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. 2017 Apr 13;292(23):9523–9539. doi: 10.1074/jbc.M116.771394

Table 1.

Multiple protein kinase inhibitors did not prevent PKD1 phosphorylation at Ser203 in IEC-18 cells

Confluent cultures of IEC-18 cells were incubated with each of the inhibitors listed below for 1 h. Then the cells were stimulated with ANG II for 60 min and lysed, and the phosphorylation of PKD1 at Ser203 was determined by immunoblotting using the antibody that detects the phosphorylated state of this residue. The inhibitors listed in this table did not prevent Ser203 phosphorylation at the concentrations tested. cPKC, conventional PKCs; nPKC, novel PKCs; aPKC, atypical PKCs; and mTOR, mechanistic target of rapamycin.

Inhibitor Primary target Concentration
μm
kb NB 142–70 PKD 1–10
CRT 0066101 PKD 1–5
Go6983 cPKC, nPKC, aPKC 1–10
GF 109203X cPKC, nPKC 3.5
KT 5720 PKA 1
KU 0063794 mTOR 1–5
GSK 690693 Akt, PKC, PKA 1–5
KU 55933 ATM 5–25
HA 1077 ROCK-II, PKA, PKG, PKCα 10
Y-27632 ROCK 10
Compound C AMPK 5–25
Aurora kinase inhibitor III Aurora A 10
Aurora kinase inhibitor II Aurora A and B 10
GSK-3 inhibitor XVI GSK-3 5
LY 294002 PI3K, mTOR 10
PP2 Src 10
AG1478 EGFR 1
U0126 MEK1/2 5
PD98059 MEK1/2 5
PIM-1 inhibitor 2 Pim-1 kinase 1–10
TG003 Clk family 1–10
Enzastaurin (LY317615) PKCβ 1–5
GO6976 cPKC, PKD 10
KN92 CaMKII 10
KN62 CaMKII 10
FAK inhibitor 14 FAK 1–5
UCN-01 Chk1 10