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Author Details

Michael J Romanowski
Sunesis Pharmaceuticals, Inc. 395 Oyster Point Boulevard
1993
38
23
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
34314938Utilizing structure based drug design and metabolic soft spot identification to optimize the in vitro potency and in vivo pharmacokinetic properties leading to the discovery of novel reversible Bruton's tyrosine kinase inhibitors.Bioorg Med Chem2021
34515462Chemoproteomics Enabled Discovery of Selective Probes for NuA4 Factor BRD8.ACS Chem Biol2021
31138459Optimization of novel reversible Bruton's tyrosine kinase inhibitors identified using Tethering-fragment-based screens.Bioorg Med Chem2019
31209353A small-molecule inhibitor of C5 complement protein.Nat Chem Biol2019
31072929Structure of lipoprotein lipase in complex with GPIHBP1.Proc Natl Acad Sci U S A2019
29475084Full-length myocilin protein is purified from mammalian cells as a dimer.Protein Expr Purif2018
22833538Naturally occurring genetic variants of human caspase-1 differ considerably in structure and the ability to activate interleukin-1β.Hum Mutat2013
21459573Discovery of a potent and highly selective PDK1 inhibitor via fragment-based drug discovery.Bioorg Med Chem Lett2011
19649632SNS-314, a pan-Aurora kinase inhibitor, shows potent anti-tumor activity and dosing flexibility in vivo.Cancer Chemother Pharmacol2010
20052711Structures of human Bruton's tyrosine kinase in active and inactive conformations suggest a mechanism of activation for TEC family kinases.Protein Sci2010
19284778Fragment-based discovery of nonpeptidic BACE-1 inhibitors using tethering.Biochemistry2009
196468662-Aminobenzimidazoles as potent Aurora kinase inhibitors.Bioorg Med Chem Lett2009
19186057Water-soluble prodrugs of an Aurora kinase inhibitor.Bioorg Med Chem Lett2009
18433722Crystal structure of unphosphorylated STAT3 core fragment.Biochem Biophys Res Commun2008
18793847Design and synthesis of 2-amino-pyrazolopyridines as Polo-like kinase 1 inhibitors.Bioorg Med Chem Lett2008
18790636Design and synthesis of 2-amino-isoxazolopyridines as Polo-like kinase inhibitors.Bioorg Med Chem Lett2008
18678489Discovery of a potent and selective aurora kinase inhibitor.Bioorg Med Chem Lett2008
18703838Structures of the wild-type and activated catalytic domains of Brachydanio rerio Polo-like kinase 1 (Plk1): changes in the active-site conformation and interactions with ligands.Acta Crystallogr D Biol Crystallogr2008
18590738An allosteric circuit in caspase-1.J Mol Biol2008
18678933Structure of the Brachydanio rerio Polo-like kinase 1 (Plk1) catalytic domain in complex with an extended inhibitor targeting the adaptive pocket of the enzyme.Acta Crystallogr Sect F Struct Biol Cryst Commun2008
17434748Mouse Aurora A: expression in Escherichia coli and purification.Protein Expr Purif2007
16274992Tethering identifies fragment that yields potent inhibitors of human caspase-1.Bioorg Med Chem Lett2006
16682620A common allosteric site and mechanism in caspases.Proc Natl Acad Sci U S A2006
15802232Malonate-assisted purification of human caspases.Protein Expr Purif2005
16511067Structural analysis of caspase-1 inhibitors derived from Tethering.Acta Crystallogr Sect F Struct Biol Cryst Commun2005
15296730Crystal structures of a ligand-free and malonate-bound human caspase-1: implications for the mechanism of substrate binding.Structure2004
12424232The kinetic mechanism of phosphomevalonate kinase.J Biol Chem2003
11948793Crystal structure of the Escherichia coli SbmC protein that protects cells from the DNA replication inhibitor microcin B17.Proteins2002
12011453Crystal structure of the Mus musculus cholesterol-regulated START protein 4 (StarD4) containing a StAR-related lipid transfer domain.Proc Natl Acad Sci U S A2002
12011452The cholesterol-regulated StarD4 gene encodes a StAR-related lipid transfer protein with two closely related homologues, StarD5 and StarD6.Proc Natl Acad Sci U S A2002
12001237Crystal structure of the Streptococcus pneumoniae phosphomevalonate kinase, a member of the GHMP kinase superfamily.Proteins2002
12001236Crystal structure of the Escherichia coli glucose-inhibited division protein B (GidB) reveals a methyltransferase fold.Proteins2002
12001235Crystal structure of the Escherichia coli shikimate kinase I (AroK) that confers sensitivity to mecillinam.Proteins2002
11118439Interaction between YY1 and the retinoblastoma protein. Regulation of cell cycle progression in differentiated cells.J Biol Chem2001
11698677Structural genomics of enzymes involved in sterol/isoprenoid biosynthesis.Proc Natl Acad Sci U S A2001
8995674Characterization of the human cytomegalovirus irs1 and trs1 genes: a second immediate-early transcription unit within irs1 whose product antagonizes transcriptional activation.J Virol1997
9188653pIRS1 and pTRS1 are present in human cytomegalovirus virions.J Virol1997
8440524Monoclonal antibody prophylaxis against the in vivo toxicity of ricin in mice.Immunol Invest1993
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Collaborators

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Albert Einstein College of Medicine
Co-authored papers 4
Department of Pharmacotherapy & Outcomes Science
Co-authored papers 3
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Co-authored papers 3
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Co-authored papers 1
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Co-authored papers 1
Carnegie Mellon University Qatar
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Beth Israel Deaconess Medical Center, Harvard Medical School
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Brookhaven National Laboratory
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University of California san francisco
Co-authored papers 1
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Co-authored papers 1