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Author Details
Full Name
Joseph D Ho
Affiliation
University of California san francisco
ORCID
Career Start Year
2000
Papers
21
H Index
14
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
35333651
Structural determinants of dual incretin receptor agonism by tirzepatide.
Proc Natl Acad Sci U S A
2022
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
32416867
Discovery and pharmacology of the covalent GLP-1 receptor (GLP-1R) allosteric modulator BETP: A novel tool to probe GLP-1R pharmacology.
Adv Pharmacol
2020
32690941
Structural insights into probe-dependent positive allosterism of the GLP-1 receptor.
Nat Chem Biol
2020
29402739
Determination 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 Lett
2018
30365309
Structural Basis for ( S)-3,4-Dicarboxyphenylglycine (DCPG) As a Potent and Subtype Selective Agonist of the mGlu<sub>8</sub> Receptor.
J Med Chem
2018
29695780
Structural basis for GPR40 allosteric agonism and incretin stimulation.
Nat Commun
2018
22119470
3-heterocyclyl quinolone inhibitors of the HCV NS5B polymerase.
Bioorg Med Chem Lett
2012
20457942
Function of human Rh based on structure of RhCG at 2.1 A.
Proc Natl Acad Sci U S A
2010
21151500
Immunodominant T cell determinants of aquaporin-4, the autoantigen associated with neuromyelitis optica.
PLoS One
2010
19383790
Crystal structure of human aquaporin 4 at 1.8 A and its mechanism of conductance.
Proc Natl Acad Sci U S A
2009
19360018
A general protocol for the crystallization of membrane proteins for X-ray structural investigation.
Nat Protoc
2009
17320904
The crystal structure of E. coli rRNA pseudouridine synthase RluE.
J Mol Biol
2007
16543221
Novel arylpyrazole compounds selectively modulate glucocorticoid receptor regulatory activity.
Genes Dev
2006
16681368
Structure-guided design of peptide-based tryptase inhibitors.
Biochemistry
2006
15242608
Structural snapshots of human HDAC8 provide insights into the class I histone deacetylases.
Structure
2004
15522303
Dissecting and designing inhibitor selectivity determinants at the S1 site using an artificial Ala190 protease (Ala190 uPA).
J Mol Biol
2004
12962630
The structure of the extracellular region of human hepsin reveals a serine protease domain and a novel scavenger receptor cysteine-rich (SRCR) domain.
Structure
2003
12454497
Expression, purification, crystallization and preliminary X-ray diffraction studies of human cathepsin F complexed with an irreversible vinyl sulfone inhibitor.
Acta Crystallogr D Biol Crystallogr
2002
12225749
The crystal structure of human cathepsin F and its implications for the development of novel immunomodulators.
J Mol Biol
2002
10956658
Induction of positive cooperativity by amino acid replacements within the C-terminal domain of Penicillium chrysogenum ATP sulfurylase.
J Biol Chem
2000
1 - 21 of 21
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Joseph D O'Connell
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University of California San Francisco
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1
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Co-authored papers
1
Mark W Knuth
Joint Center for Structural Genomics
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1
Janet Finer-Moore
University of California San Francisco
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1
Scott S Zamvil
Weill Institute for Neurosciences, University of California san francisco
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Avner Schlessinger
Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai
Co-authored papers
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David F Savage
University of California berkeley
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Sarika Chaudhary
Bennett University
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Frances Lu
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Franklin A Hays
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