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8U7L

Cryo-EM structure of LRRK2 bound to type II inhibitor GZD824

Summary for 8U7L
Entry DOI10.2210/pdb8u7l/pdb
EMDB information41985
DescriptorLeucine-rich repeat serine/threonine-protein kinase 2, GUANOSINE-5'-DIPHOSPHATE, 4-methyl-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}-3-[(1H-pyrazolo[3,4-b]pyridin-5-yl)ethynyl]benzamide (3 entities in total)
Functional Keywordscryo-em, parkinson's disease, kinase, lrrk2, type ii inhibitor, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight574806.83
Authors
Zhu, H.,Sun, J. (deposition date: 2023-09-15, release date: 2024-01-31)
Primary citationZhu, H.,Hixson, P.,Ma, W.,Sun, J.
Pharmacology of LRRK2 with type I and II kinase inhibitors revealed by cryo-EM.
Cell Discov, 10:10-10, 2024
Cited by
PubMed: 38263358
DOI: 10.1038/s41421-023-00639-8
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.6 Å)
Structure validation

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