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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：O15923 New Search
2PDB entries
3Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain A Reference sequence 1–283 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain B Reference sequence 1–283 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain D Reference sequence 1–283 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain E Reference sequence 1–283 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain A Reference sequence 1–283 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain B Reference sequence 1–283 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain D Reference sequence 1–283 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogk DEOXYURIDINE TRIPHOSPHATASE Author chain E Reference sequence 1–283 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
O15923 1ogl DEOXYURIDINE TRIPHOSPHATASE Author chain A Reference sequence 1–283 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.