Synopsis
ID23-2 is a fixed energy beamline dedicated to MX. ID23-2 offers a standard MX sample environment, but with a focused microbeam (10x4 micron).
Status:
open
Disciplines
Applications
- Macromolecular crystallography
Techniques
-
MX - macromolecular crystallography
-
Microbeam
Beam size
- Minimum (H x V) : 10.0
x 4.0
µm²
-
Maximum (H x V) : 10.0
x 4.0
µm²
Sample environments
- Microdiffractometer MD3Up
Detectors
Technical details
This beamline offers diffraction data collection on microcrystalline MX samples and on fine needle MX samples, as well as determination of the region of highest diffraction quality from larger MX samples.
Synthesis, biological properties and structural study of new halogenated azolo[4,5-b]pyridines as inhibitors of CK2 kinase
Chojnacki K., Lindenblatt D., Winska P., Wielechowska M., Toelzer C., Niefind K., Bretner M.,
Bioorganic Chemistry 106, 104502-1-104502-12 (2021)
Unveiling the dimer/monomer propensities of Smad MH1-DNA complexes
Ruiz L., Kaczmarska Z., Gomes T., Aragón E., Torner C., Freier R., Baginski B., Martin-Malpartida P., de Martin Garrido N., Márquez J.A., Cordeiro T.N., Pluta R., Macias M.J.,
Computational and Structural Biotechnology Journal 19, 632-646 (2021)
Approaching boiling point stability of an alcohol dehydrogenase through computationally-guided enzyme engineering
Aalbers F.S., Fürst M.J.L.J., Rovida S., Trajkovic M., Castellanos J.R.G., Bartsch S., Vogel A., Mattevi A., Fraaije M.W.,
eLife 9, e54639-1-e54639-18 (2020)
Distinct chromophore-protein environments enable asymmetric activation of a bacteriophytochrome-activated diguanylate cyclase
Buhrke D., Gourinchas G., Müller M., Michael N., Hildebrandt P., Winkler A.,
Journal of Biological Chemistry 295, 539-551 (2020)
Structure and catalytic regulation of Plasmodium falciparum IMP specific nucleotidase
Carrique L., Ballut L., Shukla A., Varma N., Ravi R., Violot S., Srinivasan B., Ganeshappa U.T., Kulkarni S., Balaram H., Aghajari N.,
Nature Communications 11, 3228-1-3228-11 (2020)
Mycobacterial and human Nitrobindins: Structure and function
De Simone G., di Masi A., Vita G., Polticelli F., Pesce A., Nardini M., Bolognesi M., Ciaccio C., Coletta M., Turilli E., Fasano M., Tognaccini L., Smulevich G., Abbruzzetti S., Viappiani C., Bruno S., Ascenzi P.,
Antioxidants & Redox Signaling 33, 229-246 (2020)