4DHK
Crystal structure of a deoxycytidine triphosphate deaminase (dCTP deaminase) from Burkholderia thailandensis
Summary for 4DHK
Entry DOI | 10.2210/pdb4dhk/pdb |
Descriptor | Deoxycytidine triphosphate deaminase, 1,2-ETHANEDIOL (3 entities in total) |
Functional Keywords | burkholderia thailandensis, deaminase, hydrolase, structural genomics, seattle structural genomics center for infectious disease, ssgcid |
Biological source | Burkholderia thailandensis |
Total number of polymer chains | 2 |
Total formula weight | 43449.08 |
Authors | Seattle Structural Genomics Center for Infectious Disease (SSGCID) (deposition date: 2012-01-29, release date: 2012-03-14, Last modification date: 2023-09-13) |
Primary citation | Baugh, L.,Gallagher, L.A.,Patrapuvich, R.,Clifton, M.C.,Gardberg, A.S.,Edwards, T.E.,Armour, B.,Begley, D.W.,Dieterich, S.H.,Dranow, D.M.,Abendroth, J.,Fairman, J.W.,Fox, D.,Staker, B.L.,Phan, I.,Gillespie, A.,Choi, R.,Nakazawa-Hewitt, S.,Nguyen, M.T.,Napuli, A.,Barrett, L.,Buchko, G.W.,Stacy, R.,Myler, P.J.,Stewart, L.J.,Manoil, C.,Van Voorhis, W.C. Combining functional and structural genomics to sample the essential Burkholderia structome. Plos One, 8:e53851-e53851, 2013 Cited by PubMed Abstract: The genus Burkholderia includes pathogenic gram-negative bacteria that cause melioidosis, glanders, and pulmonary infections of patients with cancer and cystic fibrosis. Drug resistance has made development of new antimicrobials critical. Many approaches to discovering new antimicrobials, such as structure-based drug design and whole cell phenotypic screens followed by lead refinement, require high-resolution structures of proteins essential to the parasite. PubMed: 23382856DOI: 10.1371/journal.pone.0053851 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.05 Å) |
Structure validation
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