6P3W

Crystal structure of the Cyclin A-CDK2-ORC1 complex

6P3W の概要

• エントリーDOI: 10.2210/pdb6p3w/pdb
• 分子名称: Cyclin-dependent kinase 2, Cyclin-A2, ORC1 Peptide, ... (5 entities in total)
• 機能のキーワード: inhibitor complex, cell cycle
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 129919.14

構造登録者

Wang, B.,Song, J. (登録日: 2019-05-24, 公開日: 2019-07-31, 最終更新日: 2024-04-03)

主引用文献

Wang, B.,Song, J.
Structural basis for the ORC1-Cyclin A association.
Protein Sci., 28:1727-1733, 2019

PubMed Abstract: Progression of cell cycle is regulated by sequential expression of cyclins, which associate with distinct cyclin kinases to drive the transition between different cell cycle phases. The complex of Cyclin A with cyclin-dependent kinase 2 (CDK2) controls the DNA replication activity through phosphorylation of a set of chromatin factors, which critically influences the S phase transition. It has been shown that the direct interaction between the Cyclin A-CDK2 complex and origin recognition complex subunit 1 (ORC1) mediates the localization of ORC1 to centrosomes, where ORC1 inhibits cyclin E-mediated centrosome reduplication. However, the molecular basis underlying the specific recognition between ORC1 and cyclins remains elusive. Here we report the crystal structure of Cyclin A-CDK2 complex bound to a peptide derived from ORC1 at 2.54 å resolution. The structure revealed that the ORC1 peptide interacts with a hydrophobic groove, termed cyclin binding groove (CBG), of Cyclin A via a KXL motif. Distinct from other identified CBG-binding sequences, an arginine residue flanking the KXL motif of ORC1 inserts into a neighboring acidic pocket, contributing to the strong ORC1-Cyclin A association. Furthermore, structural and sequence analysis of cyclins reveals divergence on the ORC1-binding sites, which may underpin their differential ORC1-binding activities. This study provides a structural basis of the specific ORC1-cyclins recognition, with implication in development of novel inhibitors against the cyclin/CDK complexes.

PubMed: 31309634
DOI: 10.1002/pro.3689

実験手法

X-RAY DIFFRACTION (2.54 Å)