← Back to search

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：P55196 New Search
5PDB entries
6Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P55196 1t2m AF-6 protein Author chain A Reference sequence 987–1077 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P55196 2ain Afadin Author chain A Reference sequence 987–1077 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P55196 2exg Afadin Author chain A Reference sequence 985–1079 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P55196 5a6c G-PROTEIN-SIGNALING MODULATOR 2, AFADIN Author chain A Reference sequence 1709–1746 1 Insufficient information Monomer Protein 1 monomeric （1） Consistent with protein count
P55196 5a6c G-PROTEIN-SIGNALING MODULATOR 2, AFADIN Author chain B Reference sequence 1709–1746 1 Insufficient information Monomer Protein 1 monomeric （1） Consistent with protein count
P55196 5a6c G-PROTEIN-SIGNALING MODULATOR 2, AFADIN Author chain A Reference sequence 1709–1746 2 Insufficient information Monomer Protein 1 monomeric （1） Consistent with protein count
P55196 5a6c G-PROTEIN-SIGNALING MODULATOR 2, AFADIN Author chain B Reference sequence 1709–1746 2 Insufficient information Monomer Protein 1 monomeric （1） Consistent with protein count
P55196 7qcr Afadin Author chain A Reference sequence 1002–1097 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P55196 7qcr Afadin Author chain B Reference sequence 1002–1097 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） 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.