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Author Details
Full Name
Michael J Romanowski
Affiliation
Sunesis Pharmaceuticals, Inc. 395 Oyster Point Boulevard
ORCID
Career Start Year
1993
Papers
38
H Index
23
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
34314938
Utilizing 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 Chem
2021
34515462
Chemoproteomics Enabled Discovery of Selective Probes for NuA4 Factor BRD8.
ACS Chem Biol
2021
31138459
Optimization of novel reversible Bruton's tyrosine kinase inhibitors identified using Tethering-fragment-based screens.
Bioorg Med Chem
2019
31209353
A small-molecule inhibitor of C5 complement protein.
Nat Chem Biol
2019
31072929
Structure of lipoprotein lipase in complex with GPIHBP1.
Proc Natl Acad Sci U S A
2019
29475084
Full-length myocilin protein is purified from mammalian cells as a dimer.
Protein Expr Purif
2018
22833538
Naturally occurring genetic variants of human caspase-1 differ considerably in structure and the ability to activate interleukin-1β.
Hum Mutat
2013
21459573
Discovery of a potent and highly selective PDK1 inhibitor via fragment-based drug discovery.
Bioorg Med Chem Lett
2011
19649632
SNS-314, a pan-Aurora kinase inhibitor, shows potent anti-tumor activity and dosing flexibility in vivo.
Cancer Chemother Pharmacol
2010
20052711
Structures of human Bruton's tyrosine kinase in active and inactive conformations suggest a mechanism of activation for TEC family kinases.
Protein Sci
2010
19284778
Fragment-based discovery of nonpeptidic BACE-1 inhibitors using tethering.
Biochemistry
2009
19646866
2-Aminobenzimidazoles as potent Aurora kinase inhibitors.
Bioorg Med Chem Lett
2009
19186057
Water-soluble prodrugs of an Aurora kinase inhibitor.
Bioorg Med Chem Lett
2009
18433722
Crystal structure of unphosphorylated STAT3 core fragment.
Biochem Biophys Res Commun
2008
18793847
Design and synthesis of 2-amino-pyrazolopyridines as Polo-like kinase 1 inhibitors.
Bioorg Med Chem Lett
2008
18790636
Design and synthesis of 2-amino-isoxazolopyridines as Polo-like kinase inhibitors.
Bioorg Med Chem Lett
2008
18678489
Discovery of a potent and selective aurora kinase inhibitor.
Bioorg Med Chem Lett
2008
18703838
Structures 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 Crystallogr
2008
18590738
An allosteric circuit in caspase-1.
J Mol Biol
2008
18678933
Structure 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 Commun
2008
17434748
Mouse Aurora A: expression in Escherichia coli and purification.
Protein Expr Purif
2007
16274992
Tethering identifies fragment that yields potent inhibitors of human caspase-1.
Bioorg Med Chem Lett
2006
16682620
A common allosteric site and mechanism in caspases.
Proc Natl Acad Sci U S A
2006
15802232
Malonate-assisted purification of human caspases.
Protein Expr Purif
2005
16511067
Structural analysis of caspase-1 inhibitors derived from Tethering.
Acta Crystallogr Sect F Struct Biol Cryst Commun
2005
15296730
Crystal structures of a ligand-free and malonate-bound human caspase-1: implications for the mechanism of substrate binding.
Structure
2004
12424232
The kinetic mechanism of phosphomevalonate kinase.
J Biol Chem
2003
11948793
Crystal structure of the Escherichia coli SbmC protein that protects cells from the DNA replication inhibitor microcin B17.
Proteins
2002
12011453
Crystal structure of the Mus musculus cholesterol-regulated START protein 4 (StarD4) containing a StAR-related lipid transfer domain.
Proc Natl Acad Sci U S A
2002
12011452
The 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 A
2002
12001237
Crystal structure of the Streptococcus pneumoniae phosphomevalonate kinase, a member of the GHMP kinase superfamily.
Proteins
2002
12001236
Crystal structure of the Escherichia coli glucose-inhibited division protein B (GidB) reveals a methyltransferase fold.
Proteins
2002
12001235
Crystal structure of the Escherichia coli shikimate kinase I (AroK) that confers sensitivity to mecillinam.
Proteins
2002
11118439
Interaction between YY1 and the retinoblastoma protein. Regulation of cell cycle progression in differentiated cells.
J Biol Chem
2001
11698677
Structural genomics of enzymes involved in sterol/isoprenoid biosynthesis.
Proc Natl Acad Sci U S A
2001
8995674
Characterization of the human cytomegalovirus irs1 and trs1 genes: a second immediate-early transcription unit within irs1 whose product antagonizes transcriptional activation.
J Virol
1997
9188653
pIRS1 and pTRS1 are present in human cytomegalovirus virions.
J Virol
1997
8440524
Monoclonal antibody prophylaxis against the in vivo toxicity of ricin in mice.
Immunol Invest
1993
1 - 38 of 38
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row(s) 1 - 30 of 30
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Co-authored papers
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Carnegie Mellon University Qatar
Co-authored papers
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C Edo
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Beth Israel Deaconess Medical Center, Harvard Medical School
Co-authored papers
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Brookhaven National Laboratory
Co-authored papers
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Ursula Pieper
University of California san francisco
Co-authored papers
1
Sue Ellen Gerchman
Brookhaven National Laboratory
Co-authored papers
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1 - 15