Structure of human cytidine deaminase bound to a potent inhibitor
about
Crystal structure of the APOBEC3G catalytic domain reveals potential oligomerization interfacesCrystal structure of the anti-viral APOBEC3G catalytic domain and functional implicationsCrystal structures of blasticidin S deaminase (BSD): implications for dynamic properties of catalytic zinc1.92 Angstrom Zinc-Free APOBEC3F Catalytic Domain Crystal StructureRNA-dependent oligomerization of APOBEC3G is required for restriction of HIV-1Crystal structure of APOBEC3A bound to single-stranded DNA reveals structural basis for cytidine deamination and specificity.Role of tyrosine 33 residue for the stabilization of the tetrameric structure of human cytidine deaminase.Contrasting behavior of conformationally locked carbocyclic nucleosides of adenosine and cytidine as substrates for deaminases.Delineation of the molecular mechanisms of nucleoside recognition by cytidine deaminase through virtual screening.New Frontiers in DruggabilityCDA directs metabolism of epigenetic nucleosides revealing a therapeutic window in cancerSynthesis and conformational analysis of locked carbocyclic analogues of 1,3-diazepinone riboside, a high-affinity cytidine deaminase inhibitor.Synthesis of conformationally locked carbocyclic 1,3-diazepinone nucleosides as inhibitors of cytidine deaminase.Human cytidine deaminase: a biochemical characterization of its naturally occurring variants.Breed and adaptive response modulate bovine peripheral blood cells' transcriptome.Validation and correction of Zn-CysxHisy complexes.Nanostructures of APOBEC3G support a hierarchical assembly model of high molecular mass ribonucleoprotein particles from dimeric subunits.NMR-based method of small changes reveals how DNA mutator APOBEC3A interacts with its single-stranded DNA substrate.Influence of the DNA sequence/length and pH on deaminase activity, as well as the roles of the amino acid residues around the catalytic center of APOBEC3F.Creation of zebularine-resistant human cytidine deaminase mutants to enhance the chemoprotection of hematopoietic stem cells.Crystal structure of Staphylococcus aureus tRNA adenosine deaminase TadA in complex with RNA.(deoxy)cytidine + H2O => (deoxy)uridine + NH4+ (CDA)O2 -independent demethylation of trimethylamine N-oxide by Tdm of Methylocella silvestris.Wobble inosine tRNA modification is essential to cell cycle progression in G(1)/S and G(2)/M transitions in fission yeast.Identification of a specific domain required for dimerization of activation-induced cytidine deaminase
P2860
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P2860
Structure of human cytidine deaminase bound to a potent inhibitor
description
2005 nî lūn-bûn
@nan
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Structure of human cytidine deaminase bound to a potent inhibitor
@ast
Structure of human cytidine deaminase bound to a potent inhibitor
@en
Structure of human cytidine deaminase bound to a potent inhibitor
@en-gb
Structure of human cytidine deaminase bound to a potent inhibitor
@nl
type
label
Structure of human cytidine deaminase bound to a potent inhibitor
@ast
Structure of human cytidine deaminase bound to a potent inhibitor
@en
Structure of human cytidine deaminase bound to a potent inhibitor
@en-gb
Structure of human cytidine deaminase bound to a potent inhibitor
@nl
prefLabel
Structure of human cytidine deaminase bound to a potent inhibitor
@ast
Structure of human cytidine deaminase bound to a potent inhibitor
@en
Structure of human cytidine deaminase bound to a potent inhibitor
@en-gb
Structure of human cytidine deaminase bound to a potent inhibitor
@nl
P356
P1476
Structure of human cytidine deaminase bound to a potent inhibitor
@en
P2093
Gregory L Verdine
Sang J Chung
P304
P356
10.1021/JM0496279
P407
P577
2005-02-01T00:00:00Z