Ravins Dohare

Prof. Ravins Dohare

Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 January 2019 in Molecular Pharmaceutics
Verified
Journal Article
Closed access
NMNeha Maurya
Neha Maurya
JMJitendra Kumar Maurya
Jitendra Kumar Maurya
USUpendra Kumar Singh
Upendra Kumar Singh
Ravins DohareRavins Dohare
Ravins Dohare
MZMohammad Zafaryab
Mohammad Zafaryab
RPRajan Patel
Rajan Patel

12 June 2019 in Frontiers in Molecular Biosciences
Verified
Journal Article
Open access
PDF file
MAMohd. Amir
Mohd. Amir
Taj MohammadTaj Mohammad
Taj Mohammad
VKVijay Kumar
Vijay Kumar
MAMohammed F. Alajmi
Mohammed F. Alajmi
TRTabish Rehman
Tabish Rehman
Md. Imtaiyaz HassanMd. Imtaiyaz Hassan
Md. Imtaiyaz Hassan
The human CST complex (CTC1–STN1–TEN1) is associated with telomere functions including genome stability. We have systemically analyzed the sequence of STN and performed structure analysis to establish its association with the Coat Plus (CP) syndrome. Many deleterious non-synonymous SNPs have been identified and subjected for structure analysis to find their pathogenic association and aggregation propensity. A 100-ns all-atom molecular dynamics simulation of WT, R135T, and D157Y structures revealed significant conformational changes in the case of mutants. Changes in hydrogen bonds, secondary structure, and principal component analysis further support the structural basis of STN1 dysfunction in such mutations. Free energy landscape analysis revealed the presence of multiple energy minima, suggesting that R135T and D157Y mutations destabilize and alter the conformational dynamics of STN1 and thus may be associated with the CP syndrome. Our study provides a valuable direction to understand the molecular basis of CP syndrome and offer a newer therapeutics approach to address CP syndrome.

5 August 2016 in Journal of Biomolecular Structure and Dynamics
Verified
Journal Article
Closed access
MKMeena Kumari
Meena Kumari
NDNeeraj Dohare
Neeraj Dohare
NMNeha Maurya
Neha Maurya
Ravins DohareRavins Dohare
Ravins Dohare
RPRajan Patel
Rajan Patel
Herein, the binding of 1-methyl-3-octylimidazolium chloride [OMIM][Cl] ionic liquid with hen egg white lysozyme (HEWL) has been studied using fluorescence, time resolved fluorescence, UV–visible and circular dichroism (CD) spectroscopy, in combination with computational study. The fluorescence results revealed that [OMIM][Cl] quenches the fluorophore of HEWL through static quenching mechanism. The calculated thermodynamic parameters show that [OMIM][Cl] bind with HEWL through hydrophobic interactions. In addition, the negative value of Gibbs energy change (∆G) indicates that the binding process was spontaneous. Furthermore, UV–vis and CD results indicate that [OMIM][Cl] induce the conformational change in HEWL and increase its enzymatic activity. Additionally, molecular docking results showed that [OMIM][Cl] binds at the active site of HEWL where both the fluorophore residues (Trp108 and Trp62) and the catalytic residues (Glu35 and Asp52) reside. Molecular dynamic simulation results show the reduction of intra-molecular hydrogen bond of HEWL when it binds with [OMIM][Cl].

1 December 2020 in Gene
Verified
Journal Article
Closed access
SAShweta Arora
Shweta Arora
PSPrithvi Singh
Prithvi Singh
Ravins DohareRavins Dohare
Ravins Dohare
RJRishabh Jha
Rishabh Jha
mansoor syedmansoor syed
mansoor syed

15 March 2016 in PLOS Neglected Tropical Diseases
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Journal Article
Open access
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NANazia Afreen
Nazia Afreen
INIrshad H. Naqvi
Irshad H. Naqvi
SBShobha Broor
Shobha Broor
AAAnwar Ahmed
Anwar Ahmed
SKSyed Naqui Kazim
Syed Naqui Kazim
SPShama Parveen
Shama Parveen
Dengue fever is the most important arboviral disease in the tropical and sub-tropical countries of the world. Delhi, the metropolitan capital state of India, has reported many dengue outbreaks, with the last outbreak occurring in 2013. We have recently reported predominance of dengue virus serotype 2 during 2011–2014 in Delhi. In the present study, we report molecular characterization and evolutionary analysis of dengue serotype 2 viruses which were detected in 2011–2014 in Delhi. Envelope genes of 42 DENV-2 strains were sequenced in the study. All DENV-2 strains grouped within the Cosmopolitan genotype and further clustered into three lineages; Lineage I, II and III. Lineage III replaced lineage I during dengue fever outbreak of 2013. Further, a novel mutation Thr404Ile was detected in the stem region of the envelope protein of a single DENV-2 strain in 2014. Nucleotide substitution rate and time to the most recent common ancestor were determined by molecular clock analysis using Bayesian methods. A change in effective population size of Indian DENV-2 viruses was investigated through Bayesian skyline plot. The study will be a vital road map for investigation of epidemiology and evolutionary pattern of dengue viruses in India. Dengue is a mosquito borne disease prevalent in more than 100 tropical and sub-tropical countries. In this study, we carried out phylogenetic and molecular clock analysis of dengue serotype 2 strains found to be circulating in Delhi, India, in 2011–2014. All the study strains were found to belong to the Cosmopolitan genotype of dengue 2 viruses. Further we also detected a lineage replacement event in the 2013 dengue fever outbreak. We identified a novel mutation in the stem region of the Envelope protein. We also determined nucleotide substitution rate and time to the most recent common ancestor of dengue 2 viruses. Further a change in the population size of dengue 2 viruses in India as depicted by Bayesian Skyline plot is reported.

12 October 2019 in Journal of Biomolecular Structure and Dynamics
Verified
Journal Article
Closed access
MAMohd Amir
Mohd Amir
Taj MohammadTaj Mohammad
Taj Mohammad
KPKartikay Prasad
Kartikay Prasad
GHGulam Mustafa Hasan
Gulam Mustafa Hasan
VKVijay Kumar
Vijay Kumar
Md. Imtaiyaz HassanMd. Imtaiyaz Hassan
Md. Imtaiyaz Hassan
Communicated by Ramaswamy H. Sarma