位置：成果数据库 > 期刊 > 期刊详情页
Exploring the relationship between sequences, structures, dynamical behaviors and functions of new t
  • ISSN号：1381-6128
  • 期刊名称：Current Pharmaceutical Design
  • 时间：2013
  • 页码：2308-2317
  • 相关项目：结合多尺度相互作用势和分子碎片生长方案的蛋白质功能预测新理论方法研究
作者： Wu, Xue|Shi, Yue|Ren, Pengyu|Wang, Deping|Li, Guohui|
同期刊论文项目
结合多尺度相互作用势和分子碎片生长方案的蛋白质功能预测新理论方法研究
期刊论文 23
同项目期刊论文
The challenge to the rule of homology modeling: folding mechanism study of protein G(A) and G(B) wit
A Structural-based Strategy for Recognition of Transcription Factor Binding Sites
Investigation of Family 18 Chitinases and Inhibitors by Computer-Aided Approaches
Exploring the structure requirement for KC theta inhibitory activity of pyridinecarbonitrile derivat
Insight into mechanism of small molecule inhibitors of the MDM2-p53 interaction: Molecular dynamics
Fast and Accurate Computation Schemes for Evaluating Vibrational Entropy of Proteins
A computational analysis of interaction mechanisms of peptide and non-peptide inhibitors with MDMX b
Molecular recognition of human angiotensin-coverting enzyme I (hACE I) and different inhibitors.
Investigation binding patterns of human carboxylesterase I (hCES I) with broad substrates by MD simu
UNDERSTANDING THE MOLECULAR MECHANISM OF BINDING MODES OF AURORA A INHIBITORS BY LONG TIME SCALE GPU
QM/MM MD and free energy simulations of the methylation reactions catalyzed by protein arginine meth
What is the role of motif D in the nucleotide incorporation catalyzed by the RNA-dependent RNA polym
Exploring the proton conductance and drug-resistance of BM2 channel through molecular dynamics simul
Computational Studies of Difference in Binding Modes of Peptide and Non-Peptide Inhibitors to MDM2/M
Coarse-grained simulations for organic molecular liquids based on Gay-Berne and electric multipole p
Molecular Dynamic Simulation Insights into the Normal State and Restoration of p53 Function
Identification of Novel Potential beta-N-Acetyl-D-Hexosaminidase Inhibitors by Virtual Screening, Mo
Binding Free Energy Estimation for Protein-Ligand Complex Based on MM-PBSwith Various Partial Charge
Role of Bivalent Cations in Structural Stabilities of New Drug Targets ——Vaccinia-relate
COMPARING FOLDING MECHANISMS OF DIFFERENT PRION PROTEINS BY Go MODEL