NOLB: Nonlinear Rigid Block Normal-Mode Analysis Method.
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[1] Martin Zacharias,et al. Rapid protein–ligand docking using soft modes from molecular dynamics simulations to account for protein deformability: Binding of FK506 to FKBP , 2004, Proteins.
[2] Pablo Chacón,et al. iMod: multipurpose normal mode analysis in internal coordinates , 2011, Bioinform..
[3] Hideaki Umeyama,et al. Algorithm for normal mode analysis with general internal coordinates , 2003, J. Comput. Chem..
[4] Y. Sanejouand,et al. Building‐block approach for determining low‐frequency normal modes of macromolecules , 2000, Proteins.
[5] Julie C. Mitchell,et al. Density‐cluster NMA: A new protein decomposition technique for coarse‐grained normal mode analysis , 2012, Proteins.
[6] Dahlia R. Weiss,et al. Optimized torsion-angle normal modes reproduce conformational changes more accurately than cartesian modes. , 2011, Biophysical journal.
[7] Junmei Wang,et al. How well does a restrained electrostatic potential (RESP) model perform in calculating conformational energies of organic and biological molecules? , 2000, J. Comput. Chem..
[8] M. Sternberg,et al. Insights into protein flexibility: The relationship between normal modes and conformational change upon protein–protein docking , 2008, Proceedings of the National Academy of Sciences.
[9] Svetlana Artemova,et al. A comparison of neighbor search algorithms for large rigid molecules , 2011, J. Comput. Chem..
[10] M. Karplus,et al. Harmonic dynamics of proteins: normal modes and fluctuations in bovine pancreatic trypsin inhibitor. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[11] Erik Lindahl,et al. Refinement of docked protein–ligand and protein–DNA structures using low frequency normal mode amplitude optimization , 2005, Nucleic acids research.
[12] Alexander D. MacKerell,et al. Development and current status of the CHARMM force field for nucleic acids , 2000, Biopolymers.
[13] C. Chennubhotla,et al. Intrinsic dynamics of enzymes in the unbound state and relation to allosteric regulation. , 2007, Current opinion in structural biology.
[14] R J Williams,et al. THE CONFORMATION PROPERTIES OF PROTEINS IN SOLUTION , 1979, Biological reviews of the Cambridge Philosophical Society.
[15] C. Pierre,et al. A NEW GALERKIN-BASED APPROACH FOR ACCURATE NON-LINEAR NORMAL MODES THROUGH INVARIANT MANIFOLDS , 2002 .
[16] M. Zacharias,et al. Accounting for global protein deformability during protein-protein and protein-ligand docking. , 2005, Biochimica et biophysica acta.
[17] Nathalie Reuter,et al. Comparing the intrinsic dynamics of multiple protein structures using elastic network models. , 2015, Biochimica et biophysica acta.
[18] K C Holmes,et al. Normal modes as refinement parameters for the F-actin model. , 1995, Biophysical journal.
[19] G. Chirikjian,et al. Efficient generation of feasible pathways for protein conformational transitions. , 2002, Biophysical journal.
[20] Y. Sanejouand,et al. A new approach for determining low‐frequency normal modes in macromolecules , 1994 .
[21] I. Bahar,et al. Normal mode analysis of biomolecular structures: functional mechanisms of membrane proteins. , 2010, Chemical reviews.
[22] M. Levitt. A simplified representation of protein conformations for rapid simulation of protein folding. , 1976, Journal of molecular biology.
[23] Tosiyuki Noguti,et al. Dynamics of Native Globular Proteins in Terms of Dihedral Angles , 1983 .
[24] I. Bahar,et al. Coarse-grained normal mode analysis in structural biology. , 2005, Current opinion in structural biology.
[25] M Karplus,et al. Dynamics of proteins: elements and function. , 1983, Annual review of biochemistry.
[26] T. N. Bhat,et al. The Protein Data Bank , 2000, Nucleic Acids Res..
[27] D. Thirumalai,et al. Low-frequency normal modes that describe allosteric transitions in biological nanomachines are robust to sequence variations , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[28] Ivet Bahar,et al. ProDy: Protein Dynamics Inferred from Theory and Experiments , 2011, Bioinform..
[29] Ilya A. Vakser,et al. Structure fluctuations and conformational Changes in protein binding , 2012, J. Bioinform. Comput. Biol..
[30] Claudio N. Cavasotto,et al. Conformational Sampling of Protein Flexibility in Generalized Coordinates: Application to Ligand Docking , 2005 .
[31] R. Jernigan,et al. Anisotropy of fluctuation dynamics of proteins with an elastic network model. , 2001, Biophysical journal.
[32] T. Siméon,et al. An NMA‐guided path planning approach for computing large‐amplitude conformational changes in proteins , 2007, Proteins.
[33] John D. Westbrook,et al. EMDataBank unified data resource for 3DEM , 2013, Nucleic Acids Res..
[34] J. Andrew McCammon,et al. The dynamic picture of protein structure , 1983 .
[35] Michael Levitt,et al. The normal modes of a protein: Native bovine pancreatic trypsin inhibitor , 2009 .
[36] Christophe Pierre,et al. Normal Modes for Non-Linear Vibratory Systems , 1993 .
[37] Dror Tobi,et al. Allosteric changes in protein structure computed by a simple mechanical model: hemoglobin T<-->R2 transition. , 2003, Journal of molecular biology.
[38] J. Carrascosa,et al. Large Terminase Conformational Change Induced by Connector Binding in Bacteriophage T7* , 2013, The Journal of Biological Chemistry.
[39] Enrique S. Quintana-Ortí,et al. Exploring large macromolecular functional motions on clusters of multicore processors , 2013, J. Comput. Phys..
[40] K. Hinsen. Analysis of domain motions by approximate normal mode calculations , 1998, Proteins.
[41] Y. Sanejouand,et al. Conformational change of proteins arising from normal mode calculations. , 2001, Protein engineering.
[42] Ivet Bahar,et al. Dynamics of proteins predicted by molecular dynamics simulations and analytical approaches: Application to α‐amylase inhibitor , 2000, Proteins.
[43] K. Hinsen,et al. Evaluation of Protein Elastic Network Models Based on an Analysis of Collective Motions. , 2013, Journal of chemical theory and computation.
[44] Alberto Cardona,et al. A LOAD-DEPENDENT BASIS FOR REDUCED NONLINEAR STRUCTURAL DYNAMICS , 1985 .
[45] Vincent B. Chen,et al. Correspondence e-mail: , 2000 .
[46] P. Bates,et al. SwarmDock and the Use of Normal Modes in Protein-Protein Docking , 2010, International journal of molecular sciences.
[47] H. Berendsen,et al. Essential dynamics of proteins , 1993, Proteins.
[48] Gregory S Chirikjian,et al. Efficient determination of low-frequency normal modes of large protein structures by cluster-NMA. , 2005, Journal of molecular graphics & modelling.
[49] Martin Zacharias,et al. Energy minimization in low‐frequency normal modes to efficiently allow for global flexibility during systematic protein–protein docking , 2008, Proteins.
[50] Daisuke Kihara,et al. Prediction of homoprotein and heteroprotein complexes by protein docking and template‐based modeling: A CASP‐CAPRI experiment , 2016, Proteins.
[51] H. Gohlke,et al. Multiscale modeling of macromolecular conformational changes combining concepts from rigidity and elastic network theory , 2006, Proteins.
[52] Guohui Li,et al. A coarse-grained normal mode approach for macromolecules: an efficient implementation and application to Ca(2+)-ATPase. , 2002, Biophysical journal.
[53] Tirion,et al. Large Amplitude Elastic Motions in Proteins from a Single-Parameter, Atomic Analysis. , 1996, Physical review letters.
[54] M. Levitt,et al. Protein normal-mode dynamics: trypsin inhibitor, crambin, ribonuclease and lysozyme. , 1985, Journal of molecular biology.
[55] Gregory S. Chirikjian,et al. Normal mode analysis of proteins: a comparison of rigid cluster modes with Cα coarse graining , 2004 .
[56] Huimin Zhao,et al. Direct observation of TALE protein dynamics reveals a two-state search mechanism , 2015, Nature Communications.
[57] Jianpeng Ma,et al. A New Method for Coarse-Grained Elastic Normal-Mode Analysis. , 2006, Journal of chemical theory and computation.
[58] K. Bastard,et al. Accounting for Large Amplitude Protein Deformation during in Silico Macromolecular Docking , 2011, International journal of molecular sciences.