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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：Q5VVY1 New Search
4PDB entries
5Biological assembly
8chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q5VVY1 5ubb Alpha N-terminal protein methyltransferase 1B Author chain A Reference sequence 58–278 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q5VVY1 6dub Alpha N-terminal protein methyltransferase 1B Author chain A Reference sequence 58–278 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q5VVY1 6dub Alpha N-terminal protein methyltransferase 1B Author chain B Reference sequence 58–278 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q5VVY1 6dub Alpha N-terminal protein methyltransferase 1B Author chain A Reference sequence 58–278 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q5VVY1 6dub Alpha N-terminal protein methyltransferase 1B Author chain B Reference sequence 58–278 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q5VVY1 6kdr Alpha N-terminal protein methyltransferase 1B Author chain A Reference sequence 61–283 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q5VVY1 6kdr Alpha N-terminal protein methyltransferase 1B Author chain B Reference sequence 61–283 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
Q5VVY1 6kds Alpha N-terminal protein methyltransferase 1B Author chain A Reference sequence 61–283 1 Protein heterocomplex Heteromer 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.