On the detection of multiple-binding modes of ligands to proteins, from biological, structural, and modeling data.
|
Hughes SH
|
|
Journal of computer-aided molecular design
|
Evaluation of natural products as inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase.
|
Hughes SH
|
|
Journal of natural products
|
Mutations in HIV-1 reverse transcriptase cause misfolding and miscleavage by the viral protease.
|
Hughes SH
|
2013
|
Virology
|
Effects of 4' - and 2-Substitutions on the Bioactivity of 4' -Ethynyl-2-Fluoro-2' -Deoxyadenosine.
|
Hughes SH
|
2013
|
Antimicrobial agents and chemotherapy
|
A comparison of the ability of rilpivirine (TMC278) and selected analogues to inhibit clinically relevant HIV-1 reverse transcriptase mutants.
|
Hughes SH
|
2012
|
Retrovirology
|
HIV-1 and HIV-2 Reverse Transcriptases: Different Mechanisms of Resistance to Nucleoside Reverse Transcriptase Inhibitors.
|
Hughes SH
|
2012
|
Journal of virology
|
HIV-1 Reverse Transcription.
|
Hughes SH
|
2012
|
Cold Spring Harbor perspectives in medicine
|
Foamy retrovirus integrase contains a Pol dimerization domain required for protease activation.
|
Hughes SH
|
2011
|
Journal of virology
|
Mutagenesis of the human immunodeficiency virus reverse transcriptase p51 subunit defines residues contributing to vinylogous urea inhibition of Ribonuclease H activity.
|
Hughes SH
|
2011
|
The Journal of biological chemistry
|
Structural basis of HIV-1 resistance to AZT by excision.
|
Hughes SH
|
2010
|
Nature structural & molecular biology
|
Nature, position, and frequency of mutations made in a single cycle of HIV-1 replication.
|
Hughes SH
|
2010
|
Journal of virology
|
The nucleoside analogue D-carba T blocks HIV-1 reverse transcription.
|
Hughes SH
|
2009
|
Journal of medicinal chemistry
|
Structural basis for the role of the K65R mutation in HIV-1 reverse transcriptase polymerization, excision antagonism, and tenofovir resistance.
|
Hughes SH
|
2009
|
The Journal of biological chemistry
|
Structure and function of HIV-1 reverse transcriptase: molecular mechanisms of polymerization and inhibition.
|
Hughes SH
|
2009
|
Journal of molecular biology
|
Mutations in the thumb allow human immunodeficiency virus type 1 reverse transcriptase to be cleaved by protease in virions.
|
Hughes SH
|
2009
|
Journal of virology
|
Structure of HIV-1 reverse transcriptase with the inhibitor beta-Thujaplicinol bound at the RNase H active site.
|
Hughes SH
|
2009
|
Structure (London, England : 1993)
|
Apparent defects in processive DNA synthesis, strand transfer, and primer elongation of Met-184 mutants of HIV-1 reverse transcriptase derive solely from a dNTP utilization defect.
|
Hughes SH
|
2008
|
The Journal of biological chemistry
|
The effects of alternate polypurine tracts (PPTs) and mutations of sequences adjacent to the PPT on viral replication and cleavage specificity of the Rous sarcoma virus reverse transcriptase.
|
Hughes SH
|
2008
|
Journal of virology
|
HIV-1 reverse transcriptase connection subdomain mutations reduce template RNA degradation and enhance AZT excision.
|
Hughes SH
|
2008
|
Proceedings of the National Academy of Sciences of the United States of America
|
Mutations in the U5 region adjacent to the primer binding site affect tRNA cleavage by human immunodeficiency virus type 1 reverse transcriptase in vivo.
|
Hughes SH
|
2008
|
Journal of virology
|
Crystal engineering of HIV-1 reverse transcriptase for structure-based drug design.
|
Hughes SH
|
2008
|
Nucleic acids research
|
High-resolution structures of HIV-1 reverse transcriptase/TMC278 complexes: strategic flexibility explains potency against resistance mutations.
|
Hughes SH
|
2008
|
Proceedings of the National Academy of Sciences of the United States of America
|
In vitro fidelity of the prototype primate foamy virus (PFV) RT compared to HIV-1 RT.
|
Hughes SH
|
2007
|
Virology
|
Targeting to the endoplasmic reticulum improves the folding of recombinant human telomerase reverse transcriptase.
|
Hughes SH
|
2007
|
Protein expression and purification
|
Synthesis, biological activity, and crystal structure of potent nonnucleoside inhibitors of HIV-1 reverse transcriptase that retain activity against mutant forms of the enzyme.
|
Hughes SH
|
2007
|
Journal of medicinal chemistry
|
Crystal structures of clinically relevant Lys103Asn/Tyr181Cys double mutant HIV-1 reverse transcriptase in complexes with ATP and non-nucleoside inhibitor HBY 097.
|
Hughes SH
|
2007
|
Journal of molecular biology
|
Analysis of amino acids in the beta7-beta8 loop of human immunodeficiency virus type 1 reverse transcriptase for their role in virus replication.
|
Hughes SH
|
2007
|
Journal of molecular biology
|
The nucleoside analogs 4'C-methyl thymidine and 4'C-ethyl thymidine block DNA synthesis by wild-type HIV-1 RT and excision proficient NRTI resistant RT variants.
|
Hughes SH
|
2007
|
Journal of molecular biology
|
The level of reverse transcriptase (RT) in human immunodeficiency virus type 1 particles affects susceptibility to nonnucleoside RT inhibitors but not to lamivudine.
|
Hughes SH
|
2006
|
Journal of virology
|
Combining mutations in HIV-1 reverse transcriptase with mutations in the HIV-1 polypurine tract affects RNase H cleavages involved in PPT utilization.
|
Hughes SH
|
2006
|
Virology
|
Why do HIV-1 and HIV-2 use different pathways to develop AZT resistance?
|
Hughes SH
|
2006
|
PLoS Pathog
|
HIV-1 reverse transcriptase structure with RNase H inhibitor dihydroxy benzoyl naphthyl hydrazone bound at a novel site.
|
Hughes SH
|
2006
|
ACS Chem Biol
|
In search of a novel anti-HIV drug: multidisciplinary coordination in the discovery of 4-[[4-[[4-[(1E)-2-cyanoethenyl]-2,6-dimethylphenyl]amino]-2- pyrimidinyl]amino]benzonitrile (R278474, rilpivirine).
|
Hughes SH
|
2005
|
J Med Chem
|
Crystal structures for HIV-1 reverse transcriptase in complexes with three pyridinone derivatives: a new class of non-nucleoside inhibitors effective against a broad range of drug-resistant strains.
|
Hughes SH
|
2005
|
J Med Chem
|
Crystallography and the design of anti-AIDS drugs: conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors.
|
Hughes SH
|
2005
|
Progress in biophysics and molecular biology
|
Effects of mutations in the G tract of the human immunodeficiency virus type 1 polypurine tract on virus replication and RNase H cleavage.
|
Hughes SH
|
2004
|
J Virol
|
Taking aim at a moving target: designing drugs to inhibit drug-resistant HIV-1 reverse transcriptases.
|
Hughes SH
|
2004
|
Current opinion in structural biology
|
A 4'-C-ethynyl-2',3'-dideoxynucleoside analogue highlights the role of the 3'-OH in anti-HIV active 4'-C-ethynyl-2'-deoxy nucleosides.
|
Hughes SH
|
2004
|
J Med Chem
|
Designing anti-AIDS drugs targeting the major mechanism of HIV-1 RT resistance to nucleoside analog drugs.
|
Hughes SH
|
2004
|
Int J Biochem Cell Biol
|
In vitro characterization of a simian immunodeficiency virus-human immunodeficiency virus (HIV) chimera expressing HIV type 1 reverse transcriptase to study antiviral resistance in pigtail macaques.
|
Hughes SH
|
2004
|
Journal of virology
|
Characterization of the polymerase and RNase H activities of human foamy virus reverse transcriptase.
|
Hughes SH
|
2004
|
Journal of virology
|
Mutations at position 184 of human immunodeficiency virus type-1 reverse transcriptase affect virus titer and viral DNA synthesis.
|
Hughes SH
|
2004
|
Virology
|
PCR amplification of DNA containing non-standard base pairs by variants of reverse transcriptase from Human Immunodeficiency Virus-1.
|
Hughes SH
|
2004
|
Nucleic acids research
|
Effects of the Delta67 complex of mutations in human immunodeficiency virus type 1 reverse transcriptase on nucleoside analog excision.
|
Hughes SH
|
2004
|
J Virol
|
Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants.
|
Hughes SH
|
2004
|
J Med Chem
|
Structures of HIV-1 RT-DNA complexes before and after incorporation of the anti-AIDS drug tenofovir.
|
Hughes SH
|
2004
|
Nature structural & molecular biology
|
Nonnucleoside inhibitor binding affects the interactions of the fingers subdomain of human immunodeficiency virus type 1 reverse transcriptase with DNA.
|
Hughes SH
|
2004
|
J Virol
|
Mutation of amino acids in the connection domain of human immunodeficiency virus type 1 reverse transcriptase that contact the template-primer affects RNase H activity.
|
Hughes SH
|
2003
|
J Virol
|
Mutations in the 5' end of the human immunodeficiency virus type 1 polypurine tract affect RNase H cleavage specificity and virus titer.
|
Hughes SH
|
2003
|
J Virol
|
A conformationally locked analogue of the anti-HIV agent stavudine. An important correlation between pseudorotation and maximum amplitude.
|
Hughes SH
|
2003
|
Journal of medicinal chemistry
|
Molecular modeling calculations of HIV-1 reverse transcriptase nonnucleoside inhibitors: correlation of binding energy with biological activity for novel 2-aryl-substituted benzimidazole analogues.
|
Hughes SH
|
2003
|
Journal of medicinal chemistry
|
HIV-1 reverse transcriptase variants: molecular modeling of Y181C, V106A, L100I, and K103N mutations with nonnucleoside inhibitors using Monte Carlo simulations in combination with a linear response method.
|
Hughes SH
|
2003
|
Drug design and discovery
|
Secondary structure in the nucleic acid affects the rate of HIV-1 nucleocapsid-mediated strand annealing.
|
Hughes SH
|
2003
|
Biochemistry
|
Mutation of the catalytic domain of the foamy virus reverse transcriptase leads to loss of processivity and infectivity.
|
Hughes SH
|
2002
|
Journal of virology
|
Mutations in the RNase H domain of HIV-1 reverse transcriptase affect the initiation of DNA synthesis and the specificity of RNase H cleavage in vivo.
|
Hughes SH
|
2002
|
Proceedings of the National Academy of Sciences of the United States of America
|
Altering the RNase H primer grip of human immunodeficiency virus reverse transcriptase modifies cleavage specificity.
|
Hughes SH
|
2002
|
Biochemistry
|
Nontemplated base addition by HIV-1 RT can induce nonspecific strand transfer in vitro.
|
Hughes SH
|
2002
|
Virology
|
The M184V mutation reduces the selective excision of zidovudine 5'-monophosphate (AZTMP) by the reverse transcriptase of human immunodeficiency virus type 1.
|
Hughes SH
|
2002
|
J Virol
|
Structures of HIV-1 reverse transcriptase with pre- and post-translocation AZTMP-terminated DNA.
|
Hughes SH
|
2002
|
The EMBO journal
|
Nucleoside analog resistance caused by insertions in the fingers of human immunodeficiency virus type 1 reverse transcriptase involves ATP-mediated excision.
|
Hughes SH
|
2002
|
J Virol
|
Nontemplated nucleotide addition by HIV-1 reverse transcriptase.
|
Hughes SH
|
2002
|
Biochemistry
|
A novel mechanism for inhibition of HIV-1 reverse transcriptase.
|
Hughes SH
|
2002
|
Bioorganic chemistry
|
The ribonuclease H activity of the reverse transcriptases of human immunodeficiency viruses type 1 and type 2 is affected by the thumb subdomain of the small protein subunits.
|
Hughes SH
|
2001
|
Journal of molecular biology
|
Molecular matchmaking: NNRTIs can enhance the dimerization of HIV type 1 reverse transcriptase.
|
Hughes SH
|
2001
|
Proceedings of the National Academy of Sciences of the United States of America
|
Replication of phenotypically mixed human immunodeficiency virus type 1 virions containing catalytically active and catalytically inactive reverse transcriptase.
|
Hughes SH
|
2001
|
Journal of virology
|
The basic loop of the RNase H domain of MLV RT is important both for RNase H and for polymerase activity.
|
Hughes SH
|
2001
|
Virology
|
In vitro analysis of human immunodeficiency virus type 1 minus-strand strong-stop DNA synthesis and genomic RNA processing.
|
Hughes SH
|
2001
|
Journal of virology
|
The Lys103Asn mutation of HIV-1 RT: a novel mechanism of drug resistance.
|
Hughes SH
|
2001
|
Journal of molecular biology
|
YADD mutants of human immunodeficiency virus type 1 and Moloney murine leukemia virus reverse transcriptase are resistant to lamivudine triphosphate (3TCTP) in vitro.
|
Hughes SH
|
2001
|
J Virol
|
RNase H cleavage of the 5' end of the human immunodeficiency virus type 1 genome.
|
Hughes SH
|
2001
|
J Virol
|
Crystal structure of HIV-1 reverse transcriptase in complex with a polypurine tract RNA:DNA.
|
Hughes SH
|
2001
|
The EMBO journal
|
Selective excision of AZTMP by drug-resistant human immunodeficiency virus reverse transcriptase.
|
Hughes SH
|
2001
|
J Virol
|
Cross-linking of the fingers subdomain of human immunodeficiency virus type 1 reverse transcriptase to template-primer.
|
Hughes SH
|
2001
|
Journal of virology
|
Self-priming of retroviral minus-strand strong-stop DNAs.
|
Hughes SH
|
2001
|
Virology
|
Analysis of mutations at positions 115 and 116 in the dNTP binding site of HIV-1 reverse transcriptase.
|
Hughes SH
|
2000
|
Proceedings of the National Academy of Sciences of the United States of America
|
Human immunodeficiency virus type 1 nucleocapsid protein can prevent self-priming of minus-strand strong stop DNA by promoting the annealing of short oligonucleotides to hairpin sequences.
|
Hughes SH
|
2000
|
Journal of virology
|
Effects of amino acid substitutions at position 115 on the fidelity of human immunodeficiency virus type 1 reverse transcriptase.
|
Hughes SH
|
2000
|
Journal of virology
|
The role of steric hindrance in 3TC resistance of human immunodeficiency virus type-1 reverse transcriptase.
|
Hughes SH
|
2000
|
Journal of molecular biology
|
Similarities and differences in the RNase H activities of human immunodeficiency virus type 1 reverse transcriptase and Moloney murine leukemia virus reverse transcriptase.
|
Hughes SH
|
1999
|
Journal of molecular biology
|
Lamivudine (3TC) resistance in HIV-1 reverse transcriptase involves steric hindrance with beta-branched amino acids.
|
Hughes SH
|
1999
|
Proceedings of the National Academy of Sciences of the United States of America
|
Analysis of amino insertion mutations in the fingers subdomain of HIV-1 reverse transcriptase.
|
Hughes SH
|
1999
|
Journal of molecular biology
|
Studies of the genomic RNA of leukosis viruses: implications for RNA dimerization.
|
Hughes SH
|
1999
|
Journal of virology
|
Touching the heart of HIV-1 drug resistance: the fingers close down on the dNTP at the polymerase active site.
|
Hughes SH
|
1999
|
Chemistry & biology
|
Structures of Tyr188Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: inhibitor flexibility is a useful design feature for reducing drug resistance.
|
Hughes SH
|
1998
|
Journal of molecular biology
|
Structure and functional implications of the polymerase active site region in a complex of HIV-1 RT with a double-stranded DNA template-primer and an antibody Fab fragment at 2.8 A resolution.
|
Hughes SH
|
1998
|
Journal of molecular biology
|
Effects of mutations in the polymerase domain on the polymerase, RNase H and strand transfer activities of human immunodeficiency virus type 1 reverse transcriptase.
|
Hughes SH
|
1998
|
Journal of molecular biology
|
Hybrid Ty1/HIV-1 elements used to detect inhibitors and monitor the activity of HIV-1 reverse transcriptase.
|
Hughes SH
|
1998
|
Proceedings of the National Academy of Sciences of the United States of America
|
A mutation at position 190 of human immunodeficiency virus type 1 reverse transcriptase interacts with mutations at positions 74 and 75 via the template primer.
|
Hughes SH
|
1998
|
Antimicrobial agents and chemotherapy
|
Placement of tRNA primer on the primer-binding site requires pol gene expression in avian but not murine retroviruses.
|
Hughes SH
|
1997
|
Journal of virology
|
Subunit-specific mutagenesis of the cysteine 280 residue of the reverse transcriptase of human immunodeficiency virus type 1: effects on sensitivity to a specific inhibitor of the RNase H activity.
|
Hughes SH
|
1997
|
Journal of virology
|
Synthesis and biological activity of novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 2-Aryl-substituted benzimidazoles.
|
Hughes SH
|
1997
|
Journal of medicinal chemistry
|
Molecular modeling of HIV-1 reverse transcriptase drug-resistant mutant strains: implications for the mechanism of polymerase action.
|
Hughes SH
|
1997
|
Protein engineering
|
Protein-nucleic acid interactions and DNA conformation in a complex of human immunodeficiency virus type 1 reverse transcriptase with a double-stranded DNA template-primer.
|
Hughes SH
|
1997
|
Biopolymers
|
In vitro anti-HIV activity of biflavonoids isolated from Rhus succedanea and Garcinia multiflora.
|
Hughes SH
|
1997
|
Journal of natural products
|
Crystal structures of 8-Cl and 9-Cl TIBO complexed with wild-type HIV-1 RT and 8-Cl TIBO complexed with the Tyr181Cys HIV-1 RT drug-resistant mutant.
|
Hughes SH
|
1996
|
Journal of molecular biology
|
Specific inhibition of human immunodeficiency virus type 1 reverse transcriptase mediated by soulattrolide, a coumarin isolated from the latex of calophyllum teysmannii.
|
Hughes SH
|
1996
|
Journal of natural products
|
Targeting HIV reverse transcriptase for anti-AIDS drug design: structural and biological considerations for chemotherapeutic strategies.
|
Hughes SH
|
1996
|
Drug design and discovery
|
Structure of unliganded HIV-1 reverse transcriptase at 2.7 A resolution: implications of conformational changes for polymerization and inhibition mechanisms.
|
Hughes SH
|
1996
|
Structure (London, England : 1993)
|
Mutagenesis in Escherichia coli by three O6-substituted guanines in double-stranded or gapped plasmids.
|
Hughes SH
|
1995
|
Biochemistry
|
Crystallization of human immunodeficiency virus type 1 reverse transcriptase with and without nucleic acid substrates, inhibitors, and an antibody Fab fragment.
|
Hughes SH
|
1995
|
Methods in enzymology
|
Structures of DNA and RNA polymerases and their interactions with nucleic acid substrates.
|
Hughes SH
|
1995
|
Current opinion in structural biology
|
Insights into DNA polymerization mechanisms from structure and function analysis of HIV-1 reverse transcriptase.
|
Hughes SH
|
1995
|
Biochemistry
|
Resistance to 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine derivatives is generated by mutations at multiple sites in the HIV-1 reverse transcriptase.
|
Hughes SH
|
1995
|
Virology
|
Molecular modeling studies of HIV-1 reverse transcriptase nonnucleoside inhibitors: total energy of complexation as a predictor of drug placement and activity.
|
Hughes SH
|
1995
|
Protein science : a publication of the Protein Society
|
Truncating alpha-helix E' of p66 human immunodeficiency virus reverse transcriptase modulates RNase H function and impairs DNA strand transfer.
|
Hughes SH
|
1995
|
The Journal of biological chemistry
|
Analysis of mutations at position 184 in reverse transcriptase of human immunodeficiency virus type 1.
|
Hughes SH
|
1995
|
Antimicrobial agents and chemotherapy
|
Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors.
|
Hughes SH
|
1995
|
Nat Struct Biol
|
Mutational analysis of the fingers and palm subdomains of human immunodeficiency virus type-1 (HIV-1) reverse transcriptase.
|
Hughes SH
|
1994
|
Journal of molecular biology
|
Sensitivity of wild-type human immunodeficiency virus type 1 reverse transcriptase to dideoxynucleotides depends on template length; the sensitivity of drug-resistant mutants does not.
|
Hughes SH
|
1994
|
Proceedings of the National Academy of Sciences of the United States of America
|
The catalytic properties of the reverse transcriptase of the lentivirus equine infectious anemia virus.
|
Hughes SH
|
1994
|
European journal of biochemistry / FEBS
|
Redesignation of the RNase D activity associated with retroviral reverse transcriptase as RNase H.
|
Hughes SH
|
1994
|
Journal of virology
|
Enzymatic properties of two mutants of reverse transcriptase of human immunodeficiency virus type 1 (tyrosine 181-->isoleucine and tyrosine 188-->leucine), resistant to nonnucleoside inhibitors.
|
Hughes SH
|
1994
|
AIDS research and human retroviruses
|
Subunit specificity of mutations that confer resistance to nonnucleoside inhibitors in human immunodeficiency virus type 1 reverse transcriptase.
|
Hughes SH
|
1994
|
Antimicrobial agents and chemotherapy
|
Locations of anti-AIDS drug binding sites and resistance mutations in the three-dimensional structure of HIV-1 reverse transcriptase. Implications for mechanisms of drug inhibition and resistance.
|
Hughes SH
|
1994
|
Journal of molecular biology
|
Analysis of nonnucleoside drug-resistant variants of human immunodeficiency virus type 1 reverse transcriptase.
|
Hughes SH
|
1993
|
Journal of virology
|
Specific inhibition of the reverse transcriptase of human immunodeficiency virus type 1 and the chimeric enzymes of human immunodeficiency virus type 1 and type 2 by nonnucleoside inhibitors.
|
Hughes SH
|
1993
|
Antimicrobial agents and chemotherapy
|
Sulfonic acid polymers are potent inhibitors of HIV-1 induced cytopathogenicity and the reverse transcriptases of both HIV-1 and HIV-2.
|
Hughes SH
|
1993
|
Biochimica et biophysica acta
|
Immunization with soluble protein-pulsed spleen cells induces class I-restricted cytotoxic T lymphocytes that recognize immunodominant epitopic peptides from Plasmodium falciparum and HIV-1.
|
Hughes SH
|
1992
|
Journal of immunology (Baltimore, Md. : 1950)
|
HIV-1 and HIV-2 reverse transcriptases: a comparative study of sensitivity to inhibition by selected natural products.
|
Hughes SH
|
1992
|
Biochemical and biophysical research communications
|
The effects of cysteine mutations on the catalytic activities of the reverse transcriptase of human immunodeficiency virus type-1.
|
Hughes SH
|
1992
|
The Journal of biological chemistry
|
Cassette mutagenesis of the reverse transcriptase of human immunodeficiency virus type 1.
|
Hughes SH
|
1992
|
Journal of virology
|
Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities.
|
Hughes SH
|
1992
|
Journal of medicinal chemistry
|
Mutational analysis of the fingers domain of human immunodeficiency virus type 1 reverse transcriptase.
|
Hughes SH
|
1992
|
Journal of virology
|
Human immunodeficiency virus reverse transcriptase T helper epitopes identified in mice and humans: correlation with a cytotoxic T cell epitope.
|
Hughes SH
|
1991
|
The Journal of infectious diseases
|
Mutational analysis of the DNA polymerase and ribonuclease H activities of human immunodeficiency virus type 2 reverse transcriptase expressed in Escherichia coli.
|
Hughes SH
|
1991
|
Virology
|
Psychotrine and its O-methyl ether are selective inhibitors of human immunodeficiency virus-1 reverse transcriptase.
|
Hughes SH
|
1991
|
The Journal of biological chemistry
|
The destiny of reverse transcriptase anatomy.
|
Hughes SH
|
1991
|
Current biology : CB
|
Crystals of a ternary complex of human immunodeficiency virus type 1 reverse transcriptase with a monoclonal antibody Fab fragment and double-stranded DNA diffract x-rays to 3.5-A resolution.
|
Hughes SH
|
1991
|
Proceedings of the National Academy of Sciences of the United States of America
|
Protein-protein interactions of HIV-1 reverse transcriptase: implication of central and C-terminal regions in subunit binding.
|
Hughes SH
|
1991
|
Biochemistry
|
HIV-1 reverse transcriptase: structure predictions for the polymerase domain.
|
Hughes SH
|
1990
|
AIDS research and human retroviruses
|
Immunologic and proteolytic analysis of HIV-1 reverse transcriptase structure.
|
Hughes SH
|
1990
|
Virology
|
Mutational analysis of the ribonuclease H activity of human immunodeficiency virus 1 reverse transcriptase.
|
Hughes SH
|
1990
|
Virology
|
Effects of small insertions on the RNA-dependent DNA polymerase activity of HIV-1 reverse transcriptase.
|
Hughes SH
|
1989
|
Virology
|
Comparison of inhibitory activities of various antiretroviral agents against particle-derived and recombinant human immunodeficiency virus type 1 reverse transcriptases.
|
Hughes SH
|
1989
|
Antimicrobial agents and chemotherapy
|
Expression of soluble, enzymatically active, human immunodeficiency virus reverse transcriptase in Escherichia coli and analysis of mutants.
|
Hughes SH
|
1988
|
Proceedings of the National Academy of Sciences of the United States of America
|
Expression in Escherichia coli of a Moloney murine leukemia virus reverse transcriptase whose structure closely resembles the viral enzyme.
|
Hughes SH
|
1988
|
Gene
|
Mapping unintegrated avian sarcoma virus DNA: termini of linear DNA bear 300 nucleotides present once or twice in two species of circular DNA.
|
Hughes SH
|
1978
|
Cell
|