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A structure-based method for identifying DNA-binding proteins and their sites of DNA-interaction.

作者信息

McLaughlin William A, Kulp Daniel W, de la Cruz Joanna, Lu Xiang-Jun, Lawson Catherine L, Berman Helen M

机构信息

Department of Chemistry and Chemical Biology, Rutgers-The State University of New Jersey, 610 Taylor Road, Piscataway, NJ 08854-8087, USA.

出版信息

J Struct Funct Genomics. 2004;5(4):255-65. doi: 10.1007/s10969-005-4902-1.

Abstract

A classification model of a DNA-binding protein chain was created based on identification of alpha helices within the chain likely to bind to DNA. Using the model, all chains in the Protein Data Bank were classified. For many of the chains classified with high confidence, previous documentation for DNA-binding was found, yet no sequence homology to the structures used to train the model was detected. The result indicates that the chain model can be used to supplement sequence based methods for annotating the function of DNA-binding. Four new candidates for DNA-binding were found, including two structures solved through structural genomics efforts. For each of the candidate structures, possible sites of DNA-binding are indicated by listing the residue ranges of alpha helices likely to interact with DNA.

摘要

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