Alpha 2.0
Login Register
» Authors » Aditi G Muddebihalkar

Aditi G Muddebihalkar

Explore the profile of Aditi G Muddebihalkar including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 7
Citations 53
Followers 0
Related Specialties
Biology
Molecular Biology
General Medicine
Top 10 Co-Authors
Vidya Niranjan
Sinosh Skariyachan
Akshay Uttarkar
Dharshini Gopal
Pratyoosh Shukla
Tejaswini Venkatesan
Shweta Chakrabarti
Roshini Ravi Shankar
Prinith Kaveramma Uluvangada Praveen
Ulluvangada Praveen
Published In
J Biomol Struct Dyn
Infect Genet Evol
Comput Biol Med
Mol Biotechnol
Affiliations
Soon will be listed here.
Recent Articles
1.
Understanding the Xylooligosaccharides Utilization Mechanism of Lactobacillus brevis and Bifidobacterium adolescentis: Proteins Involved and Their Conformational Stabilities for Effectual Binding
Khangwal I, Skariyachan S, Uttarkar A, Muddebihalkar A, Niranjan V, Shukla P
Mol Biotechnol . 2021 Sep; 64(1):75-89. PMID: 34542815
Xylooligosaccharides having various degrees of polymerization such as xylobiose, xylotriose, and xylotetraose positively affect human health by interacting with gut proteins. The present study aimed to identify proteins present in...
2.
Structural insights on the interaction potential of natural leads against major protein targets of SARS-CoV-2: Molecular modelling, docking and dynamic simulation studies
Skariyachan S, Gopal D, Muddebihalkar A, Uttarkar A, Niranjan V
Comput Biol Med . 2021 Mar; 132:104325. PMID: 33751995
Though significant efforts are in progress for developing drugs and vaccines against COVID-19, limited therapeutic agents are available currently. Thus, it is essential to undertake COVID-19 research and to identify...
3.
Structural and molecular basis of the interaction mechanism of selected drugs towards multiple targets of SARS-CoV-2 by molecular docking and dynamic simulation studies- deciphering the scope of repurposed drugs
Skariyachan S, Gopal D, Chakrabarti S, Kempanna P, Uttarkar A, Muddebihalkar A, et al.
Comput Biol Med . 2020 Oct; 126:104054. PMID: 33074111
The repurposing of FDA approved drugs is presently receiving attention for COVID-19 drug discovery. Previous studies revealed the binding potential of several FDA-approved drugs towards specific targets of SARS-CoV-2; however,...
4.
Response regulator GacA and transcriptional activator RhlR proteins involved in biofilm formation of Pseudomonas aeruginosa are prospective targets for natural lead molecules: Computational modelling, molecular docking and dynamic simulation studies
Skariyachan S, Ravishankar R, Gopal D, Muddebihalkar A, Uttarkar A, Praveen P, et al.
Infect Genet Evol . 2020 Jul; 85:104448. PMID: 32622078
Pseudomonas aeruginosa has become a global concern due to its extreme resistance to most of the last resort antibiotics. Present study focuses on the screening of potential molecular targets involved...
5.
Natural epiestriol-16 act as potential lead molecule against prospective molecular targets of multidrug resistant Acinetobacter baumannii-Insight from in silico modelling and in vitro investigations
Skariyachan S, Muddebihalkar A, Badrinath V, Umashankar B, Eram D, Uttarkar A, et al.
Infect Genet Evol . 2020 Apr; 82:104314. PMID: 32268193
The current study aimed to identify putative drug targets of multidrug resistant Acinetobacter baumannii (MDRAb) and study the therapeutic potential of natural epiestriol-16 by computer aided virtual screening and in...
6.
Carbon fullerene acts as potential lead molecule against prospective molecular targets of biofilm-producing multidrug-resistant and : computational modeling and MD simulation studies
Skariyachan S, Gopal D, Kadam S, Muddebihalkar A, Uttarkar A, Niranjan V
J Biomol Struct Dyn . 2020 Feb; 39(3):1121-1137. PMID: 32036742
This study aimed to screen putative drug targets associated with biofilm formation of multidrug-resistant and and prioritize carbon nano-fullerene as potential lead molecule by structure-based virtual screening. Based on the...
7.
Mitogen activated protein kinase-1 and cell division control protein-42 are putative targets for the binding of novel natural lead molecules: a therapeutic intervention against
Gopal D, Muddebihalkar A, Skariyachan S, C A, Kaveramma P, Praveen U, et al.
J Biomol Struct Dyn . 2019 Oct; 38(15):4584-4599. PMID: 31625462
, fungal yeast causes several lethal infections in immune-suppressed patients and recently emerged as drug-resistant pathogens worldwide. The present study aimed to screen putative drug targets of and to study...