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[磷酸核糖焦磷酸合成酶超活性]

[PRPP synthetase superactivity].

作者信息

Fujimori S

机构信息

Second Department of Internal Medicine, Teikyo University School of Medicine.

出版信息

Nihon Rinsho. 1996 Dec;54(12):3309-14.

PMID:8976111
Abstract

Phosphoribosylpyrophosphate(PRPP) synthetase(PRS) catalyzes the formation of PRPP from ATP and ribose-5-phosphate. PRPP is an important substrate for the synthesis of purine, pyrimidine, and pyridine dinucleotides. Human PRS exists as complex aggregates composed of the 34 kDa catalytic subunits(PRS1 and PRS2) and other 39 kDa component designated PRPP synthetase-associated protein (PAP39). PRS superactivity is an X-chromosome linked disorder, characterized by gout and uric acid overproduction resulting from accelerated synthesis of PRPP and purine nucleotides. Among the nearly 30 affected families identified to date, there are several families in which PRS superactivity with purine nucleotide feedback resistance are associated with neurodevelopmental abnormalities in addition to hyperuricemia and gout. Different nucleotide substitutions in the PRPS1 gene encoding PRS1 have identified in six unrelated affected families with purine nucleotide feedback-resistant PRS superactivity.

摘要

磷酸核糖焦磷酸(PRPP)合成酶(PRS)催化由ATP和5-磷酸核糖形成PRPP。PRPP是嘌呤、嘧啶和吡啶二核苷酸合成的重要底物。人PRS以由34 kDa催化亚基(PRS1和PRS2)和另一种39 kDa组分(称为PRPP合成酶相关蛋白(PAP39))组成的复合聚集体形式存在。PRS超活性是一种X染色体连锁疾病,其特征是痛风和尿酸过度产生,这是由PRPP和嘌呤核苷酸合成加速所致。在迄今确定的近30个受影响家族中,有几个家族中,具有嘌呤核苷酸反馈抗性的PRS超活性除了伴有高尿酸血症和痛风外,还与神经发育异常有关。在六个患有嘌呤核苷酸反馈抗性PRS超活性的无关受影响家族中,已鉴定出编码PRS1的PRPS1基因中的不同核苷酸取代。

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