1t4w

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1t4w, resolution 2.10Å

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Structural Differences in the DNA Binding Domains of Human p53 and its C. elegans Ortholog Cep-1: Structure of C. elegans Cep-1

Overview

The DNA binding domains of human p53 and Cep-1, its C. elegans ortholog, recognize essentially identical DNA sequences despite poor sequence, similarity. We solved the three-dimensional structure of the Cep-1 DNA, binding domain in the absence of DNA and compared it to that of human p53., The two domains have similar overall folds. However, three loops, involved, in DNA and Zn binding in human p53, contain small alpha helices in Cep-1., The alpha helix in loop L3 of Cep-1 orients the side chains of two, conserved arginines toward DNA; in human p53, both arginines are mutation, hotspots, but only one contacts DNA. The alpha helix in loop L1 of Cep-1, repositions the entire loop, making it unlikely for residues of this loop, to contact bases in the major groove of DNA, as occurs in human p53. Thus, during evolution there have been considerable changes in the structure of, the p53 DNA binding domain.

About this Structure

1T4W is a Single protein structure of sequence from Caenorhabditis elegans with ZN as ligand. Full crystallographic information is available from OCA.

Reference

Structural differences in the DNA binding domains of human p53 and its C. elegans ortholog Cep-1., Huyen Y, Jeffrey PD, Derry WB, Rothman JH, Pavletich NP, Stavridi ES, Halazonetis TD, Structure. 2004 Jul;12(7):1237-43. PMID:15242600

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