Search Results - "Yee, Vivien C."
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Structural Basis of Substrate Recognition in Human Nicotinamide N-Methyltransferase
Published in Biochemistry (Easton) (13-09-2011)“…Nicotinamide N-methyltransferase (NNMT) catalyzes the N-methylation of nicotinamide, pyridines, and other analogues using S-adenosyl-l-methionine as donor…”
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2
Crystal structure of the human prion protein reveals a mechanism for oligomerization
Published in Nature structural biology (01-09-2001)“…The pathogenesis of transmissible encephalopathies is associated with the conversion of the cellular prion protein, PrPC, into a conformationally altered…”
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3
Bora downregulation results in radioresistance by promoting repair of double strand breaks
Published in PloS one (05-03-2015)“…Following DNA double-strand breaks cells activate several DNA-damage response protein kinases, which then trigger histone H2AX phosphorylation and the…”
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4
Crystal Structure of the 2′-Specific and Double-Stranded RNA-Activated Interferon-Induced Antiviral Protein 2′-5′-Oligoadenylate Synthetase
Published in Molecular cell (01-11-2003)“…2′-5′-oligoadenylate synthetases are interferon-induced, double-stranded RNA-activated antiviral enzymes which are the only proteins known to catalyze…”
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5
Crystal Structure of the Deglycating Enzyme Fructosamine Oxidase (Amadoriase II)
Published in The Journal of biological chemistry (03-10-2008)“…Fructosamine oxidases (FAOX) catalyze the oxidative deglycation of low molecular weight fructosamines (Amadori products). These proteins are of interest in…”
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6
Cytosolic 5′-nucleotidase III (NT5C3): gene sequence variation and functional genomics
Published in Pharmacogenetics and genomics (01-08-2009)“…BACKGROUND5′-Nucleotidases play a critical role in nucleotide pool balance and in the metabolism of nucleoside analogs such as gemcitabine and cytosine…”
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7
Impaired dimer assembly and decreased stability of naturally recurring R260C mutant A subunit for coagulation factor XIII
Published in Journal of biochemistry (Tokyo) (01-11-2012)“…Factor XIII (FXIII) consists of catalytic A subunits (FXIII-A) and carrier B subunits. Congenital FXIII deficiency is a severe bleeding disorder. We previously…”
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8
Characterization of Four Variant Forms of Human Propionyl-CoA Carboxylase Expressed in Escherichia coli
Published in The Journal of biological chemistry (29-07-2005)“…Propionyl-CoA carboxylase (PCC) is a biotin-dependent mitochondrial enzyme that catalyzes the conversion of propionyl-CoA to d-methylmalonyl-CoA. PCC consists…”
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9
Structure of the dimerized hormone-binding domain of a guanylyl- cyclase-coupled receptor
Published in Nature (London) (06-07-2000)“…The atrial natriuretic peptide (ANP) hormone is secreted by the heart in response to an increase in blood pressure. ANP exhibits several potent…”
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10
Crystal Structures of Polymorphic Prion Protein β1 Peptides Reveal Variable Steric Zipper Conformations
Published in Biochemistry (Easton) (16-06-2015)“…The pathogenesis of prion diseases is associated with the conformational conversion of normal, predominantly α-helical prion protein (PrPC) into a pathogenic…”
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11
An ultra-stable single-chain insulin analog resists thermal inactivation and exhibits biological signaling duration equivalent to the native protein
Published in The Journal of biological chemistry (05-01-2018)“…Thermal degradation of insulin complicates its delivery and use. Previous efforts to engineer ultra-stable analogs were confounded by prolonged cellular…”
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12
Structure-based stabilization of insulin as a therapeutic protein assembly via enhanced aromatic–aromatic interactions
Published in The Journal of biological chemistry (13-07-2018)“…Key contributions to protein structure and stability are provided by weakly polar interactions, which arise from asymmetric electronic distributions within…”
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13
Conformational diversity in prion protein variants influences intermolecular β-sheet formation
Published in The EMBO journal (06-01-2010)“…A conformational transition of normal cellular prion protein (PrP C ) to its pathogenic form (PrP Sc ) is believed to be a central event in the transmission of…”
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14
The Dual Regulatory Role of Amino Acids Leu480 and Gln481 of Prothrombin
Published in The Journal of biological chemistry (22-01-2016)“…Prothrombin (FII) is activated to α-thrombin (IIa) by prothrombinase. Prothrombinase is composed of a catalytic subunit, factor Xa (fXa), and a regulatory…”
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Targeting Bcl-2 based on the interaction of its BH4 domain with the inositol 1,4,5-trisphosphate receptor
Published in Biochimica et biophysica acta (01-06-2009)“…Bcl-2 is the founding member of a large family of apoptosis regulating proteins. Bcl-2 is a prime target for novel therapeutics because it is elevated in many…”
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16
Aggresome formation and pharmacogenetics: sulfotransferase 1A3 as a model system
Published in Biochemical and biophysical research communications (10-12-2004)“…A common cause for pharmacogenetic alteration in drug response is genetic variation in encoded amino acid sequence. We have used the catecholamine and…”
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A chimeric prokaryotic pentameric ligand-gated channel reveals distinct pathways of activation
Published in The Journal of general physiology (01-10-2015)“…Recent high resolution structures of several pentameric ligand-gated ion channels have provided unprecedented details of their molecular architecture. However,…”
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Thiopurine S-methyltransferase pharmacogenetics: variant allele functional and comparative genomics
Published in Pharmacogenetics and genomics (01-11-2005)“…Thiopurine S-methyltransferase (TPMT) catalyses the S-methylation of thiopurine drugs. Genetic polymorphisms for TPMT are a major factor responsible for large…”
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Residues required for phosphorylation of translation initiation factor eIF2α under diverse stress conditions are divergent between yeast and human
Published in The international journal of biochemistry & cell biology (01-02-2015)“…•eIF2α phosphorylation is the master signal of the cellular response to stress.•Four stress-activated kinases phosphorylate eIF2α on Ser51.•Phosphorylation…”
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Molecular modeling predicts structural changes in the A subunit of factor XIII caused by two novel mutations identified in a neonate with severe congenital factor XIII deficiency
Published in Thrombosis research (01-09-2012)“…Abstract Introduction Coagulation factor XIII (FXIII) is a fibrin-stabilizing factor, which contributes to hemostasis, wound healing, and maintenance of…”
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