Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Arch Biochem Biophys ; 404(2): 197-209, 2002 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-12147257

RESUMO

We have cloned and overexpressed a truncated, recombinant form of beta-carbonic anhydrase from Arabidopsis thaliana. The wild-type enzyme and two site-directed variants, H216N and Y212F, have been kinetically characterized both at steady state by stopped-flow spectrophotometry and at chemical equilibrium by (18)O isotope exchange methods. The wild-type enzyme has a maximal k(cat) for CO2 hydration of 320 ms(-1) and is rate limited by proton transfer involving two residues with apparent pK(a) values of 6.0 and 8.7. The mutant enzyme H216N has a maximal k(cat) at high pH that is 43% that of wild type, but is only 5% that of wild type at pH 7.0. (18)O exchange studies reveal that the effect of the mutations H216N or Y212F is primarily on proton transfer steps in the catalytic mechanism and not in the rate of CO2-HCO3- exchange. These results suggest that residues His-216 and Tyr-212 are both important for efficient proton transfer in A. thaliana carbonic anhydrase.


Assuntos
Arabidopsis/enzimologia , Anidrases Carbônicas/química , Anidrases Carbônicas/genética , Substituição de Aminoácidos , Proteínas de Arabidopsis/química , Proteínas de Arabidopsis/genética , Sítios de Ligação/fisiologia , Dióxido de Carbono/química , Catálise , Ativação Enzimática/fisiologia , Escherichia coli/genética , Concentração de Íons de Hidrogênio , Imidazóis/química , Isoenzimas/química , Isoenzimas/genética , Cinética , Peso Molecular , Mutagênese Sítio-Dirigida , Isótopos de Oxigênio , Prótons , Especificidade por Substrato , Zinco/análise
2.
J Biol Chem ; 277(43): 40397-402, 2002 Oct 25.
Artigo em Inglês | MEDLINE | ID: mdl-12183462

RESUMO

Entry of most primary human immunodeficiency virus, type 1 (HIV-1) isolates into their target cells requires the cellular receptor CD4 and the G protein-coupled chemokine coreceptor CCR5. An acidic, tyrosine-rich, and tyrosine-sulfated domain of the CCR5 amino terminus plays a critical role in the ability of CCR5 to serve as an HIV-1 coreceptor, and tyrosine-sulfated peptides based on this region physically associate with the HIV-1 envelope glycoprotein gp120 and slow HIV-1 entry into CCR5-expressing cells. Here we show that the same tyrosine-sulfated peptides, but not their unsulfated analogs, can restore the HIV-1 coreceptor activity of a CCR5 variant lacking residues 2-17 of its amino terminus. Additionally, these sulfated peptides restored the ability of this CCR5 variant to mobilize calcium in response to the chemokines macrophage inflammatory factors 1alpha and 1beta. These observations show that a tyrosine-sulfated region of the CCR5 amino terminus can function independently to mediate association of chemokines and the HIV-1 envelope glycoprotein with the remaining domains of CCR5.


Assuntos
Peptídeos/metabolismo , Receptores CCR5/metabolismo , Sulfatos/metabolismo , Tirosina/metabolismo , Sequência de Aminoácidos , Cálcio/metabolismo , HIV-1/metabolismo , Dados de Sequência Molecular , Receptores CCR5/química , Receptores CCR5/genética
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa