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5VGM

Crystal structure of dihydroorotase pyrC from Vibrio cholerae in complex with zinc at 1.95 A resolution.

Summary for 5VGM
Entry DOI10.2210/pdb5vgm/pdb
DescriptorDihydroorotase, ZINC ION, ACETATE ION, ... (5 entities in total)
Functional Keywordsstructural genomics, psi-biology, center for structural genomics of infectious diseases, csgid, hydrolase
Biological sourceVibrio cholerae
Total number of polymer chains2
Total formula weight76241.15
Authors
Primary citationLipowska, J.,Miks, C.D.,Kwon, K.,Shuvalova, L.,Zheng, H.,Lewinski, K.,Cooper, D.R.,Shabalin, I.G.,Minor, W.
Pyrimidine biosynthesis in pathogens - Structures and analysis of dihydroorotases from Yersinia pestis and Vibrio cholerae.
Int.J.Biol.Macromol., 136:1176-1187, 2019
Cited by
PubMed Abstract: The de novo pyrimidine biosynthesis pathway is essential for the proliferation of many pathogens. One of the pathway enzymes, dihydroorotase (DHO), catalyzes the reversible interconversion of N-carbamoyl-l-aspartate to 4,5-dihydroorotate. The substantial difference between bacterial and mammalian DHOs makes it a promising drug target for disrupting bacterial growth and thus an important candidate to evaluate as a response to antimicrobial resistance on a molecular level. Here, we present two novel three-dimensional structures of DHOs from Yersinia pestis (YpDHO), the plague-causing pathogen, and Vibrio cholerae (VcDHO), the causative agent of cholera. The evaluations of these two structures led to an analysis of all available DHO structures and their classification into known DHO types. Comparison of all the DHO active sites containing ligands that are listed in DrugBank was facilitated by a new interactive, structure-comparison and presentation platform. In addition, we examined the genetic context of characterized DHOs, which revealed characteristic patterns for different types of DHOs. We also generated a homology model for DHO from Plasmodium falciparum.
PubMed: 31207330
DOI: 10.1016/j.ijbiomac.2019.05.149
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

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