拟杆菌二肽基肽酶III催化肽水解的机理

IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY Croatica Chemica Acta Pub Date : 2018-06-04 DOI:10.5562/CCA3343
M. Tomin, A. Tomić, B. Kovačević, S. Tomić
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引用次数: 1

摘要

二肽基肽酶III (DPP III)是一种锌依赖性肽酶,可将二肽从其底物的n端切割下来。前人对人DPP III的研究表明其反应机制与热溶素相似。由于活性位点在DPP III家族中保守,因此确定的Bacteroides thetaiotaomicron DPP III (BtDPP III)的机制与hDPP III非常相似也就不足为奇了。然而,模型中的氢键网络与人类同源物中的氢键网络略有不同,这导致了两种被提出的途径。计算得到的吉布斯活化能为90.1 kJ mol-1,大于优选底物arg2 -2-萘酰胺在室温下的活化能(69 kJ mol-1),表明在计算中处理整个DPP III酶的重要性。
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The Mechanism of Peptide Hydrolysis Catalysed by Dipeptidyl Peptidase III from Bacteroides thetaiotaomicron
Dipeptidyl peptidase III (DPP III) is a zinc- dependent peptidase that cleaves dipeptides off of N-termini of its substrates. Previous studies on human DPP III reveal a reaction mechanism similar to that of thermolysin. Since the active site is conserved within the DPP III family, it is not surprising that the mechanism determined for Bacteroides thetaiotaomicron DPP III (BtDPP III) closely resembles that of hDPP III. However, the hydrogen bond network within the model differs slightly from that in the human ortholog, which results in two proposed pathways. The calculated Gibbs activation energy of 90.1 kJ mol–1 is larger than the one calculated from kinetic data for the preferred substrate Arg2-2-naphthylamide at room temperature (69 kJ mol–1), suggesting the importance of treating the whole DPP III enzyme in the calculations.
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来源期刊
Croatica Chemica Acta
Croatica Chemica Acta 化学-化学综合
CiteScore
0.60
自引率
0.00%
发文量
3
审稿时长
18 months
期刊介绍: Croatica Chemica Acta (Croat. Chem. Acta, CCA), is an international journal of the Croatian Chemical Society publishing scientific articles of general interest to chemistry.
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