3GK3

Crystal structure of acetoacetyl-CoA reductase from Burkholderia pseudomallei 1710b

3GK3 の概要

• エントリーDOI: 10.2210/pdb3gk3/pdb
• 分子名称: Acetoacetyl-CoA reductase, PHOSPHATE ION (3 entities in total)
• 機能のキーワード: acetoacetyl-co reductase, oxidoreductase, structural genomics, seattle structural genomics center for infectious disease, ssgcid
• 由来する生物種: Burkholderia pseudomallei 1710b
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 115499.24

構造登録者

Seattle Structural Genomics Center for Infectious Disease (SSGCID) (登録日: 2009-03-09, 公開日: 2009-03-24, 最終更新日: 2024-02-21)

主引用文献

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

実験手法

X-RAY DIFFRACTION (2.1 Å)