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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：Q8IY92 New Search
7PDB entries
7Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q8IY92 4m7c Peptide from Structure-specific endonuclease subunit SLX4 Author chain C Reference sequence 1014–1025 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q8IY92 4m7c Peptide from Structure-specific endonuclease subunit SLX4 Author chain D Reference sequence 1014–1025 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q8IY92 4uyi STRUCTURE-SPECIFIC ENDONUCLEASE SUBUNIT SLX4 Author chain A Reference sequence 668–796 1 Protein homooligomer Homooligomer Protein 6 hexameric （6） Consistent with protein count
Q8IY92 4zou Structure-specific endonuclease subunit SLX4 Author chain A Reference sequence 669–787 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q8IY92 7bu5 Structure-specific endonuclease subunit SLX4 Author chain B Reference sequence 1550–1610 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q8IY92 7tuj Structure-specific endonuclease subunit SLX4 Author chain A Reference sequence 1528–1613 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q8IY92 9qed Structure-specific endonuclease subunit SLX4 Author chain D Reference sequence 330–555 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q8IY92 9qee Structure-specific endonuclease subunit SLX4 Author chain D Reference sequence 330–555 1 Protein–DNA Heteromer Protein 4 DNA 2 hexameric （6） Consistent with all polymers

“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.