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A Protocol for Computer-Based Protein Structure and Function Prediction
Published on: November 3, 2011
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Structure modeling to function prediction of Uncharacterized Human Protein C15orf41
Md Shakil Ahmed1, Md Shahjaman2, Enamul Kabir3
1Department of Statistics, University of Rajshahi, Rajshahi-6205, Bangladesh.
Bioinformation
|August 16, 2018
Summary
Genetic mutations in the C15orf41 gene cause dyserythropoietic anemia, a disorder affecting red blood cell formation. This study characterizes the C15orf41 protein
Area of Science:
- Genetics
- Molecular Biology
- Hematology
Background:
- Dyserythropoietic anemia is a genetic disorder characterized by abnormal erythroblast morphology.
- The human gene C15orf41 is implicated in the pathogenesis of this anemia.
- The C15orf41 protein's function remains largely uncharacterized.
Purpose of the Study:
- To functionally characterize the human C15orf41 gene and its protein product.
- To investigate the structural and interaction properties of C15orf41.
- To provide insights into the molecular mechanisms underlying C15orf41-related dyserythropoietic anemia.
Main Methods:
- Bioinformatic analysis of the C15orf41 gene and protein sequence.
- Identification of protein domains and post-translational modification (PTM) sites.
- Protein-protein interaction (PPI) network analysis to identify interacting partners.
Main Results:
- The C15orf41 protein possesses a Treponema Pallidum (TPD) domain and exhibits thermostability, instability, and acidic properties.
- Identified PTM sites include K50 (Acetylation), T114 (Phosphorylation), and K176 (Ubiquitination).
- Protein-protein interaction analysis revealed a significant interaction with human ATP binding domain 4 (ATPBD4).
Conclusions:
- The C15orf41 protein plays a role in erythropoiesis and complex formation.
- Understanding C15orf41's interactions and modifications is crucial for elucidating dyserythropoietic anemia.
- This study provides foundational data for further research into C15orf41 function and therapeutic strategies.
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