A user-friendly web portal for analyzing conformational changes in structures of Mycobacterium tuberculosis

Verfasser / Beitragende:
[Sameer Hassan, Manonanthini Thangam, Praveen Vasudevan, G. Kumar, Rahul Unni, P. Devi, Luke Hanna]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Molecular Modeling, 21/10(2015-10-01), 1-10
Format:
Artikel (online)
ID: 605512310
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024 7 0 |a 10.1007/s00894-015-2799-6  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00894-015-2799-6 
245 0 2 |a A user-friendly web portal for analyzing conformational changes in structures of Mycobacterium tuberculosis  |h [Elektronische Daten]  |c [Sameer Hassan, Manonanthini Thangam, Praveen Vasudevan, G. Kumar, Rahul Unni, P. Devi, Luke Hanna] 
520 3 |a Initiation of the Tuberculosis Structural Consortium has resulted in the expansion of the Mycobacterium tuberculosis (MTB) protein structural database. Currently, 969 experimentally solved structures are available for 354 MTB proteins. This includes multiple crystal structures for a given protein under different functional conditions, such as the presence of different ligands or mutations. In depth analysis of the multiple structures reveal that subtle differences exist in conformations of a given protein under varied conditions. Therefore, it is immensely important to understand the conformational differences between the multiple structures of a given protein in order to select the most suitable structure for molecular docking and structure-based drug designing. Here, we introduce a web portal ( http://bmi.icmr.org.in/mtbsd/torsion.php ) that we developed to provide comparative data on the ensemble of available structures of MTB proteins, such as Cα root means square deviation (RMSD), sequence identity, presence of mutations and torsion angles. Additionally, torsion angles were used to perform principal component analysis (PCA) to identify the conformational differences between the structures. Additionally, we present a few case studies to demonstrate this database. Graphical Abstract Conformational changes seen in the structures of the enoyl-ACP reductase protein encoded by the Mycobacterial gene inhA 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Principal component analysis  |2 nationallicence 
690 7 |a Proteins  |2 nationallicence 
690 7 |a RMSD  |2 nationallicence 
690 7 |a Structures  |2 nationallicence 
690 7 |a Torsion angles  |2 nationallicence 
700 1 |a Hassan  |D Sameer  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
700 1 |a Thangam  |D Manonanthini  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
700 1 |a Vasudevan  |D Praveen  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
700 1 |a Kumar  |D G.  |u AU-KBC Research Centre, Madras Institute of Technology, Anna University, Chromepet, Chennai, India  |4 aut 
700 1 |a Unni  |D Rahul  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
700 1 |a Devi  |D P.  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
700 1 |a Hanna  |D Luke  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
773 0 |t Journal of Molecular Modeling  |d Springer Berlin Heidelberg  |g 21/10(2015-10-01), 1-10  |x 1610-2940  |q 21:10<1  |1 2015  |2 21  |o 894 
856 4 0 |u https://doi.org/10.1007/s00894-015-2799-6  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00894-015-2799-6  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hassan  |D Sameer  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Thangam  |D Manonanthini  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Vasudevan  |D Praveen  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kumar  |D G.  |u AU-KBC Research Centre, Madras Institute of Technology, Anna University, Chromepet, Chennai, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Unni  |D Rahul  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Devi  |D P.  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hanna  |D Luke  |u Department of Biomedical Informatics, National Institute for Research in Tuberculosis, Chetpet, 600 031, Chennai, India  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Molecular Modeling  |d Springer Berlin Heidelberg  |g 21/10(2015-10-01), 1-10  |x 1610-2940  |q 21:10<1  |1 2015  |2 21  |o 894