Investigating structural changes induced by nucleotide binding to RecA using difference FTIR

Biophysical Journal

Volumn 82, Issue 4, 2002, Pages 2198-2210

  Butler, Blaine C ^a   Hanchett, Ross H ^a   Rafailov, Helena ^a   MacDonald, Gina ^a  

^a JAMES MADISON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEOTIDE BINDING PROTEIN; RECA PROTEIN;

ARTICLE; BINDING AFFINITY; CRYSTAL STRUCTURE; DNA REPAIR; FOURIER TRANSFORMATION; GENETIC RECOMBINATION; OLIGOMERIZATION; PHOTOCHEMISTRY; PROTEIN CONFORMATION; PROTEIN STRUCTURE; RECEPTOR AFFINITY; STRUCTURE ANALYSIS; X RAY CRYSTALLOGRAPHY;

EID: 0036217489     PISSN: 00063495     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3495(02)75566-5     Document Type: Article

References (49)

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9. Examination of the secondary structure of proteins by deconvolved FTIR spectra
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11. Fourier transform infrared photolysis studies of caged compounds
12. Estimation of amino acid residue side-chain absorption in the infrared spectra of protein solutions in heavy water
13. Phe217 regulates the transfer of allosteric information across the subunit interface of the RecA protein filament
14. Fourier transform infrared difference spectroscopy of bacteriorhodopsin and its photoproducts regenerated with deuterated tyrosine
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17. Mutations in the N-terminal region of RecA that disrupt the stability of free protein oligomers but not RecA-DNA complexes
18. Evidence for elongation of the helical pitch of the RecA filament upon ATP and ADP binding using small-angle neutron scattering
19. A comparative study of ATP and GTP complexation with trivalent Al, Ga and Fe cations. Determination of cation binding site and nucleotide conformation by FTIR difference spectroscopy
20. Saturation mutagenesis of the E. coli RecA loop L2 homologous DNA pairing region reveals residues essential for recombination and recombinational repair
21. The use and misuse of FTIR spectroscopy in the determination of protein structure
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26. Inhibition of RecA protein promoted ATP hydrolysis. 1. ATPγS and ADP are antagonistic inhibitors
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28. RecA protein has extremely high cooperativity for substrate in its ATPase activity
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43. 2O) solutions. I. Spectral parameters of amino acid residue absorption bands
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45. 2+-ATPase upon nucleotide binding studied by Fourier transform infrared spectroscopy
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48. Structural data suggest that the active and inactive forms of the RecA filament are not simply interconvertible