Interferon induced Mx protein from Indian snow trout Schizothorax richardsonii (Gray) lacks critical functional features unlike its mammalian homologues. (April 2018)
- Record Type:
- Journal Article
- Title:
- Interferon induced Mx protein from Indian snow trout Schizothorax richardsonii (Gray) lacks critical functional features unlike its mammalian homologues. (April 2018)
- Main Title:
- Interferon induced Mx protein from Indian snow trout Schizothorax richardsonii (Gray) lacks critical functional features unlike its mammalian homologues
- Authors:
- Saxena, Ankur
Belwal, Kiran
Chauhan, Ankita
Pande, Amit - Abstract:
- Graphical abstract: Highlights: Snow trout Mx protein carries the signature of dynamin family (LPRGTGIVTR) and a tripartite GTP-binding domain (GDQSSGKS, DLPG, and TKPD). Mx protein is an elongated structure with a G domain, bundle signaling element (BSE) and a GTPase effector domain with two highly conserved leucine zippers at C treminal. Snow trout Mx lacks the crucial functional features of its mammalian homologues. A potential ligand binding site was identified in G-domain of Mx. Abstract: Viral attack within host cells triggers the production of type I interferons and leads to the induction of interferon stimulated genes (ISGs). One of the ISG Mx, encodes type I interferon inducible GTPase that is responsible for the establishment of an anti-viral state within cells. Intriguingly, several isoforms of Mx have been reported in fish, but the structural analysis of fish Mx proteins remains unexplored. For the first time, we have identified and unraveled the molecular structure of Mx protein from Indian snow trout, Schizothorax richardsonii (Gray) a Coldwater fish that inhabits the water bodies in the sub-Himalayan region. The snow trout Mx coding region consists of 2518 nucleotides with an open reading frame (ORF) of 1854 nucleotides. It codes for a polypeptide of 617 amino acids with a predicted molecular weight of 70 kDa. In silico analysis of snow trout Mx protein revealed signature of dynamin family (LPRGTGIVTR) along with a tripartite GTP-binding domain (GDQSSGKS,Graphical abstract: Highlights: Snow trout Mx protein carries the signature of dynamin family (LPRGTGIVTR) and a tripartite GTP-binding domain (GDQSSGKS, DLPG, and TKPD). Mx protein is an elongated structure with a G domain, bundle signaling element (BSE) and a GTPase effector domain with two highly conserved leucine zippers at C treminal. Snow trout Mx lacks the crucial functional features of its mammalian homologues. A potential ligand binding site was identified in G-domain of Mx. Abstract: Viral attack within host cells triggers the production of type I interferons and leads to the induction of interferon stimulated genes (ISGs). One of the ISG Mx, encodes type I interferon inducible GTPase that is responsible for the establishment of an anti-viral state within cells. Intriguingly, several isoforms of Mx have been reported in fish, but the structural analysis of fish Mx proteins remains unexplored. For the first time, we have identified and unraveled the molecular structure of Mx protein from Indian snow trout, Schizothorax richardsonii (Gray) a Coldwater fish that inhabits the water bodies in the sub-Himalayan region. The snow trout Mx coding region consists of 2518 nucleotides with an open reading frame (ORF) of 1854 nucleotides. It codes for a polypeptide of 617 amino acids with a predicted molecular weight of 70 kDa. In silico analysis of snow trout Mx protein revealed signature of dynamin family (LPRGTGIVTR) along with a tripartite GTP-binding domain (GDQSSGKS, DLPG, and TKPD). Homology modelling established that the Mx protein is an elongated structure with a G domain, bundle signaling element (BSE) and a GTPase effector domain (GED). Moreover, the GED of Mx contains two highly conserved leucine zippers at the COOH-terminal of the protein suggesting its structural similarity with human homologues. However, snow trout Mx lacks the essential features of its mammalian homologues questioning its functional characteristics. Further, a ligand binding site in the said protein has also been predicted adjacent to the GTPase switch within the G domain. … (more)
- Is Part Of:
- Computational biology and chemistry. Volume 73(2018)
- Journal:
- Computational biology and chemistry
- Issue:
- Volume 73(2018)
- Issue Display:
- Volume 73, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 73
- Issue:
- 2018
- Issue Sort Value:
- 2018-0073-2018-0000
- Page Start:
- 31
- Page End:
- 40
- Publication Date:
- 2018-04
- Subjects:
- ISGs interferon stimulated genes -- GED GTPase effector domain -- ORF open reading frame -- BSE bundle signaling element -- Poly (I:C) polyinosinic:polycytidylic acid -- UTRs untranslated regions
Schizothorax richardsonii -- Interferon stimulated genes -- Mx protein -- Antiviral state -- Homology modelling
Chemistry -- Data processing -- Periodicals
Biology -- Data processing -- Periodicals
Biochemistry -- Data processing
Biology -- Data processing
Molecular biology -- Data processing
Periodicals
Electronic journals
542.85 - Journal URLs:
- http://www.sciencedirect.com/science/journal/14769271 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.compbiolchem.2017.12.011 ↗
- Languages:
- English
- ISSNs:
- 1476-9271
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- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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