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. Author manuscript; available in PMC: 2010 Aug 1.
Published in final edited form as: Arch Biochem Biophys. 2009 Jun 21;488(1):14–22. doi: 10.1016/j.abb.2009.06.010

Table 2.

Kinetic constants for PAD substrates

Substrate Km
(µM)
Relative Vmax
(%)
kcat
(sec−1)
kcat/Km
(µM−1sec−1)
L-Arginine (1.2 ± 0.5)×103 100 0.22 1.9×10−4
Nα-Benzoyl-L-arginine (Nα-BA) 10–20 54.5 0.12 (6–12)×10−3
D-Arginine (1.9 ± 0.5)×103 26.4 0.058 3.1×10−5
BK (R-P-P-G-F-S-P-F-R) 21 ± 1 18.8 0.043 2.1×10−3
BK antagonist (K-R-P-P-G-F-S-P-L) 33 ±1 3.1 6.8×10−3 2.1×10−4
P-R-F 70 ± 1 3.4 7.5×10−3 1.1×10−4
P-F-R 89 ± 1 78.2 0.17 1.9×10−3
L-Canavanine (6 ± 1)×103 2.5 5.2×10−3 9.3×10−7
L-Arginine hydroxamate (6.9 ± 0.5)×103 68.2 0.15 2.2×10−5
Benzoyl arginine ethyl ester (BAEE) (18 ± 1)×103 8.1 0.019 9.9×10−7
Agmatine (31 ± 1)×103 3.2 7.0×10−3 2.3×10−7
Homoarginine (4.7 ± 0.8)×103 50 0.11 2.4×10−5
Nω-Hydroxy-L-arginine (1.5 ± 0.5)×103 2.1 4.6×10−3 3.0×10−6
Nω,Nω-Dimethyl-L-arginine >1×106 a <0.0017
a

No activity detected with 100mM Nω,Nω-dimethyl-L-arginine. Products from Nω-hydroxy-L-arginine and Nω, Nω-dimethyl-L-arginine have been previously measured using the citrulline colorimetric assay [33].