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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：A0A218NFC2 New Search
3PDB entries
4Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
A0A218NFC2 9m71 AcrIE10 Author chain A Reference sequence 4–116 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
A0A218NFC2 9m71 AcrIE10 Author chain B Reference sequence 4–116 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
A0A218NFC2 9m71 AcrIE10 Author chain A Reference sequence 4–116 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
A0A218NFC2 9m71 AcrIE10 Author chain B Reference sequence 4–116 2 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
A0A218NFC2 9m7t AcrIE10 Author chain A Reference sequence 1–116 1 Protein–DNA Homooligomer Protein 2 DNA 2 tetrameric （4） Consistent with all polymers
A0A218NFC2 9m7t AcrIE10 Author chain B Reference sequence 1–116 1 Protein–DNA Homooligomer Protein 2 DNA 2 tetrameric （4） Consistent with all polymers
A0A218NFC2 9uer AcrIE10 Author chain A Reference sequence 1–116 1 Protein–DNA Heteromer Protein 6 DNA 2 octameric （8） Consistent with all polymers
A0A218NFC2 9uer AcrIE10 Author chain B Reference sequence 1–116 1 Protein–DNA Heteromer Protein 6 DNA 2 octameric （8） Consistent with all polymers
A0A218NFC2 9uer AcrIE10 Author chain C Reference sequence 1–116 1 Protein–DNA Heteromer Protein 6 DNA 2 octameric （8） Consistent with all polymers
A0A218NFC2 9uer AcrIE10 Author chain D Reference sequence 1–116 1 Protein–DNA Heteromer Protein 6 DNA 2 octameric （8） 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.