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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：Q49AH0 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
Q49AH0 2lpn Cerebral dopamine neurotrophic factor Author chain A Reference sequence 27–131 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q49AH0 2w50 ARMET-LIKE PROTEIN 1 Author chain A Reference sequence 32–133 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q49AH0 2w50 ARMET-LIKE PROTEIN 1 Author chain B Reference sequence 32–133 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q49AH0 2w50 ARMET-LIKE PROTEIN 1 Author chain A Reference sequence 32–133 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q49AH0 2w50 ARMET-LIKE PROTEIN 1 Author chain B Reference sequence 32–133 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q49AH0 4bit CEREBRAL DOPAMINE NEUROTROPHIC FACTOR Author chain A Reference sequence 27–187 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q49AH0 8qaj Cerebral dopamine neurotrophic factor Author chain A Reference sequence 127–187 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q49AH0 9h0c Cerebral dopamine neurotrophic factor Author chain B Reference sequence 127–187 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q49AH0 9i5y Cerebral dopamine neurotrophic factor Author chain B Reference sequence 127–187 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.