PoPMuSiC 2.1: a web server for the estimation of protein stability changes upon mutation and sequence optimality
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Analyzing effects of naturally occurring missense mutationsComputational enzyme design approaches with significant biological outcomes: progress and challengesA novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndromeTECPR2 Associated Neuroaxonal Dystrophy in Spanish Water DogsMetabolic and Target-Site Mechanisms Combine to Confer Strong DDT Resistance in Anopheles gambiaeDesign of thermostable rhamnogalacturonan lyase mutants from Bacillus licheniformis by combination of targeted single point mutationsIdentification and glycerol-induced correction of misfolding mutations in the X-linked mental retardation gene CASKStructure-based engineering of alkaline α-amylase from alkaliphilic Alkalimonas amylolytica for improved thermostability.Association between PARP-1 V762A polymorphism and breast cancer susceptibility in Saudi population.Evolution- and structure-based computational strategy reveals the impact of deleterious missense mutations on MODY 2 (maturity-onset diabetes of the young, type 2)SDS, a structural disruption score for assessment of missense variant deleteriousness.GALT protein database: querying structural and functional features of GALT enzyme.Structure-PPi: a module for the annotation of cancer-related single-nucleotide variants at protein-protein interfacesExome analysis reveals differentially mutated gene signatures of stage, grade and subtype in breast cancers.Association of DNA Repair Gene APE1 Asp148Glu Polymorphism with Breast Cancer Risk.Crysalis: an integrated server for computational analysis and design of protein crystallization.Predicting protein thermal stability changes upon point mutations using statistical potentials: Introducing HoTMuSiC.STRUM: structure-based prediction of protein stability changes upon single-point mutation.Large scale analysis of protein stability in OMIM disease related human protein variantsCorrelation assessment among clinical phenotypes, expression analysis and molecular modeling of 14 novel variations in the human galactose-1-phosphate uridylyltransferase gene.Residue mutations and their impact on protein structure and function: detecting beneficial and pathogenic changes.Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients.A frequent splicing mutation and novel missense mutations color the updated mutational spectrum of classic galactosemia in Portugal.Bioengineered protein phosphatase 2A: update on needImproving landscape inference by integrating heterogeneous data in the inverse Ising problem.Enzyme Efficiency but Not Thermostability Drives Cefotaxime Resistance Evolution in TEM-1 β-Lactamase.ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients.A comprehensive, high-resolution map of a gene's fitness landscapeMolecular and Functional Bases of Selection against a Mutation Bias in an RNA Virus.Genetic and pharmacological strategies to refunctionalize the von Hippel Lindau R167Q mutant protein.Computational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnosticsThe X-Ray Crystal Structure of the Keratin 1-Keratin 10 Helix 2B Heterodimer Reveals Molecular Surface Properties and Biochemical Insights into Human Skin Disease.Adaptive evolution of the matrix extracellular phosphoglycoprotein in mammalsCommunity-wide evaluation of methods for predicting the effect of mutations on protein-protein interactions.On the effect of protein conformation diversity in discriminating among neutral and disease related single amino acid substitutions.Evaluating caveolin interactions: do proteins interact with the caveolin scaffolding domain through a widespread aromatic residue-rich motif?Coevolutionary Landscape Inference and the Context-Dependence of Mutations in Beta-Lactamase TEM-1.Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyPrincipal component analysis of binding energies for single-point mutants of hT2R16 bound to an agonist correlate with experimental mutant cell responseSubdomain interactions foster the design of two protein pairs with ∼80% sequence identity but different folds.
P2860
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P2860
PoPMuSiC 2.1: a web server for the estimation of protein stability changes upon mutation and sequence optimality
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին 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
PoPMuSiC 2.1: a web server for ...... tation and sequence optimality
@ast
PoPMuSiC 2.1: a web server for ...... tation and sequence optimality
@en
type
label
PoPMuSiC 2.1: a web server for ...... tation and sequence optimality
@ast
PoPMuSiC 2.1: a web server for ...... tation and sequence optimality
@en
prefLabel
PoPMuSiC 2.1: a web server for ...... tation and sequence optimality
@ast
PoPMuSiC 2.1: a web server for ...... tation and sequence optimality
@en
P2860
P356
P1433
P1476
PoPMuSiC 2.1: a web server for ...... tation and sequence optimality
@en
P2093
Jean Marc Kwasigroch
Marianne Rooman
P2860
P2888
P356
10.1186/1471-2105-12-151
P577
2011-05-13T00:00:00Z
P5875
P6179
1007018062