunoglobulin heavy variable 1-8,chain H of P5A-2F11_2B,Epididymis luminal protein 214,Epididymis luminal protein 214 ; Author chain J Reference sequence 20–117 1 Insufficient information Heteromer Protein 7 其他 23 heptameric （7） Consistent with protein count
P0DP01 7czz ;Immunoglobulin heavy variable 1-8,Immunoglobulin heavy variable 1-8,chain H of P5A-2F11_3B,Epididymis luminal protein 214,Epididymis luminal protein 214 ; Author chain H Reference sequence 20–117 1 Insufficient information Heteromer Protein 9 其他 25 nonameric （9） Consistent with protein count
P0DP01 7czz ;Immunoglobulin heavy variable 1-8,Immunoglobulin heavy variable 1-8,chain H of P5A-2F11_3B,Epididymis luminal protein 214,Epididymis luminal protein 214 ; Author chain I Reference sequence 20–117 1 Insufficient information Heteromer Protein 9 其他 25 nonameric （9） Consistent with protein count
P0DP01 7czz ;Immunoglobulin heavy variable 1-8,Immunoglobulin heavy variable 1-8,chain H of P5A-2F11_3B,Epididymis luminal protein 214,Epididymis luminal protein 214 ; Author chain J Reference sequence 20–117 1 Insufficient information Heteromer Protein 9 其他 25 nonameric （9） 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.