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8OWC

Crystal structure of Hen Egg White Lysozyme co-crystallized with 10 mM TbXo4

Summary for 8OWC
Entry DOI10.2210/pdb8owc/pdb
DescriptorLysozyme C, TERBIUM(III) ION, Tb-Xo4, ... (6 entities in total)
Functional Keywordshewl, crystallophore, nucleating agent, hydrolase
Biological sourceGallus gallus (chicken)
Total number of polymer chains1
Total formula weight17244.10
Authors
Alsalman, Z.,Girard, E. (deposition date: 2023-04-27, release date: 2024-07-17, Last modification date: 2024-11-13)
Primary citationRoux, A.,Alsalman, Z.,Jiang, T.,Mulatier, J.C.,Pitrat, D.,Dumont, E.,Riobe, F.,Gillet, N.,Girard, E.,Maury, O.
Influence of Chemical Modifications of the Crystallophore on Protein Nucleating Properties and Supramolecular Interactions Network.
Chemistry, 30:e202400900-e202400900, 2024
Cited by
PubMed Abstract: Crystallophores are lanthanide complexes that have demonstrated outstanding induction of crystallization for various proteins. This article explores the effect of tailored modifications of the crystallophore first generation and their impact on the nucleating properties and protein crystal structures. Through high-throughput crystallization experiments and dataset analysis, we evaluated the effectiveness of these variants, in comparison to the first crystallophore generation G. In particular, the V variant, featuring a propanol pendant arm, demonstrated the ability to produce new crystallization conditions for the proteins tested (hen-egg white lysozyme, proteinase K and thaumatin). Structural analysis performed in the case of hen egg-white lysozyme along with Molecular Dynamics simulations, highlights V's unique behavior, taking advantage of the flexibility of its propanol arm to explore different protein surfaces and form versatile supramolecular interactions.
PubMed: 38738452
DOI: 10.1002/chem.202400900
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.7 Å)
Structure validation

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數據於2024-11-13公開中

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