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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：A0A366UU94 New Search
8PDB entries
8Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
A0A366UU94 8spr Outer membrane protein assembly factor BamE Author chain E Reference sequence 21–113 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
A0A366UU94 8sqa Outer membrane protein assembly factor BamE Author chain E Reference sequence 21–113 1 Insufficient information Heteromer Protein 6 hexameric （6） Consistent with protein count
A0A366UU94 8sqb Outer membrane protein assembly factor BamE Author chain E Reference sequence 21–113 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
A0A366UU94 9cnw Outer membrane protein assembly factor BamE Author chain E Reference sequence 1–113 1 Protein heterocomplex Heteromer Protein 5 pentameric （5） Consistent with protein count
A0A366UU94 9cnx Outer membrane protein assembly factor BamE Author chain E Reference sequence 1–113 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
A0A366UU94 9cny Outer membrane protein assembly factor BamE Author chain E Reference sequence 1–113 1 Protein heterocomplex Heteromer Protein 5 pentameric （5） Consistent with protein count
A0A366UU94 9cnz Outer membrane protein assembly factor BamE Author chain E Reference sequence 1–113 1 Protein heterocomplex Heteromer Protein 8 octameric （8） Consistent with protein count
A0A366UU94 9co0 Outer membrane protein assembly factor BamE Author chain E Reference sequence 1–113 1 Protein heterocomplex Heteromer Protein 8 octameric （8） 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.