Prokineticin receptors in GtoPdb v.2023.1

R. Hills, Adam J. Pawson, P. Rondard, O. Sbai, Q. Zhou
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Abstract

Prokineticin receptors, PKR1 and PKR2 (provisional nomenclature as recommended by NC-IUPHAR [26]) respond to the cysteine-rich 81-86 amino-acid peptides prokineticin-1 (also known as endocrine gland-derived vascular endothelial growth factor, mambakine) and prokineticin-2 (protein Bv8 homologue). An orthologue of PROK1 from black mamba (Dendroaspis polylepis) venom, mamba intestinal toxin 1 (MIT1, [71]) is a potent, non-selective agonist at prokineticin receptors [46], while Bv8, an orthologue of PROK2 from amphibians (Bombina sp., [49]), is equipotent at recombinant PKR1 and PKR2 [53], and has high potency in macrophage chemotaxis assays, which are lost in PKR1-null mice.
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促动素受体在GtoPdb v.2023.1
促运动素受体PKR1和PKR2 (NC-IUPHAR推荐的临时命名[26])对富含半胱氨酸的81-86氨基酸肽prokinetic -1(也称为内分泌腺源性血管内皮生长因子,mambakine)和prokinetic -2(蛋白Bv8同源物)有反应。黑曼巴(Dendroaspis polylepis)毒液中PROK1的同源物,曼巴肠毒素1 (MIT1,[71])是促动素受体的有效非选择性激动剂[46],而两栖动物(Bombina sp.,[49])中PROK2的同源物Bv8在重组PKR1和PKR2中具有同等效力[53],并且在巨噬细胞趋化试验中具有高效力,在PKR1缺失的小鼠中缺失。
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