Pie charts in Fig. 3. Subtype-selective molecules were slightly more prevalent between

Pie charts in Fig. 3. Subtype-selective molecules were slightly more prevalent between A1 and A3 than between A1 and A2A: 66 and 58 of the ligands were more than 10-fold selective in either direction, respectively. The ligands emerging from this screen tended to be more selective for A2A and A3 than A1, as can be seen from the larger areas for theIn Silico Screening for A1AR Antagonistscorresponding selectivity ratios (inner donuts in Fig. 3). Although the numbers have to be viewed with caution because of the limitations of statistics of small numbers, these observations contrast those for the ChEMBL ligands, which tended to be more selective for A1.DiscussionThree main results emerge from this study. First, as has been shown previously [45,46], different models (or X-ray structures) of the same receptor yield different ligand sets, even when screening the same diverse library. Interestingly, the performance of the various models, both in absolute number of actual ligands as well as in terms of selectivity, differed widely. This fact is both en- and discouraging. It is encouraging, because it means that even using models with large structural deviations from a closely related template (i.e. the conformation of ECL3, the lack of the conserved salt bridge between His2647.29 and Glu172, and the orientation of Trp2476.48) such as model A, docking is likely to find pharmacologically validated ligands. Conversely, it is discouraging, as the presumably refined model C did not yield any ligands. This is particularly striking considering the small differences between models C and D. We did not exclude the molecules tested in earlier rounds of screening during the subsequent ones, yet the vast majority of ligands identified in one model did not appear in the top ranks of a screen against another one (data not shown). Such behavior is a testament to the conformational flexibility of GPCRs, but also to the sensitivity of docking to small changes in the protein structure. In combination, it can be exploited to identify larger numbers of ligands by docking to more than one protein conformation. Any model of a protein structure (including the X-ray solution) represents only one possibility from the continuum of conformations. Thus, using differently optimized models (e.g. obtained by slightly different ligand placements or different force field BI 78D3 supplier parameters), the set of identified ligands would have changed. Yet, the overall performance, with some models being able to recognize ligands and some not, would be similar. This fact might also be considered disheartening for approaches that aim to include receptor flexibility via docking to multiple conformations of a receptor and calculating the average rank of a molecule across all structures. Second, docking to GPCRs, even using “only” homology models, works well. The screen against the A1AR was successful by all Tramiprosate site criteria, with a hit rate of 21 and potent compounds with Ki values as low as 400 nM for the 2H-chromen-2-imine derivative 17. Some of the ligands also represent novel chemotypes for the A1AR, such as 17 and related, albeit only weakly active, derivatives quinazolin-4(3H)-ones (14, 22, 25) and a pyrido[2,3d]pyrimidin-4(3H)-one (26). In particular, the ligands identified with model D tend to have ECFP4 Tanimoto similarity values of less than 0.40 when compared to the 7173 AR ligands in the ChEMBL database. The reason for the relatively few genuinely novel ligands presumably lies in the bias of.Pie charts in Fig. 3. Subtype-selective molecules were slightly more prevalent between A1 and A3 than between A1 and A2A: 66 and 58 of the ligands were more than 10-fold selective in either direction, respectively. The ligands emerging from this screen tended to be more selective for A2A and A3 than A1, as can be seen from the larger areas for theIn Silico Screening for A1AR Antagonistscorresponding selectivity ratios (inner donuts in Fig. 3). Although the numbers have to be viewed with caution because of the limitations of statistics of small numbers, these observations contrast those for the ChEMBL ligands, which tended to be more selective for A1.DiscussionThree main results emerge from this study. First, as has been shown previously [45,46], different models (or X-ray structures) of the same receptor yield different ligand sets, even when screening the same diverse library. Interestingly, the performance of the various models, both in absolute number of actual ligands as well as in terms of selectivity, differed widely. This fact is both en- and discouraging. It is encouraging, because it means that even using models with large structural deviations from a closely related template (i.e. the conformation of ECL3, the lack of the conserved salt bridge between His2647.29 and Glu172, and the orientation of Trp2476.48) such as model A, docking is likely to find pharmacologically validated ligands. Conversely, it is discouraging, as the presumably refined model C did not yield any ligands. This is particularly striking considering the small differences between models C and D. We did not exclude the molecules tested in earlier rounds of screening during the subsequent ones, yet the vast majority of ligands identified in one model did not appear in the top ranks of a screen against another one (data not shown). Such behavior is a testament to the conformational flexibility of GPCRs, but also to the sensitivity of docking to small changes in the protein structure. In combination, it can be exploited to identify larger numbers of ligands by docking to more than one protein conformation. Any model of a protein structure (including the X-ray solution) represents only one possibility from the continuum of conformations. Thus, using differently optimized models (e.g. obtained by slightly different ligand placements or different force field parameters), the set of identified ligands would have changed. Yet, the overall performance, with some models being able to recognize ligands and some not, would be similar. This fact might also be considered disheartening for approaches that aim to include receptor flexibility via docking to multiple conformations of a receptor and calculating the average rank of a molecule across all structures. Second, docking to GPCRs, even using “only” homology models, works well. The screen against the A1AR was successful by all criteria, with a hit rate of 21 and potent compounds with Ki values as low as 400 nM for the 2H-chromen-2-imine derivative 17. Some of the ligands also represent novel chemotypes for the A1AR, such as 17 and related, albeit only weakly active, derivatives quinazolin-4(3H)-ones (14, 22, 25) and a pyrido[2,3d]pyrimidin-4(3H)-one (26). In particular, the ligands identified with model D tend to have ECFP4 Tanimoto similarity values of less than 0.40 when compared to the 7173 AR ligands in the ChEMBL database. The reason for the relatively few genuinely novel ligands presumably lies in the bias of.