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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：Q72J73 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
Q72J73 5gar V-type ATP synthase beta chain Author chain D Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 26 26-meric （26） Consistent with protein count
Q72J73 5gar V-type ATP synthase beta chain Author chain E Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 26 26-meric （26） Consistent with protein count
Q72J73 5gar V-type ATP synthase beta chain Author chain F Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 26 26-meric （26） Consistent with protein count
Q72J73 5gas V-type ATP synthase beta chain Author chain D Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 26 26-meric （26） Consistent with protein count
Q72J73 5gas V-type ATP synthase beta chain Author chain E Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 26 26-meric （26） Consistent with protein count
Q72J73 5gas V-type ATP synthase beta chain Author chain F Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 26 26-meric （26） Consistent with protein count
Q72J73 5tsj V-type ATP synthase beta chain Author chain D Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
Q72J73 5tsj V-type ATP synthase beta chain Author chain E Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） Consistent with protein count
Q72J73 5tsj V-type ATP synthase beta chain Author chain F Reference sequence 7–463 1 Protein heterocomplex Heteromer Protein 28 28-meric （28） 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.