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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：Q62838 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
Q62838 1luf muscle-specific tyrosine kinase receptor musk Author chain A Reference sequence 529–868 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q62838 2iep Muscle-specific kinase receptor Author chain A Reference sequence 22–212 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q62838 2iep Muscle-specific kinase receptor Author chain B Reference sequence 22–212 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q62838 2iep Muscle-specific kinase receptor Author chain A Reference sequence 22–212 2 Protein homooligomer Homooligomer Protein 3 trimeric （3） Consistent with protein count
Q62838 2iep Muscle-specific kinase receptor Author chain B Reference sequence 22–212 2 Protein homooligomer Homooligomer Protein 3 trimeric （3） Consistent with protein count
Q62838 2iep Muscle-specific kinase receptor Author chain A Reference sequence 22–212 3 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q62838 2iep Muscle-specific kinase receptor Author chain B Reference sequence 22–212 3 Protein homooligomer Homooligomer Protein 4 tetrameric （4） Consistent with protein count
Q62838 3hkl Muscle, skeletal receptor tyrosine protein kinase Author chain A Reference sequence 313–494 1 Other combination Homooligomer Protein 2 其他 2 dimeric （2） Consistent with protein count
Q62838 3hkl Muscle, skeletal receptor tyrosine protein kinase Author chain B Reference sequence 313–494 1 Other combination Homooligomer Protein 2 其他 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.