2f1h: Difference between revisions
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|PDB= 2f1h |SIZE=350|CAPTION= <scene name='initialview01'>2f1h</scene>, resolution 2.70Å | |PDB= 2f1h |SIZE=350|CAPTION= <scene name='initialview01'>2f1h</scene>, resolution 2.70Å | ||
|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand= | |LIGAND= <scene name='pdbligand=ANP:PHOSPHOAMINOPHOSPHONIC+ACID-ADENYLATE+ESTER'>ANP</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene> | ||
|ACTIVITY= | |ACTIVITY= | ||
|GENE= radA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=2188 Methanococcus voltae]) | |GENE= radA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=2188 Methanococcus voltae]) | ||
|DOMAIN= | |||
|RELATEDENTRY=[[1xu4|1XU4]] | |||
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2f1h FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2f1h OCA], [http://www.ebi.ac.uk/pdbsum/2f1h PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2f1h RCSB]</span> | |||
}} | }} | ||
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[[Category: Qian, X.]] | [[Category: Qian, X.]] | ||
[[Category: Wu, Y.]] | [[Category: Wu, Y.]] | ||
[[Category: atpase]] | [[Category: atpase]] | ||
[[Category: protein-atp complex]] | [[Category: protein-atp complex]] | ||
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[[Category: recombinase]] | [[Category: recombinase]] | ||
''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 02:56:39 2008'' | ||
Revision as of 02:56, 31 March 2008
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| , resolution 2.70Å | |||||||
|---|---|---|---|---|---|---|---|
| Ligands: | , , | ||||||
| Gene: | radA (Methanococcus voltae) | ||||||
| Related: | 1XU4
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| Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
RECOMBINASE IN COMPLEX WITH AMP-PNP and Potassium
OverviewOverview
Archaeal RadA/Rad51 are close homologues of eukaryal Rad51/DMC1. Such recombinases, as well as their bacterial RecA orthologues, form helical nucleoprotein filaments in which a hallmark strand exchange reaction occurs between homologous DNA substrates. Our recent ATPase and structure studies on RadA recombinase from Methanococcus voltae have suggested that not only magnesium but also potassium ions are absorbed at the ATPase center. Potassium, but not sodium, stimulates the ATP hydrolysis reaction with an apparent dissociation constant of approximately 40 mM. The minimal inhibitory effect by 40 mM NaCl further suggests that the protein does not have adequate affinity for sodium. The wild-type protein's strand exchange activity is also stimulated by potassium with an apparent dissociation constant of approximately 35 mM. We made site-directed mutations at the potassium-contacting residues Glu151 and Asp302. The mutant proteins are expectedly defective in promoting ATP hydrolysis. Similar potassium preference in strand exchange is observed for the E151D and E151K proteins. The D302K protein, however, shows comparable strand exchange efficiencies in the presence of either potassium or sodium. Crystallized E151D filaments reveal a potassium-dependent conformational change similar to what has previously been observed with the wild-type protein. We interpret these data as suggesting that both ATP hydrolysis and DNA strand exchange requires accessibility to an "active" conformation similar to the crystallized ATPase-active form in the presence of ATP, Mg2+ and K+.
About this StructureAbout this Structure
2F1H is a Single protein structure of sequence from Methanococcus voltae. Full crystallographic information is available from OCA.
ReferenceReference
Asp302 determines potassium dependence of a RadA recombinase from Methanococcus voltae., Qian X, He Y, Wu Y, Luo Y, J Mol Biol. 2006 Jul 14;360(3):537-47. Epub 2006 Jun 9. PMID:16782126
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