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9F5B

Identification of zinc ions in LMO4.

Summary for 9F5B
Entry DOI10.2210/pdb9f5b/pdb
DescriptorLIM domain transcription factor LMO4,LIM domain-binding protein 1, ZINC ION (3 entities in total)
Functional Keywordsprotease, hydrolase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains1
Total formula weight20457.28
Authors
El Omari, K.,Forsyth, I.,Mancini, E.J.,Wagner, A. (deposition date: 2024-04-28, release date: 2024-10-02, Last modification date: 2024-10-16)
Primary citationEl Omari, K.,Forsyth, I.,Duman, R.,Orr, C.M.,Mykhaylyk, V.,Mancini, E.J.,Wagner, A.
Utilizing anomalous signals for element identification in macromolecular crystallography.
Acta Crystallogr D Struct Biol, 80:713-721, 2024
Cited by
PubMed Abstract: AlphaFold2 has revolutionized structural biology by offering unparalleled accuracy in predicting protein structures. Traditional methods for determining protein structures, such as X-ray crystallography and cryo-electron microscopy, are often time-consuming and resource-intensive. AlphaFold2 provides models that are valuable for molecular replacement, aiding in model building and docking into electron density or potential maps. However, despite its capabilities, models from AlphaFold2 do not consistently match the accuracy of experimentally determined structures, need to be validated experimentally and currently miss some crucial information, such as post-translational modifications, ligands and bound ions. In this paper, the advantages are explored of collecting X-ray anomalous data to identify chemical elements, such as metal ions, which are key to understanding certain structures and functions of proteins. This is achieved through methods such as calculating anomalous difference Fourier maps or refining the imaginary component of the anomalous scattering factor f''. Anomalous data can serve as a valuable complement to the information provided by AlphaFold2 models and this is particularly significant in elucidating the roles of metal ions.
PubMed: 39291627
DOI: 10.1107/S2059798324008659
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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