Cysteine Proteinase  (Cp- 30) Protein of Trichomonas Vaginalis: In-silico Homology Modeling and Docking Study - Surya Prakash Dwivedi - Libros - LAP LAMBERT Academic Publishing - 9783843386289 - 20 de diciembre de 2010
En caso de que portada y título no coincidan, el título será el correcto

Cysteine Proteinase (Cp- 30) Protein of Trichomonas Vaginalis: In-silico Homology Modeling and Docking Study

Surya Prakash Dwivedi

Los regalos de Navidad se podrán canjear hasta el 31 de enero
Añadir a tu lista de deseos de iMusic

Cysteine Proteinase (Cp- 30) Protein of Trichomonas Vaginalis: In-silico Homology Modeling and Docking Study

CP30 protein plays an important role in the establishment of host parasite relationship in Trichomoniasis. In the present work, single letter amino acid sequence of CP30 protein of T. vaginalis (ACC. No. NP_057852) was retrieved from protein database of NCBI, taken as a target protein sequence. Modeling of 3D structure of CP30 protein performed related to the target sequence using PSI-BLAST. As a consequence of number of hits, potential template structure (PDB-ID: 1K30), followed by calculation for energy and root mean square deviation (RMSD) of the specific model. Subsequently, various inhibitors were docked employing AutoDock to CP30 protein structure determined by comparative homology modeling. Auto Dock 3.05' was used for docking and calculation of the energy maps. From inhibitor optimization and docking studies, suitable inhibitor sphingosine is hunted. CP30 binds by the designed inhibitor; it may be very successful drug for CP30 protein inhibition. This work on inhibitor optimization will be a platform for the further studies on molecular mechanism of HIV infection & for most cost effective drug designing & for finding the inhibitor against this sexual transmitting disease.

Medios de comunicación Libros     Paperback Book   (Libro con tapa blanda y lomo encolado)
Publicado 20 de diciembre de 2010
ISBN13 9783843386289
Editores LAP LAMBERT Academic Publishing
Páginas 72
Dimensiones 226 × 4 × 150 mm   ·   117 g
Lengua English