Kang H, Yang H-S, Ki AY, Ko S-B, Kim KW, Shim CY, Kim K, Choi H-J*, Chung KY*. Conformational dynamics and functional implications of phosphorylated beta-arrestins.

Lee S-M, Jeong Y, Simms J, Warner ML, Poyner DR, Chung KY, Pioszak AA. Calcitonin receptor N-glycosylation enhances peptide hormone affinity by controlling receptor dynamics.

Ghosh E, Dwivedi H, Baidya M, Srivastava A, Kumari P, Stepniewski T, Kim HR, Lee M-H, Gstel J, Chaturvedi M, Roy D, Pandey S, Maharana J, Guixà‐Gonzàlez R, Luttrell LM, Chung KY, Dutta S, Selent J, Shukla AK. Conformational sensors and domain-swapping reveal structural and functional differences between the beta-arrestin isoforms.

Du Y, Duc NM, Rasmussen SGF, Hilger D, Kubiak X, Wang L, Bohon J, Kim HR, Wegrecki M, Asuru A, Jeong KM, Lee JM, Chance MR, Lodowski DT*, Kobilka BK*, Chung KY*. Assembly of a GPCR-G protein complex.

Park JY, Qu C, Li R, Yang F, Tian Z, Shen Y, Cai B, Yun Y, Sun J*, Chung KY*. Structural mechanism of the arrestin-3/JNK3 interaction.

Yang H-S, Sun N, Zhao X, Kim HR, Park H-J, Kim K-M*, Chung KY*. Role of helix 8 in dopamine receptor signaling.

Ki AY, Park JY, Chung KY*. Conformational changes of JNK3 splice variants upon ATP binding.

Lisnyansky Bar-El M, Lee SY, Ki AY, Kapelushnik N, Loewenstein A, Chung KY, Schneidman-Duhovny D, Giladi M, Newman H, Haitin Y. Structural characterization of full-length human dehydrodolichyl diphosphate synthase using an integrative computational and experimental approach.

Ham S, Kim H, Hwang S, Kang H, Yun SP, Kim S, Kim D, Kwon HS, Lee YS, Cho M, Shin HM, Choi H, Chung KY, Ko HS, Lee GH, Lee Y. Cell-Based Screen Using Amyloid Mimic β23 Expression Identifies Peucedanocoumarin III as a Novel Inhibitor of α-Synuclein and Huntingtin Aggregates.

Park BB, Choi JW, Park Y, Choi D, Paek J, Kim HJ, Son S-Y, Mushtaq AU, Shin H, Kim SH, Zhou Y, Lim TH, Park JY, Baek J-Y, Kim K, Kwon H, Son SH, Chung KY, Jeong H-J, Kim H-M, Jung WY, Lee K, Lee K, Byun Y, Jeon YH. Structure-activity relationships of Baicalein and its analogs as novel TSLP inhibitors.