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  2. Protein–ligand docking - Wikipedia

    en.wikipedia.org/wiki/Proteinligand_docking

    The ability to accurately predict target binding sites is a new phenomena, however, which expands on the ability to simply parse a data set of chemical compounds; now due to increasing computational capability, it is possible to inspect the actual geometries of the protein-ligand binding site in vitro.

  3. Docking (molecular) - Wikipedia

    en.wikipedia.org/wiki/Docking_(molecular)

    A binding interaction between a small molecule ligand and an enzyme protein may result in activation or inhibition of the enzyme. If the protein is a receptor, ligand binding may result in agonism or antagonism. Docking is most commonly used in the field of drug design — most drugs are small organic molecules, and docking may be applied to:

  4. Ligand (biochemistry) - Wikipedia

    en.wikipedia.org/wiki/Ligand_(biochemistry)

    In protein-ligand binding, the ligand is usually a molecule which produces a signal by binding to a site on a target protein. The binding typically results in a change of conformational isomerism (conformation) of the target protein. In DNA-ligand binding studies, the ligand can be a small molecule, ion, [1] or protein [2] which binds to the ...

  5. PDBbind database - Wikipedia

    en.wikipedia.org/wiki/PDBbind_database

    The PDBbind database is a comprehensive collection of experimentally measured binding affinity data (Kd, Ki, and IC50) for the protein-ligand complexes deposited in the Protein Data Bank (PDB). [ 1 ] [ 2 ] It thus provides a link between energetic and structural information of protein-ligand complexes, which is of great value to various studies ...

  6. I-TASSER - Wikipedia

    en.wikipedia.org/wiki/I-TASSER

    TM-SITE: A structure-based approach for ligand-binding site prediction. S-SITE: A sequence-based approach for ligand-binding site prediction. LOMETS: A set of locally installed threading programs for meta-server protein fold-recognition. MUSTER: A threading program to identify templates from a non-redundant protein structure library.

  7. Scoring functions for docking - Wikipedia

    en.wikipedia.org/wiki/Scoring_functions_for_docking

    Protein structures may be determined by experimental techniques such as X-ray crystallography or solution phase NMR methods or predicted by homology modelling. Ligand active conformation – three-dimensional shape of the ligand when bound to the protein; Binding-mode – orientation of the two binding partners relative to each other in the complex

  8. Binding site - Wikipedia

    en.wikipedia.org/wiki/Binding_site

    Binding of a ligand to a binding site on protein often triggers a change in conformation in the protein and results in altered cellular function. Hence binding site on protein are critical parts of signal transduction pathways. [10] Types of ligands include neurotransmitters, toxins, neuropeptides, and steroid hormones. [11]

  9. ProBiS - Wikipedia

    en.wikipedia.org/wiki/ProBiS

    ProBiS is a computer software which allows prediction of binding sites and their corresponding ligands for a given protein structure. Initially ProBiS was developed as a ProBiS algorithm by Janez Konc and Dušanka Janežič in 2010 [1] and is now available as ProBiS server, ProBiS CHARMMing server, ProBiS algorithm and ProBiS plugin.