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Department of Chemistry

Computational rationale for the selective inhibition of the herpes simplex virus type 1 uracil-DNA glycosylase enzyme

Abstract

dc:description.abstract

In this thesis I will investigate the binding pocket and analyse the nature of binding of the 6-(4-Alkylanilino)-uracil inhibitors in hsvUDG and hUDG to provide a platform for the development of improved inhibitors.

Degree

thesis:*
Grantor dc:publisher.institution
Department of Chemistry
Year dc:date.issued
2011

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Hendricks, Umraan
Advisor dc:contributor.advisor
  • Naidoo, Kevin J

Rights

Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/11427/11049
OAI identifier oai:identifier
oai:open.uct.ac.za:11427/11049

Chain of custody

source
Harvested from
University of Cape Town
Base URL
open.uct.ac.za/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
related terms
citation

Hendricks, Umraan. Computational rationale for the selective inhibition of the herpes simplex virus type 1 uracil-DNA glycosylase enzyme. Department of Chemistry, 2011. http://hdl.handle.net/11427/11049