Binding mechanisms of 1,4-dihydropyridine derivatives to L-type calcium channel Cav1.2: a molecular modeling study.
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Dan Li | Tingjun Hou | Youyong Li | Dan Li | Tingjun Hou | Lei Xu | Youyong Li | Lei Xu | Li Tao | Yanling Yang | Linfen Tao | Yanling Yang
[1] G. Ciccotti,et al. Numerical Integration of the Cartesian Equations of Motion of a System with Constraints: Molecular Dynamics of n-Alkanes , 1977 .
[2] W. L. Jorgensen,et al. Comparison of simple potential functions for simulating liquid water , 1983 .
[3] A. Cm,et al. Two distinct populations of calcium channels in a clonal line of pituitary cells. , 1985 .
[4] J. Arrowsmith,et al. Long-acting dihydropyridine calcium antagonists. 1. 2-Alkoxymethyl derivatives incorporating basic substituents. , 1986, Journal of medicinal chemistry.
[5] M. Karplus,et al. Collective motions in proteins: A covariance analysis of atomic fluctuations in molecular dynamics and normal mode simulations , 1991, Proteins.
[6] D. Eisenberg,et al. Assessment of protein models with three-dimensional profiles , 1992, Nature.
[7] P. Kollman,et al. A well-behaved electrostatic potential-based method using charge restraints for deriving atomic char , 1993 .
[8] T. Darden,et al. Particle mesh Ewald: An N⋅log(N) method for Ewald sums in large systems , 1993 .
[9] W. Catterall,et al. Molecular Determinants of High Affinity Phenylalkylamine Block of L-type Calcium Channels (*) , 1995, The Journal of Biological Chemistry.
[10] W. Catterall,et al. Calcium Binding in the Pore of L-type Calcium Channels Modulates High Affinity Dihydropyridine Binding (*) , 1995, The Journal of Biological Chemistry.
[11] N. Klugbauer,et al. The IVS6 segment of the L‐type calcium channel is critical for the action of dihydropyridines and phenylalkylamines. , 1996, The EMBO journal.
[12] H. Glossmann,et al. Transfer of 1,4-Dihydropyridine Sensitivity from L-Type to Class A (BI) Calcium Channels , 1996, Neuron.
[13] W. Catterall,et al. Molecular determinants of drug binding and action on L-type calcium channels. , 1997, Annual review of pharmacology and toxicology.
[14] A. Schwartz,et al. Motif III S5 of L-type Calcium Channels Is Involved in the Dihydropyridine Binding Site , 1997, The Journal of Biological Chemistry.
[15] Alexander D. MacKerell,et al. All-atom empirical potential for molecular modeling and dynamics studies of proteins. , 1998, The journal of physical chemistry. B.
[16] W. C. Still,et al. Approximate atomic surfaces from linear combinations of pairwise overlaps (LCPO) , 1999 .
[17] Y. Okamura,et al. Serine Residue in the IIIS5-S6 Linker of the L-type Ca2+ Channel α1C Subunit Is the Critical Determinant of the Action of Dihydropyridine Ca2+Channel Agonists* , 2000, The Journal of Biological Chemistry.
[18] P. Kollman,et al. Calculating structures and free energies of complex molecules: combining molecular mechanics and continuum models. , 2000, Accounts of chemical research.
[19] V. Ananthanarayanan,et al. Homology model of dihydropyridine receptor: implications for L-type Ca(2+) channel modulation by agonists and antagonists. , 2001, Archives of biochemistry and biophysics.
[20] R. Friesner,et al. Evaluation and Reparametrization of the OPLS-AA Force Field for Proteins via Comparison with Accurate Quantum Chemical Calculations on Peptides† , 2001 .
[21] D. Case,et al. Insights into protein-protein binding by binding free energy calculation and free energy decomposition for the Ras-Raf and Ras-RalGDS complexes. , 2003, Journal of molecular biology.
[22] H. Ichijo,et al. Key roles of Phe1112 and Ser1115 in the pore-forming IIIS5-S6 linker of L-type Ca2+ channel alpha1C subunit (CaV 1.2) in binding of dihydropyridines and action of Ca2+ channel agonists. , 2003, Molecular pharmacology.
[23] H. Fozzard,et al. Molecular modeling of interactions of dihydropyridines and phenylalkylamines with the inner pore of the L-type Ca2+ channel. , 2003, Molecular pharmacology.
[24] D. Case,et al. Exploring protein native states and large‐scale conformational changes with a modified generalized born model , 2004, Proteins.
[25] Junmei Wang,et al. Development and testing of a general amber force field , 2004, J. Comput. Chem..
[26] Laxmikant V. Kalé,et al. Scalable molecular dynamics with NAMD , 2005, J. Comput. Chem..
[27] W. Catterall,et al. Allosteric Interactions Required for High-Affinity Binding of Dihydropyridine Antagonists to CaV1.1 Channels Are Modulated by Calcium in the Pore , 2006, Molecular Pharmacology.
[28] Xiaojie Xu,et al. Recent Advances in Free Energy Calculations with a Combination of Molecular Mechanics and Continuum Models , 2006 .
[29] V. Hornak,et al. Comparison of multiple Amber force fields and development of improved protein backbone parameters , 2006, Proteins.
[30] Ettore Novellino,et al. Characterizing the 1,4-dihydropyridines binding interactions in the L-type Ca2+ channel: model construction and docking calculations. , 2007, Journal of medicinal chemistry.
[31] Tingjun Hou,et al. Molecular dynamics and free energy studies on the wild-type and double mutant HIV-1 protease complexed with amprenavir and two amprenavir-related inhibitors: mechanism for binding and drug resistance. , 2007, Journal of medicinal chemistry.
[32] Boris S Zhorov,et al. Molecular Modeling of Benzothiazepine Binding in the L-type Calcium Channel* , 2008, Journal of Biological Chemistry.
[33] D. Case,et al. Characterization of domain-peptide interaction interface: a case study on the amphiphysin-1 SH3 domain. , 2008, Journal of molecular biology.
[34] Boris S Zhorov,et al. Structural Model for Dihydropyridine Binding to L-type Calcium Channels* , 2009, The Journal of Biological Chemistry.
[35] A. Mehdipour,et al. Dihydropyridines: evaluation of their current and future pharmacological applications. , 2009, Drug discovery today.
[36] Oliver Beckstein,et al. Lipidbook: A Public Repository for Force-Field Parameters Used in Membrane Simulations , 2010, The Journal of Membrane Biology.
[37] Kenneth M Merz,et al. Structural Survey of Zinc Containing Proteins and the Development of the Zinc AMBER Force Field (ZAFF). , 2010, Journal of chemical theory and computation.
[38] G. Cruciani,et al. 1,4-Dihydropyridine scaffold in medicinal chemistry, the story so far and perspectives (part 1): action in ion channels and GPCRs. , 2011, Current medicinal chemistry.
[39] Tingjun Hou,et al. Assessing the Performance of the MM/PBSA and MM/GBSA Methods. 1. The Accuracy of Binding Free Energy Calculations Based on Molecular Dynamics Simulations , 2011, J. Chem. Inf. Model..
[40] P. Lory,et al. Hallmarks of the channelopathies associated with L-type calcium channels: a focus on the Timothy mutations in Ca(v)1.2 channels. , 2011, Biochimie.
[41] Tingjun Hou,et al. Structural Bioinformatics Prediction of Peptides Binding to the Pka Riiα Subunit Using a Hierarchical Strategy , 2022 .
[42] Tingjun Hou,et al. Assessing the performance of the molecular mechanics/Poisson Boltzmann surface area and molecular mechanics/generalized Born surface area methods. II. The accuracy of ranking poses generated from docking , 2011, J. Comput. Chem..
[43] Tingjun Hou,et al. Concerted Movement in pH-Dependent Gating of FocA from Molecular Dynamics Simulations , 2012, J. Chem. Inf. Model..
[44] Wei Wang,et al. Characterization of domain-peptide interaction interface: prediction of SH3 domain-mediated protein-protein interaction network in yeast by generic structure-based models. , 2012, Journal of proteome research.
[45] Xiong Cao,et al. An L-Type Calcium Channel Agonist, Bay K8644, Extends the Window of Intervention Against Ischemic Neuronal Injury , 2012, Molecular Neurobiology.
[46] Tingjun Hou,et al. Studies on the Interactions between β2 Adrenergic Receptor and Gs Protein by Molecular Dynamics Simulations , 2012, J. Chem. Inf. Model..
[47] Xiaojie Jin,et al. Exploring the Molecular Mechanism of Cross-Resistance to HIV-1 Integrase Strand Transfer Inhibitors by Molecular Dynamics Simulation and Residue Interaction Network Analysis , 2013, J. Chem. Inf. Model..
[48] Dan Li,et al. Structural basis of the interactions between CXCR4 and CXCL12/SDF-1 revealed by theoretical approaches. , 2013, Molecular bioSystems.
[49] Youyong Li,et al. Assessing the performance of MM/PBSA and MM/GBSA methods. 3. The impact of force fields and ligand charge models. , 2013, The journal of physical chemistry. B.
[50] T. Stockner,et al. What can naturally occurring mutations tell us about Cav1.x channel function? , 2013, Biochimica et biophysica acta.
[51] W. Catterall,et al. Structural basis for Ca2+ selectivity of a voltage-gated calcium channel , 2013, Nature.
[52] Peng Yang,et al. Modeling, Molecular Dynamics Simulation, and Mutation Validation for Structure of Cannabinoid Receptor 2 Based on Known Crystal Structures of GPCRs , 2014, J. Chem. Inf. Model..
[53] G. Zamponi,et al. Neuronal Voltage-Gated Calcium Channels: Structure, Function, and Dysfunction , 2014, Neuron.
[54] R. Gust,et al. Pyrimidine-2,4,6-triones are a new class of voltage-gated L-type Ca2+ channel activators , 2014, Nature Communications.
[55] Tingjun Hou,et al. Assessing the performance of MM/PBSA and MM/GBSA methods. 5. Improved docking performance using high solute dielectric constant MM/GBSA and MM/PBSA rescoring. , 2014, Physical chemistry chemical physics : PCCP.
[56] Huanxiang Liu,et al. Computational Study on the Inhibitor Binding Mode and Allosteric Regulation Mechanism in Hepatitis C Virus NS3/4A Protein , 2014, PloS one.
[57] Youyong Li,et al. Assessing the performance of MM/PBSA and MM/GBSA methods. 4. Accuracies of MM/PBSA and MM/GBSA methodologies evaluated by various simulation protocols using PDBbind data set. , 2014, Physical chemistry chemical physics : PCCP.
[58] Huanxiang Liu,et al. Molecular modeling and residue interaction network studies on the mechanism of binding and resistance of the HCV NS5B polymerase mutants to VX-222 and ANA598. , 2014, Antiviral research.
[59] J. Hescheler,et al. Voltage-gated calcium channels: Determinants of channel function and modulation by inorganic cations , 2015, Progress in Neurobiology.