Please use this identifier to cite or link to this item: http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/455
Full metadata record
DC FieldValueLanguage
dc.contributor.authorChhakchhuak, Liansangmawii-
dc.date.accessioned2024-06-10T09:29:42Z-
dc.date.available2024-06-10T09:29:42Z-
dc.date.issued2011-
dc.identifier.issnISSN (print) 0975-6175 ISSN (online) 2229-6026-
dc.identifier.urihttp://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/455-
dc.description.abstractThe protein sequence of aspartate aminotransferase of pig was retrieved from the Swiss-Prot data-base. The appropriate template for homology modeling was determined using Blastp. 3D structures were determined by homology modeling softwares such as Swiss Model and EsyPred3D which passed quality test by ProQ software and set for further analysis. The pockets determined by CASTp server for the predicted structures showed a significant difference in the pocket area and volume, which were due to structural deviation between the residues 30-40 found in the 3d-ss software. Both the structures were analyzed using ProFunc tool which showed different functions as they had different structures and active sites. Thus the structure plays a vital role in determining its function.en_US
dc.language.isoen_USen_US
dc.subjectAspartate aminotransferase; Blastp; CASTp; 3D structure; ProQ.en_US
dc.titleProtein 3D structure determination using homology modeling and structure analysisen_US
dc.typeOtheren_US
Appears in Collections:Research Paper

Files in This Item:
File Description SizeFormat 
Ku4aesKIwvW1K27sF6KT.pdf595.49 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.