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Author Details
Full Name
John G Luz
Affiliation
Beth Israel Deaconess Medical Center and Harvard Medical School
ORCID
Career Start Year
1994
Papers
27
H Index
18
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
33246032
Structure-based, multi-targeted drug discovery approach to eicosanoid inhibition: Dual inhibitors of mPGES-1 and 5-lipoxygenase activating protein (FLAP).
Biochim Biophys Acta Gen Subj
2021
33724805
Crystal Structure of the Carbohydrate Recognition Domain of the Human Macrophage Galactose C-Type Lectin Bound to GalNAc and the Tumor-Associated Tn Antigen.
Biochemistry
2021
32690595
The structural basis for monoclonal antibody 5D2 binding to the tryptophan-rich loop of lipoprotein lipase.
J Lipid Res
2020
28190634
Discovery and characterization of [(cyclopentyl)ethyl]benzoic acid inhibitors of microsomal prostaglandin E synthase-1.
Bioorg Med Chem Lett
2017
26882000
Correction to The 2.5 ÿ Crystal Structure of the SIRT1 Catalytic Domain Bound to Nicotinamide Adenine Dinucleotide (NAD(+)) and an Indole (EX527 Analogue) Reveals a Novel Mechanism of Histone Deacetylase Inhibition.
J Med Chem
2016
26653180
Discovery and Characterization of 2-Acylaminoimidazole Microsomal Prostaglandin E Synthase-1 Inhibitors.
J Med Chem
2016
27554445
Characterization of 3,3-dimethyl substituted N-aryl piperidines as potent microsomal prostaglandin E synthase-1 inhibitors.
Bioorg Med Chem Lett
2016
26683992
2-Chloro-4-[[(1R,2R)-2-hydroxy-2-methyl-cyclopentyl]amino]-3-methyl-benzonitrile: A Transdermal Selective Androgen Receptor Modulator (SARM) for Muscle Atrophy.
J Med Chem
2016
25961169
Crystal Structures of mPGES-1 Inhibitor Complexes Form a Basis for the Rational Design of Potent Analgesic and Anti-Inflammatory Therapeutics.
J Med Chem
2015
26218343
Indole Glucocorticoid Receptor Antagonists Active in a Model of Dyslipidemia Act via a Unique Association with an Agonist Binding Site.
J Med Chem
2015
24446728
Glucocorticoid receptor modulators informed by crystallography lead to a new rationale for receptor selectivity, function, and implications for structure-based design.
J Med Chem
2014
23311358
The 2.5 ÿ crystal structure of the SIRT1 catalytic domain bound to nicotinamide adenine dinucleotide (NAD+) and an indole (EX527 analogue) reveals a novel mechanism of histone deacetylase inhibition.
J Med Chem
2013
24367637
Structural context of disease-associated mutations and putative mechanism of autoinhibition revealed by X-ray crystallographic analysis of the EZH2-SET domain.
PLoS One
2013
20156452
Structures of PHR domains from Mus musculus Phr1 (Mycbp2) explain the loss-of-function mutation (Gly1092-->Glu) of the C. elegans ortholog RPM-1.
J Mol Biol
2010
18235434
Protein production and purification.
Nat Methods
2008
16140327
Crystal structure of viral macrophage inflammatory protein I encoded by Kaposi's sarcoma-associated herpesvirus at 1.7A.
J Mol Biol
2005
15084288
Supine orientation of a murine MHC class I molecule on the membrane bilayer.
Curr Biol
2004
15476818
Analysis of the class I aldolase binding site architecture based on the crystal structure of 2-deoxyribose-5-phosphate aldolase at 0.99A resolution.
J Mol Biol
2004
14978103
A peptide that antagonizes TCR-mediated reactions with both syngeneic and allogeneic agonists: functional and structural aspects.
J Immunol
2004
12672694
XOL-1, primary determinant of sexual fate in C. elegans, is a GHMP kinase family member and a structural prototype for a class of developmental regulators.
Genes Dev
2003
11988465
Structural and thermodynamic correlates of T cell signaling.
Annu Rev Biophys Biomol Struct
2002
11994422
Structural comparison of allogeneic and syngeneic T cell receptor-peptide-major histocompatibility complex complexes: a buried alloreactive mutation subtly alters peptide presentation substantially increasing V(beta) Interactions.
J Exp Med
2002
11598300
Observation of covalent intermediates in an enzyme mechanism at atomic resolution.
Science
2001
11092933
Crystallization of retinol dehydratase from Spodoptera frugiperda: improvement of crystal quality by modification by ethylmercurythiosalicylate.
Acta Crystallogr D Biol Crystallogr
2000
9857081
Substrate specificity and kinetic mechanism of the insect sulfotransferase, retinol dehydratase.
J Biol Chem
1998
7916210
Novel Cl(-)-dependent intracellular pH regulation in murine MDR 1 transfectants and potential implications.
Biochemistry
1994
7911682
Transfection of mu MDR 1 inhibits Na(+)-independent Cl-/-HCO3 exchange in Chinese hamster ovary cells.
Biochemistry
1994
1 - 27 of 27
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Co-authored papers
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Co-authored papers
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Mei Jiang
The University of Texas MD Anderson Cancer Center
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Kristin C Gunsalus
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Robert Wood Johnson Medical School, Rutgers University
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Gaetano T Montelione
Rensselaer Polytechnic Institute
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Ritu Shastry
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Yingchun Wang
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