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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：Q12906 New Search
4PDB entries
6Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q12906 2l33 Interleukin enhancer-binding factor 3 Author chain A Reference sequence 521–600 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q12906 3p1x Interleukin enhancer-binding factor 3 Author chain A Reference sequence 520–594 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q12906 3p1x Interleukin enhancer-binding factor 3 Author chain B Reference sequence 520–594 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q12906 3p1x Interleukin enhancer-binding factor 3 Author chain A Reference sequence 520–594 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q12906 3p1x Interleukin enhancer-binding factor 3 Author chain B Reference sequence 520–594 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q12906 3p1x Interleukin enhancer-binding factor 3 Author chain A Reference sequence 520–594 3 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q12906 3p1x Interleukin enhancer-binding factor 3 Author chain B Reference sequence 520–594 3 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
Q12906 7rjm Interleukin enhancer-binding factor 3 Author chain C Reference sequence 99–106 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q12906 7rjq Interleukin enhancer-binding factor 3 Author chain B Reference sequence 99–106 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.