1iz3: Difference between revisions

Revision as of 14:15, 1 July 2008

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File:1iz3.png

Template:STRUCTURE 1iz3

Dimeric structure of FIH (Factor inhibiting HIF)Dimeric structure of FIH (Factor inhibiting HIF)

Template:ABSTRACT PUBMED 12482756

About this StructureAbout this Structure

1IZ3 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Structure of human FIH-1 reveals a unique active site pocket and interaction sites for HIF-1 and von Hippel-Lindau., Lee C, Kim SJ, Jeong DG, Lee SM, Ryu SE, J Biol Chem. 2003 Feb 28;278(9):7558-63. Epub 2002 Dec 12. PMID:12482756

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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-'''Dimeric structure of FIH (Factor inhibiting HIF)'''
+===Dimeric structure of FIH (Factor inhibiting HIF)===
-==Overview==
+<!--
-The master switch of cellular hypoxia responses, hypoxia-inducible factor 1 (HIF-1), is hydroxylated by factor inhibiting HIF-1 (FIH-1) at a conserved asparagine residue under normoxia, which suppresses transcriptional activity of HIF-1 by abrogating its interaction with transcription coactivators. Here we report the crystal structure of human FIH-1 at 2.8-A resolution. The structural core of FIH-1 consists of a jellyroll-like beta-barrel containing the conserved ferrous-binding triad residues, confirming that FIH-1 is a member of the 2-oxoglutarate-dependent dioxygenase family. Except for the core structure and triad residues, FIH-1 has many structural deviations from other family members including N- and C-terminal insertions and various deletions in the middle of the structure. The ferrous-binding triad region is highly exposed to the solvent, which is connected to a prominent groove that may bind to a helix near the hydroxylation site of HIF-1. The structure, which is in a dimeric state, also reveals the putative von Hippel-Lindau-binding site that is distinctive to the putative HIF-1-binding site, supporting the formation of the ternary complex by FIH-1, HIF-1, and von Hippel-Lindau. The unique environment of the active site and cofactor-binding region revealed in the structure should allow design of selective drugs that can be used in ischemic diseases to promote hypoxia responses.
+The line below this paragraph, {{ABSTRACT_PUBMED_12482756}}, adds the Publication Abstract to the page
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+{{ABSTRACT_PUBMED_12482756}}
 ==About this Structure==
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 [[Category: Ryu, S E.]]
 [[Category: Double beta-sheet helix]]
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