1i4v

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[[Image:1i4v.gif|left|200px]]
[[Image:1i4v.gif|left|200px]]
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{{Structure
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|PDB= 1i4v |SIZE=350|CAPTION= <scene name='initialview01'>1i4v</scene>
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The line below this paragraph, containing "STRUCTURE_1i4v", creates the "Structure Box" on the page.
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|SITE=
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|GENE= UMUD ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=562 Escherichia coli])
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|DOMAIN=
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{{STRUCTURE_1i4v| PDB=1i4v | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1i4v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1i4v OCA], [http://www.ebi.ac.uk/pdbsum/1i4v PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1i4v RCSB]</span>
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'''SOLUTION STRUCTURE OF THE UMUD' HOMODIMER'''
'''SOLUTION STRUCTURE OF THE UMUD' HOMODIMER'''
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[[Category: Wagner, G.]]
[[Category: Wagner, G.]]
[[Category: Walker, G C.]]
[[Category: Walker, G C.]]
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[[Category: autocatalytic cleavage]]
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[[Category: Autocatalytic cleavage]]
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[[Category: dna polymerase accessory protein]]
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[[Category: Dna polymerase accessory protein]]
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[[Category: dna polymerase v]]
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[[Category: Dna polymerase v]]
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[[Category: dna repair]]
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[[Category: Dna repair]]
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[[Category: lambda ci]]
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[[Category: Lambda ci]]
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[[Category: lexa repressor]]
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[[Category: Lexa repressor]]
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[[Category: serine protease]]
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[[Category: Serine protease]]
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[[Category: serine-lysine dyad]]
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[[Category: Serine-lysine dyad]]
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[[Category: signal peptidase]]
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[[Category: Signal peptidase]]
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[[Category: sos mutagenesis]]
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[[Category: Sos mutagenesis]]
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[[Category: sos response]]
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[[Category: Sos response]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 19:34:27 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:14:39 2008''
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Revision as of 16:34, 2 May 2008

Image:1i4v.gif

Template:STRUCTURE 1i4v

SOLUTION STRUCTURE OF THE UMUD' HOMODIMER


Overview

During the SOS response of Escherichia coli to DNA damage, the umuDC operon is induced, producing the trimeric protein complexes UmuD2C, a DNA damage checkpoint effector, and UmuD'2C (DNA polymerase V), which carries out translesion synthesis, the basis of 'SOS mutagenesis'. UmuD'2, the homodimeric component of DNA pol V, is produced from UmuD by RecA-facilitated self-cleavage, which removes the 24 N-terminal residues of UmuD. We report the solution structure of UmuD'2 (PDB ID 1I4V) and interactions within UmuD'-UmuD, a heterodimer inactive in translesion synthesis. The overall shape of UmuD'2 in solution differs substantially from the previously reported crystal structure, even though the topologies of the two structures are quite similar. Most significantly, the active site residues S60 and K97 do not point directly at one another in solution as they do in the crystal, suggesting that self-cleavage of UmuD might require RecA to assemble the active site. Structural differences between UmuD'2 and UmuD'- UmuD suggest that UmuD'2C and UmuD2C might achieve their different biological activities through distinct interactions with RecA and DNA pol III.

About this Structure

1I4V is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.

Reference

Converting a DNA damage checkpoint effector (UmuD2C) into a lesion bypass polymerase (UmuD'2C)., Ferentz AE, Walker GC, Wagner G, EMBO J. 2001 Aug 1;20(15):4287-98. PMID:11483531 Page seeded by OCA on Fri May 2 19:34:27 2008

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