DUET: a server for predicting effects of mutations on protein stability using an integrated computational approach.
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Essential but not vulnerable: indazole sulfonamides targeting inosine monophosphate dehydrogenase as potential leads against Mycobacterium tuberculosisStructure of the bovine COPI δ subunit μ homology domain at 2.15 Å resolutionThe Inosine Monophosphate Dehydrogenase, GuaB2, Is a Vulnerable New Bactericidal Drug Target for Tuberculosis.Mutations in the NHEJ component XRCC4 cause primordial dwarfismThe Presence, Persistence and Functional Properties of Plasmodium vivax Duffy Binding Protein II Antibodies Are Influenced by HLA Class II Allelic VariantsVariation in Human Cytochrome P-450 Drug-Metabolism Genes: A Gateway to the Understanding of Plasmodium vivax RelapsesTP53 copy number expansion is associated with the evolution of increased body size and an enhanced DNA damage response in elephantsIn silico predicted structural and functional insights of all missense mutations on 2B domain of K1/K10 causing genodermatoses.mCSM-lig: quantifying the effects of mutations on protein-small molecule affinity in genetic disease and emergence of drug resistanceMECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis DisorderMutation-Structure-Function Relationship Based Integrated Strategy Reveals the Potential Impact of Deleterious Missense Mutations in Autophagy Related Proteins on Hepatocellular Carcinoma (HCC): A Comprehensive Informatics ApproachPlatinum: a database of experimentally measured effects of mutations on structurally defined protein-ligand complexes.INPS: predicting the impact of non-synonymous variations on protein stability from sequence.In silico functional dissection of saturation mutagenesis: Interpreting the relationship between phenotypes and changes in protein stability, interactions and activity.Mycobacterium tuberculosis whole genome sequencing and protein structure modelling provides insights into anti-tuberculosis drug resistance.PinSnps: structural and functional analysis of SNPs in the context of protein interaction networksA Novel Mutation in a Critical Region for the Methyl Donor Binding in DNMT3B Causes Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome (ICF).mCSM-NA: predicting the effects of mutations on protein-nucleic acids interactions.Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.Simulation based investigation of deleterious nsSNP's in ATXN2 gene and its structural consequence towards Spinocerebellar Ataxia.Impact of genetic variation on three dimensional structure and function of proteins.MAESTRO--multi agent stability prediction upon point mutations.Increased Biological Activity of Aneurinibacillus migulanus Strains Correlates with the Production of New Gramicidin Secondary Metabolites.Prediction and visualization data for the interpretation of sarcomeric and non-sarcomeric DNA variants found in patients with hypertrophic cardiomyopathy.Molecular Determinants of Mutant Phenotypes, Inferred from Saturation Mutagenesis DataSDHA related tumorigenesis: a new case series and literature review for variant interpretation and pathogenicity.Mycobacterium tuberculosis Glyceraldehyde-3-Phosphate Dehydrogenase (GAPDH) Functions as a Receptor for Human Lactoferrin.Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing.Variation Interpretation Predictors: Principles, Types, Performance, and Choice.pkCSM: Predicting Small-Molecule Pharmacokinetic and Toxicity Properties Using Graph-Based Signatures.Dancing through Life: Molecular Dynamics Simulations and Network-Centric Modeling of Allosteric Mechanisms in Hsp70 and Hsp110 Chaperone Proteins.Analysis of HGD Gene Mutations in Patients with Alkaptonuria from the United Kingdom: Identification of Novel MutationsSequence analysis of four vitamin D family genes (VDR, CYP24A1, CYP27B1 and CYP2R1) in Vogt-Koyanagi-Harada (VKH) patients: identification of a potentially pathogenic variant in CYP2R1Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip.Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease.A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome.MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability.Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy.Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinomaMolecular Basis of Transient Neonatal Zinc Deficiency: NOVEL ZnT2 MUTATIONS DISRUPTING ZINC BINDING AND PERMEATION.
P2860
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P2860
DUET: a server for predicting effects of mutations on protein stability using an integrated computational approach.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
DUET: a server for predicting ...... grated computational approach.
@en
type
label
DUET: a server for predicting ...... grated computational approach.
@en
prefLabel
DUET: a server for predicting ...... grated computational approach.
@en
P2860
P50
P356
P1476
DUET: a server for predicting ...... egrated computational approach
@en
P2860
P304
P356
10.1093/NAR/GKU411
P433
Web Server issue
P577
2014-05-14T00:00:00Z