Targeting Metalloenzymes for Therapeutic Intervention

被引:216
作者
Chen, Allie Y. [1 ]
Adamek, Rebecca N. [1 ]
Dick, Benjamin L. [1 ]
Credille, Cy V. [1 ]
Morrison, Christine N. [1 ]
Cohen, Seth M. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
CATECHOL-O-METHYLTRANSFERASE; ANGIOTENSIN-CONVERTING ENZYME; HIV-1; REVERSE-TRANSCRIPTASE; D-ALANINE LIGASE; ALANYL-D-ALANINE; ANTHRAX LETHAL FACTOR; 1-DEOXY-D-XYLULOSE 5-PHOSPHATE REDUCTOISOMERASE; HISTONE DEACETYLASE INHIBITORS; KETOL-ACID REDUCTOISOMERASE; SMALL-MOLECULE INHIBITORS;
D O I
10.1021/acs.chemrev.8b00201
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metalloenzymes are central to a wide range of essential biological activities, including nucleic acid modification, protein degradation, and many others. The role of metalloenzymes in these processes also makes them central for the progression of many diseases and, as such, makes metalloenzymes attractive targets for therapeutic intervention. Increasing awareness of the role metalloenzymes play in disease and their importance as a class of targets has amplified interest in the development of new strategies to develop inhibitors and ultimately useful drugs. In this Review, we provide a broad overview of several drug discovery efforts focused on metalloenzymes and attempt to map out the current landscape of high-value metalloenzyme targets.
引用
收藏
页码:1323 / 1455
页数:133
相关论文
共 1228 条
[51]   Structure of the deacetylase LpxC bound to the antibiotic CHIR-090: Time-dependent inhibition and specificity in ligand binding [J].
Barb, Adam W. ;
Jiang, Ling ;
Raetz, Christian R. H. ;
Zhou, Pei .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (47) :18433-18438
[52]   Inhibition of lipid A biosynthesis as the primary mechanism of CHIR-090 antibiotic activity in Escherichia coli [J].
Barb, Adam W. ;
McClerren, Amanda L. ;
Snehelatha, Karnem ;
Reynolds, C. Michael ;
Zhou, Pei ;
Raetz, Christian R. H. .
BIOCHEMISTRY, 2007, 46 (12) :3793-3802
[53]  
Barceloux DG, 1999, J TOXICOL-CLIN TOXIC, V37, P537
[54]   INVESTIGATION ON GLYOXALASE-I INHIBITORS [J].
BARNARD, JF ;
HONEK, JF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (01) :118-124
[55]  
Barrett A. J., 2012, Handbook of proteolytic enzymes, V1
[56]   Inhibition of D-Ala:D-Ala ligase through a phosphorylated form of the antibiotic D-cycloserine [J].
Batson, Sarah ;
de Chiara, Cesira ;
Majce, Vita ;
Lloyd, Adrian J. ;
Gobec, Stanislav ;
Rea, Dean ;
Fulop, Vilmos ;
Thoroughgood, Christopher W. ;
Simmons, Katie J. ;
Dowson, Christopher G. ;
Fishwick, Colin W. G. ;
de Carvalho, Luiz Pedro S. ;
Roper, David I. .
NATURE COMMUNICATIONS, 2017, 8
[57]   Inhibition of the catecholase activity of biomimetic dinuclear copper complexes by kojic acid [J].
Battaini, G ;
Monzani, E ;
Casella, L ;
Santagostini, L ;
Pagliarin, R .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2000, 5 (02) :262-268
[58]   TREATMENT OF ETHYLENE-GLYCOL POISONING WITH INTRAVENOUS 4-METHYLPYRAZOLE [J].
BAUD, FJ ;
GALLIOT, M ;
ASTIER, A ;
BIEN, DV ;
GARNIER, R ;
LIKFORMAN, J ;
BISMUTH, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 319 (02) :97-100
[59]   Crystallographic Fragment Screening and Structure-Based Optimization Yields a New Class of Influenza Endonuclease Inhibitors [J].
Bauman, Joseph D. ;
Patel, Disha ;
Baker, Steven F. ;
Vijayan, R. S. K. ;
Xiang, Amy ;
Parhi, Ajit K. ;
Martinez-Sobrido, Luis ;
LaVoie, Edmond J. ;
Das, Kalyan ;
Arnold, Eddy .
ACS CHEMICAL BIOLOGY, 2013, 8 (11) :2501-2508
[60]   SEQUENCE AND STRUCTURE COMPARISON SUGGEST THAT METHIONINE AMINOPEPTIDASE, PROLIDASE, AMINOPEPTIDASE-P, AND CREATINASE SHARE A COMMON FOLD [J].
BAZAN, JF ;
WEAVER, LH ;
RODERICK, SL ;
HUBER, R ;
MATTHEWS, BW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (07) :2473-2477