7ELG
LC3B modificated with a covalent probe
Summary for 7ELG
| Entry DOI | 10.2210/pdb7elg/pdb |
| Descriptor | Microtubule-associated proteins 1A/1B light chain 3B, 2-methylidene-5-thiophen-2-yl-cyclohexane-1,3-dione, SULFATE ION, ... (4 entities in total) |
| Functional Keywords | inhibitor, complex, protein binding |
| Biological source | Homo sapiens (Human) |
| Total number of polymer chains | 1 |
| Total formula weight | 14781.89 |
| Authors | |
| Primary citation | Fan, S.,Yue, L.,Wan, W.,Zhang, Y.,Zhang, B.,Otomo, C.,Li, Q.,Lin, T.,Hu, J.,Xu, P.,Zhu, M.,Tao, H.,Chen, Z.,Li, L.,Ding, H.,Yao, Z.,Lu, J.,Wen, Y.,Zhang, N.,Tan, M.,Chen, K.,Xie, Y.,Otomo, T.,Zhou, B.,Jiang, H.,Dang, Y.,Luo, C. Inhibition of Autophagy by a Small Molecule through Covalent Modification of the LC3 Protein. Angew.Chem.Int.Ed.Engl., 60:26105-26114, 2021 Cited by PubMed Abstract: The autophagic ubiquitin-like protein LC3 functions through interactions with LC3-interaction regions (LIRs) of other autophagy proteins, including autophagy receptors, which stands out as a promising protein-protein interaction (PPI) target for the intervention of autophagy. Post-translational modifications like acetylation of Lys49 on the LIR-interacting surface could disrupt the interaction, offering an opportunity to design covalent small molecules interfering with the interface. Through screening covalent compounds, we discovered a small molecule modulator of LC3A/B that covalently modifies LC3A/B protein at Lys49. Activity-based protein profiling (ABPP) based evaluations reveal that a derivative molecule DC-LC3in-D5 exhibits a potent covalent reactivity and selectivity to LC3A/B in HeLa cells. DC-LC3in-D5 compromises LC3B lipidation in vitro and in HeLa cells, leading to deficiency in the formation of autophagic structures and autophagic substrate degradation. DC-LC3in-D5 could serve as a powerful tool for autophagy research as well as for therapeutic interventions. PubMed: 34590387DOI: 10.1002/anie.202109464 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.599 Å) |
Structure validation
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