Comparison of the specificity of interaction of cellular and viral zinc-binding domains with 2-mercaptobenzamide thioesters
- Author
- JENKINS, Lisa M. Miller1 ; DURELL, Stewart R2 ; MAYNARD, Andrew T3 ; STAHL, Stephen J4 ; INMAN, John K5 ; APPELLA, Ettore2 ; LEGAULT, Pascale1 6 ; OMICHINSKI, James G1 6 7
[1] Departments of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia, 30602, United States
[2] Laboratory of Cell Biology, NCI, National Institutes of Health, Bethesda, Maryland 20892, United States
[3] Computational Chemistry and Informatics, Icagen, Research Triangle Park, North Carolina 27709, United States
[4] Protein Expression Laboratory, NIAMSD, National Institutes of Health, Bethesda, Maryland 20892, United States
[5] Laboratory of Immunology, NIAID, National Institutes of Health, Bethesda, Maryland 20892, United States
[6] Département de Biochimie, Université de Montréal, Montréal, Québec H3C 3J7, Canada
[7] Department of Chemistry, University of Georgia, Athens, Georgia, 30602, United States - Source
Journal of the American Chemical Society. 2006, Vol 128, Num 36, pp 11964-11976, 13 p ; ref : 62 ref
- CODEN
- JACSAT
- ISSN
- 0002-7863
- Scientific domain
- Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide nucléique Amine Aminoacide soufré Benzamide dérivé Complexation Composé benzénique Criblage Cystéine DNA Effet stérique Etude comparative Interaction moléculaire Protein kinase C Protéine Réactivité chimique Souris Spectrométrie RMN Spectrométrie UV visible Spectrométrie UV Spectrométrie visible Stabilité chimique Structure moléculaire Sélectivité Thioester Tumeur Virus HIV1 Zinc Enzyme Lentivirus Mammalia Métal transition Retroviridae Rodentia Transferases Vertebrata Virus immunodéficience humaine Virus
- Keyword (en)
- Nucleic acid Amine Sulfur containing aminoacid Benzamide derivatives Complexation Benzenic compound Screening Cysteine DNA Steric effect Comparative study Molecular interaction Protein kinase C Protein Chemical reactivity Mouse NMR spectrometry Ultraviolet visible spectrometry Ultraviolet spectrometry Visible spectrometry Chemical stability Molecular structure Selectivity Thioester Tumor HIV-1 virus Zinc Enzyme Lentivirus Mammalia Transition metal Retroviridae Rodentia Transferases Vertebrata Human immunodeficiency virus Virus
- Keyword (es)
- Acido nucleico Amina Aminoácido azufrado Benzamida derivado Complexación Compuesto bencénico Cernido Cisteína DNA Efecto estérico Estudio comparativo Interacción molecular Protein kinase C Proteína Reactividad química Ratón Espectrometría RMN Espectrometría UV visible Espectrometría UV Espectrometría visible Estabilidad química Estructura molecular Selectividad Tioester Tumor HIV-1 virus Zinc Enzima Lentivirus Mammalia Metal transición Retroviridae Rodentia Transferases Vertebrata Human immunodeficiency virus Virus
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C02 Inorganic chemistry and origins of life / 001C02B Preparations and properties / 001C02B04 Coordination compounds
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A02 Analytical, structural and metabolic biochemistry / 002A02C Nucleic acids / 002A02C03 Dna, deoxyribonucleoproteins
- Discipline
- Analytical, structural and metabolic biochemistry General chemistry and physical chemistry Mineral chemistry and origin of life
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18099302
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1021/ja063329e 
https://dx.doi.org/10.1021/ja063329e
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