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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：A0A086KR31 New Search
1PDB entries
1Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A1 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A2 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A3 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A4 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A5 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A6 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A7 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A8 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） Consistent with protein count
A0A086KR31 9y9z CF4, TGME49_246720 Author chain A9 Reference sequence 1–502 1 Protein heterocomplex Heteromer Protein 378 378-meric （378） 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.