Important interactions stabilizing the transition state | However, probably the most interesting of all the active site residues is Trp331. |
Introduction | The authors have scanned potential energy along a single predefined reaction coordinate, using a very modest quantum-chemical description of the active site , namely the Becke-Perdew pure density functional together with a small basis (SVP) and a small quantum region (80 atoms). |
Methods | Visual inspection of the active site showed near perfect overlap of the UDP molecules and neighboring side chains, allowing the coordinates of GalNAc to be directly transferred from 2D7I into 2FFU. |
Methods | Furthermore, water molecules present in the active site were manually rotated to create a network of hydrogen bonds where possible. |
Methods | Three of these water molecules are located close to the metal ion with one of them directly serving as a ligand and the other two forming a hydrogen bond network between the first water molecule and neighboring active site residues. |
Reactant and product structures | The native enzyme structure contains a manganese ion in the active site , coordinating the diphosphate fragment of UDP. |
Reactant and product structures | [26] Because this fact would entail a spin-unrestrict-ed treatment of the active site , leading to an almost twofold increase in computational cost and possible convergence problems, we opted for replacing it with magnesium. |
Abstract | The most stabilizing point mutation was D27F, which is located in the active site of the protein, rendering it inactive. |
Abstract | However for the rest of mutations outside of the active site we observed a weak yet statistically significant positive correlation between thermal stability and catalytic activity indicating the lack of a stability-activity tradeoff for DHFR. |
Discussion | This conclusion was reached in [53,58], based on the exploration of stability effects of mutations in the active site of beta-lactamase [53] and rubisco [58]. |
Discussion | Fersht and coauthors also found several stabilizing mutations in the active site of Barnase rendering the protein inactive [59]. |
Discussion | 9 shows that exploring only mutations in the active site provides a biased view on the tradeoff between activity and stability. |
Stability and activity do not trade-off for DHFR | Our data, however, paints a different picture for DHFR—of a weak positive correlation between Tm and kcat or kcat/KM (r = 0.46, p = 0.02 and r = 0.41, p = 0.03 respectively) with one notable outlier D27F, where the stabilizing mutation is made right in the active site (Fig. |
Abstract | Formation of a cyclic sulfenyl amide residue at the active site of redox-regulated proteins has been proposed as a protection mechanism against irreversible oxidation as the sulfenyl amide intermediate has been identified in several proteins. |
Protein topology and Cysteine reactivity | In this work we have also identified two PFAM families, Glutamine amidotransferase and Carbon-ni-trogen hydrolase, that lack experimental evidence of cysteine oxidation but have a relevant Cys in the active site . |
Protein topology and Cysteine reactivity | On the other hand, pth has an extra domain called “lid domain” which acts as a gate to the active site of this enzyme, protecting it from oxidative stress. |
Results | Because of its pathological relevance and protective role in oxidative stress DI-l has been intensively studied and oxidation of the active site cysteine has been described several times [78,85]. |
The formation of sulfenic acid and the following cyclic sulfenyl amide reaction mechanism | Proteins that have a reactive cysteine in their active site that has a low pKa are susceptible to inactivation by radical species like H202. |
Discussion | By combining this information with protein structure information, we found that all (10 out of 10) such identified hotspots, where they fell within known oncoproteins, are ‘functional hotspots’ in the sense that all fell within ligand-binding or active sites . |
Mutational trends of oncoproteins and tumor suppressor proteins | For oncoproteins, of 40 mutational hotspots, 15 (38%) fell at functional sites, including GTP/ ATP binding sites and other active sites of enzymes. |
Oncogenic mutational hotspots appearing in multiple cancer types | Here, we collectively analyzed the domain position-based hotspots for K-RAS, H-RAS, and N-RAS, finding that at least one of the GTP binding site residues p.G12 or p.G13, or the active site residue p.R61 show a relatively high mutation rate in at least five cancer types (Fig. |