Related Experiment Video
Updated: Jun 15, 2026

11:44
A High Resolution Method to Monitor Phosphorylation-dependent Activation of IRF3
Published on: January 24, 2016
Molecular interactions between Bos taurus interferon-tau1c and human type I interferon receptor
Vishawdeep Singh Jamwal1, Gourav Modi, Aman George
1Embryo Biotechnology Lab, Animal Biotechnology Centre, National Dairy Research Institute, Karnal-132001, Haryana, India.
Bioinformation
|March 4, 2010
Summary
Interferon-tau1c, crucial for pregnancy recognition in ruminants, has its 3D structure predicted. This study explores its interaction with the human interferon Type 1 receptor (IFNAR1).
Area of Science:
- Structural biology
- Immunology
- Reproductive biology
Background:
- Interferon-tau (IFN-tau) is vital for maternal recognition of pregnancy in ruminants.
- IFN-tau exhibits antiviral and antiproliferative properties.
- IFN-tau1c and IFN-tau3a are the most abundant isoforms.
Purpose of the Study:
- To predict the 3D structure of bovine Interferon-tau1c (IFN-tau1c).
- To investigate the potential molecular interactions between bovine IFN-tau1c and the human interferon Type 1 receptor (IFNAR1).
Main Methods:
- Homology modeling was employed to predict the IFN-tau1c structure.
- Ovine interferon-tau (PDB ID: 1B5L_A) served as the template for modeling.
- Stereochemical quality assessment was used to select the best structural model.
- Molecular interactions with human IFNAR1 were explored computationally.
Main Results:
- A 3D model of bovine IFN-tau1c was successfully generated.
- The predicted structure consists of 5 alpha helices and loop regions, consistent with other interferons.
- Potential binding sites of bovine IFN-tau1c on human IFNAR1 were identified.
Conclusions:
- The study provides a structural model for bovine IFN-tau1c.
- The findings offer insights into the potential interaction of bovine IFN-tau1c with the human IFNAR1, suggesting possible conserved binding mechanisms across species.
- This structural information can facilitate further research into IFN-tau function and therapeutic applications.
More Related Videos
Related Concept Videos
TGF - β Signaling Pathway
The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors are of three kinds RI, RII, and RIII. The RI...
Inhibitors of Viral Protein Synthesis
Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...
Protein-protein Interfaces
Many proteins form complexes to carry out their functions, making protein-protein interactions (PPIs) essential for an organism's survival. Most PPIs are stabilized by numerous weak noncovalent chemical forces. The physical shape of the interfaces determines the way two proteins interact. Many globular proteins have closely-matching shapes on their surfaces, which form a large number of weak bonds. Additionally, many PPIs occur between two helices or between a surface cleft and a polypeptide...

