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8U7H

Cryo-EM structure of LRRK2 bound to type I inhibitor GNE-7915

Summary for 8U7H
Entry DOI10.2210/pdb8u7h/pdb
EMDB information41982
Descriptornon-specific serine/threonine protein kinase, GUANOSINE-5'-DIPHOSPHATE, [4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-2-fluoranyl-5-methoxy-phenyl]-morpholin-4-yl-methanone (3 entities in total)
Functional Keywordscryo-em, parkinson's disease, kinase, lrrk2, type i inhibitor, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight137730.07
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 (3.8 Å)
Structure validation

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