T. Holler

发表

5,6-Dihydropyran-2-ones possessing various sulfonyl functionalities: potent nonpeptidic inhibitors of HIV protease.

G. Zeikus, E. Lunney, S. Gulnik, 2000, Journal of medicinal chemistry.

Trypanosoma brucei Glycogen Synthase Kinase-3, A Target for Anti-Trypanosomal Drug Development: A Public-Private Partnership to Identify Novel Leads

Tod P. Holler, L. Maes, Richard O. Oduor, 2011, PLoS neglected tropical diseases.

Analysis of the Arabinose-5-Phosphate Isomerase of Bacteroides fragilis Provides Insight into Regulation of Single-Domain Arabinose Phosphate Isomerases

Pan-Fen Wang, R. Woodard, T. Holler, 2014, Journal of bacteriology.

Arabinose 5-phosphate isomerase as a target for antibacterial design: studies with substrate analogues and inhibitors.

F. Nicotra, L. Cipolla, R. Woodard, 2014, Bioorganic & medicinal chemistry.

A Novel Glucose 6-Phosphate Isomerase from Listeria monocytogenes

Pan-Fen Wang, R. Woodard, Victoria A. Assimon, 2014, The Protein Journal.

Nonpeptidic HIV protease inhibitors possessing excellent antiviral activities and therapeutic indices. PD 178390: a lead HIV protease inhibitor.

G. Zeikus, C. Humblet, E. Lunney, 1999, Bioorganic & medicinal chemistry.

A new class of anti-HIV-1 agents targeted toward the nucleocapsid protein NCp7: the 2,2'-dithiobisbenzamides.

J. Domagala, D. Hupe, R. Schultz, 1997, Bioorganic & medicinal chemistry.

The in vitro ejection of zinc from human immunodeficiency virus (HIV) type 1 nucleocapsid protein by disulfide benzamides with cellular anti-HIV activity.

J. Domagala, D. Hupe, P. Harvey, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Ovothiols as free-radical scavengers and the mechanism of ovothiol-promoted NAD(P)H-O2 oxidoreductase activity.

T. Holler, P. B. Hopkins, 1990, Biochemistry.

Bacterial 1,4-α-glucan branching enzymes: characteristics, preparation and commercial applications

Abhishek S. Dhoble, Zhengbiao Gu, Yan Hong, 2020, Critical reviews in biotechnology.

Synthesis and structure-activity relationship study of potent trypanocidal thio semicarbazone inhibitors of the trypanosomal cysteine protease cruzain.

F. Cohen, J. McKerrow, C. Caffrey, 2002, Journal of medicinal chemistry.

Biophysical characterization of zinc ejection from HIV nucleocapsid protein by anti-HIV 2,2'-dithiobis[benzamides] and benzisothiazolones.

M. Reily, J. Loo, T. Holler, 1996, Journal of medicinal chemistry.

Polyethylene glycols enhance the thermostability of β-cyclodextrin glycosyltransferase from Bacillus circulans.

Caiming Li, Tod P. Holler, Zhengbiao Gu, 2014, Food chemistry.

Chemiluminescent method for determination of hydrogen peroxide in the ambient atmosphere

G. Kok, T. Holler, M. B. López, 1978 .

Identification of a Slow Tight-Binding Inhibitor of 3-Deoxy-d-manno-octulosonic Acid 8-Phosphate Synthase

R. Woodard, T. Holler, M. Birck, 2000 .

New synthesis of 4- and 5-imidazolethiols

A. Spaltenstein, T. Holler, P. B. Hopkins, 1987 .

Escherichia coli requires the protease activity of FtsH for growth.

E. Olson, T. Holler, M. M. Jayasekera, 2000, Archives of biochemistry and biophysics.

Rational protein engineering in action: the first crystal structure of a phenylalanine tRNA synthetase from Staphylococcus haemolyticus.

B. Beattie, E. Fauman, B. Finzel, 2008, Journal of structural biology.

Synthesis and structure reassignment of mercaptohistidines of marine origin: syntheses of L-ovothiols A and C

R. Klevit, B. Shapiro, A. Spaltenstein, 1987 .

Total synthesis of marine mercaptohistidines: ovothiols A, B, and C

A. Spaltenstein, T. Holler, Fuqiang Ruan, 1989 .

Novel nonpeptidic inhibitors of peptide deformylase.

M. Shapiro, T. Holler, M. Dermyer, 2000, Archives of biochemistry and biophysics.

Ovothiols as biological antioxidants. The thiol groups of ovothiol and glutathione are chemically distinct

T. Holler, P. B. Hopkins, 1988 .

A systematic review of rice noodles: Raw material, processing method and quality improvement

Caiming Li, You Yuxian, Chen Di, 2020 .

A Unique Arabinose 5-Phosphate Isomerase Found within a Genomic Island Associated with the Uropathogenicity of Escherichia coli CFT073

Timothy C. Meredith, H. Mobley, J. A. Mosberg, 2011, Journal of bacteriology.

A qualitative fluorescence-based assay for tyrosyl radical scavenging activity: ovothiol A is an efficient scavenger.

T. Holler, P. B. Hopkins, 1989, Analytical biochemistry.

Targeting the non-structural proteins of hepatitis C virus: beyond hepatitis C virus protease and polymerase

D. Pryde, T. Parkinson, T. Holler, 2009, Expert opinion on drug discovery.

A model for the role of multiple cysteine residues involved in ribonucleotide reduction: amazing and still confusing.

J. Bollinger, J. Stubbe, S. Booker, 1992, Biochemistry.

HIV1 integrase expressed in Escherichia coli from a synthetic gene.

D. Hupe, T. Holler, D J Hupe, 1993, Gene.

Maltooligosaccharide-forming amylase: Characteristics, preparation, and application.

Yan Hong, Li Cheng, Caiming Li, 2017, Biotechnology advances.

Structural biology approaches to antibacterial drug discovery

A. Evdokimov, Tod P Holler, Artem G Evdokimov, 2007, Expert opinion on drug discovery.

Interaction of C225SR1 mutant subunit of ribonucleotide reductase with R2 and nucleoside diphosphates: tales of a suicidal enzyme.

J. Bollinger, J. Stubbe, T. Holler, 1992, Biochemistry.

A simple assay for 3-deoxy-d-manno-octulosonate cytidylyltransferase and its use as a pathway screen.

R. Woodard, T. Holler, Li Yi, 2011, Analytical biochemistry.

4-hydroxy-5,6-dihydro-2H-pyran-2-ones.3. Bicyclic and hetero-aromatic ring systems as 3-position scaffolds to bind to S1' and S2' of the HIV-1 protease enzyme.

G. Zeikus, E. Lunney, S. Hagen, 1999, Bioorganic & medicinal chemistry letters.

In vivo labeling: A glimpse of the dynamic proteome and additional constraints for protein identification

J. Loo, R. Loo, T. Holler, 2002, Journal of the American Society for Mass Spectrometry.

Application of electrospray ionization mass spectrometry for studying human immunodeficiency virus protein complexes

D. P. Mack, J. Loo, P. McConnell, 1998, Proteins.

Leu600 mutations decrease product inhibition of the β-cyclodextrin glycosyltransferase from Bacillus circulans STB01.

Yan Hong, Li Cheng, Caiming Li, 2018, International journal of biological macromolecules.

Simultaneous screening of multiple bacterial tRNA synthetases using an Escherichia coli S30-based transcription and translation assay.

T. Holler, S. Wise, M. Dermyer, 2007, Assay and drug development technologies.

Asp577 mutations enhance the catalytic efficiency of cyclodextrin glycosyltransferase from Bacillus circulans.

Yan Hong, Li Cheng, Caiming Li, 2016, International journal of biological macromolecules.

Nonpeptidic HIV protease inhibitors: 6-alkyl-5,6-dihydropyran-2-ones possessing achiral 3-(4-amino/carboxamide-2-t-butyl,5-methylphenyl thio) moiety: antiviral activities and pharmacokinetic properties.

E. Lunney, S. Hagen, J. Domagala, 1999, Bioorganic & medicinal chemistry letters.

Synthesis and Structure−Activity Relationship Study of Potent Trypanocidal Thio Semicarbazone Inhibitors of the Trypanosomal Cysteine Protease Cruzain

J. McKerrow, C. Caffrey, T. Holler, 2002 .

A Unique Arabinose 5-Phosphate Isomerase Found within a Genomic Island Associated with the Uropathogenicity of Escherichia coli CFT073

Timothy C. Meredith, H. Mobley, R. Woodard, 2011, Journal of Bacteriology.

Arabinose 5-phosphate isomerase as a target for antibacterial design: studies with substrate analogues and inhibitors.

F. Nicotra, L. Cipolla, R. Woodard, 2014, Bioorganic & medicinal chemistry.

Application of electrospray ionization mass spectrometry for studying human immunodeficiency virus protein complexes

D. P. Mack, J. Loo, P. McConnell, 1998, Proteins.