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Target subfamilies

Bioinformatics Discovery of Target Subfamilies with Conserved Molecular Recognition 145... [Pg.145]

Cheminformatics Discovery of Potential Ligands of Target Subfamilies 1149... [Pg.149]

Knowledge-based Combinatorial Library Design Strategies within Homogenous Target Subfamilies... [Pg.155]

This family contains more than 40 members subdivided into five subfamilies [4]. The NCS have been involved in phototransduction and regulation of neurotransmitter release. The NCS have two pairs of EF-hands and, unlike CaM and SI00 proteins, possess a consensus myristoylation sequence at the N-terminal responsible for the targeting of the NCS to the membrane. [Pg.293]

A subfamily of Rho proteins, the Rnd family of small GTPases, are always GTP-bound and seem to be regulated by expression and localization rather than by nucleotide exchange and hydrolysis. Many Rho GTPase effectors have been identified, including protein and lipid kinases, phospholipase D and numerous adaptor proteins. One of the best characterized effector of RhoA is Rho kinase, which phosphorylates and inactivates myosin phosphatase thereby RhoA causes activation of actomyosin complexes. Rho proteins are preferred targets of bacterial protein toxins ( bacterial toxins). [Pg.1141]

The carboxyl proteases are so called because they have two catalytically essential aspartate residues. They were formerly called acid proteases because most of them are active at low pH. The best-known member of the family is pepsin, which has the distinction of being the first enzyme to be named (in 1825, by T. Schwann). Other members are chymosin (rennin) cathepsin D Rhizopus-pepsin (from Rhizopus chinensis) penicillinopepsin (from Penicillium janthinel-lum) the enzyme from Endothia parasitica and renin, which is involved in the regulation of blood pressure. These constitute a homologous family, and all have an Mr of about 35 000. The aspartyl proteases have been thrown into prominence by the discovery of a retroviral subfamily, including one from HIV that is the target of therapy for AIDS. These are homodimers of subunits of about 100 residues.156,157 All the aspartyl proteases contain the two essential aspartyl residues. Their reaction mechanism is the most obscure of all the proteases, and there are no simple chemical models for guidance. [Pg.1]


See other pages where Target subfamilies is mentioned: [Pg.139]    [Pg.157]    [Pg.139]    [Pg.157]    [Pg.71]    [Pg.246]    [Pg.401]    [Pg.743]    [Pg.1163]    [Pg.1245]    [Pg.4]    [Pg.34]    [Pg.411]    [Pg.102]    [Pg.375]    [Pg.67]    [Pg.151]    [Pg.84]    [Pg.221]    [Pg.480]    [Pg.74]    [Pg.96]    [Pg.90]    [Pg.128]    [Pg.155]    [Pg.182]    [Pg.183]    [Pg.506]    [Pg.293]    [Pg.283]    [Pg.248]    [Pg.249]    [Pg.432]    [Pg.344]    [Pg.455]    [Pg.108]    [Pg.9]    [Pg.128]    [Pg.457]   
See also in sourсe #XX -- [ Pg.145 , Pg.151 , Pg.157 ]




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Knowledge-based Combinatorial Library Design Strategies within Homogenous Target Subfamilies

Subfamilies

Target Genes of the NR4A Subfamily

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