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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：P41662 New Search
5PDB entries
7Biological assembly
10chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
P41662 8vwi Protein AC109 Author chain N Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 36 36-meric （36） Consistent with protein count
P41662 8vwi Protein AC109 Author chain i Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 36 36-meric （36） Consistent with protein count
P41662 8vwj Protein AC109 Author chain N Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 36 36-meric （36） Consistent with protein count
P41662 8vwj Protein AC109 Author chain i Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 36 36-meric （36） Consistent with protein count
P41662 9h2a Protein AC109 Author chain L Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 224 224-meric （224） Consistent with protein count
P41662 9h2a Protein AC109 Author chain d Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 224 224-meric （224） Consistent with protein count
P41662 9h2b Protein AC109 Author chain L Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 196 196-meric （196） Consistent with protein count
P41662 9h2b Protein AC109 Author chain L Reference sequence 1–390 2 Protein heterocomplex Heteromer Protein 14 tetradecameric （14） Consistent with protein count
P41662 9h2b Protein AC109 Author chain L Reference sequence 1–390 3 Protein heterocomplex Heteromer Protein 14 tetradecameric （14） Consistent with protein count
P41662 9h2j Protein AC109 Author chain K Reference sequence 1–390 1 Protein heterocomplex Heteromer Protein 224 112-meric （112） Review required

“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.