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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：P47992 New Search
7PDB entries
7Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P47992 1j8i Lymphotactin Author chain A Reference sequence 22–114 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P47992 1j9o LYMPHOTACTIN Author chain A Reference sequence 22–114 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P47992 2hdm Lymphotactin Author chain A Reference sequence 23–114 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
P47992 2jp1 Lymphotactin Author chain A Reference sequence 22–114 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P47992 2jp1 Lymphotactin Author chain B Reference sequence 22–114 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P47992 2n54 Lymphotactin Author chain A Reference sequence 22–114 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P47992 2n54 Lymphotactin Author chain B Reference sequence 22–114 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P47992 2nyz Lymphotactin Author chain D Reference sequence 22–114 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P47992 2nyz Lymphotactin Author chain E Reference sequence 22–114 1 Protein heterocomplex Heteromer Protein 4 tetrameric （4） Consistent with protein count
P47992 9ast Lymphotactin Author chain L Reference sequence 22–114 1 Insufficient information Heteromer Protein 6 hexameric （6） 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.