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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：Q09490 New Search
4PDB entries
6Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q09490 5azf Protein lgg-1 Author chain A Reference sequence 1–116 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 5azf Protein lgg-1 Author chain B Reference sequence 1–116 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 5azf Protein lgg-1 Author chain A Reference sequence 1–116 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 5azf Protein lgg-1 Author chain B Reference sequence 1–116 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 5azg Protein lgg-1 Author chain A Reference sequence 1–116 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 5azg Protein lgg-1 Author chain B Reference sequence 1–116 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 5azg Protein lgg-1 Author chain A Reference sequence 1–116 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 5azg Protein lgg-1 Author chain B Reference sequence 1–116 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 8tgf Protein lgg-1 Author chain A Reference sequence 1–123 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q09490 8tgx Protein lgg-1 Author chain A Reference sequence 1–123 1 Protein monomer Monomer Protein 1 monomeric （1） 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.