5fzp

Structure of the dispase autolysis inducing protein from Streptomyces mobaraensis

spinqualitylabelsall models 5fzp, resolution 1.70Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 5fzp is a 2 chain structure with sequence from Streptomyces mobaraensis. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: CA, GOL Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function [DAIP_STRMB] Induces autolysis of dispase and thermolysin. Publication Abstract from PubMed Transglutaminase from Streptomyces mobaraensis (MTG) is an important enzyme for cross-linking and modifying proteins. An intrinsic substrate of MTG is the dispase autolysis inducing protein (DAIP). The amino acid sequence of DAIP contains five potential glutamines and ten lysines for MTG mediated cross-linking. Aim of the study was to determine the structure and glutamine cross-linking sites of the first physiological MTG substrate. A production procedure was established in E. coli BL21 (DE3) to obtain high yields of recombinant DAIP. DAIP variants were prepared by replacing four out of five glutamines for asparagines in various combinations via site-directed mutagenesis. Incorporation of biotin cadaverine revealed preference of MTG for the DAIP glutamines in the order of Q39>>Q298>Q345~Q65>>Q144. In the structure of DAIP the preferred glutamines do cluster at the top of the seven-bladed beta-propeller. This suggests a targeted cross-linking of DAIP by MTG that may occur after self-assembly in the bacterial cell wall. Based on our biochemical and the structural data of the first physiological MTG substrate, we further provide novel insight into determinants of MTG-mediated modification, specificity and efficiency. Structure of the Dispase Autolysis Inducing Protein from Streptomyces mobaraensis and Glutamine Cross-linking Sites for Transglutaminase.,Fiebig D, Schmelz S, Zindel S, Ehret V, Beck J, Ebenig A, Ehret M, Frols S, Pfeifer F, Kolmar H, Fuchsbauer HL, Scrima A J Biol Chem. 2016 Aug 4. pii: jbc.M116.731109. PMID:27493205 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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