about
Insights into -Lactamases from Burkholderia Species, Two Phylogenetically Related yet Distinct Resistance DeterminantsDendritic cell immunoreceptor is a new target for anti-AIDS drug development: identification of DCIR/HIV-1 inhibitorsDeciphering the signaling mechanisms of the plant cell wall degradation machinery in Aspergillus oryzaeOutcome of a workshop on applications of protein models in biomedical researchBenchmarking sets for molecular dockingApplication of the 4D fingerprint method with a robust scoring function for scaffold-hopping and drug repurposing strategies.Comprehensive structural and functional characterization of the human kinome by protein structure modeling and ligand virtual screening.Virtual ligand screening against comparative protein structure models.Benchmarking methods and data sets for ligand enrichment assessment in virtual screening.kinDOCK: a tool for comparative docking of protein kinase ligands.Recent advances in computer-aided drug design.Molecular docking screens using comparative models of proteinsMolecular modeling and ligand docking for solute carrier (SLC) transportersLigand-based virtual screening approach using a new scoring functionPredicting the accuracy of protein-ligand docking on homology models.Structure-based systems biology for analyzing off-target bindingPrediction of substrates for glutathione transferases by covalent docking.A method to enhance the hit ratio by a combination of structure-based drug screening and ligand-based screening.Chemical approaches to the discovery and development of cancer therapies.Virtual interactomics of proteins from biochemical standpoint.Towards the development of universal, fast and highly accurate docking/scoring methods: a long way to go.In silico fragment-based drug design.A lazy learning-based QSAR classification study for screening potential histone deacetylase 8 (HDAC8) inhibitors.A critical assessment of the performance of protein-ligand scoring functions based on NMR chemical shift perturbations.An integrated structure- and system-based framework to identify new targets of metabolites and known drugs.A novel and efficient ligand-based virtual screening approach using the HWZ scoring function and an enhanced shape-density model.Decoys Selection in Benchmarking Datasets: Overview and Perspectives.High-throughput structural characterisation of therapeutic protein targets
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Kinases, homology models, and high throughput docking.
@ast
Kinases, homology models, and high throughput docking.
@en
type
label
Kinases, homology models, and high throughput docking.
@ast
Kinases, homology models, and high throughput docking.
@en
prefLabel
Kinases, homology models, and high throughput docking.
@ast
Kinases, homology models, and high throughput docking.
@en
P356
P1476
Kinases, homology models, and high throughput docking.
@en
P2093
David J Diller
P304
P356
10.1021/JM020503A
P407
P577
2003-10-01T00:00:00Z