Structure of a putative succinyl-diaminopimelate desuccinylase from Corynebacterium glutamicum
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 A ̊ 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.
A.T.Brunger, D.Das, A.M.Deacon, J.Grant,T.C.Terwilliger, R.J.Read, P.D.Adams, M.Levitt, G.F.Schroeder. 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 Cryst. D68, 391-403 (2012).

Primary data
3tx8-sf.cif.zip (2.8 MB bytes): Deposited data file
3TX8.pdb (479.2 KB bytes): Deposited coordinates
Image of 3TX8