TY - JOUR
T1 - An Improved Integration of Template-Based and Template-Free Protein Structure Modeling Methods and its Assessment in CASP11
AU - Li, Jilong
AU - Adhikari, Badri
AU - Cheng, Jianlin
N1 - The tertiary structure of a protein is important for understanding its functions. Experimental techniques such as x-ray crystallography and nucleic magnetic resonance can determine protein structure with high-resolution, however, they are too expensive to be applied to all the proteins.
PY - 2015/6/17
Y1 - 2015/6/17
N2 - Most computational protein structure prediction methods are designed for either templatebased or template-free (ab initio) structure prediction. The approaches that integrate the prediction capabilities of both template-based modeling and template-free modeling are needed to synergistically combine the two kinds of methods to improve protein structure prediction. In this work, we develop a new method to integrate several protein structure prediction methods including our template-based MULTICOM server, our ab initio contact-based protein structure prediction method CONFOLD, our multi-template-based model generation tool MTMG, and locally installed external Rosetta, I-TASSER and RaptorX protein structure prediction tools to improve protein structure prediction of a fullspectrum difficulty ranging from easy, to medium and to hard. Our method participated in the 11 th community-wide Critical Assessment of Techniques for Protein Structure Prediction (CASP11) in 2014 as MULTICOM-NOVEL server. It was ranked among top 10 methods for protein tertiary structure prediction according to the official CASP11 assessment, which demonstrates that integrating complementary modeling methods is useful for advancing protein structure prediction.
AB - Most computational protein structure prediction methods are designed for either templatebased or template-free (ab initio) structure prediction. The approaches that integrate the prediction capabilities of both template-based modeling and template-free modeling are needed to synergistically combine the two kinds of methods to improve protein structure prediction. In this work, we develop a new method to integrate several protein structure prediction methods including our template-based MULTICOM server, our ab initio contact-based protein structure prediction method CONFOLD, our multi-template-based model generation tool MTMG, and locally installed external Rosetta, I-TASSER and RaptorX protein structure prediction tools to improve protein structure prediction of a fullspectrum difficulty ranging from easy, to medium and to hard. Our method participated in the 11 th community-wide Critical Assessment of Techniques for Protein Structure Prediction (CASP11) in 2014 as MULTICOM-NOVEL server. It was ranked among top 10 methods for protein tertiary structure prediction according to the official CASP11 assessment, which demonstrates that integrating complementary modeling methods is useful for advancing protein structure prediction.
KW - Model generation
KW - model selection
KW - protein structure prediction
KW - sequence alignment
KW - template-based modeling
KW - template-free modeling.
UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593487/
UR - http://www.eurekaselect.com/131520/article
U2 - 10.2174/0929866522666150520145717
DO - 10.2174/0929866522666150520145717
M3 - Article
VL - 22
JO - Protein and Peptide Letters
JF - Protein and Peptide Letters
ER -