SAAMBE: Webserver to Predict the Charge of Binding Free Energy Caused by Amino Acids Mutations (Q36847179)

16 August 2017

SAAMBE: Webserver to Predict the Charge of Binding Free Energy Caused by Amino Acids Mutations (English)

1 reference

16 August 2017

Marharyta Petukh

1

1 reference

16 August 2017

Luogeng Dai

series ordinal

2

1 reference

16 August 2017

Emil Alexov

series ordinal

3

1 reference

16 August 2017

language of work or name

English

0 references

publication date

12 April 2016

1 reference

International Journal of Molecular Sciences

16 August 2017

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16 August 2017

17

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16 August 2017

4

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16 August 2017

547

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Creative Commons Attribution 4.0 International

16 August 2017

start time

12 April 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease

29 September 2017

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Predicting Binding Free Energy Change Caused by Point Mutations with Knowledge-Modified MM/PBSA Method

29 September 2017

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On human disease-causing amino acid variants: statistical study of sequence and structural patterns

29 September 2017

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Structural and physico-chemical effects of disease and non-disease nsSNPs on proteins

29 September 2017

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Chronic Beryllium Disease: revealing the role of beryllium ion and small peptides binding to HLA-DP2

29 September 2017

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Computational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnostics

29 September 2017

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Predicting the Impact of Missense Mutations on Protein-Protein Binding Affinity.

29 September 2017

1 reference

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ClinVar: public archive of relationships among sequence variation and human phenotype

29 September 2017

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Molecular mechanisms of disease-causing missense mutations

29 September 2017

1 reference

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Scoring functions for protein-protein interactions

29 September 2017

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Cancer missense mutations alter binding properties of proteins and their interaction networks

29 September 2017

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SKEMPI: a Structural Kinetic and Energetic database of Mutant Protein Interactions and its use in empirical models.

29 September 2017

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An X-linked channelopathy with cardiomegaly due to a CLIC2 mutation enhancing ryanodine receptor channel activity.

29 September 2017

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Proteome-wide prediction of protein-protein interactions from high-throughput data

29 September 2017

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Analyzing effects of naturally occurring missense mutations

29 September 2017

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Predicting protein-protein interactions on a proteome scale by matching evolutionary and structural similarities at interfaces using PRISM.

29 September 2017

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In silico and in vitro investigations of the mutability of disease-causing missense mutation sites in spermine synthase

29 September 2017

1 reference

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A missense mutation in CLIC2 associated with intellectual disability is predicted by in silico modeling to affect protein stability and dynamics

29 September 2017

1 reference

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Mutations in the promoter region of the aldolase B gene that cause hereditary fructose intolerance.

29 September 2017

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Computational analysis of missense mutations causing Snyder-Robinson syndrome

29 September 2017

1 reference

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Performance of protein stability predictors.

29 September 2017

1 reference

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Modeling effects of human single nucleotide polymorphisms on protein-protein interactions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Approaches and resources for prediction of the effects of non-synonymous single nucleotide polymorphism on protein function and interactions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

The worldwide Protein Data Bank (wwPDB): ensuring a single, uniform archive of PDB data

29 September 2017

1 reference

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The FoldX web server: an online force field

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

The structure of human liver fructose-1,6-bisphosphate aldolase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Molecular recognition of human angiogenin by placental ribonuclease inhibitor--an X-ray crystallographic study at 2.0 A resolution.

29 September 2017

1 reference

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mCSM: predicting the effects of mutations in proteins using graph-based signatures.

29 September 2017

1 reference

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BeAtMuSiC: Prediction of changes in protein-protein binding affinity on mutations.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Investigating the linkage between disease-causing amino acid variants and their effect on protein stability and binding

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Understanding molecular effects of naturally occurring genetic differences.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Immunohistochemical studies of angiogenin in the skin of patients with amyotrophic lateral sclerosis

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Physics approaches to protein interactions and gene regulation

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Hereditary fructose intolerance: frequency and spectrum mutations of the aldolase B gene in a large patients cohort from France--identification of eight new mutations

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Protein-protein interactions

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Aldolase B mutations and prevalence of hereditary fructose intolerance in a Polish population

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4849003

Editorial overview: Linking protein sequence and structural changes to function in the era of next-generation sequencing

5 September 2018

1 reference

12 December 2020

Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort

1 reference

12 December 2020

Calculation of the relative change in binding free energy of a protein-inhibitor complex

1 reference

12 December 2020

Association between the Angiogenin (ANG) K17I variant and amyotrophic lateral sclerosis risk in Caucasian: a meta-analysis

1 reference

12 December 2020

Identifiers

DOI

10.3390/IJMS17040547

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

27077847

1 reference