First author:
Seattle Structural Genomics Center for Infectious Disease (SSGCID) Seattle Structural Genomics Center for Infectious Disease Resolution: 1.60 Å R/Rfree: 0.16/0.20
X-ray diffraction data for the Crystal Structure of Dihydrofolate reductase (DHFR) from Mycobacterium ulcerans Agy99 in complex with NADP and inhibitor SDDC-0001914, orthorhombic crystal from
X-ray diffraction data for the Crystal Structure of Dihydrofolate reductase (DHFR) from Mycobacterium ulcerans Agy99 in complex with NADP and inhibitor SDDC-0001913, tetragonal crystal from
X-ray diffraction data for the Crystal Structure of Dihydrofolate reductase (DHFR) from Mycobacterium ulcerans Agy99 in complex with NADP and inhibitor SDDC-0001912
X-ray diffraction data for the Crystal Structure of Dihydrofolate reductase (DHFR) from Mycobacterium ulcerans Agy99 in complex with NADP and inhibitor SDDC-0001580
X-ray diffraction data for the Crystal Structure of Dihydrofolate reductase (DHFR) from Mycobacterium ulcerans Agy99 in complex with NADP and inhibitor SDDC-0001914, tetragonal crystal from
X-ray diffraction data for the Crystal Structure of deoxyuridine 5'-triphosphate nucleotidohydrolase from Rickettsia prowazekii str. Madrid E in complex with 2'-deoxyuridine 5'-monophoephate (dUMP)
First author:
Seattle Structural Genomics Center for Infectious Disease (SSGCID) Seattle Structural Genomics Center for Infectious Disease Resolution: 2.40 Å R/Rfree: 0.15/0.19
First author:
Seattle Structural Genomics Center for Infectious Disease (SSGCID) Seattle Structural Genomics Center for Infectious Disease Resolution: 2.30 Å R/Rfree: 0.21/0.25
X-ray diffraction data for the Structure of USP5 zinc-finger ubiquitin binding domain co-crystallized with (5-((4-(4-chlorophenyl)piperidin-1-yl)sulfonyl)picolinoyl)glycine
X-ray diffraction data for the Structure of USP5 zinc-finger ubiquitin binding domain co-crystallized with (2-fluoro-4-((4-phenylpiperidin-1-yl)sulfonyl)benzoyl)glycine
X-ray diffraction data for the Structure of USP5 zinc-finger ubiquitin binding domain co-crystallized with 4-(4-(4-(3,4-difluoro-phenyl)-piperidin-1-ylsulfonyl)-phenyl)-4-oxo-butanoic acid