PDB files of induced fit docking results for selected reference, N10- and Tail-modified pteridines in LmPTR1 without water molecules
Zip-archive with induced fit docking results for reference compounds methotrexate, 1b and 1c as well as the N10-modified compound 2e in their neutral and N1-protonated variants and the N10-modified compound 2a and Tail-modified compounds 4e, 4f, 4i and 4j in neutral form as individual ligand:receptor complex PDB files. The files are ordered as ranked by Glide docking scores. The LmPTR1 receptor was based on PDB-ID 1e92 without additional water molecules. Docking results were obtained by Induced Fit docking with Schrödinger Glide and Prime in the Induced Fit docking workflow (Schrödinger, LLC, New York, NY, Schrödinger Release 2015-4, 2015, Induced Fit Docking Protocol, Glide v6.9 and Prime v4.2). For details and naming conventions also refer to the README file.
SEEK ID: https://fairdomhub.org/data_files/3853?version=1
Filename:
LmPTR1-noHOH.zip
Format: Zip file
Size: 13.9 MB
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Created: 22nd Sep 2020 at 14:31
Last updated: 16th Jul 2021 at 11:21
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Version 2 (latest) Created 16th Jul 2021 at 11:21 by Ina Poehner
Updated nomenclature
Version 1 (earliest) Created 22nd Sep 2020 at 14:31 by Ina Poehner
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https://orcid.org/0000-0002-2801-8902
Group Leader, Molecular and Cellular Modeling Group, EML Research, Heidelberg
Projects: NMTrypI - New Medicines for Trypanosomatidic Infections
Web page: https://cordis.europa.eu/programme/id/FP7_HEALTH.2013.2.3.4-2
The New Medicines for Trypanosomatidic Infections - NMTrypI project aimed at obtaining new candidate drugs against Trypanosomatidic infections with appropriate efficiency from the lead phase to the final preclinical phase that are more accessible to patients.
Programme: Drug development for neglected parasitic diseases
Public web page: https://fp7-nmtrypi.eu/
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Studies: Docking to PTR1 and DHFR targets and off-targets, In silico property and correlation analysis
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Docking results of pteridine-based compounds in different target PTR1 and DHFR receptors and the off-target human DHFR when using an induced fit docking routine with an initial crude ligand placement step, subsequent receptor optimization in response to ligand binding and another docking step into the optimized receptor.
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