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5W72

Impact of IR active probes on PDZ3 and its ligand binding studied by NMR and X-ray crystallography

Summary for 5W72
Entry DOI10.2210/pdb5w72/pdb
NMR InformationBMRB: 30307
DescriptorDisks large homolog 4 (1 entity in total)
Functional Keywordssignaling protein
Biological sourceRattus norvegicus (Norway Rat)
Total number of polymer chains1
Total formula weight11006.23
Authors
Lehner, F.,Kudlinzki, D.,Schwalbe, H.,Silvers, R. (deposition date: 2017-06-19, release date: 2017-12-13, Last modification date: 2023-11-15)
Primary citationLehner, F.,Kudlinzki, D.,Richter, C.,Muller-Werkmeister, H.M.,Eberl, K.B.,Bredenbeck, J.,Schwalbe, H.,Silvers, R.
Impact of Azidohomoalanine Incorporation on Protein Structure and Ligand Binding.
Chembiochem, 18:2340-2350, 2017
Cited by
PubMed Abstract: The impact of the incorporation of a non-natural amino acid (NNAA) on protein structure, dynamics, and ligand binding has not been studied rigorously so far. NNAAs are regularly used to modify proteins post-translationally in vivo and in vitro through click chemistry. Herein, structural characterisation of the impact of the incorporation of azidohomoalanine (AZH) into the model protein domain PDZ3 is examined by means of NMR spectroscopy and X-ray crystallography. The structure and dynamics of the apo state of AZH-modified PDZ3 remain mostly unperturbed. Furthermore, the binding of two PDZ3 binding peptides are unchanged upon incorporation of AZH. The interface of the AZH-modified PDZ3 and an azulene-linked peptide for vibrational energy transfer studies has been mapped by means of chemical shift perturbations and NOEs between the unlabelled azulene-linked peptide and the isotopically labelled protein. Co-crystallisation and soaking failed for the peptide-bound holo complex. NMR spectroscopy, however, allowed determination of the protein-ligand interface. Although the incorporation of AZH was minimally invasive for PDZ3, structural analysis of NNAA-modified proteins through the methodology presented herein should be performed to ensure structural integrity of the studied target.
PubMed: 28950050
DOI: 10.1002/cbic.201700437
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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数据于2024-10-30公开中

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