The synthesis of inhibitors for processing proteinases and their action on the Kex2 proteinase of yeast.
about
The neuroendocrine polypeptide 7B2 is an endogenous inhibitor of prohormone convertase PC2Characterization of structural determinants and molecular mechanisms involved in pro-stromelysin-3 activation by 4-aminophenylmercuric acetate and furin-type convertasesProtection from anthrax toxin-mediated killing of macrophages by the combined effects of furin inhibitors and chloroquine.Proprotein convertase inhibition results in decreased skin cell proliferation, tumorigenesis, and metastasisFurin overexpression suppresses tumor growth and predicts a better postoperative disease-free survival in hepatocellular carcinomaProteolysis during tumor cell extravasation in vitro: metalloproteinase involvement across tumor cell types.Analysis of cathepsin and furin proteolytic enzymes involved in viral fusion protein activation in cells of the bat reservoir host.Increased furin activity enhances the malignant phenotype of human head and neck cancer cellsInhibition of prohormone convertases PC1/3 and PC2 by 2,5-dideoxystreptamine derivatives.Inhibition of proprotein convertases: approaches to block squamous carcinoma development and progression.On the cutting edge of proprotein convertase pharmacology: from molecular concepts to clinical applications.Polyarginine peptide IND-1 enhances recombinant human bone morphogenetic protein-2 yield in mammalian cells.Selective and potent furin inhibitors protect cells from anthrax without significant toxicityProteolytic cleavage of wild type and mutants of the F protein of human parainfluenza virus type 3 by two subtilisin-like endoproteases, furin and Kex2.Effects of L- and D-REKR amino acid-containing peptides on HIV and SIV envelope glycoprotein precursor maturation and HIV and SIV replication.Endocytic delivery of intramolecularly quenched substrates and inhibitors to the intracellular yeast Kex2 protease1.Comparative study of the binding pockets of mammalian proprotein convertases and its implications for the design of specific small molecule inhibitors.Synthetic small-molecule prohormone convertase 2 inhibitors.Activation of MMP-2 in response to vascular injury is mediated by phosphatidylinositol 3-kinase-dependent expression of MT1-MMP.Furin-independent pathway of membrane type 1-matrix metalloproteinase activation in rabbit dermal fibroblasts.Homology modelling of the catalytic domain of human furin. A model for the eukaryotic subtilisin-like proprotein convertases.Subtilisin-like proprotein convertase activity is necessary for left-right axis determination in Xenopus neurula embryos.
P2860
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P2860
The synthesis of inhibitors for processing proteinases and their action on the Kex2 proteinase of yeast.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
The synthesis of inhibitors fo ...... the Kex2 proteinase of yeast.
@en
The synthesis of inhibitors fo ...... the Kex2 proteinase of yeast.
@nl
type
label
The synthesis of inhibitors fo ...... the Kex2 proteinase of yeast.
@en
The synthesis of inhibitors fo ...... the Kex2 proteinase of yeast.
@nl
prefLabel
The synthesis of inhibitors fo ...... the Kex2 proteinase of yeast.
@en
The synthesis of inhibitors fo ...... the Kex2 proteinase of yeast.
@nl
P2093
P2860
P356
P1433
P1476
The synthesis of inhibitors fo ...... the Kex2 proteinase of yeast.
@en
P2093
P2860
P356
10.1042/BJ2930075
P407
P478
293 ( Pt 1)
P577
1993-07-01T00:00:00Z