Literature DB >> 22574683

FINDSITE(X): a structure-based, small molecule virtual screening approach with application to all identified human GPCRs.

Hongyi Zhou1, Jeffrey Skolnick.   

Abstract

We have developed FINDSITE(X), an extension of FINDSITE, a protein threading based algorithm for the inference of protein binding sites, biochemical function and virtual ligand screening, that removes the limitation that holo protein structures (those containing bound ligands) of a sufficiently large set of distant evolutionarily related proteins to the target be solved; rather, predicted protein structures and experimental ligand binding information are employed. To provide the predicted protein structures, a fast and accurate version of our recently developed TASSER(VMT), TASSER(VMT)-lite, for template-based protein structural modeling applicable up to 1000 residues is developed and tested, with comparable performance to the top CASP9 servers. Then, a hybrid approach that combines structure alignments with an evolutionary similarity score for identifying functional relationships between target and proteins with binding data has been developed. By way of illustration, FINDSITE(X) is applied to 998 identified human G-protein coupled receptors (GPCRs). First, TASSER(VMT)-lite provides updates of all human GPCR structures previously modeled in our lab. We then use these structures and the new function similarity detection algorithm to screen all human GPCRs against the ZINC8 nonredundant (TC < 0.7) ligand set combined with ligands from the GLIDA database (a total of 88,949 compounds). Testing (excluding GPCRs whose sequence identity > 30% to the target from the binding data library) on a 168 human GPCR set with known binding data, the average enrichment factor in the top 1% of the compound library (EF(0.01)) is 22.7, whereas EF(0.01) by FINDSITE is 7.1. For virtual screening when just the target and its native ligands are excluded, the average EF(0.01) reaches 41.4. We also analyze off-target interactions for the 168 protein test set. All predicted structures, virtual screening data and off-target interactions for the 998 human GPCRs are available at http://cssb.biology.gatech.edu/skolnick/webservice/gpcr/index.html .

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Year:  2012        PMID: 22574683      PMCID: PMC3396429          DOI: 10.1021/mp3000716

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  65 in total

1.  Protein structure prediction and structural genomics.

Authors:  D Baker; A Sali
Journal:  Science       Date:  2001-10-05       Impact factor: 47.728

2.  Scoring function for automated assessment of protein structure template quality.

Authors:  Yang Zhang; Jeffrey Skolnick
Journal:  Proteins       Date:  2004-12-01

Review 3.  Homology modeling of G-protein-coupled receptors with X-ray structures on the rise.

Authors:  Talia Yarnitzky; Anat Levit; Masha Y Niv
Journal:  Curr Opin Drug Discov Devel       Date:  2010-05

4.  A threading-based method (FINDSITE) for ligand-binding site prediction and functional annotation.

Authors:  Michal Brylinski; Jeffrey Skolnick
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-28       Impact factor: 11.205

5.  3DLigandSite: predicting ligand-binding sites using similar structures.

Authors:  Mark N Wass; Lawrence A Kelley; Michael J E Sternberg
Journal:  Nucleic Acids Res       Date:  2010-05-31       Impact factor: 16.971

6.  DEPTH: a web server to compute depth and predict small-molecule binding cavities in proteins.

Authors:  Kuan Pern Tan; Raghavan Varadarajan; M S Madhusudhan
Journal:  Nucleic Acids Res       Date:  2011-05-16       Impact factor: 16.971

7.  PubChem's BioAssay Database.

Authors:  Yanli Wang; Jewen Xiao; Tugba O Suzek; Jian Zhang; Jiyao Wang; Zhigang Zhou; Lianyi Han; Karen Karapetyan; Svetlana Dracheva; Benjamin A Shoemaker; Evan Bolton; Asta Gindulyte; Stephen H Bryant
Journal:  Nucleic Acids Res       Date:  2011-12-02       Impact factor: 16.971

8.  DrugBank: a comprehensive resource for in silico drug discovery and exploration.

Authors:  David S Wishart; Craig Knox; An Chi Guo; Savita Shrivastava; Murtaza Hassanali; Paul Stothard; Zhan Chang; Jennifer Woolsey
Journal:  Nucleic Acids Res       Date:  2006-01-01       Impact factor: 16.971

9.  TM-align: a protein structure alignment algorithm based on the TM-score.

Authors:  Yang Zhang; Jeffrey Skolnick
Journal:  Nucleic Acids Res       Date:  2005-04-22       Impact factor: 16.971

10.  Sequence-similar, structure-dissimilar protein pairs in the PDB.

Authors:  Mickey Kosloff; Rachel Kolodny
Journal:  Proteins       Date:  2008-05-01
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  16 in total

1.  Pocket detection and interaction-weighted ligand-similarity search yields novel high-affinity binders for Myocilin-OLF, a protein implicated in glaucoma.

Authors:  Bharath Srinivasan; Sam Tonddast-Navaei; Jeffrey Skolnick
Journal:  Bioorg Med Chem Lett       Date:  2017-07-12       Impact factor: 2.823

2.  GLASS: a comprehensive database for experimentally validated GPCR-ligand associations.

Authors:  Wallace K B Chan; Hongjiu Zhang; Jianyi Yang; Jeffrey R Brender; Junguk Hur; Arzucan Özgür; Yang Zhang
Journal:  Bioinformatics       Date:  2015-05-13       Impact factor: 6.937

Review 3.  Are predicted protein structures of any value for binding site prediction and virtual ligand screening?

Authors:  Jeffrey Skolnick; Hongyi Zhou; Mu Gao
Journal:  Curr Opin Struct Biol       Date:  2013-02-14       Impact factor: 6.809

4.  FINDSITEcomb2.0: A New Approach for Virtual Ligand Screening of Proteins and Virtual Target Screening of Biomolecules.

Authors:  Hongyi Zhou; Hongnan Cao; Jeffrey Skolnick
Journal:  J Chem Inf Model       Date:  2018-10-16       Impact factor: 4.956

5.  FINDSITE(comb): a threading/structure-based, proteomic-scale virtual ligand screening approach.

Authors:  Hongyi Zhou; Jeffrey Skolnick
Journal:  J Chem Inf Model       Date:  2012-12-28       Impact factor: 4.956

6.  Novel small molecule binders of human N-glycanase 1, a key player in the endoplasmic reticulum associated degradation pathway.

Authors:  Bharath Srinivasan; Hongyi Zhou; Sreyoshi Mitra; Jeffrey Skolnick
Journal:  Bioorg Med Chem       Date:  2016-08-13       Impact factor: 3.641

7.  PoLi: A Virtual Screening Pipeline Based on Template Pocket and Ligand Similarity.

Authors:  Ambrish Roy; Bharath Srinivasan; Jeffrey Skolnick
Journal:  J Chem Inf Model       Date:  2015-08-12       Impact factor: 4.956

8.  Virtual Screening of Human Class-A GPCRs Using Ligand Profiles Built on Multiple Ligand-Receptor Interactions.

Authors:  Wallace K B Chan; Yang Zhang
Journal:  J Mol Biol       Date:  2020-07-09       Impact factor: 5.469

9.  FRAGSITE: A Fragment-Based Approach for Virtual Ligand Screening.

Authors:  Hongyi Zhou; Hongnan Cao; Jeffrey Skolnick
Journal:  J Chem Inf Model       Date:  2021-03-16       Impact factor: 4.956

10.  BioLiP: a semi-manually curated database for biologically relevant ligand-protein interactions.

Authors:  Jianyi Yang; Ambrish Roy; Yang Zhang
Journal:  Nucleic Acids Res       Date:  2012-10-18       Impact factor: 16.971

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