Program in Biophysics (A.G.B., E.E.S.) and Departments of Medicinal Chemistry and Pharmacology (E.E.S.), University of Michigan, Ann Arbor, Michigan; and Department of Drug Metabolism and Pharmacokinetics (R.H.T.) and Department of Discovery Chemistry (X.W.), Genentech Inc., South San Francisco, California.
Program in Biophysics (A.G.B., E.E.S.) and Departments of Medicinal Chemistry and Pharmacology (E.E.S.), University of Michigan, Ann Arbor, Michigan; and Department of Drug Metabolism and Pharmacokinetics (R.H.T.) and Department of Discovery Chemistry (X.W.), Genentech Inc., South San Francisco, California
Drug Metab Dispos. 2020 Feb;48(2):86-92. doi: 10.1124/dmd.119.089607. Epub 2019 Nov 22.
The human cytochrome P450 1A1 (CYP1A1) is well known for chemical activation of procarcinogens and often has a substrate scope of small and highly planar compounds. Substrates deviating from these characteristics are certainly known, but how these larger and nonplanar substrates are accommodated and oriented within the CYP1A1 active site is not understood. Herein a new X-ray structure of CYP1A1 bound to the pan-Pim kinase inhibitor GDC-0339 reveals how the CYP1A1 active site cavity is reconfigured to bind larger and nonplanar compounds. The shape and size of the cavity are controlled by structural elements in the active site roof, with major changes in the conformation of the F helix break and relocation of Phe224 from the active site to the protein surface. This altered CYP1A1 active site architecture is consistent with the proposed mechanism for CYP1A1 generation of an unusual aminoazepane-rearranged metabolite for this substrate. SIGNIFICANCE STATEMENT: Cytochrome P450 1A1 metabolizes drugs, procarcinogens, and toxins and although previous structures have revealed how its stereotypical planar, aromatic compounds are accommodated in the CYP1A1 active site, this is not the case for flexible and nonplanar compounds. The current work determines the X-ray structure of CYP1A1 with such a flexible, nonplanar Pim kinase inhibitor, revealing significant modification of the CYP1A1 roof that accommodate this preclinical candidate and support an unusual intramolecular rearrangement reaction.
人细胞色素 P450 1A1(CYP1A1)以化学激活前致癌物而闻名,通常具有小分子和高度平面化合物的底物范围。偏离这些特征的底物是已知的,但这些较大和非平面底物如何在 CYP1A1 活性部位内被容纳和定向还不清楚。本文报道了 CYP1A1 与泛 Pim 激酶抑制剂 GDC-0339 结合的新 X 射线结构,揭示了 CYP1A1 活性部位腔如何重新配置以结合较大和非平面化合物。腔的形状和大小由活性部位屋顶中的结构元件控制,F 螺旋的构象发生重大变化,断裂并将 Phe224 从活性部位重新定位到蛋白质表面。这种改变的 CYP1A1 活性部位结构与 CYP1A1 生成这种底物的不寻常氨基氮杂环庚烷重排代谢物的提出机制一致。意义陈述:细胞色素 P450 1A1 代谢药物、前致癌物和毒素,尽管以前的结构已经揭示了其典型的平面、芳香化合物如何在 CYP1A1 活性部位中被容纳,但对于灵活和非平面化合物则不是这样。目前的工作确定了具有这种灵活、非平面 Pim 激酶抑制剂的 CYP1A1 的 X 射线结构,揭示了 CYP1A1 屋顶的显著修饰,以容纳这种临床前候选物,并支持不寻常的分子内重排反应。