2fez: Difference between revisions

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[[Image:2fez.gif|left|200px]]
{{Seed}}
[[Image:2fez.png|left|200px]]


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{{STRUCTURE_2fez|  PDB=2fez  |  SCENE=  }}  
{{STRUCTURE_2fez|  PDB=2fez  |  SCENE=  }}  


'''Mycobacterium tuberculosis EmbR'''
===Mycobacterium tuberculosis EmbR===




==Overview==
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Ser/Thr phosphorylation has emerged as a critical regulatory mechanism in a number of bacteria, including Mycobacterium tuberculosis. This problematic pathogen encodes 11 eukaryotic-like Ser/Thr kinases, yet few substrates or signaling targets have been characterized. Here, we report the structure of EmbR (2.0 A), a putative transcriptional regulator of key arabinosyltransferases (EmbC, -A, and -B), and an endogenous substrate of the Ser/Thr-kinase PknH. EmbR presents a unique domain architecture: the N-terminal winged-helix DNA-binding domain forms an extensive interface with the all-helical central bacterial transcriptional activation domain and is positioned adjacent to the regulatory C-terminal forkhead-associated (FHA) domain, which mediates binding to a Thr-phosphorylated site in PknH. The structure in complex with a phospho-peptide (1.9 A) reveals a conserved mode of phospho-threonine recognition by the FHA domain and evidence for specific recognition of the cognate kinase. The present structures suggest hypotheses as to how EmbR might propagate the phospho-relay signal from its cognate kinase, while serving as a template for the structurally uncharacterized Streptomyces antibiotic regulatory protein family of transcription factors.
The line below this paragraph, {{ABSTRACT_PUBMED_16477027}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 16477027 is the PubMed ID number.
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{{ABSTRACT_PUBMED_16477027}}


==About this Structure==
==About this Structure==
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[[Category: Transcriptional regulator]]
[[Category: Transcriptional regulator]]
[[Category: Winged-helix]]
[[Category: Winged-helix]]
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