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Author Details

Joseph D Ho
University of California san francisco
2000
21
14
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
35333651Structural determinants of dual incretin receptor agonism by tirzepatide.Proc Natl Acad Sci U S A2022
33246032Structure-based, multi-targeted drug discovery approach to eicosanoid inhibition: Dual inhibitors of mPGES-1 and 5-lipoxygenase activating protein (FLAP).Biochim Biophys Acta Gen Subj2021
32416867Discovery and pharmacology of the covalent GLP-1 receptor (GLP-1R) allosteric modulator BETP: A novel tool to probe GLP-1R pharmacology.Adv Pharmacol2020
32690941Structural insights into probe-dependent positive allosterism of the GLP-1 receptor.Nat Chem Biol2020
29402739Determination of L-AP4-bound human mGlu8 receptor amino terminal domain structure and the molecular basis for L-AP4's group III mGlu receptor functional potency and selectivity.Bioorg Med Chem Lett2018
30365309Structural Basis for ( S)-3,4-Dicarboxyphenylglycine (DCPG) As a Potent and Subtype Selective Agonist of the mGlu<sub>8</sub> Receptor.J Med Chem2018
29695780Structural basis for GPR40 allosteric agonism and incretin stimulation.Nat Commun2018
221194703-heterocyclyl quinolone inhibitors of the HCV NS5B polymerase.Bioorg Med Chem Lett2012
20457942Function of human Rh based on structure of RhCG at 2.1 A.Proc Natl Acad Sci U S A2010
21151500Immunodominant T cell determinants of aquaporin-4, the autoantigen associated with neuromyelitis optica.PLoS One2010
19383790Crystal structure of human aquaporin 4 at 1.8 A and its mechanism of conductance.Proc Natl Acad Sci U S A2009
19360018A general protocol for the crystallization of membrane proteins for X-ray structural investigation.Nat Protoc2009
17320904The crystal structure of E. coli rRNA pseudouridine synthase RluE.J Mol Biol2007
16543221Novel arylpyrazole compounds selectively modulate glucocorticoid receptor regulatory activity.Genes Dev2006
16681368Structure-guided design of peptide-based tryptase inhibitors.Biochemistry2006
15242608Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases.Structure2004
15522303Dissecting and designing inhibitor selectivity determinants at the S1 site using an artificial Ala190 protease (Ala190 uPA).J Mol Biol2004
12962630The structure of the extracellular region of human hepsin reveals a serine protease domain and a novel scavenger receptor cysteine-rich (SRCR) domain.Structure2003
12454497Expression, purification, crystallization and preliminary X-ray diffraction studies of human cathepsin F complexed with an irreversible vinyl sulfone inhibitor.Acta Crystallogr D Biol Crystallogr2002
12225749The crystal structure of human cathepsin F and its implications for the development of novel immunomodulators.J Mol Biol2002
10956658Induction of positive cooperativity by amino acid replacements within the C-terminal domain of Penicillium chrysogenum ATP sulfurylase.J Biol Chem2000
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Collaborators

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Lilly Research Laboratories
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Weill Institute for Neurosciences, University of California san francisco
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Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai
Co-authored papers 1
University of California berkeley
Co-authored papers 1
Bennett University
Co-authored papers 1
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University of Oklahoma Health Sciences Center
Co-authored papers 1
New York SGX Research Center for Structural Genomics
Co-authored papers 1
Vagelos College of Physicians and Surgeons, Columbia University
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Beth Israel Deaconess Medical Center and Harvard Medical School
Co-authored papers 1
Icahn School of Medicine at Mount Sinai
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