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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：B8YB59 New Search
3PDB entries
5Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
B8YB59 2y0s RNA POLYMERASE SUBUNIT 8 Author chain G Reference sequence 1–132 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
B8YB59 2y0s RNA POLYMERASE SUBUNIT 8 Author chain V Reference sequence 1–132 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
B8YB59 2y0s RNA POLYMERASE SUBUNIT 8 Author chain G Reference sequence 1–132 2 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
B8YB59 2y0s RNA POLYMERASE SUBUNIT 8 Author chain V Reference sequence 1–132 2 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
B8YB59 4ayb DNA-DIRECTED RNA POLYMERASE Author chain G Reference sequence 1–132 1 Protein heterocomplex Heteromer Protein 13 tridecameric （13） Consistent with protein count
B8YB59 4v8s RNA POLYMERASE SUBUNIT 8 Author chain AV Reference sequence 1–132 1 Protein–DNA Heteromer Protein 13 DNA 2 pentadecameric （15） Consistent with all polymers
B8YB59 4v8s RNA POLYMERASE SUBUNIT 8 Author chain BG Reference sequence 1–132 1 Protein–DNA Heteromer Protein 13 DNA 2 pentadecameric （15） Consistent with all polymers
B8YB59 4v8s RNA POLYMERASE SUBUNIT 8 Author chain AV Reference sequence 1–132 2 Protein–DNA Heteromer Protein 13 DNA 2 pentadecameric （15） Consistent with all polymers
B8YB59 4v8s RNA POLYMERASE SUBUNIT 8 Author chain BG Reference sequence 1–132 2 Protein–DNA Heteromer Protein 13 DNA 2 pentadecameric （15） Consistent with all polymers

“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.