5W6O

Choline Kinase Alpha in Complex with TCD-717

5W6O の概要

• エントリーDOI: 10.2210/pdb5w6o/pdb
• 分子名称: Choline kinase alpha, 1,1'-[[1,1'-biphenyl]-4,4'-diylbis(methylene)]bis{4-[(4-chlorophenyl)(methyl)amino]quinolin-1-ium}, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, ... (5 entities in total)
• 機能のキーワード: enzyme, inhibitor, drug, transferase-inhibitor complex, transferase/inhibitor
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 91002.00

構造登録者

Kall, S.K.,Lavie, A. (登録日: 2017-06-16, 公開日: 2018-02-14, 最終更新日: 2024-12-25)

主引用文献

Kall, S.L.,Delikatny, E.J.,Lavie, A.
Identification of a Unique Inhibitor-Binding Site on Choline Kinase alpha.
Biochemistry, 57:1316-1325, 2018

PubMed Abstract: Choline kinase α (ChoKα) is an enzyme that is upregulated in many types of cancer and has been shown to be tumorigenic. As such, it makes a promising target for inhibiting tumor growth. Though there have been several inhibitors synthesized for ChoKα, not all of them demonstrate the same efficacy in vivo, though the reasons behind this difference in potency are not clear. One particular inhibitor, designated TCD-717, has recently completed phase I clinical trials. Cell culture and in vitro studies support the powerful inhibitory effect TCD-717 has on ChoKα, but an examination of the inhibitor's interaction with the ChoKα enzyme has been missing prior to this work. Here we detail the 2.35 Å structure of ChoKα in complex with TCD-717. Examination of this structure in conjunction with kinetic assays reveals that TCD-717 does not bind directly in the choline pocket as do previously characterized ChoKα inhibitors, but rather in a proximal but novel location near the surface of the enzyme. The unique binding site identified for TCD-717 lends insight for the future design of more potent in vivo inhibitors for ChoKα.

PubMed: 29389115
DOI: 10.1021/acs.biochem.7b01257

実験手法

X-RAY DIFFRACTION (2.35 Å)