Lead Finder

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Lead Finder is a computational chemistry tool designed for modeling protein-ligand interactions. It is used for conducting molecular docking studies and quantitatively assessing ligand binding and biological activity. It offers free access to users in commercial, academic, or other settings.

About[edit]

The original docking algorithm integrated into Lead Finder can be tailored for either quick but less accurate virtual screening applications or slower but more in-depth analyses.[1]

Lead Finder is used by computational and medicinal chemists for drug discovery, pharmacologists, and toxicologists involved in in silico assessment of ADMET properties. Additionally, it is used by biochemists and enzymologists working on modeling protein-ligand interactions, enzyme specificity, and rational enzyme design. Lead Finder's specialization in ligand docking and binding energy estimation is a result of its advanced docking algorithm and the precision with which it represents protein-ligand interactions.[2]

Docking algorithm[edit]

From a mathematical perspective, ligand docking involves the modelling of a multidimensional surface that describes the free energy associated with protein-ligand binding. This surface can be highly complex, with ligands possessing as many as 15-20 degrees of freedom, such as freely rotatable bonds.

Lead Finder's approach combines the use of genetic algorithm search, local optimization techniques, and knowledge gathered during the search process.

Scoring function[edit]

The Lead Finder scoring function represents protein-ligand interactions more precisely. The scoring function's model considers various types of molecular interactions.

In this scoring function, individual energy contributions are carefully adjusted with empirically derived coefficients tailored to objectives. such as the prediction of binding energies, the ranking of energy for docked ligand poses, and the ordering of active and inactive compounds during virtual screening experiments. To achieve these goals, Lead Finder employs three types of scoring functions, based on the same set of energy contributions but with different sets of energy-scaling coefficients.[3]

Docking success rate[edit]

Docking success rate was benchmarked as a percentage of correctly docked ligands (for which top-scored pose was within 2 Å RMSD from the reference ligand coordinates) for a set of protein-ligand complexes extracted from PDB. A set of 407 protein-ligand complexes was used for current docking success rate measurements. This set of complexes was combined from test sets used in original benchmarking studies of such docking programs as: FlexX,[4] Glide SP,[5] Glide XP,[6] Gold,[7][8][9] LigandFit,[10] MolDock,[11] Surflex.[12]

Accuracy of binding energy estimations[edit]

The ability of Lead Finder to estimate free energy of protein-ligand binding was benchmarked against the set of 330 diverse protein-ligand complexes. Lead Finder predicted bond energy precisely (RMSD = 1.5 kcal/mol) in less than one second per compound, on average.

References[edit]

  1. ^ Stroganov O (2008). "Lead Finder: An Approach To Improve Accuracy of Protein−Ligand Docking, Binding Energy Estimation, and Virtual Screening". J. Chem. Inf. Model. 48 (12): 2371–2385. doi:10.1021/ci800166p. PMID 19007114.
  2. ^ "Benchmarking Lead Finder's Performance in Virtual Screening". www.biomoltech.com. Retrieved 2023-11-12.
  3. ^ Novikov, Fedor N.; Stroylov, Viktor S.; Zeifman, Alexey A.; Stroganov, Oleg V.; Kulkov, Val; Chilov, Ghermes G. (2012-05-09). "Lead Finder docking and virtual screening evaluation with Astex and DUD test sets". Journal of Computer-Aided Molecular Design. 26 (6): 725–735. doi:10.1007/s10822-012-9549-y. ISSN 0920-654X.
  4. ^ M. Rarey; B. Kramer; T. Lengauer (1997). "Multiple automatic base selection: Protein-ligand docking based on incremental construction without manual intervention". J Comp Aid Mol Des. 11 (4): 369–384. Bibcode:1997JCAMD..11..369R. doi:10.1023/A:1007913026166. PMID 9334903. S2CID 5987558.
  5. ^ R. A. Friesner; R. B. Murphy; M. P. Repasky; L. L. Frye; J. R. Greenwood; T. A. Halgren; P. C. Sanschagrin; D. T. Mainz (2004). "Glide: A New Approach for Rapid, Accurate Docking and Scoring. 1. Method and Assessment of Docking Accuracy". Journal of Medicinal Chemistry. 47 (7): 1739–1749. doi:10.1021/jm0306430. PMID 15027865.
  6. ^ R. A. Friesner; J. L. Banks; R. B. Murphy; T. A. Halgren; J. J. Klicic; D. T. Mainz; M. P. Repasky; E. H. Knoll; M. Shelley; J. K. Perry; D. E. Shaw; P. Francis; P. S. Shenkin (2006). "Glide: extra Precision Glide: Docking and Scoring incorporating a Model of Hydrophobic Enclosure for Protein-Ligand Complexes". Journal of Medicinal Chemistry. 49 (21): 6177–6196. CiteSeerX 10.1.1.619.3600. doi:10.1021/jm051256o. PMID 17034125. S2CID 6369255.
  7. ^ G. Jones; P. Willett; R. C. Glen; A. R. Leach; R. Taylor (1997). "Development and Validation of a Genetic Algorithm for Flexible Docking". J Mol Biol. 267 (3): 727–748. CiteSeerX 10.1.1.130.3377. doi:10.1006/jmbi.1996.0897. PMID 9126849.
  8. ^ M. J. Hartshorn; M. L. Verdonk; G. Chessari; S. C. Brewerton; W.T..M. Mooij; P. N. Mortenson; C. W. Murray (2007). "Diverse, High-Quality Test Set for the Validation of Protein-Ligand Docking Performance". Journal of Medicinal Chemistry. 50 (4): 726–741. doi:10.1021/jm061277y. PMID 17300160.
  9. ^ J.W.M. Nissink; C. Murray; M. Hartshorn; M. L. Verdonk; J. C. Cole; R. Taylor (2002). "A New Test Set for Validating Predictions of Protein-Ligand Interaction". Proteins: Structure, Function, and Genetics. 49 (4): 457–471. doi:10.1002/prot.10232. PMID 12402356. S2CID 37136109.
  10. ^ C. M. Venkatachalam; X. Jiang; T. Oldfield; M. Waldman (2003). "LigandFit: a novel method for the shape-directed rapid docking of ligands to protein active sites". J Mol Graph Model. 21 (4): 289–307. doi:10.1016/s1093-3263(02)00164-x. PMID 12479928.
  11. ^ R. Thomsen; M. H. Christensen (2006). "MolDock: A new technique for high-accuracy molecular docking". Journal of Medicinal Chemistry. 49 (11): 3315–3321. CiteSeerX 10.1.1.116.2126. doi:10.1021/jm051197e. PMID 16722650.
  12. ^ A. N. Jain (2003). "Surflex: Fully Automatic Flexible Molecular Docking Using a Molecular Similarity-Based Search Engine". Journal of Medicinal Chemistry. 46 (4): 499–511. doi:10.1021/jm020406h. PMID 12570372.
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