Combinatorial Clustering of Residue Position Subsets Predicts Inhibitor Affinity across the Human Kinome

doi:10.1371/journal.pcbi.1003087

Combinatorial Clustering of Residue Position Subsets Predicts Inhibitor Affinity across the Human Kinome

Figure 9

Per inhibitor Precision-Recall (PR) curves.

The - and -axis plot the recall and precision, respectively, both ranging from 0 to 1. The Area Under Curve () per drug can be found in Table 3. As shown above, ccorps is demonstrated to have very high precision across a wide range of inhibitors when tested for targets spanning the kinome.

doi: https://doi.org/10.1371/journal.pcbi.1003087.g009