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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：P69902 New Search
6PDB entries
6Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P69902 1pqy Hypothetical protein yfdW Author chain A Reference sequence 2–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1pt5 Hypothetical protein yfdW Author chain A Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1pt5 Hypothetical protein yfdW Author chain B Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1pt7 Hypothetical protein yfdW Author chain A Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1pt7 Hypothetical protein yfdW Author chain B Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1pt8 Hypothetical protein yfdW Author chain A Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1pt8 Hypothetical protein yfdW Author chain B Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1q6y Hypothetical protein yfdW Author chain A Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P69902 1q7e Hypothetical protein yfdW Author chain A Reference sequence 1–416 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） 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.