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Volumn 82, Issue 10, 2014, Pages 2671-2680

Extracting representative structures from protein conformational ensembles

Author keywords

Averaging; CASP; Clustering; Ensembles; Molecular dynamics; Protein; Root mean square deviation

Indexed keywords

PROTEIN; MULTIPROTEIN COMPLEX;

EID: 84940214914     PISSN: 08873585     EISSN: 10970134     Source Type: Journal    
DOI: 10.1002/prot.24633     Document Type: Article
Times cited : (5)

References (35)
  • 2
    • 0024094768 scopus 로고
    • Accurate simulation of protein dynamics in solution
    • Levitt M, Sharon R. Accurate simulation of protein dynamics in solution. Proc Natl Acad Sci USA 1988;85:7557-7561.
    • (1988) Proc Natl Acad Sci USA , vol.85 , pp. 7557-7561
    • Levitt, M.1    Sharon, R.2
  • 3
    • 80055081145 scopus 로고    scopus 로고
    • How fast-folding proteins fold
    • Piana S, Dror RO, Shaw DE. How fast-folding proteins fold. Science 2011;334:517-520.
    • (2011) Science , vol.334 , pp. 517-520
    • Piana, S.1    Dror, R.O.2    Shaw, D.E.3
  • 4
    • 0025681549 scopus 로고
    • Protein structure determination in solution by NMR spectroscopy
    • Wüthrich K. Protein structure determination in solution by NMR spectroscopy. J Biol Chem 1990.
    • (1990) J Biol Chem
    • Wüthrich, K.1
  • 6
    • 0032612579 scopus 로고    scopus 로고
    • Ab initio protein structure prediction of CASP III targets using ROSETTA
    • Simons KT, Bonneau R, Ruczinski I, Baker D. Ab initio protein structure prediction of CASP III targets using ROSETTA. Proteins 1999 (Suppl 3):171-176.
    • (1999) Proteins , pp. 171-176
    • Simons, K.T.1    Bonneau, R.2    Ruczinski, I.3    Baker, D.4
  • 8
    • 77954065271 scopus 로고    scopus 로고
    • I-TASSER: a unified platform for automated protein structure and function prediction
    • Roy A, Kucukural A, Zhang Y. I-TASSER: a unified platform for automated protein structure and function prediction. Nat Protoc 2010;5:725-738.
    • (2010) Nat Protoc , vol.5 , pp. 725-738
    • Roy, A.1    Kucukural, A.2    Zhang, Y.3
  • 9
    • 84867347204 scopus 로고    scopus 로고
    • FlexE: using elastic network models to compare models of protein structure
    • Perez A, Yang Z, Bahar I, Dill KA, FlexE: using elastic network models to compare models of protein structure. J Chem Theory Comput 2012;8:3985-3991.
    • (2012) J Chem Theory Comput , vol.8 , pp. 3985-3991
    • Perez, A.1    Yang, Z.2    Bahar, I.3    Dill, K.A.4
  • 10
    • 84892957566 scopus 로고    scopus 로고
    • Evaluation of predictions in the CASP10 model refinement category
    • Nugent T, Cozzetto D, Jones DT. Evaluation of predictions in the CASP10 model refinement category. Proteins 2014;82:98-111.
    • (2014) Proteins , vol.82 , pp. 98-111
    • Nugent, T.1    Cozzetto, D.2    Jones, D.T.3
  • 11
    • 0035283159 scopus 로고    scopus 로고
    • Conformation spaces of proteins
    • Sullivan DC, Kuntz ID. Conformation spaces of proteins. Proteins 2001;42:495-511.
    • (2001) Proteins , vol.42 , pp. 495-511
    • Sullivan, D.C.1    Kuntz, I.D.2
  • 12
    • 36649006642 scopus 로고    scopus 로고
    • Clustering molecular dynamics trajectories: 1. Characterizing the performance of different clustering algorithms
    • Shao J, Tanner SW, Thompson N, Cheatham TE. Clustering molecular dynamics trajectories: 1. Characterizing the performance of different clustering algorithms. J Chem Theory Comput 2007; 3:2312-2334.
    • (2007) J Chem Theory Comput , vol.3 , pp. 2312-2334
    • Shao, J.1    Tanner, S.W.2    Thompson, N.3    Cheatham, T.E.4
  • 13
    • 77149131242 scopus 로고    scopus 로고
    • Comparing geometric and kinetic cluster algorithms for molecular simulation data
    • Keller B, Daura X, van Gunsteren WF. Comparing geometric and kinetic cluster algorithms for molecular simulation data. J Chem Phys 2010;132:074110.
    • (2010) J Chem Phys , vol.132 , pp. 074110
    • Keller, B.1    Daura, X.2    van Gunsteren, W.F.3
  • 15
    • 77954826067 scopus 로고    scopus 로고
    • Google Books, Oxford University Press, New York, NY
    • Newman M. Networks: an introduction, Google Books, Oxford University Press, New York, NY (2010).
    • (2010) Networks: an introduction
    • Newman, M.1
  • 16
  • 17
    • 46249092554 scopus 로고    scopus 로고
    • GROMACS 4: algorithms for highly efficient, load-balanced, and scalable molecular simulation
    • Hess B, Kutzner C, van der Spoel D, Lindahl E. GROMACS 4: algorithms for highly efficient, load-balanced, and scalable molecular simulation. J Chem Theory Comput 2008;48:435-447.
    • (2008) J Chem Theory Comput , vol.48 , pp. 435-447
    • Hess, B.1    Kutzner, C.2    van der Spoel, D.3    Lindahl, E.4
  • 18
    • 33748518255 scopus 로고    scopus 로고
    • Comparison of multiple Amber force fields and development of improved protein backbone parameters
    • Hornak V, Abel R, Okur A, Strockbine B, Roitberg A, Simmerling C. Comparison of multiple Amber force fields and development of improved protein backbone parameters. Proteins 2006;65:712-725.
    • (2006) Proteins , vol.65 , pp. 712-725
    • Hornak, V.1    Abel, R.2    Okur, A.3    Strockbine, B.4    Roitberg, A.5    Simmerling, C.6
  • 20
    • 1842479952 scopus 로고    scopus 로고
    • Exploring protein native states and large-scale conformational changes with a modified generalized born model
    • Onufriev A, Bashford D, Case DA. Exploring protein native states and large-scale conformational changes with a modified generalized born model. Proteins 2004;55:383-394.
    • (2004) Proteins , vol.55 , pp. 383-394
    • Onufriev, A.1    Bashford, D.2    Case, D.A.3
  • 21
    • 0031552370 scopus 로고    scopus 로고
    • Determination of atomic desolvation energies from the structures of crystallized proteins
    • Zhang C, Vasmatzis G, Cornette JL, DeLisi C. Determination of atomic desolvation energies from the structures of crystallized proteins. J Mol Biol 1997;267:707-726.
    • (1997) J Mol Biol , vol.267 , pp. 707-726
    • Zhang, C.1    Vasmatzis, G.2    Cornette, J.L.3    DeLisi, C.4
  • 22
    • 33646887390 scopus 로고
    • On the limited memory BFGS method for large scale optimization
    • Liu DC, Nocedal J. On the limited memory BFGS method for large scale optimization. Math Program 1989;45:503-528.
    • (1989) Math Program , vol.45 , pp. 503-528
    • Liu, D.C.1    Nocedal, J.2
  • 23
  • 24
    • 0042622381 scopus 로고    scopus 로고
    • LGA: a method for finding 3D similarities in protein structures
    • Zemla A. LGA: a method for finding 3D similarities in protein structures. Nucleic Acids Res 2003;31:3370-3374.
    • (2003) Nucleic Acids Res , vol.31 , pp. 3370-3374
    • Zemla, A.1
  • 25
    • 84871040640 scopus 로고    scopus 로고
    • CAD-score: a new contact area difference-based function for evaluation of protein structural models
    • Olechnovič K, Kulberkyte E, Venclovas C. CAD-score: a new contact area difference-based function for evaluation of protein structural models. Proteins 2013;81;149-162.
    • (2013) Proteins , vol.81 , pp. 149-162
    • Olechnovič, K.1    Kulberkyte, E.2    Venclovas, C.3
  • 26
    • 3242886389 scopus 로고    scopus 로고
    • MolProbity: structure validation and all-atom contact analysis for nucleic acids and their complexes
    • Davis IW, Murray LW, Richardson JS, Richardson DC. MolProbity: structure validation and all-atom contact analysis for nucleic acids and their complexes. Nucleic Acids 2004;32:W615-W619.
    • (2004) Nucleic Acids , vol.32 , pp. W615-W619
    • Davis, I.W.1    Murray, L.W.2    Richardson, J.S.3    Richardson, D.C.4
  • 27
    • 18344362394 scopus 로고
    • On the use of classical statistical mechanics in the treatment of polymer chain conformation
    • Go N, Scheraga HA. On the use of classical statistical mechanics in the treatment of polymer chain conformation. Macromolecules 1976;9:535-542.
    • (1976) Macromolecules , vol.9 , pp. 535-542
    • Go, N.1    Scheraga, H.A.2
  • 31
    • 33846823909 scopus 로고
    • Particle mesh Ewald: an N{dot operator}log(N) method for Ewald sums in large systems
    • Darden T, York D, Pedersen L. Particle mesh Ewald: an N{dot operator}log(N) method for Ewald sums in large systems. J Chem Phys 1993;98:10089-10092.
    • (1993) J Chem Phys , vol.98 , pp. 10089-10092
    • Darden, T.1    York, D.2    Pedersen, L.3
  • 32
    • 84873657174 scopus 로고    scopus 로고
    • Protein structure refinement through structure selection and averaging from molecular dynamics ensembles
    • Mirjalili V, Feig M. Protein structure refinement through structure selection and averaging from molecular dynamics ensembles. J Chem Theory Comput 2013;9:1294-1303.
    • (2013) J Chem Theory Comput , vol.9 , pp. 1294-1303
    • Mirjalili, V.1    Feig, M.2
  • 33
    • 84893021599 scopus 로고    scopus 로고
    • Critical assessment of methods of protein structure prediction (CASP)-round X
    • Moult J, Fidelis K, Kryshtafovych A, Schwede T, Tramontano A. Critical assessment of methods of protein structure prediction (CASP)-round X. Proteins 2014;82(Suppl 2):1-6.
    • (2014) Proteins , vol.82 , pp. 1-6
    • Moult, J.1    Fidelis, K.2    Kryshtafovych, A.3    Schwede, T.4    Tramontano, A.5
  • 34
    • 46449139781 scopus 로고    scopus 로고
    • Ab initio folding of terminal segments with secondary structures reveals the fine difference between two closely related all-atom statistical energy functions
    • Yang Y, Zhou Y. Ab initio folding of terminal segments with secondary structures reveals the fine difference between two closely related all-atom statistical energy functions. Protein Sci 2008;17:1212-1219.
    • (2008) Protein Sci , vol.17 , pp. 1212-1219
    • Yang, Y.1    Zhou, Y.2
  • 35
    • 46449132707 scopus 로고    scopus 로고
    • Specific interactions for ab initio folding of protein terminal regions with secondary structures
    • Yang Y, Zhou Y. Specific interactions for ab initio folding of protein terminal regions with secondary structures. Proteins 2008;72:793-803.
    • (2008) Proteins , vol.72 , pp. 793-803
    • Yang, Y.1    Zhou, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.