3TX8
Crystal structure of a succinyl-diaminopimelate desuccinylase (ArgE) from Corynebacterium glutamicum ATCC 13032 at 2.97 A resolution
3TX8 の概要
| エントリーDOI | 10.2210/pdb3tx8/pdb |
| 分子名称 | Succinyl-diaminopimelate desuccinylase, PHOSPHATE ION, CHLORIDE ION (3 entities in total) |
| 機能のキーワード | peptidase, structural genomics, joint center for structural genomics, jcsg, protein structure initiative, psi-biology, hydrolase |
| 由来する生物種 | Corynebacterium glutamicum |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 40401.61 |
| 構造登録者 | Joint Center for Structural Genomics (JCSG),Brunger, A.T.,Terwilliger, T.C.,Read, R.J.,Adams, P.D.,Levitt, M.,Schroder, G.F. (登録日: 2011-09-22, 公開日: 2011-10-26, 最終更新日: 2024-11-27) |
| 主引用文献 | Brunger, A.T.,Das, D.,Deacon, A.M.,Grant, J.,Terwilliger, T.C.,Read, R.J.,Adams, P.D.,Levitt, M.,Schroder, G.F. Application of DEN refinement and automated model building to a difficult case of molecular-replacement phasing: the structure of a putative succinyl-diaminopimelate desuccinylase from Corynebacterium glutamicum. Acta Crystallogr.,Sect.D, 68:391-403, 2012 Cited by PubMed Abstract: Phasing by molecular replacement remains difficult for targets that are far from the search model or in situations where the crystal diffracts only weakly or to low resolution. Here, the process of determining and refining the structure of Cgl1109, a putative succinyl-diaminopimelate desuccinylase from Corynebacterium glutamicum, at ∼3 Å resolution is described using a combination of homology modeling with MODELLER, molecular-replacement phasing with Phaser, deformable elastic network (DEN) refinement and automated model building using AutoBuild in a semi-automated fashion, followed by final refinement cycles with phenix.refine and Coot. This difficult molecular-replacement case illustrates the power of including DEN restraints derived from a starting model to guide the movements of the model during refinement. The resulting improved model phases provide better starting points for automated model building and produce more significant difference peaks in anomalous difference Fourier maps to locate anomalous scatterers than does standard refinement. This example also illustrates a current limitation of automated procedures that require manual adjustment of local sequence misalignments between the homology model and the target sequence. PubMed: 22505259DOI: 10.1107/S090744491104978X 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.972 Å) |
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