Noyon M Rafiul O K, Hematian Shabnam
Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, Greensboro, NC 27402, United States.
Trends Chem. 2024 Nov;6(11):649-655. doi: 10.1016/j.trechm.2024.09.002. Epub 2024 Oct 22.
BURP domain peptide cyclases, or BpCs (an abbreviation we recommend in this opinion), are an emerging class of copper enzymes which catalyze the oxidative macrocyclization of peptides in plants. A close examination of their novel protein fold, along with the unique dicopper active site that meticulously controls crosslinking within peptides, highlights how nature exploits intricate mechanistic strategies to achieve diverse functionalities. Here, we summarize recent discoveries regarding the sequence, structure, function, and proposed chemistry of BpCs. We also present plausible mechanistic ideas and recommend important structural considerations that could advance investigations and discussions surrounding their reactivity and underlying mechanisms.
BURP结构域肽环化酶,即BpC(我们在此观点中推荐使用的缩写),是一类新兴的铜酶,可催化植物中肽的氧化大环化反应。对其新颖的蛋白质折叠结构以及精心控制肽内交联的独特双铜活性位点进行仔细研究,凸显了自然界如何利用复杂的机制策略来实现多样的功能。在此,我们总结了关于BpC的序列、结构、功能及推测化学性质的最新发现。我们还提出了合理的机制观点,并推荐了重要的结构考量因素,这些因素可能推动围绕其反应性及潜在机制的研究和讨论。