5Y80

Complex structure of cyclin G-associated kinase with gefitinib

Summary for 5Y80

• Entry DOI: 10.2210/pdb5y80/pdb
• Descriptor: Cyclin-G-associated kinase, NANOBODY, Gefitinib, ... (4 entities in total)
• Functional Keywords: kinase, complex, transferase-immune system complex, transferase/immune system
• Biological source: Homo sapiens (Human); More
• Total number of polymer chains: 2
• Total formula weight: 52741.30

Authors

Ohbayashi, N.,Murayama, K.,Kato-Murayama, M.,Shirouzu, M. (deposition date: 2017-08-18, release date: 2018-08-29, Last modification date: 2024-10-23)

Primary citation

Ohbayashi, N.,Murayama, K.,Kato-Murayama, M.,Kukimoto-Niino, M.,Uejima, T.,Matsuda, T.,Ohsawa, N.,Yokoyoma, S.,Nojima, H.,Shirouzu, M.
Structural Basis for the Inhibition of Cyclin G-Associated Kinase by Gefitinib.
ChemistryOpen, 7:721-727, 2018

PubMed Abstract: Gefitinib is the molecular target drug for advanced non-small-cell lung cancer. The primary target of gefitinib is the positive mutation of epidermal growth factor receptor, but it also inhibits cyclin G-associated kinase (GAK). To reveal the molecular bases of GAK and gefitinib binding, structure analyses were conducted and determined two forms of the gefitinib-bound nanobody⋅GAK kinase domain complex structures. The first form, GAK_1, has one gefitinib at the ATP binding pocket, whereas the second form, GAK_2, binds one each in the ATP binding site and a novel binding site adjacent to the activation segment C-terminal helix, a unique element of the Numb-associated kinase family. In the novel binding site, gefitinib binds in the hydrophobic groove around the activation segment, disrupting the conserved hydrogen bonds for the catalytic activity. These structures suggest possibilities for the development of selective GAK inhibitors for viral infections, such as the hepatitis C virus.

PubMed: 30214852
DOI: 10.1002/open.201800177

Experimental method

X-RAY DIFFRACTION (2.5 Å)