← Back to search

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：P40701 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
P40701 6pem Surface presentation of antigens protein SpaR Author chain 5 Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 74 74-meric （74） Consistent with protein count
P40701 6pep Surface presentation of antigens protein SpaR Author chain 5 Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 69 69-meric （69） Consistent with protein count
P40701 6q14 Surface presentation of antigens protein SpaR Author chain 5 Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 74 74-meric （74） Consistent with protein count
P40701 6q15 Surface presentation of antigens protein SpaR Author chain 5 Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 110 110-meric （110） Consistent with protein count
P40701 6q16 Surface presentation of antigens protein SpaR Author chain 5 Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 93 93-meric （93） Consistent with protein count
P40701 7agx Surface presentation of antigens protein SpaR Author chain 1F Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 33 33-meric （33） Consistent with protein count
P40701 7ah9 Surface presentation of antigens protein SpaR Author chain 1F Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 153 153-meric （153） Consistent with protein count
P40701 7ahi Surface presentation of antigens protein SpaR Author chain 1F Reference sequence 1–263 1 Protein heterocomplex Heteromer Protein 153 153-meric （153） 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.