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These simulations revealed that the derivatives predominantly form hydrophobic interactions with key residues in the active site: Phe53, Phe110, and Phe89 (467)

Inactivation is caused by oxidation of the cluster followed by release of Fe a (which is required to coordinate OH on C 3 position of citrate) and cluster disassembly (Gardner, 1997)

Toxicity and biochemical effects of spirotetramat and its binary mixtures with nanosilica against Aphis gossypii Glover, Bemisia tabaci Gennadius and the earthworm, Eisenia fetida

Ethics declarations Ethics approval and consent to participate This animal study was approved by the Ethics Committee for Experimental Animals of Dongzhimen Hospital, Beijing University of Chinese Medicine (Approval No

We combined data from all trials to estimate the pooled risk ratio (RR) with 95% confidence intervals (CIs) for mortality, infectious complications, VAP and overall weighted mean difference (WMD) with 95% CIs for LOS data