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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：P45448 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
P45448 1pk5 Orphan nuclear receptor NR5A2 Author chain A Reference sequence 318–560 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P45448 1pk5 Orphan nuclear receptor NR5A2 Author chain B Reference sequence 318–560 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P45448 1pk5 Orphan nuclear receptor NR5A2 Author chain A Reference sequence 318–560 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P45448 1pk5 Orphan nuclear receptor NR5A2 Author chain B Reference sequence 318–560 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P45448 1zh7 Orphan nuclear receptor NR5A2 Author chain A Reference sequence 318–560 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P45448 1zh7 Orphan nuclear receptor NR5A2 Author chain B Reference sequence 318–560 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P45448 1zh7 Orphan nuclear receptor NR5A2 Author chain A Reference sequence 318–560 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P45448 1zh7 Orphan nuclear receptor NR5A2 Author chain B Reference sequence 318–560 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P45448 3f5c Nuclear receptor subfamily 5 group A member 2 Author chain A Reference sequence 313–560 1 Protein heterocomplex Heteromer Protein 3 trimeric （3） 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.