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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：Q58435 New Search
6PDB entries
7Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q58435 3fyc Probable dimethyladenosine transferase Author chain A Reference sequence 10–272 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3fyc Probable dimethyladenosine transferase Author chain B Reference sequence 10–272 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3fyc Probable dimethyladenosine transferase Author chain A Reference sequence 10–272 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3fyc Probable dimethyladenosine transferase Author chain B Reference sequence 10–272 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3fyd Probable dimethyladenosine transferase Author chain A Reference sequence 10–272 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3grr Dimethyladenosine transferase Author chain A Reference sequence 1–275 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3gru Dimethyladenosine transferase Author chain A Reference sequence 1–275 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3grv Dimethyladenosine transferase Author chain A Reference sequence 1–275 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q58435 3gry Dimethyladenosine transferase Author chain A Reference sequence 1–275 1 Protein monomer Monomer Protein 1 monomeric （1） 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.