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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：Q96GD0 New Search
9PDB entries
9Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q96GD0 2cfr PYRIDOXAL PHOSPHATE PHOSPHATASE Author chain A Reference sequence 1–296 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q96GD0 2cfs PYRIDOXAL PHOSPHATE PHOSPHATASE Author chain A Reference sequence 1–296 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q96GD0 2cft PYRIDOXAL PHOSPHATE PHOSPHATASE Author chain A Reference sequence 1–296 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q96GD0 2oyc Pyridoxal phosphate phosphatase Author chain A Reference sequence 2–296 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q96GD0 2p27 Pyridoxal phosphate phosphatase Author chain A Reference sequence 2–296 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q96GD0 2p69 Pyridoxal phosphate phosphatase Author chain A Reference sequence 2–296 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q96GD0 5gyn Pyridoxal phosphate phosphatase Author chain A Reference sequence 1–296 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q96GD0 8s8a Chronophin Author chain A Reference sequence 1–296 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q96GD0 9em1 Chronophin Author chain A Reference sequence 1–296 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.