Daniel K. Nomura
Associate Professor of Chemistry, Molecular and Cell Biology, and Nutritional Sciences and Toxicology
About Daniel K. Nomura
Dan Nomura is an associate professor in the Departments of Chemistry, Molecular and Cell Biology, and Nutritional Sciences and Toxicology at UC Berkeley. He is also an associate adjunct professor in the Department of Pharmaceutical Chemistry at UCSF. He earned his Ph.D. in Molecular Toxicology at UC Berkeley with Professor John Casida and was a postdoctoral fellow in chemical physiology at The Scripps Research Institute with Professor Ben Cravatt before returning to Berkeley as a faculty member in 2011. Among his honors are selection as a Searle Scholar, American Cancer Society Research Scholar Award, and the Department of Defense Breakthroughs Award. The Nomura Research Group is focused on mapping metabolic and chemical drivers of human disease through the development and application of chemical biology approaches including chemoproteomic and metabolomic platforms.
Research Description
The Nomura Research Group is focused on developing and applying chemical proteomic and
metabolomic platforms to identify and pharmacologically target metabolic drivers of human disease. Our
laboratory currently has three major research areas. Our first research area focuses on developing and
applying chemoproteomic and metabolomic platforms to map metabolic drivers of complex human
diseases, including cancer, neurodegenerative diseases, and inflammatory disorders, towards developing
novel therapeutic strategies to cure these complex human pathologies. Our second research area
focuses on developing chemoproteomic tools and technologies to map proteome-wide hyper-reactive and
ligandable hotspots towards massively expanding our capability of developing pharmacological tools and
eventually therapeutics against the entirety of the proteome. Our third research area is around developing
innovative chemoproteomic and metabolomic strategies for comprehensive assessment of chemical
toxicology ranging from small-molecule target identification, target characterization, and predictive and
mechanistic toxicological assessment.
For more information, visit The Nomura Research Group
Mapping Metabolic Drivers of Cancer. Cancer cells possess fundamentally altered cellular metabolism
that not only leads to a re-wiring of cellular biochemistry, but also drives nearly every aspect of cancer
pathogenicity. While targeting dysregulated metabolism is a promising strategy for cancer treatment,
much of research in cancer metabolism has focused on well-understood metabolic pathways in central
carbon metabolism underlying cellular transformation and early-stages of cancer, and has largely ignored
the majority of cellular metabolic pathways or those networks involved in cancer progression, despite
clear genetic or metabolic evidence of their involvement in cancer. This is in-part because our efforts are
hindered by our largely incomplete understanding of metabolic networks in normal physiology, let alone in
human cancers. This includes the large number of uncharacterized or misannotated metabolic enzymes,
undiscovered metabolites, and orphan metabolic networks. Historically, scientists have shied away from
uncovering the oncological roles of these uncharacterized enzymes and metabolic pathways, leaving
untapped the large therapeutic potential that remains in the majority of the unexplored metabolic genome.
A major focus of our research group is to massively expand the arsenal of targets, mechanisms, and
drugs to combat cancer by mapping the unexplored and untapped novel metabolic drivers of cancer using
chemoproteomic and functional metabolomic platforms. We have already made substantial progress
towards this goal by using integrated platforms that incorporate: 1) activity-based protein profiling (ABPP)
platform, which uses active-site directed chemical probes coupled to proteomics to enrich, detect, and
quantify dysregulated metabolic enzyme activities en masse in cancer; 2) functional targeted and
discovery-based metabolomic platforms to identify novel dysregulated metabolic pathways and
functionally annotate the metabolic and pathophysiological roles of cancer-relevant enzymes; and 3) a
competitive ABPP inhibitor/drug-discovery platform based on competing small-molecule inhibitors against
activity-based probe binding to enzyme active sites to discover potent, selective, and in vivo active
compounds for further biological validation.
Using Reactivity-Based Chemoproteomic Platforms to Expand the Druggable Proteome through
High-Throughput Pharmacological Mapping of Ligandable Sites. Despite the completion of human
genome sequencing efforts nearly 15 years ago and the promise of genome-based discoveries that would
cure human diseases, more than 75% of all protein research still focuses on the same 10% of proteins
characterized before the sequencing of the human genome. Even with the identification of many novel
protein targets that control disease, these potential drug targets have remained largely untranslated, in-
part because most protein targets are “undruggable,” and the majority of the proteome is devoid of
pharmacological tools, hindering and oftentimes paralyzing translational research efforts in drug
discovery. Development of high-quality chemical tools for proteins catalyzes research into the function
and therapeutic exploitation of those proteins, thus correlating the development of chemical tools for
specific proteins with their associated research activity. Thus, developing pharmacological tools for every
protein in the proteome would radically expand our ability to understand protein function, mine the entirety
of the proteome for drug targets, and accelerate the drug discovery process to cure complex diseases.
However, “drugging” all proteins simultaneously, has remained practically impossible. Furthermore,
assessing the quality and selectivity of small-molecule modulators of protein function has remained
challenging. We have been using the reactivity-based chemoproteomic platforms to enable simultaneous
high-throughput discovery of small-molecule leads for drug discovery across the entire proteome by
globally profiling and pharmacologically interrogating proteome-wide hyper-reactive hotspots. We have
been combining the screening of reactive small-molecule fragment libraries against the profiling of
proteome-wide hyper-reactive hotspots with reactivity-based probes directly in complex proteomesto
enable: 1) the identification of proteome-wide hyper-reactive and functional hotspots with reactivity-based
probes, which in-turn serve as sites that can be pharmacologically interrogated; 2) accelerated and
massively parallel development of small-molecule modulators of large numbers of protein targets and the
assessment of their proteome-wide selectivity; and 3) chemical genomics coupled with facile target
identification to identify novel therapeutic targets.
Mapping Proteome-Wide Interactions of Environmental Chemicals to Uncover Novel Toxicological
Mechanisms. We are environmentally exposed to countless synthetic chemicals on a daily basis, with an
increasing number of these chemical exposures linked to adverse health effects. However, our
understanding of the (patho)physiological effects of these chemicals remains poorly understood, due in
part to a general lack of effort to systematically and comprehensively identify the direct interactions of
environmental chemicals with biological macromolecules in mammalian systems in vivo. Understanding
the direct protein targets of chemicals provides critical information on the types of biochemical and
(patho)physiological effects that may be expected from exposure to the chemical. Our lab has been using
the activity-based and reactivity-based chemoproteomic strategies to comprehensively identify chemical-
protein interactions in complex biological systems, which has in-turn allowed us to identify unique and
novel toxicological mechanisms for many widely used chemicals in our environment.
Education
Publications
Louie SM, Grossman EA, Crawford LA, Ding L, Camarda R, Huffman TR, Miyamoto DK, Goga A, Weerapana E, Nomura DK. (2016) GSTP1 is a driver of triple-negative breast cancer cell metabolism and pathogenicity. Cell Chemical Biology 23, 1-12.
Counihan JC, Ford B, Nomura DK. (2016) Mapping Proteome-Wide Interactions of Reactive
Chemicals using Chemoproteomic Platforms. Current Opinions in Chemical Biology 30, 68-
76.Medina-Cleghorn D, Bateman LA, Ford B, Heslin A, Fisher KJ, Dalvie ED, Nomura DK.
(2015) Mapping proteome-wide targets of environmental chemicals using reactivity-based
chemoproteomic platforms. Chemistry and Biology 22, 1394-1405. PMID26496688Piano V#, Benjamin DI#, Valente S, Nenci S, Mai A, Aliverti A, Nomura DK*, Mattevi A*.
(2015) Discovery of inhibitors for the ether lipid-generating enzyme AGPS as anti-cancer
agents. ACS Chemical Biology doi: 10.1021/acschembio.5b00466. PMID 26322624 (#co-first
authors; * co-corresponding authors).Queiroz A, Medina-Cleghorn D, Marjanovic O, Nomura DK, Riley LW. (2015) Comparative
metabolic profiling of Mycobacterium tuberculosis: cell wall lipid reorganization as a
virulence factor. Pathogens and Disease pii: ftv066. PMID26319139.Sanchez-Alavez M, Nguyen W, Mori S, Moroncini G, Viader A, Nomura DK, Cravatt BF,
Conti B. (2015) Monoacylglycerol lipase regulates fever response. Plos One 10, e0134437.
PMID: 26287872.Kohnz RA, Mulvihill MM, Chang JW, Hsu K-L, Sorrentino A, Cravatt BF, Bandyopadhyay S,
Goga A, Nomura DK. (2015) Activity-based protein profiling of oncogene-driven changes in
metabolism reveals PAFAH1B2 and 1B3 as broad-spectrum cancer therapy targets. ACS
Chemical Biology 10, 1624-1630. PMID: 25945974.Benjamin DI, Li DS, Lowe, W, Heuer T, Kemble G, Nomura DK. (2015) Diacylglycerol
metabolism and signaling is a predictive and driving force underlying FASN inhibitor
sensitivity in cancer cells. ACS Chemical Biology 10, 1616-1623. PMID: 25871544Rashidian J, Le Scolan E, Ji X, Mulvihill MM, Nomura DK, Luo K. (2015) Ski regulates
Hippo and TAZ signaling to suppress breast cancer progression. Science Signaling 10,
ra14. PMID: 25670202Anderson CM, Kazantzis M, Wang J, Venkatraman S, Goncalves RLS, Quinlan CL, Ng R,
Jastroch, M, Benjamin DI, Nie B, Herber C, Van A-AN, Park MK, Yun D, Chan K, Yu A,
Vuong P, Febbraio M, Nomura DK, Napoli JL, Brand MD, Stahl A. (2015) Dependence of
brown adipose tissue function on CD36-mediated coenzyme Q uptake. Cell Reports 10,
505-515. PMID 25620701Chang JW, Zuhl AM, Speers AE, Niessen S, Brown SJ, Mulvihill MM, Fan YC, Spicer TP,
Southern M, Scampavia L, Fernandez-Vega V, Dix MM, Cameron MD, Hodder PS, Rosen
H, Nomura DK, Kwon O, Hsu K-L, Cravatt BF. (2015) A selective inhibitor of platelet-
activating factor acetylhydrolases 1b2 and 1b3 that impairs cancer cell survival. ACS
Chemical Biology 10, 925-932. PMID: 25602368Lysenko LV, Kim J, Henry C, Tyrtyshnaia A, Kohnz RA, Madamba F, Simon GM,
Kleschevnikova NE, Nomura DK, Ezekowitz RAB, Kleschevnikov AM. (2014)
Monoacylglycerol lipase inhibitor JZL184 improves behavior and neural properties in aged
Ts65Dn mice, a model of Down Syndrome. Plos One 9, e114521. PMID: 25474204.Valdearcos M, Robblee M, Benjamin DI, Nomura DK, Xu AW, Koliwad SK. (2014) Microglia
Dictate the Impact of Saturated Fat Consumption on Hypothalamic Inflammation and
Neuronal Function. Cell Reports 9, 1-15. PMID: 25497089Hunerdosse D, Morris PJ, Miyamoto DK, Fisher KJ, Bateman LA, Ghazaleh J, Zhong S,
Nomura DK. (2014) Chemical Genetics Screening Reveals KIAA1363 as a Cytokine-
Lowering Target. ACS Chemical Biology. Doi: 10.1021/cb500717g. PMID: 25343321.Medina-Cleghorn D, Nomura DK. (2014) Exploring metabolic pathways and regulation
through functional chemoproteomic and metabolomic platforms. Chemistry & Biology 21,
1171-1184. PMID: 25237861.Cai X, Perttula K, Pajouh SK, Hubbard A, Nomura DK, Rappaport SM. (2014) Untargeted
lipidomic profiling of human plasma reveals differences due to race, gender, and smoking
status. Metabolomics: Open Access 4, 1000131.Mulvihill MM, Nomura DK. (2014) Metabolomic Strategies to Map Functions of Metabolic
Pathways. AJP Metabolism and Endocrinology 307, E237-E244. PMID: 24918200Latimer LN, Lee MR, Medina-Cleghorn D, Kohnz RA, Nomura DK, Dueber JE. (2014)
Employing a combinatorial expression approach to characterize xylose utilization in
Saccharomyces cerevisiae. Metabolic Engineering 25, 20-29. PMID: 24930894.Mulvihill MM, Benjamin DI, LeScolan E, Ji X, Shieh A, Green M, Narasimhalu T, Morris PJ,
Luo K, Nomura DK. (2014) Metabolic Profiling Reveals PAFAH1B3 as a critical driver of
breast cancer pathogenicity. Chemistry & Biology 21, 831-840. PMID: 24954006Benjamin DI, Louie S, Mulvihill MM, Kohnz RA, Li DS, Chan LG, Sorrentino A,
Bandhyopadhyay S, Cozzo A, Ohiri A, Goga A, Ng-SW, Nomura DK. (2014) INPP1
Promotes Cancer Aggressiveness by Linking Inositol Phosphate Recycling to Glycolytic and
Lipid Metabolism. ACS Chemical Biology 20, 1340-1350. PMID: 24738946Kohnz RK, Nomura DK. (2014) Chemical approaches to therapeutically target the
metabolism and signaling of the endocannabinoid 2-AG and eicosanoids. Chemical Society
Reviews 43, 6859-6869. PMID: 24676249Morris PJ*, Medina-Cleghorn D*, Heslin A, King S, Orr J, Krauss RM, Nomura DK. (2014)
Organophosphorus flame retardants inhibit specific liver carboxylesterases and cause
serum hypertriglyceridemia. ACS Chemical Biology 9, 1097-1103. (*authors contributed
equally to the work) PMID: 24597639Hunerdosse D, Nomura DK. (2014) Activity-based proteomic and metabolomic approaches
for understanding metabolism. Current Opinion in Biotechnology 28C, 116-126. PMID
24594637Poole D, Lee M, Tso P, Bunnett N, Yo S, Lieu T, Shiu A, Wang J-C, Nomura DK, and
Aponte GW. (2014) Feeding dependent activation of enteric cells and sensory neurons by
lymphatic fluid: evidence for a neurolymphocrine system. AJP-Gastrointestinal and Liver
Physiology 306, G686-G698. PMID: 24578341Dominguez E, Galmozzi A, Chang JW, Hsu K-L, Pawlak J, Li W, Godio C, Thomas J,
Partida D, Niessen S, O’Brien PE, Russell AP, Watt MJ, Nomura DK, Cravatt BF, Saez E.
(2014) Integrated phenotypic screening and activity-based proteomics defines a role for
carboxylesterase 3 in obesity and diabetes. Nature Chemical Biology 10, 113-121. PMID:
24362705Medina-Cleghorn D, Heslin A, Morris PJ, Mulvihill MM, Nomura DK. (2014)
Multidimensional profiling platforms reveal metabolic dysregulation caused by
organophosphorus pesticides. ACS Chemical Biology 9, 423-432. PMID: 24205821Nomura DK, Cravatt BF. (2013) Lipid Metabolism in Cancer. Biochimica et Biophysica
Acta—Molecular and Cell Biology of Lipids 1831, 1497-1498. PMID: 23921253Benjamin DI, Cozzo A, Ji X, Roberts LS, Louie SM, Luo K, Nomura DK. (2013) The ether
lipid generating enzyme AGPS alters the balance of structural and signaling lipids that fuel
cancer pathogenicity. Proceedings of the National Academy of Sciences, USA 110, 14912-
14917. PMID: 23980144Louie SM*, Roberts LS*, Mulvihill MM, Luo K, Nomura DK. (2013) Cancer cells incorporate
and remodel exogenous fatty acids into structural and oncogenic signaling lipids. Biochimica
et Biophysica Acta—Molecular and Cell Biology of Lipids 1831, 1566-1572. PMID:
23872477 (* authors contributed equally to the work)Louie SM, Roberts LS, Nomura DK. (2013) Mechanisms linking obesity and cancer.
Biochimica et Biophysica Acta—Molecular and Cell Biology of Lipids 1831, 1499-1508.
PMID: 23470257Medina-Cleghorn D, Nomura DK. (2013) Chemical Approaches to Study Metabolic
Networks. Pflugers Archive 465,427-440. PMID: 23296751Cao Z, Mulvihill MM, Mukhopadhyay P, Xu H, Erdelyi K, Hao E, Holovac E, Hasko G, Cravatt
BF, Nomura DK#, Pal Pacher#. (2013) Monoacylglycerol lipase controls endocannabinoid
and eicosanoid signaling and hepatic injury in mice. Gastroenterology 144, 808-817. PMID:
23295443 (# co-corresponding authors)Mulvihill MM, Nomura DK. (2013) Therapeutic Potential of Monoacylglycerol Lipase
Inhibitors. Life Sciences 92, 492-497. PMID: 23142242Morrison BE, Garibaldi Marcondes MC, Nomura DK, Sanchez-Alavez M, Saar I, Bartfai T,
Maher P, Sugama S, Conti B. (2012) IL-13Ralpha1 expression in dopaminergic neurons
contributes to their oxidative stress-mediates loss following chronic systemic treatment with
LPS. Journal of Immunology 189, 5498-5502. PMID: 23169588Benjamin DI, Cravatt BF, Nomura DK. (2012) Global Profiling Strategies towards Mapping
Dysregulated Metabolic Pathways in Cancer. Cell Metabolism 16, 565-567. PMID:
23063552Piro JR, Benjamin DI, Duerr JM, Pi YQ, Gonzales C, Schwartz JW, Nomura DK#, Samad
TA#. (2012) A Dysregulated Endocannabinoid-Eicosanoid Network Supports Pathogenesis
in a Mouse Model of Alzheimer's Disease. Cell Reports 1, 617-623. PMID: 22813736 (# co-
corresponding author)Nomura DK#, Morrison BE, Blankman JL, Long JZ, Kinsey SG, Marcondes MC, Ward AM,
Hahn YK, Lichtman AH, Conti B, Cravatt BF#. (2011) Endocannabinoid hydrolysis generates
brain eicosanoids that promote neuroinflammation. Science 334, 809-813. PMID: 22021672
(# co-corresponding author)Ruby MA, Nomura DK, Hudak CSS, Barber A, Casida JE, Krauss RM. (2011) Overactive
endocannabinoid signaling induces hepatic steatosis, insulin resistance, and global
transcriptional changes. Plos One 6, e26415. PMID: 22073164Nomura DK#, Lombardi DP, Chang JW, Niessen S, Ward AM, Long JZ, Hoover HH, Cravatt
BF#. (2011) Monoacylglycerol lipase exerts bidirectional control over endocannabinoid and
fatty acid pathways to support prostate cancer pathogenesis. Chemistry & Biology 18, 848-
856. PMID: 21802006 (# co-corresponding author)Ramesh D, Ross GR, Schlosburg JE, Abdullah RA, Kinsey SG, Long JZ, Nomura DK, Sim-
Selley LJ, Cravatt BF. (2011) Blockade of endocannabinoid hydrolytic enzymes attenuates
precipitated withdrawal symptoms in mice. Journal of Pharmacology and Experimental
Therapeutics 339, 173-185. PMID: 21719468Kinsey SG, Nomura DK, O'Neal ST, Long JZ, Cravatt BF, Lichtman AH. (2011) Inhibition of
monoacylglycerol lipase (MAGL) attenuates NSAID-induced gastric hemorrhages in mice.
Journal of Pharmacology and Experimental Therapeutics 338, 795-802. PMID: 21659471Chang JW, Nomura DK, Cravatt BF. (2011) A potent and selective inhibitor of
KIAA1363/AADACL1 that impairs prostate cancer pathogenesis. Chemistry & Biology 18,
476-484. PMID: 21513884Ahn K, Smith SE, Liimata MB, Sadagopan N, Dudley D, Young T, Wren P, Zhang Y,
Swaney S, Van Becelaere K, Blankman JL, Nomura DK, Bhattachar SN, Stif C,
Nomanbhoy TK, Weerapana E, Johnson DS, Cravatt BF. (2011) Mechanistic and
pharmacological characterization of PF-04457845: a highly potent and selective FAAH
inhibitor that reduces inflammatory and noninflammatory pain. Journal of Pharmacology and
Experimental Therapeutics 338, 114-124. PMID: 21505060Nomura DK#, Casida JE#. (2011) Activity-based protein profiling of organophosphorus and
thiocarbamate pesticides reveals multiple secondary targets in the mammalian nervous
system. Journal of Agricultural and Food Chemistry 59, 2808-2815. PMID: 21341672 (# co-
corresponding author)Nicolaou KC, Sanchini S, Sarlah D, Lu G, Wu R, Nomura DK, Cravatt BF, Cubitt B, de la
Torre JC, Hessell AJ, Burton DR. (2011) Design, synthesis and biological evaluation of a
biyouyanagin compound library. Proceedings of the National Academy of Sciences, USA
108, 6715-6720. PMID: 21245351Bachovchin DA, Mohr JT, Speers AE, Wang C, Berlin JM, Spicer TP, Fernandez-Vega V,
Chase P, Hodder PS, Schűrer, Nomura DK, Rosen H, Fu GC, Cravatt BF. (2011) Academic
cross-fertilization by public screening yields a remarkable class of protein phosphatase
methylesterase-1 inhibitors. Proceedings of the National Academy of Sciences, USA 108,
6811-6816. PMID: 21398589Kopp F, Komatsu T, Nomura DK, Trauger SA, Thomas JR, Simon GM, Cravatt BF. (2010)
The glycerophospho-metabolome and its influence on amino acid homeostasis by brain
metabolomics of GDE1(-/-) mice. Chemistry & Biology 17, 831-840. PMID: 20797612Schlosburg JE, Blankman JL, Long JZ, Nomura DK, Nguyen PT, Ramesh D, Kinsey SG,
Booker L, Burston JK, Wise LE, Ghosh S, Selley DE, Sim-Selley LJ, Liu Q, Cravatt BF,
Lichtman AH. (2010) Sustained inactivation of monoacylglycerol lipase produces functional
antagonism of the brain endocannabinoid system. Nature Neuroscience 13, 1113-1119.
PMID: 20729846Nomura DK, Dix MM, Cravatt BF. (2010) Chemoproteomic Approaches for Biochemical
Pathway Discovery in Cancer. Nature Reviews Cancer 10, 630-638. PMID: 20703252Nomura DK, Long JZ, Niessen S, Hoover HS, Ng S-W, Cravatt BF. (2010)
Monoacylglycerol lipase regulates a fatty acid network that promotes cancer pathogenesis.
Cell 140, 49-61. PMID: 20079333Long JZ, Nomura DK, Vann RE, Walentiny DM, Booker L, Jin X, Burston JJ, Sim-Selley LJ,
Lichtman AH, Wiley JL, Cravatt BF. (2009) Dual blockade of FAAH and MAGL identifies
behavioral processes regulated by endocannabinoid crosstalk in vivo. Proceedings of the
National Academy of Sciences, USA 106, 20270-20275. PMID: 19918051Long JZ, Nomura DK, Cravatt BF. (2009) Mechanistic characterization of selective
monoacylglycerol lipase inhibition reveals differences in central and peripheral
endocannabinoid metabolism. Chemistry & Biology 16, 744-753. PMID: 19635411Ruby M*, Nomura DK*, Hudak CS, Mangravite LM, Chiu S, Casida JE, Krauss RM. (2008)
Overactive endocannabinoid signaling impairs apolipoprotein E-mediated clearance of
triglyceride-rich lipoproteins. Proceedings of the National Academy of Sciences, USA 105,
14561-14566. PMID: 18794527 (* co-first author)Nomura DK, Ward AM, Hudak CS, Burston JJ, Issa RS, Fisher KJ, Abood ME, Wiley JL,
Lichtman A, Casida JE. (2008) Monoacylglycerol lipase regulates 2-arachidonoylglycerol
action and arachidonic acid levels. Bioorganic Medicinal Chemistry Letters 18, 5875-5878.
PMID: 18752948Casida JE, Nomura DK, Vose SC, Fujioka K. (2008) Organophosphate-Sensitive Lipases
Modulate Brain Lysophospholipids, Ether Lipids and Endocannabinoids. Chemico-Biological
Interactions 175, 355-64. PMID: 18495101Nomura DK, Blankman JL, Simon GM, Fujioka K, Issa RS, Ward AM, Cravatt BF, Casida
JE. (2008) Activation of the endocannabinoid system by organophosphorus nerve agents.
Nature Chemical Biology 4, 373-378. PMID: 18438404Nomura DK, Fujioka K, Issa RS, Ward AM, Cravatt BF, Casida JE. (2008) Dual Roles of
Brain Serine Hydrolase KIAA1363 in Ether Lipid Metabolism and Organophosphate
Detoxification. Toxicology and Applied Pharmacology 228, 42-482. PMID: 18154358Nomura DK, Durkin KA, Chiang KP, Quistad GB, Cravatt BF, Casida JE. (2006) Serine
Hydrolase KIAA1363: Toxicological and Structural Features with Emphasis on
Organophosphate Interactions. Chemical Research in Toxicology 19, 1142-1150. PMID:
16978018Quistad GB, Liang SN, Fisher KJ, Nomura DK, Casida JE. (2006) Each Lipase has a
Unique Sensitivity Profile for Organophosphorus Inhibitors. Toxicological Sciences 91,166-
172. PMID: 16449251Nomura DK, Leung D, Chiang KP, Quistad GB, Cravatt BF, Casida JE. (2005) A Brain
Detoxifying Enzyme for Organophosphorus Nerve Poisons. Proceedings of the National
Academy of Sciences, USA 102, 6195-6200. PMID: 15840715Segall Y, Quistad GB, Sparks SE, Nomura DK, Casida JE. (2003) Toxicological and
Structural Features of Organophosphorus and Organosulfur Cannabinoid CB1 Receptor
Ligands. Toxicological Sciences 76, 131-137. PMID: 12944568Segall Y, Quistad GB, Nomura DK, Casida JE. (2003) Arachidonylsulfonyl Derivatives as
Cannabinoid CB1 Receptor and Fatty Acid Amide Hydrolase Inhibitors. Bioorganic Medicinal
Chemistry Letters 13,3301-3303. PMID: 12951114Quistad GB, Nomura DK, Sparks SE, Segall Y, Casida JE. (2002) Cannabinoid CB1
Receptor as a Target for Chlorpyrifos Oxon and Organophosphorus Pesticides. Toxicology
Letters 135, 89-93. PMID: 12243867Quistad GB, Sparks SE, Segall Y, Nomura DK, Casida JE. (2002) Selective Inhibitors of
Fatty Acid Amide Hydrolase Relative to Neuropathy Target Esterase and
Acetylcholinesterase: Toxicological Implications. Toxicology and Applied Pharmacology 179,
57-63. PMID: 11884237Saghatelian A, Nomura DK, Weerapana E (2016) Omics: The maturation of chemical biology. Current Opinions in Chemical Biology 30: v-vi. PMID 26739665
Camarda R, Zhou AY, Kohnz RA, Balakrishnan S, Mahieu C, Anderton B, Eyob H, Kajimura S, Tward A, Krings G, Nomura DK, Goga A. (2016) Inhibition of fatty-acid oxidation as a therapy for MYC-overexpressing triple-negative breast cancer. Nature Medicine Doi: 10.1038/nm.4055. PMID 26950360
Nikkanen J, Forsstrom S, Euro L, Paetau I, Kohnz RA, Wang L, Chilov D, Viinamaki J, Roivainen A, Marjamaki P, Liljenback H, Ahola S, Buzkova J, Terzioglu M, Khan NA, Pirnes-Karhu S, Paetau A, Lonnqvist T, Sajantila A, Isohanni P, Tyynaismaa H, Nomura DK, Battersby B, Velagapudi V, Carroll CJ, Suomalainen A (2016) Mitochondrial DNA replication defects disturb cellular dNTP pools and remodel one-carbon metabolism. Cell Metabolism. Feb 23. pii: S1550-4131(16)30012-2. doi: 10.1016/j.cmet.2016.01.019. PMID 26924217
Zhang J, Medina-Cleghorn D, Bernal-Mizrachi L, Bracci PM, Hubbard A, Conde L, Riby J, Nomura DK, Skibola C (2016) The potential relevance of the endocannabinoid, 2-arachidonoylglycerol, in diffuse large B-cell lymphoma. Oncoscience 3, 31-41.
Nomura DK, Casida JE (2016) Lipases and their inhibitors in health and disease. Chemico-Biological Interactions doi: 10.1016/j.cbi.2016.04.004. PMID 27067293.
Long JZ, Svensson KJ, Bateman LA, Lin H, Kamenecka T, Lokurkar IA, Lou J, Rao RR, Chang MT, Jedrychowski MP, Paolo J, Griffin PR, Nomura DK*, Spiegelman BM* (2016) PM20D1 secretion by thermogenic adipose cells regulates lipidated amino acid uncouplers of mitochondrial respiration. Cell 166, 424-435. PMID 27374330 (*co-corresponding authorship)
Kohnz RA, Roberts, LS, DeTomaso D, Badyopadhyay S, Yosef N, Nomura DK. (2016) Protein sialylation regulates a gene expression signature that promotes breast cancer cell pathogenicity. ACS Chemical Biology doi: 10.1021/acschembio.6b00433. PMID 27380425
Braverman J, Sogi KM, Benjamin D, Nomura DK, Stanley SA. (2016) HIF-1alpha is an essential mediator of IFA-gamma-dependent immunity to Mycobacterium tuberculosis. Journal of Immunology doi: 10.4049/jimmunol.1600266. PMID 27430718
Sogi K, Holsclaw C, Fragiadakis G, Nomura DK, Leary J, Bertozzi C. (2016) Biosynthesis and regulation of sulfomenaquinone, a metabolite associated with virulence in Mycobacterium tuberculosis. ACS Infectious Diseases DOI: 10.1021/acsinfecdis.6b00106.
