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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：Q6F0T5 New Search
5PDB entries
5Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q6F0T5 6gp2 Ribonucleoside-diphosphate reductase beta chain Author chain A Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q6F0T5 6gp2 Ribonucleoside-diphosphate reductase beta chain Author chain B Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q6F0T5 6gp3 Ribonucleoside-diphosphate reductase beta chain Author chain A Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q6F0T5 6gp3 Ribonucleoside-diphosphate reductase beta chain Author chain B Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q6F0T5 8bt3 Ribonucleoside-diphosphate reductase beta chain Author chain A Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q6F0T5 8bt4 Ribonucleoside-diphosphate reductase Author chain A Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q6F0T5 8bt4 Ribonucleoside-diphosphate reductase Author chain B Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q6F0T5 9r5l ribonucleoside-diphosphate reductase Author chain A Reference sequence 1–340 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） 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.