A docking score function for estimating ligand-protein interactions: application to acetylcholinesterase inhibition.
暂无分享,去创建一个
Gerald H Lushington | Margaret M Hurley | G. Lushington | Jianxin Guo | J. B. Wright | Jianxin Guo | Jeffery B Wright | M. Hurley | Jian-xin Guo
[1] J. Borak,et al. Chemical warfare agents: II. Nerve agents. , 1992, Annals of emergency medicine.
[2] S. Gray,et al. Donepezil Use in Alzheimer Disease , 1998, The Annals of pharmacotherapy.
[3] Gerhard Klebe,et al. Predicting binding modes, binding affinities and ‘hot spots’ for protein-ligand complexes using a knowledge-based scoring function , 2000 .
[4] P Willett,et al. Development and validation of a genetic algorithm for flexible docking. , 1997, Journal of molecular biology.
[5] Andres D. Ramirez,et al. 5,7‐Dihydro‐3‐(2‐(1‐(phenylmethyl)‐4‐piperidinyl)ethyl)‐6H‐pyrrolo(3,2‐ f)‐1,2‐benzisoxazol‐6‐one: A Potent and Centrally‐Selective Inhibitor of Acetylcholinesterase with an Improved Margin of Safety. , 1995 .
[6] Satu M. Somani,et al. Chemical warfare agents , 1992 .
[7] A. Goldman,et al. Atomic structure of acetylcholinesterase from Torpedo californica: a prototypic acetylcholine-binding protein , 1991, Science.
[8] T. Marrs. Organophosphate poisoning. , 1993, Pharmacology & therapeutics.
[9] F. Vallette,et al. Molecular and cellular biology of cholinesterases , 1993, Progress in Neurobiology.
[10] Wolfgang Sippl,et al. Structure-based 3D QSAR and design of novel acetylcholinesterase inhibitors , 2001, J. Comput. Aided Mol. Des..
[11] N. Ariel,et al. Structures of recombinant native and E202Q mutant human acetylcholinesterase complexed with the snake-venom toxin fasciculin-II. , 2000, Acta crystallographica. Section D, Biological crystallography.
[12] Ting Wang,et al. Comparative binding energy (COMBINE) analysis of OppA-peptide complexes to relate structure to binding thermodynamics. , 2002, Journal of medicinal chemistry.
[13] G. V. Paolini,et al. Empirical scoring functions: I. The development of a fast empirical scoring function to estimate the binding affinity of ligands in receptor complexes , 1997, J. Comput. Aided Mol. Des..
[14] J. Sussman,et al. Structure of acetylcholinesterase complexed with E2020 (Aricept): implications for the design of new anti-Alzheimer drugs. , 1999, Structure.
[15] Thomas Lengauer,et al. A fast flexible docking method using an incremental construction algorithm. , 1996, Journal of molecular biology.
[16] T. Halgren. MMFF VI. MMFF94s option for energy minimization studies , 1999, J. Comput. Chem..
[17] Jirí Damborský,et al. Comparative binding energy analysis of haloalkane dehalogenase substrates: Modelling of enzyme-substrate complexes by molecular docking and quantum mechanical calculations , 2003, J. Comput. Aided Mol. Des..
[18] Thomas Hughes,et al. Inhibitors Tethered Near the Acetylcholinesterase Active Site Serve as Molecular Rulers of the Peripheral and Acylation Sites* , 2003, Journal of Biological Chemistry.
[19] S. Wold,et al. Comparative molecular field analysis , 1991 .
[20] Philippe Bernard,et al. Automated docking of 82 N-benzylpiperidine derivatives to mouse acetylcholinesterase and comparative molecular field analysis with 'natural' alignment , 1999, J. Comput. Aided Mol. Des..
[21] Zoran Radić,et al. Structural insights into ligand interactions at the acetylcholinesterase peripheral anionic site , 2003, The EMBO journal.
[22] B Velan,et al. The Architecture of Human Acetylcholinesterase Active Center Probed by Interactions with Selected Organophosphate Inhibitors , 1996, The Journal of Biological Chemistry.
[23] P Taylor,et al. The cholinesterases: from genes to proteins. , 1994, Annual review of pharmacology and toxicology.
[24] J M Blaney,et al. A geometric approach to macromolecule-ligand interactions. , 1982, Journal of molecular biology.
[25] J. Sussman,et al. The X-ray structure of a transition state analog complex reveals the molecular origins of the catalytic power and substrate specificity of acetylcholinesterase. , 1996 .
[26] F. J. Luque,et al. Towards improved acetylcholinesterase inhibitors: a structural and computational approach. , 2001, Mini reviews in medicinal chemistry.
[27] R. Cramer,et al. Comparative molecular field analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins. , 1988, Journal of the American Chemical Society.
[28] Y. Li,et al. Molecular cloning of mouse acetylcholinesterase: Tissue distribution of alternatively spliced mRNA species , 1990, Neuron.
[29] Y. Martin,et al. A general and fast scoring function for protein-ligand interactions: a simplified potential approach. , 1999, Journal of medicinal chemistry.
[30] N. Ariel,et al. Substrate inhibition of acetylcholinesterase: residues affecting signal transduction from the surface to the catalytic center. , 1992, The EMBO journal.
[31] Klaus R Liedl,et al. Molecular docking studies of natural cholinesterase-inhibiting steroidal alkaloids from Sarcococca saligna. , 2003, Journal of medicinal chemistry.
[32] P. Cowley,et al. Quaternary salts of E2020 analogues as acetylcholinesterase inhibitors for the reversal of neuromuscular block. , 2002, Bioorganic & medicinal chemistry letters.
[33] Wolfgang Sippl,et al. Development of biologically active compounds by combining 3D QSAR and structure-based design methods , 2002, J. Comput. Aided Mol. Des..
[34] J. Blake,et al. Novel benzisoxazole derivatives as potent and selective inhibitors of acetylcholinesterase. , 1994, Journal of medicinal chemistry.
[35] J Andrew McCammon,et al. Studying enzyme binding specificity in acetylcholinesterase using a combined molecular dynamics and multiple docking approach. , 2002, Journal of the American Chemical Society.
[36] M. Crismon,et al. Tacrine: First Drug Approved for Alzheimer's Disease , 1994, The Annals of pharmacotherapy.
[37] A Tropsha,et al. Structure-based alignment and comparative molecular field analysis of acetylcholinesterase inhibitors. , 1996, Journal of medicinal chemistry.
[38] Marta Murcia,et al. Virtual screening with flexible docking and COMBINE-based models. Application to a series of factor Xa inhibitors. , 2004, Journal of medicinal chemistry.