Titlebook: Reversible Protein Phosphorylation in Cell Regulation; R. L. Khandelwal,J. H. Wang Book 1993 Springer Science+Business Media Dordrecht 199

HAVEN

書目名稱Reversible Protein Phosphorylation in Cell Regulation影響因子(影響力)




書目名稱Reversible Protein Phosphorylation in Cell Regulation影響因子(影響力)學(xué)科排名




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書目名稱Reversible Protein Phosphorylation in Cell Regulation讀者反饋




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Transfusion

Mutagenesis of the catalytic subunit of rabbit muscle protein phosphatase-1. These results indicate that the catalytic mechanism of ppase-1 is different from that of the protein tyrosine phosphatases which involve a cysteinyl phosphate intermediate. (Mol Cell Biochem . 113–119, 1993)

健壯

The phosphorylation of stathmin by MAP kinasestathmin kinases detected in PC12 cells after stimulation by nerve growth factor (NGF). The results suggest that MAP kinases are the enzymes responsible for increasing the level of phosphorylation of Ser-25, which has been observed previously in PC12 cells following stimulation by NGF. (Mol Cell Biochem . 151–156, 1993)

最有利

Autophosphorylation: a salient feature of protein kinasesffects the functional properties of most protein kinases. Members of the protein kinase family exhibit diversity in the characteristics and functions of autophosphorylation, but certain common themes are emerging. (Mol Cell Biochem . 51–70, 1993)

有法律效應(yīng)

Vulnerable

Negligible

碌碌之人

Development and characterization of fluorescently-labeled myosin light chain kinase calmodulin-bindies responsible for binding calmodulin. These regions are known as calmodulin-binding domains and in many cases are contained within sequences that are short enough to be synthesized by solid-phase techniques. The ability to chemically-synthesize target enzyme calmodulin-binding domains has permitted

Additive

政府

Expression of cGMP-dependent protein kinase in ,ic cell lines but so far not in prokaryotic cells. Three vectors were constructed for the expression of Iα cGMP kinase in .. Transformation with the pET3a/cgk vector which uses the T7 RNA polymerase/promotor system resulted in efficient accumulation of cGMP kinase. Most of the protein was in an inso