Biochemical mechanism of human immunodeficiency virus type 1 reverse transcriptase resistance to stavudine

被引:38
作者
Lennerstrand, J
Stammers, DK
Larder, BA
机构
[1] Virco UK Ltd, Cambridge CB4 0GA, England
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
关键词
D O I
10.1128/AAC.45.7.2144-2146.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have found a close correlation between viral stavudine (d4T) resistance and resistance to d4T-triphosphate at the human immunodeficiency virus type 1 reverse transcriptase (RT) level, RT from site-directed mutants with 69S-XX codon insertions and/or conventional zidovudine resistance mutations seems to be involved in an ATP-dependent resistance mechanism analogous to pyrophosphorolysis, whereas the mechanism for RT with the Q151M or V75T mutation appears to be independent of added ATP for reducing binding to d4T-triphosphate.
引用
收藏
页码:2144 / 2146
页数:3
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