2b2n
From Proteopedia
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|PDB= 2b2n |SIZE=350|CAPTION= <scene name='initialview01'>2b2n</scene>, resolution 2.10Å | |PDB= 2b2n |SIZE=350|CAPTION= <scene name='initialview01'>2b2n</scene>, resolution 2.10Å | ||
|SITE= | |SITE= | ||
- | |LIGAND= <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand= | + | |LIGAND= <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=P4C:O-ACETALDEHYDYL-HEXAETHYLENE+GLYCOL'>P4C</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene> |
|ACTIVITY= | |ACTIVITY= | ||
|GENE= mfd ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=562 Escherichia coli]) | |GENE= mfd ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=562 Escherichia coli]) | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY= | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2b2n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2b2n OCA], [http://www.ebi.ac.uk/pdbsum/2b2n PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2b2n RCSB]</span> | ||
}} | }} | ||
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[[Category: Lammens, A.]] | [[Category: Lammens, A.]] | ||
[[Category: Wenig, K.]] | [[Category: Wenig, K.]] | ||
- | [[Category: | + | [[Category: rna polymerase]] |
- | [[Category: | + | [[Category: rnap]] |
- | [[Category: | + | [[Category: strand-specific repair]] |
- | [[Category: | + | [[Category: template strand]] |
+ | [[Category: uvra/b/c repair system]] | ||
+ | [[Category: x-ray crystallography]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:00:39 2008'' |
Revision as of 23:00, 30 March 2008
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, resolution 2.10Å | |||||||
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Ligands: | , , | ||||||
Gene: | mfd (Escherichia coli) | ||||||
Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Structure of transcription-repair coupling factor
Overview
The transcription repair coupling factor Mfd removes stalled RNA polymerase from DNA lesions and links transcription to UvrABC-dependent nucleotide excision repair in prokaryotes. We report the 2.1A crystal structure of the UvrA-binding N terminus (residues 1-333) of Escherichia coli Mfd (Mfd-N). Remarkably, Mfd-N reveals a fold that resembles the three N-terminal domains of the repair enzyme UvrB. Domain 1A of Mfd adopts a typical RecA fold, domain 1B matches the damage-binding domain of the UvrB, and domain 2 highly resembles the implicated UvrA-binding domain of UvrB. However, Mfd apparently lacks a functional ATP-binding site and does not contain the DNA damage-binding motifs of UvrB. Thus, our results suggest that Mfd might form a UvrA recruitment factor at stalled transcription complexes that architecturally but not catalytically resembles UvrB.
About this Structure
2B2N is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.
Reference
Structural basis for transcription-coupled repair: the N terminus of Mfd resembles UvrB with degenerate ATPase motifs., Assenmacher N, Wenig K, Lammens A, Hopfner KP, J Mol Biol. 2006 Jan 27;355(4):675-83. Epub 2005 Nov 8. PMID:16309703
Page seeded by OCA on Mon Mar 31 02:00:39 2008