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The structure of the first representative of Pfam family PF09836 reveals a two‐domain organization and suggests involvement in transcriptional regulation
Author(s) -
Das Debanu,
Grishin Nick V.,
Kumar Abhinav,
Carlton Dennis,
Bakolitsa Constantina,
Miller Mitchell D.,
Abdubek Polat,
Astakhova Tamara,
Axelrod Herbert L.,
Burra Prasad,
Chen Connie,
Chiu HsiuJu,
Chiu Michelle,
Clayton Thomas,
Deller Marc C.,
Duan Lian,
Ellrott Kyle,
Ernst Dustin,
Farr Carol L.,
Feuerhelm Julie,
Grzechnik Anna,
Grzechnik Slawomir K.,
Grant Joanna C.,
Han Gye Won,
Jaroszewski Lukasz,
Jin Kevin K.,
Johnson Hope A.,
Klock Heath E.,
Knuth Mark W.,
Kozbial Piotr,
Krishna S. Sri,
Marciano David,
McMullan Daniel,
Morse Andrew T.,
Nigoghossian Edward,
Nopakun Amanda,
Okach Linda,
Oommachen Silvya,
Paulsen Jessica,
Puckett Christina,
Reyes Ron,
Rife Christopher L.,
Sefcovic Natasha,
Tien Henry J.,
Trame Christine B.,
Van Den Bedem Henry,
Weekes Dana,
Wooten Tiffany,
Xu Qingping,
Hodgson Keith O.,
Wooley John,
Elsliger MarcAndré,
Deacon Ashley M.,
Godzik Adam,
Lesley Scott A.,
Wilson Ian A.
Publication year - 2010
Publication title -
acta crystallographica section f
Language(s) - English
Resource type - Journals
ISSN - 1744-3091
DOI - 10.1107/s1744309109022672
Subject(s) - biology , computational biology , genetics , protein family , neisseria , domain (mathematical analysis) , protein domain , transcriptional regulation , neisseria gonorrhoeae , sequence alignment , gene , peptide sequence , bacteria , transcription factor , mathematical analysis , mathematics
Proteins with the DUF2063 domain constitute a new Pfam family, PF09836. The crystal structure of a member of this family, NGO1945 from Neisseria gonorrhoeae , has been determined and reveals that the N‐terminal DUF2063 domain is likely to be a DNA‐binding domain. In conjunction with the rest of the protein, NGO1945 is likely to be involved in transcriptional regulation, which is consistent with genomic neighborhood analysis. Of the 216 currently known proteins that contain a DUF2063 domain, the most significant sequence homologs of NGO1945 (∼40–99% sequence identity) are from various Neisseria and Haemophilus species. As these are important human pathogens, NGO1945 represents an interesting candidate for further exploration via biochemical studies and possible therapeutic intervention.

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