Molecular modelling and dynamic simulations of sequestosome 1 (SQSTM1) missense mutations linked to Paget disease of bone-Reference-Cited by-同舟云学术

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Molecular modelling and dynamic simulations of sequestosome 1 (SQSTM1) missense mutations linked to Paget disease of bone

Published:2020-05-13 Issue:8 Volume:39 Page:2873-2884
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Shaik Noor Ahmad¹²^ORCID,Nasser Khalidah K.²³,Alruwaili Muteb Muidh¹,Alallasi Sami Raja¹,Elango Ramu¹²,Banaganapalli Babajan¹²

Affiliation:

1. Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Saudi Arabia

2. Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia

3. Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia

Funder

Deanship of Scientific Research (DSR) at King Abdulaziz University

Publisher

Informa UK Limited

Subject

Molecular Biology,General Medicine,Structural Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/07391102.2020.1758212

Reference60 articles.

1. Integration of New Genes into Cellular Networks, and Their Structural Maturation

2. Alpha Helices Are More Robust to Mutations than Beta Strands

3. Genetics of Paget’s disease of bone

4. Common susceptibility alleles andSQSTM1mutations predict disease extent and severity in a multinational study of patients with Paget's disease

5. Genome-wide association identifies three new susceptibility loci for Paget's disease of bone

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1. Genotype–phenotype correlation ofSQSTM1variants in patients with amyotrophic lateral sclerosis;Journal of Medical Genetics;2024-08-08

2. Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment;Frontiers in Genetics;2023-04-26

3. Combining machine learning and structure-based approaches to develop oncogene PIM kinase inhibitors;Frontiers in Chemistry;2023-03-10

4. Genotype-protein phenotype characterization of NOD2 and IL23R missense variants associated with inflammatory bowel disease: A paradigm from molecular modelling, dynamics, and docking simulations;Frontiers in Medicine;2023-01-10

5. Structural characterization and conformational dynamics of alpha-1 antitrypsin pathogenic variants causing alpha-1-antitrypsin deficiency;Frontiers in Molecular Biosciences;2022-11-24

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