Abstract
Amino acid mutations may have diverse effects on protein structure and function. Thus reliable information about the protein sequence variations is essential to gain insights into disease genotype-phenotype correlations. With the recent availability of the complete genome sequence and the accumulation of variation data, determining the effects of amino acid substitution will be the next challenge in mutation research. The molecular consequences of amino acid mutations can readily be predicted by numerous bioinformatic methods, which analyze the mutation effects from different points of view. In this review, these approaches are categorized according to their analysis principles. The applicability of these tools for inference of mutation-structure-function relationship is also recapitulated. When the human diseases are likely to involve defects in multiple genes, most of the current mutation analysis focuses on single point mutation and lacks an expansive proteome-wide perspective. We propose in this review the application of the existing computational tools in the analysis of correlated mutations at a system level. Directions for future developments and implications are discussed, which will help to understand the networks underlying human disease.
Keywords: Proteome, amino acid mutation, computational analysis, missense mutation, multiple sequence alignment
Current Proteomics
Title: Computational Analysis of Amino Acid Mutation: A Proteome Wide Perspective
Volume: 6 Issue: 4
Author(s): Jiajia Chen and Bairong Shen
Affiliation:
Keywords: Proteome, amino acid mutation, computational analysis, missense mutation, multiple sequence alignment
Abstract: Amino acid mutations may have diverse effects on protein structure and function. Thus reliable information about the protein sequence variations is essential to gain insights into disease genotype-phenotype correlations. With the recent availability of the complete genome sequence and the accumulation of variation data, determining the effects of amino acid substitution will be the next challenge in mutation research. The molecular consequences of amino acid mutations can readily be predicted by numerous bioinformatic methods, which analyze the mutation effects from different points of view. In this review, these approaches are categorized according to their analysis principles. The applicability of these tools for inference of mutation-structure-function relationship is also recapitulated. When the human diseases are likely to involve defects in multiple genes, most of the current mutation analysis focuses on single point mutation and lacks an expansive proteome-wide perspective. We propose in this review the application of the existing computational tools in the analysis of correlated mutations at a system level. Directions for future developments and implications are discussed, which will help to understand the networks underlying human disease.
Export Options
About this article
Cite this article as:
Chen Jiajia and Shen Bairong, Computational Analysis of Amino Acid Mutation: A Proteome Wide Perspective, Current Proteomics 2009; 6 (4) . https://dx.doi.org/10.2174/157016409789973734
DOI https://dx.doi.org/10.2174/157016409789973734 |
Print ISSN 1570-1646 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6247 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
Related Articles
-
Personalized Medicine for Glioblastoma: Current Challenges and Future Opportunities
Current Molecular Medicine New Insights into HLA-G and Inflammatory Diseases
Inflammation & Allergy - Drug Targets (Discontinued) Serum Carboxypeptidase N1 Serves as a Potential Biomarker Complementing CA15-3 for Breast Cancer
Anti-Cancer Agents in Medicinal Chemistry CC Chemokine Receptor Small Molecule Antagonists in the Treatment of Rheumatoid Arthritis and Other Diseases: A Current View
Current Topics in Medicinal Chemistry Triazene Compounds in the Treatment of Acute Myeloid Leukemia: A Short Review and a Case Report
Current Medicinal Chemistry Stem Cell Differentiation Stage Factors and their Role in Triggering Symmetry Breaking Processes during Cancer Development: A Quantum Field Theory Model for Reprogramming Cancer Cells to Healthy Phenotypes
Current Medicinal Chemistry Histidine Rich Glycoprotein, an Endogenous Regulator of Macrophage and Endothelial Biology
Current Angiogenesis (Discontinued) Saccharomyces Cerevisiae as a Genetic Model in Anticancer Therapy
Current Pharmacogenomics GSK-3 Inhibitors: Discoveries and Developments
Current Medicinal Chemistry NPY and Receptors in Immune and Inflammatory Diseases
Current Topics in Medicinal Chemistry ACAT1 as a Therapeutic Target and its Genetic Relationship with Alzheimer's Disease
Current Alzheimer Research Targeted Ultrasound Imaging of Cancer: An Emerging Technology on its Way to Clinics
Current Pharmaceutical Design Cancer Stem Cells: Current Status and Therapeutic Implications in Cancer Therapy-A New Paradigm
Current Stem Cell Research & Therapy Cytostatic and Cytotoxic Activity of Synthetic Diterpene Derivatives Obtained from (-)-Kaur-9(11), 16-Dien-19-Oic Acid Against Human Cancer Cell Lines
Letters in Drug Design & Discovery Wnt Signaling and Cell-Matrix Adhesion
Current Molecular Medicine Does Phosphodiesterase 11A (PDE11A) Hold Promise as a Future Therapeutic Target?
Current Pharmaceutical Design Methylenetetrahydrofolate Reductase (MTHFR): A Novel Target for Cancer Therapy
Current Pharmaceutical Design Synthesis of 1<i>H</i>-1,2,3-Triazole-Linked Quinoline-Isatin Molecular Hybrids as Anti-Breast Cancer and Anti-Methicillin-Resistant <i>Staphylococcus aureus</i> (MRSA) Agents
Anti-Cancer Agents in Medicinal Chemistry Give Boron a Chance: Boron Containing Compounds Reach Ionotropic and Metabotropic Transmembrane Receptors
Mini-Reviews in Medicinal Chemistry Novel Reverse-Phase High-Performance Liquid Chromatography (RPHPLC) Method for the Quantification of Apigenin in Ocimum Basilicum Linn Seeds (Tukmaria)
Current Analytical Chemistry