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8TZC

Structure of C-terminal LRRK2 bound to MLi-2 (G2019S mutant)

Summary for 8TZC
Entry DOI10.2210/pdb8tzc/pdb
Related8TXZ
EMDB information41754
DescriptorLeucine-rich repeat serine/threonine-protein kinase 2, E11 DARPin, (2~{R},6~{S})-2,6-dimethyl-4-[6-[5-(1-methylcyclopropyl)oxy-1~{H}-indazol-3-yl]pyrimidin-4-yl]morpholine, ... (5 entities in total)
Functional Keywordsgtpase, kinase, inhibitors, protein binding
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight156794.37
Authors
Sanz-Murillo, M.,Villagran-Suarez, A.,Alegrio-Louro, J.,Leschziner, A. (deposition date: 2023-08-26, release date: 2023-12-06, Last modification date: 2023-12-13)
Primary citationSanz Murillo, M.,Villagran Suarez, A.,Dederer, V.,Chatterjee, D.,Alegrio Louro, J.,Knapp, S.,Mathea, S.,Leschziner, A.E.
Inhibition of Parkinson's disease-related LRRK2 by type I and type II kinase inhibitors: Activity and structures.
Sci Adv, 9:eadk6191-eadk6191, 2023
Cited by
PubMed: 38039358
DOI: 10.1126/sciadv.adk6191
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.7 Å)
Structure validation

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