Table 1.
Substrate phosphorylation by ATP, kcat/Km, IC50 and predicted interaction energy for protein–ligand pairs
| Kinases | Ligands | Experimental data | Predicted interaction energies (kcal/mol) |
|---|---|---|---|
| JNK kinase | % Substrate phosphorylation | ||
| JNK | N6-(benzyl) | 99 | 0a |
| N6-(2-phenythyl) | 98 | 0a | |
| N6-(cyclopentyl) | 97 | 0a | |
| N6-(1-methylbutyl) | 93 | 0a | |
| JNKM108GL168A | N6-(benzyl) | 62 | −17.34 |
| N6-(cyclopentyl) | 59 | −14.42 | |
| N6-(1-methylbutyl) | 47 | −20.42 | |
| N6-(2-phenythyl) | 8 | −33.0 | |
| v-Src tyrosine kinase | kcat/Km (min −1 M −1 ) | ||
| v-Src | ATP | 1.6*105 | −21.35 |
| v-SrcI338A | 1.4*104 | −19.91 | |
| v-SrcI338G | 1*104 | −19.01 | |
| v-Src | N6-(benzyl) ATP | 0 | 0a |
| v-SrcI338A | 2.5*104 | −14.92 | |
| v-SrcI338G | 4.0*104 | −29.17 | |
| Tyrosine and serine/threonine kinases | IC 50 (μM) | ||
| v-Src | PP1 | 5 ± 2 | 0a |
| v-SrcI338F | 8 ± 2 | 0a | |
| v-SrcI338 M | 8 ± 1 | 0a | |
| v-SrcI338S | 0.4 ± 0.05 | −28.78 | |
| v-SrcI338T | 0.1 ± 0.02 | −33.32 | |
| v-SrcI338 V | 0.1 ± 0.02 | −27.41 | |
| v-SrcI338C | 0.07 ± 0.02 | −27.44 | |
| v-SrcI338A | 0.005 ± 0.002 | −39.26 | |
| v-SrcI338G | 0.005 ± 0.002 | −38.56 | |
| Fyn | 0.05 ± 0.02 | −36.81 | |
| FynT339A | 0.005 ± 0.002 | −36.21 | |
| Abl | 0.3 ± 0.03 | −32.93 | |
| AblT334A | 0.03 ± 0.005 | −33.86 | |
| CamKII | 80 ± 10 | 0a | |
| CamKIIF89G | 0.5 ± 0.1 | −15.74 | |
| Cdk2 | 50 ± 10 | 0a | |
| Cdk2F80G | 0.16 ± 0.03 | −24.85 | |
| P38 | 0.82 ± 0.2 | −34.61 | |
| P38T106A | 0.0027 ± 0.005 | −33.43 | |
| P38T106G | 0.0027 ± 0.005 | −32.78 |
aInteraction energies of 0 kcal/mol represent positive interaction energies