4JOP
CFTR Associated Ligand (CAL) PDZ bound to HPV16 E6 oncoprotein C-terminal peptide (TRRETQL)
Summary for 4JOP
Entry DOI | 10.2210/pdb4jop/pdb |
Related | 4JOE 4JOF 4JOG 4JOH 4JOJ 4JOK 4JOR |
Descriptor | Golgi-associated PDZ and coiled-coil motif-containing protein, Protein E6 (3 entities in total) |
Functional Keywords | pdz, cftr associated ligand, cal, fig, pist, human papillomavirus type 16, hpv16, e6 oncoprotein, peptide binding protein |
Biological source | Homo sapiens (human) More |
Cellular location | Cytoplasm: Q9HD26 Host nucleus matrix: P03126 |
Total number of polymer chains | 4 |
Total formula weight | 20517.47 |
Authors | Amacher, J.F.,Madden, D.R. (deposition date: 2013-03-18, release date: 2014-01-22, Last modification date: 2023-09-20) |
Primary citation | Amacher, J.F.,Cushing, P.R.,Brooks, L.,Boisguerin, P.,Madden, D.R. Stereochemical Preferences Modulate Affinity and Selectivity among Five PDZ Domains that Bind CFTR: Comparative Structural and Sequence Analyses. Structure, 22:82-93, 2014 Cited by PubMed Abstract: PDZ domain interactions are involved in signaling and trafficking pathways that coordinate crucial cellular processes. Alignment-based PDZ binding motifs identify the few most favorable residues at certain positions along the peptide backbone. However, sequences that bind the CAL (CFTR-associated ligand) PDZ domain reveal only a degenerate motif that overpredicts the true number of high-affinity interactors. Here, we combine extended peptide-array motif analysis with biochemical techniques to show that non-motif "modulator" residues influence CAL binding. The crystallographic structures of 13 CAL:peptide complexes reveal defined, but accommodating stereochemical environments at non-motif positions, which are reflected in modulator preferences uncovered by multisequence substitutional arrays. These preferences facilitate the identification of high-affinity CAL binding sequences and differentially affect CAL and NHERF PDZ binding. As a result, they also help determine the specificity of a PDZ domain network that regulates the trafficking of CFTR at the apical membrane. PubMed: 24210758DOI: 10.1016/j.str.2013.09.019 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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