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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：Q9NQT8 New Search
3PDB entries
5Biological assembly
9chain/assembly records
UNP PDB Protein and construct Assembly Composition class Protein state Molecular copy count PDB declaration Consistency status
Q9NQT8 2cow Kinesin-like protein KIF13B Author chain A Reference sequence 1685–1771 1 Protein monomer Monomer Protein 1 monomeric （1） Consistent with protein count
Q9NQT8 3fm8 Kinesin-like protein KIF13B Author chain A Reference sequence 440–545 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NQT8 3fm8 Kinesin-like protein KIF13B Author chain B Reference sequence 440–545 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NQT8 3fm8 Kinesin-like protein KIF13B Author chain A Reference sequence 440–545 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NQT8 3fm8 Kinesin-like protein KIF13B Author chain B Reference sequence 440–545 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NQT8 3mdb Kinesin-like protein KIF13B Author chain A Reference sequence 440–545 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NQT8 3mdb Kinesin-like protein KIF13B Author chain B Reference sequence 440–545 1 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NQT8 3mdb Kinesin-like protein KIF13B Author chain A Reference sequence 440–545 2 Protein heterocomplex Heteromer Protein 2 dimeric （2） Consistent with protein count
Q9NQT8 3mdb Kinesin-like protein KIF13B Author chain B Reference sequence 440–545 2 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.