about
TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathyMutations in SCO2 are associated with autosomal-dominant high-grade myopiaCrystal Structure of Inhibitor of Growth 4 (ING4) Dimerization Domain Reveals Functional Organization of ING Family of Chromatin-binding ProteinsTitin kinase is an inactive pseudokinase scaffold that supports MuRF1 recruitment to the sarcomeric M-lineCrystal structure of Arabidopsis thaliana calmodulin7 and insight into its mode of DNA bindingNeu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathwayEndonuclease G interacts with histone H2B and DNA topoisomerase II alpha during apoptosisBinding of N-methylscopolamine to the extracellular domain of muscarinic acetylcholine receptorsAlternative splice variants in TIM barrel proteins from human genome correlate with the structural and evolutionary modularity of this versatile protein foldThe structural pathway of interleukin 1 (IL-1) initiated signaling reveals mechanisms of oncogenic mutations and SNPs in inflammation and cancerSpecific Interaction between eEF1A and HIV RT Is Critical for HIV-1 Reverse Transcription and a Potential Anti-HIV TargetExploration of pathomechanisms triggered by a single-nucleotide polymorphism in titin's I-band: the cardiomyopathy-linked mutation T2580I.Mutations I117V and I117M and oseltamivir sensitivity of pandemic (H1N1) 2009 viruses.Probing impact of active site residue mutations on stability and activity of Neisseria polysaccharea amylosucrase.Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.Enzyme Efficiency but Not Thermostability Drives Cefotaxime Resistance Evolution in TEM-1 β-Lactamase.Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing lossThe structural network of Interleukin-10 and its implications in inflammation and cancerImproving the anti-toxin abilities of the CMG2-Fc fusion protein with the aid of computational designNLRP7 inter-domain interactions: the NACHT-associated domain is the physical mediator for oligomeric assemblyStabilizing proteins from sequence statistics: the interplay of conservation and correlation in triosephosphate isomerase stability.Structure-energy-based predictions and network modelling of RASopathy and cancer missense mutationsMolecular modeling of the human hemoglobin-haptoglobin complex sheds light on the protective mechanisms of haptoglobin.Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.Environmental dependence of genetic constraint.Directed evolution of the substrate specificity of dialkylglycine decarboxylaseComputer-Aided Protein Directed Evolution: a Review of Web Servers, Databases and other Computational Tools for Protein EngineeringConservancy of mAb Epitopes in Ebolavirus Glycoproteins of Previous and 2014 OutbreaksA first continuous 4-aminoantipyrine (4-AAP)-based screening system for directed esterase evolution.Dancing through Life: Molecular Dynamics Simulations and Network-Centric Modeling of Allosteric Mechanisms in Hsp70 and Hsp110 Chaperone Proteins.The Architecture of the TIR Domain Signalosome in the Toll-like Receptor-4 Signaling PathwayMolecular modeling and molecular dynamic simulation of the effects of variants in the TGFBR2 kinase domain as a paradigm for interpretation of variants obtained by next generation sequencing.Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.Structural Basis of Neuronal Nitric-oxide Synthase Interaction with Dystrophin Repeats 16 and 17.The size and conservation of a coiled-coil structure in the ectodomain of human BST-2/tetherin is dispensable for inhibition of HIV-1 virion release.Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic featuresMutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand disease.A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's diseaseAnalysis of protein thermostability enhancing factors in industrially important thermus bacteria species.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
A graphical interface for the FoldX forcefield.
@ast
A graphical interface for the FoldX forcefield.
@en
type
label
A graphical interface for the FoldX forcefield.
@ast
A graphical interface for the FoldX forcefield.
@en
prefLabel
A graphical interface for the FoldX forcefield.
@ast
A graphical interface for the FoldX forcefield.
@en
P2093
P2860
P356
P1433
P1476
A graphical interface for the FoldX forcefield.
@en
P2093
Francois Stricher
Frederic Rousseau
Javier Delgado
Joost Van Durme
Luis Serrano
P2860
P304
P356
10.1093/BIOINFORMATICS/BTR254
P407
P577
2011-04-19T00:00:00Z