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©The Author(s) 2025.
World J Gastroenterol. Jul 7, 2025; 31(25): 107893
Published online Jul 7, 2025. doi: 10.3748/wjg.v31.i25.107893
Published online Jul 7, 2025. doi: 10.3748/wjg.v31.i25.107893
Figure 4 Drug binding affinity to leucine-rich repeat-containing 19 drug and molecular docking.
A: Amuvatinib binding affinity to leucine-rich repeat-containing 19 (LRRC19) drug and molecular docking; B: Ciclopirox binding affinity to LRRC19 drug and molecular docking; C: Docetaxel binding affinity to LRRC19 drug and molecular docking; D: Elesclomol binding affinity to LRRC19 drug and molecular docking; E: JNK Inhibitor VIII binding affinity to LRRC19 drug and molecular docking; F: Piperlongumine binding affinity to LRRC19 drug and molecular docking; G: Sepantronium bromide binding affinity to LRRC19 drug and molecular docking; H: STF-62247 binding affinity to LRRC19 drug and molecular docking.
- Citation: Huang SS, Chen W, Vaishnani DK, Huang LJ, Li JZ, Huang SR, Li YZ, Xie QP. Leucine-rich repeat-containing protein 19 suppresses colorectal cancer by targeting cyclin-dependent kinase 6/E2F1 and remodeling the immune microenvironment. World J Gastroenterol 2025; 31(25): 107893
- URL: https://www.wjgnet.com/1007-9327/full/v31/i25/107893.htm
- DOI: https://dx.doi.org/10.3748/wjg.v31.i25.107893