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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：Q0T8Y8 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
Q0T8Y8 3jwn FimH protein Author chain H Reference sequence 25–303 1 Protein heterocomplex Heteromer Protein 5 pentameric （5） Consistent with protein count
Q0T8Y8 3jwn FimH protein Author chain N Reference sequence 25–303 1 Protein heterocomplex Heteromer Protein 5 pentameric （5） Consistent with protein count
Q0T8Y8 3jwn FimH protein Author chain H Reference sequence 25–303 2 Protein heterocomplex Heteromer Protein 5 pentameric （5） Consistent with protein count
Q0T8Y8 3jwn FimH protein Author chain N Reference sequence 25–303 2 Protein heterocomplex Heteromer Protein 5 pentameric （5） Consistent with protein count
Q0T8Y8 4xoc FimH protein Author chain A Reference sequence 25–183 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q0T8Y8 4xoc FimH protein Author chain B Reference sequence 25–183 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q0T8Y8 4xoc FimH protein Author chain A Reference sequence 25–183 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q0T8Y8 4xoc FimH protein Author chain B Reference sequence 25–183 2 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q0T8Y8 4xod FimH protein Author chain A Reference sequence 25–303 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q0T8Y8 4xoe FimH protein Author chain A Reference sequence 25–303 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.