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A molecular model for diacylglycerol acyltransferase from Mortierella ramanniana var. angulispora.
Mishra, Sanjay; Dwivedi, Surya Prakash; Dwivedi, Neeraja; Kumar, Ajay; Rawat, Anil; Kamisaka, Yasushi.
Afiliação
  • Mishra S; Department of Biotechnology, College of Engineering and Technology, IFTM Campus, Lodhipur-Rajput, Delhi Road, Moradabad 244 001, U.P., India. sanjaymishra66@gmail.com
Bioinformation ; 3(9): 394-8, 2009 Jun 28.
Article em En | MEDLINE | ID: mdl-19759814
ABSTRACT
Acyl CoA diacylglycerol acyltransferase (DGAT, EC 2.3.120) is recognized as a key player of cellular diacylglycerol metabolism. It catalyzes the terminal, yet the committed step in triacylglycerol synthesis using diacylglycerol and fatty acyl CoA as substrates. The protein sequence of diacylglycerol acyltransferse (DGAT) Type 2B in Moretierella ramanniana var. angulispora (Protein_ID = AAK84180.1) was retrieved from GenBank. However, a structure is not yet available for this sequence. The 3D structure of DGAT Type 2B was modeled using a template structure (PDB ID 1K30) obtained from Protein databank (PDB) identified by searching with position specific iterative BLAST (PSI-BLAST). The template (PDB ID 1K30) describes the structure of DGAT from Cucurbita moschata. Modeling was performed using Modeller 9v2 and protein model is hence generated. The DGAT type 2B protein model was subsequently docked with six inhibitors (sphingosine; trifluoroperazine; phosphatidic acid; lysophospatidylserine; KCl; 1, 2-diolein) using AutoDock (a molecular docking program). The binding of inhibitors to the protein model of DGAT type 2B is discussed.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Bioinformation Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Bioinformation Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Índia