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. Author manuscript; available in PMC: 2019 Dec 28.
Published in final edited form as: J Am Chem Soc. 2019 Apr 16;141(16):6553–6560. doi: 10.1021/jacs.8b13248

Table 1.

Retro- and prospectively predicted reactive lysines and cysteines in the human protein kinasesa

Kinase Name Kinase Group PDB ID Catalytic Lys Calc pKa Other Reactive Lys Calc pKa All Reactive Cys Calc pKa Inhibitor Type
ABL1 TK 2G2F C305 (β4–β5) 8.0 II
EGFR TK 5U8L K745 7.3 C781 (β4–β5) 8.1 II
EGFRmt TK 5UG8 K745 7.1 C781 (β4–β5) 8.1 II
MET TK 4MXC K1110 7.7 II
c-SRC TK 5K9I K295 8.1 C277 (P-loop) 6.8 II
LIMK2 TKL 4TPT C365 3–αC) 5.8 III
RIPK1 TKL 4ITJ K45 6.7 C53 (β3–αC) 8.3 III
LOK STE 4USD C206 (A-loop) 7.6 II
PAK1 STE 4ZLO C411 (DFG+2, built) 5.0 II
PDK1 AGC 3NAX K111 7.0 C260 (A-loop to αF) 6.0 II
CDK6 CMGC 1G3N K43 6.1 K147 (HRD+2) 6.0 C15 (β1) 7.9 II
NEK2 Other 2XNM K37 7.8 II
Aurora Other 4JAI K162 7.9 C290 (A-loop, built) 5.4 II
IRE1α Other 4YZ9 C747 (A-loop, built) 7.9 II
C715 (DFG+2) 5.8
PEK Other 4X7N K622 7.6 K939 (HRD+2) 7.3 C1049 (αH) 5.2 II
a

Only kinases with at least one reactive lysine or cysteine (see main text for definitions) are listed. The complete list is given in Table S1. Locations for non-catalytic residues are indicated in parentheses. EGFRmt refers to the mutant L858R/T790M. c-SRC is included as a part of the validation set. The pKa calculations for cysteines used the second halves of the simulations. Cys290 in Aurora and Cys747 in IRE1α were missing in the PDB les and the positions were built using SWISS-MODEL.39 For CDK6 and PEK, Asp in the commonly-known HRD motif is replaced with Asn.