7MS7

Structure of USP5 zinc-finger ubiquitin binding domain co-crystallized with (5-((4-(4-chlorophenyl)piperidin-1-yl)sulfonyl)picolinoyl)glycine

Summary for 7MS7

Entry DOI	10.2210/pdb7ms7/pdb
Descriptor	Ubiquitin carboxyl-terminal hydrolase 5, ZINC ION, N-{5-[4-(4-chlorophenyl)piperidine-1-sulfonyl]pyridine-2-carbonyl}glycine, ... (6 entities in total)
Functional Keywords	usp5, ubiquitin, usp, ubiquitin specific protease, hydrolase, hydrolase-inhibitor complex, hydrolase/inhibitor
Biological source	Homo sapiens (Human)
Total number of polymer chains	2
Total formula weight	27760.23
Authors	Mann, M.K.,Zepeda-Velazquez, C.A.,Alvarez, H.G.,Dong, A.,Kiyota, T.,Aman, A.,Arrowsmith, C.H.,Al-Awar, R.,Harding, R.J.,Schapira, M. (deposition date: 2021-05-10, release date: 2021-06-09, Last modification date: 2023-10-18)
Primary citation	Mann, M.K.,Zepeda-Velazquez, C.A.,Gonzalez-Alvarez, H.,Dong, A.,Kiyota, T.,Aman, A.M.,Loppnau, P.,Li, Y.,Wilson, B.,Arrowsmith, C.H.,Al-Awar, R.,Harding, R.J.,Schapira, M. Structure-Activity Relationship of USP5 Inhibitors. J.Med.Chem., 64:15017-15036, 2021 Cited by PubMed: 34648286 DOI: 10.1021/acs.jmedchem.1c00889 PDB entries with the same primary citation
Experimental method	X-RAY DIFFRACTION (1.45 Å)

Structure validation