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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：P35568 New Search
8PDB entries
8Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P35568 1irs IRS-1 Author chain A Reference sequence 157–267 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P35568 1k3a insulin receptor substrate 1 Author chain B Reference sequence 891–902 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P35568 1qqg INSULIN RECEPTOR SUBSTRATE 1 Author chain A Reference sequence 4–267 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P35568 1qqg INSULIN RECEPTOR SUBSTRATE 1 Author chain B Reference sequence 4–267 1 Protein homooligomer Homooligomer Protein 2 dimeric （2） Consistent with protein count
P35568 2z8c 6-mer peptide from Insulin receptor substrate 1 Author chain B Reference sequence 731–736 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P35568 5u1m Insulin receptor substrate 1 Author chain A Reference sequence 161–265 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P35568 6bnt Insulin receptor substrate 1 Author chain B Reference sequence 607–620 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P35568 7ppl Insulin receptor substrate 1 Author chain B Reference sequence 625–639 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
P35568 7ppm Insulin receptor substrate 1 Author chain B Reference sequence 889–901 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.