Computational investigation of the human SOD1 mutant, Cys146Arg, that directs familial amyotrophic lateral sclerosis
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Title
Computational investigation of the human SOD1 mutant, Cys146Arg, that directs familial amyotrophic lateral sclerosis
Authors
Keywords
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Journal
Molecular BioSystems
Volume 13, Issue 8, Pages 1495-1503
Publisher
Royal Society of Chemistry (RSC)
Online
2017-06-02
DOI
10.1039/c7mb00106a
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Note: Only part of the references are listed.- SAAFEC: Predicting the Effect of Single Point Mutations on Protein Folding Free Energy Using a Knowledge-Modified MM/PBSA Approach
- (2016) Ivan Getov et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
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- (2016) Sarah Pickles et al. Acta Neuropathologica Communications
- The mechanisms of flavonoids inhibiting conformational transition of amyloid-β42 monomer: a comparative molecular dynamics simulation study
- (2015) Ling Wang et al. RSC Advances
- Role of mitochondria in mutant SOD1 linked amyotrophic lateral sclerosis
- (2014) Wenzhi Tan et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Insights into the Role of the Unusual Disulfide Bond in Copper-Zinc Superoxide Dismutase
- (2014) Kevin Sea et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Study on the disulfide bond and disulfide loop of native and mutated SOD1 protein
- (2014) S.P. Keerthana et al. JOURNAL OF MOLECULAR GRAPHICS & MODELLING
- DUET: a server for predicting effects of mutations on protein stability using an integrated computational approach
- (2014) D. E. V. Pires et al. NUCLEIC ACIDS RESEARCH
- PredictSNP: Robust and Accurate Consensus Classifier for Prediction of Disease-Related Mutations
- (2014) Jaroslav Bendl et al. PLoS Computational Biology
- Structures of the E46K Mutant-Type α-Synuclein Protein and Impact of E46K Mutation on the Structures of the Wild-Type α-Synuclein Protein
- (2013) Olivia Wise-Scira et al. ACS Chemical Neuroscience
- mCSM: predicting the effects of mutations in proteins using graph-based signatures
- (2013) Douglas E. V. Pires et al. BIOINFORMATICS
- Bioinformatics analysis of the epitope regions for norovirus capsid protein
- (2013) Liping Chen et al. BMC BIOINFORMATICS
- Drug resistance mechanism of PncA inMycobacterium tuberculosis
- (2013) Vidya Rajendran et al. JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
- Role of ELA region in auto-activation of mutant KIT receptor: a molecular dynamics simulation insight
- (2013) Rituraj Purohit JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
- Features of wild-type human SOD1 limit interactions with misfolded aggregates of mouse G86R Sod1
- (2013) David A Qualls et al. Molecular Neurodegeneration
- Identification of a novel Cys146X mutation of SOD1 in familial amyotrophic lateral sclerosis by whole-exome sequencing
- (2012) Jinyu Wu et al. GENETICS IN MEDICINE
- Disulfide Scrambling Describes the Oligomer Formation of Superoxide Dismutase (SOD1) Proteins in the Familial Form of Amyotrophic Lateral Sclerosis
- (2012) Keisuke Toichi et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Computational screening and molecular dynamics simulation of disease associated nsSNPs in CENP-E
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- Role of Disulfide Cross-Linking of Mutant SOD1 in the Formation of Inclusion-Body-Like Structures
- (2012) Brittany L. T. Roberts et al. PLoS One
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- SDM--a server for predicting effects of mutations on protein stability and malfunction
- (2011) C. L. Worth et al. NUCLEIC ACIDS RESEARCH
- Roles of zinc and copper in modulating the oxidative refolding of bovine copper, zinc superoxide dismutase
- (2010) H.-T. Li et al. ACTA BIOCHIMICA ET BIOPHYSICA SINICA
- Relationship between mutation of serine residue at 315th position in M. tuberculosis catalase-peroxidase enzyme and Isoniazid susceptibility: An in silico analysis
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- Aggregation of Copper–Zinc Superoxide Dismutase in Familial and Sporadic ALS
- (2009) Madhuri Chattopadhyay et al. ANTIOXIDANTS & REDOX SIGNALING
- ALSOD: The Amyotrophic Lateral Sclerosis Online Database
- (2008) Richard Wroe et al. Amyotrophic Lateral Sclerosis
- A Limited Role for Disulfide Cross-linking in the Aggregation of Mutant SOD1 Linked to Familial Amyotrophic Lateral Sclerosis
- (2008) Celeste M. Karch et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Complete Loss of Post-translational Modifications Triggers Fibrillar Aggregation of SOD1 in the Familial Form of Amyotrophic Lateral Sclerosis
- (2008) Yoshiaki Furukawa et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- GROMACS 4: Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation
- (2008) Berk Hess et al. Journal of Chemical Theory and Computation
- SOD1 and Amyotrophic Lateral Sclerosis: Mutations and Oligomerization
- (2008) Lucia Banci et al. PLoS One
- Structure and dynamics of copper-free SOD: The protein before binding copper
- (2002) Lucia Banci et al. PROTEIN SCIENCE
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