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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：B1MLW2 New Search
3PDB entries
3Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
B1MLW2 9vkp ATP synthase subunit beta Author chain D Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkp ATP synthase subunit beta Author chain E Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkp ATP synthase subunit beta Author chain F Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkq ATP synthase subunit beta Author chain D Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkq ATP synthase subunit beta Author chain E Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkq ATP synthase subunit beta Author chain F Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkr ATP synthase subunit beta Author chain D Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkr ATP synthase subunit beta Author chain E Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） Consistent with protein count
B1MLW2 9vkr ATP synthase subunit beta Author chain F Reference sequence 1–476 1 Protein heterocomplex Heteromer Protein 10 decameric （10） 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.