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. 2009 Jul 9;284(38):25620–25629. doi: 10.1074/jbc.M109.000042

TABLE 1.

Km, kcat, and kcat/Km values for thrombin hydrolysis of chromogenic substrates in the presence of exosite ligands

The rates of thrombin cleavage of various chromogenic substrates were used to determine the kinetic parameters by Michaelis-Menten analysis. Experiments were performed in the absence or presence of 10 μm HD1, HD22, or hirudin-(54–65). The experiments were repeated three times in duplicate, and the values represent means ± S.E.

Substrate Addition Km kcat kcat/Km
μm s1 μm1s1
tGPR-pNA
None 16.4 ± 1.2 234.5 ± 4.1 14.3 ± 1.0
HD1 14.2 ± 1.4 240.3 ± 9.6 16.9 ± 1.8
HD22 8.5 ± 0.7 192.8 ± 16.3 22.7 ± 2.8
Hirudin-(54–65) 11.7 ± 2.0 251.6 ± 20.3 21.5 ± 4.1
S2238
None 2.6 ± 0.4 101.9 ± 6.8 39.8 ± 6.5
HD1 14.3 ± 0.6 209.4 ± 6.7 14.7 ± 0.8
HD22 12.1 ± 1.7 106.8 ± 4.1 8.8 ± 1.3
Hirudin-(54–65) 3.1 ± 0.1 156.5 ± 1.8 51.0 ± 2.1
S2366
None 282.9 ± 30.6 249.5 ± 11.3 0.9 ± 0.1
HD1 195.0 ± 18.3 217.1 ± 9.4 1.1 ± 0.1
HD22 155.4 ± 14.1 231.1 ± 13.4 1.5 ± 0.2
Hirudin-(54–65) 147.1 ± 6.0 278.6 ± 3.5 1.9 ± 0.1