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8UTS

KIF1A[1-393] APO in complex with a microtubule

Summary for 8UTS
Entry DOI10.2210/pdb8uts/pdb
EMDB information42548
DescriptorKinesin-like protein KIF1A, Tubulin alpha-1B chain, Tubulin beta-2B chain, ... (7 entities in total)
Functional Keywordskif1a, kinesin, motility, microtubule, tubulin, motor protein
Biological sourceHomo sapiens (human)
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Total number of polymer chains3
Total formula weight151337.36
Authors
Benoit, M.P.M.H.,Rao, L.,Asenjo, A.B.,Gennerich, A.,Sosa, H. (deposition date: 2023-10-31, release date: 2024-06-12, Last modification date: 2024-07-31)
Primary citationBenoit, M.P.M.H.,Rao, L.,Asenjo, A.B.,Gennerich, A.,Sosa, H.
Cryo-EM unveils kinesin KIF1A's processivity mechanism and the impact of its pathogenic variant P305L.
Nat Commun, 15:5530-5530, 2024
Cited by
PubMed Abstract: Mutations in the microtubule-associated motor protein KIF1A lead to severe neurological conditions known as KIF1A-associated neurological disorders (KAND). Despite insights into its molecular mechanism, high-resolution structures of KIF1A-microtubule complexes remain undefined. Here, we present 2.7-3.5 Å resolution structures of dimeric microtubule-bound KIF1A, including the pathogenic P305L mutant, across various nucleotide states. Our structures reveal that KIF1A binds microtubules in one- and two-heads-bound configurations, with both heads exhibiting distinct conformations with tight inter-head connection. Notably, KIF1A's class-specific loop 12 (K-loop) forms electrostatic interactions with the C-terminal tails of both α- and β-tubulin. The P305L mutation does not disrupt these interactions but alters loop-12's conformation, impairing strong microtubule-binding. Structure-function analysis reveals the K-loop and head-head coordination as major determinants of KIF1A's superprocessive motility. Our findings advance the understanding of KIF1A's molecular mechanism and provide a basis for developing structure-guided therapeutics against KAND.
PubMed: 38956021
DOI: 10.1038/s41467-024-48720-4
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.7 Å)
Structure validation

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