4E4T

Crystal structure of Phosphoribosylaminoimidazole carboxylase, ATPase subunit from Burkholderia ambifaria

Replaces:  3UVZ

Summary for 4E4T

• Entry DOI: 10.2210/pdb4e4t/pdb
• Descriptor: Phosphoribosylaminoimidazole carboxylase, ATPase subunit, SULFATE ION (3 entities in total)
• Functional Keywords: structural genomics, seattle structural genomics center for infectious disease, ssgcid, purine biosynthesis, atp binding, lyase, acair, cair
• Biological source: Burkholderia ambifaria
• Total number of polymer chains: 2
• Total formula weight: 88392.15

Authors

Seattle Structural Genomics Center for Infectious Disease (SSGCID) (deposition date: 2012-03-13, release date: 2012-03-28, 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

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: 23382856
DOI: 10.1371/journal.pone.0053851

Experimental method

X-RAY DIFFRACTION (1.55 Å)