(Q27729427)

3

0 references

Yvonne Jones

object named as

Y Jones

9

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David Ian Stuart

object named as

D Stuart

10

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author name string

R Esnouf

2

0 references

D Somers

4

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C Ross

5

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I Kirby

6

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J Keeling

7

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G Darby

Nature structural biology

8

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publication date

April 1995

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published in

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volume

2

0 references

page(s)

293-302

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issue

4

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exact match

https://scigraph.springernature.com/pub.10.1038/nsb0495-293

0 references

cites work

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Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for Acquired Immune Deficiency Syndrome (AIDS)

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Multiple mutations in HIV-1 reverse transcriptase confer high-level resistance to zidovudine (AZT)

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Highly specific inhibition of human immunodeficiency virus type 1 by a novel 6-substituted acyclouridine derivative

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Inhibition of HIV-1 Replication by a Nonnucleoside Reverse Transcriptase Inhibitor

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Potent and highly selective human immunodeficiency virus type 1 (HIV-1) inhibition by a series of alpha-anilinophenylacetamide derivatives targeted at HIV-1 reverse transcriptase

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A novel dipyridodiazepinone inhibitor of HIV-1 reverse transcriptase acts through a nonsubstrate binding site

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An antiviral target on reverse transcriptase of human immunodeficiency virus type 1 revealed by tetrahydroimidazo-[4,5,1-jk] [1,4]benzodiazepin-2 (1H)-one and -thione derivatives

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Crystal structure at 3.5 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor

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Human immunodeficiency virus type 1 mutants resistant to nonnucleoside inhibitors of reverse transcriptase arise in tissue culture

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The growth and characterization of crystals of human immunodeficiency virus (HIV) reverse transcriptase

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Structure of the binding site for nonnucleoside inhibitors of the reverse transcriptase of human immunodeficiency virus type 1

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Crystal structure of human immunodeficiency virus type 1 reverse transcriptase complexed with double-stranded DNA at 3.0 A resolution shows bent DNA

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2.2 A resolution structure of the amino-terminal half of HIV-1 reverse transcriptase (fingers and palm subdomains)

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Crystal structure of the ribonuclease H domain of HIV-1 reverse transcriptase

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Crystals of HIV-1 Reverse Transcriptase Diffracting to 2·2 Å Resolution

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Comprehensive mutant enzyme and viral variant assessment of human immunodeficiency virus type 1 reverse transcriptase resistance to nonnucleoside inhibitors

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HIV-1-specific reverse transcriptase inhibitors show differential activity against HIV-1 mutant strains containing different amino acid substitutions in the reverse transcriptase

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Human immunodeficiency virus 1 (HIV-1)-specific reverse transcriptase (RT) inhibitors may suppress the replication of specific drug-resistant (E138K)RT HIV-1 mutants or select for highly resistant (Y181C-->C181I)RT HIV-1 mutants

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A mutation in reverse transcriptase of bis(heteroaryl)piperazine-resistant human immunodeficiency virus type 1 that confers increased sensitivity to other nonnucleoside inhibitors

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Viral resistance to the thiazolo-iso-indolinones, a new class of nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase

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Characterization of HIV-1 strains isolated from patients treated with TIBO R82913.

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