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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：Q38950 New Search
5PDB entries
5Biological assembly
7chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q38950 7xvk Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform Author chain A Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q38950 9j5i Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform Author chain A Reference sequence 1–587 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q38950 9j5i Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform Author chain D Reference sequence 1–587 1 Protein heterocomplex Heteromer Protein 6 hexameric （6） Consistent with protein count
Q38950 9j5k Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform Author chain A Reference sequence 1–587 1 Protein heterocomplex Heteromer Protein 8 octameric （8） Consistent with protein count
Q38950 9j5k Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform Author chain D Reference sequence 1–587 1 Protein heterocomplex Heteromer Protein 8 octameric （8） Consistent with protein count
Q38950 9j5n Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform Author chain A Reference sequence 1–587 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） Consistent with protein count
Q38950 9j5r Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform Author chain A Reference sequence 1–587 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） 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.