A crystal of Escherichia coli dihydrofolate reductase (ecDHFR) complexed with folate and NADP+ of 4 x 1.3 x 0.7 mm (3.6 mm3) in size was obtained by sequential application of microseeding and macroseeding. A neutron diffraction data set was collected to 2.0 A resolution using the IMAGINE diffractometer at the High Flux Isotope Reactor within Oak Ridge National Laboratory. A 1.6 A resolution X-ray data set was also collected from a smaller crystal at room temperature. The neutron and X-ray data were used together for joint refinement of the ecDHFR–folate–NADP+ ternary-complex structure in order to examine the protonation state, protein dynamics and solvent structure of the complex, furthering understanding of the catalytic mechanism
Crystal diffraction data of heart fatty acid binding protein (H-FABP) in complex with oleic acid wer...
International audienceBackgroundHydrogen atoms represent about half of the total number of atoms in ...
AbstractThe structure of the complex between E. coli (RT500) form I dihydrofolate reductase, the ant...
A crystal of Escherichia coli dihydrofolate reductase (ecDHFR) complexed with folate and NADP+ of 4 ...
Dihydrofolate Reductases (DHFRs) have been identified in nearly every proteome and are essential for...
Dihydrofolate reductase from Pneumocystis carinii has been crystallized in a form suitable for high ...
Many redox proteins possess cofactors, such as heme, FAD, and Fe-S cluster and the cofactors are inv...
Neutron crystallography is a powerful technique to obtain accurate positions of hydrogen atoms in pr...
Hydrogen atoms and hydration water molecules in proteins are essential for many biochemical processe...
Information about hydrogen atoms and valence electrons is important to understand functions of elect...
AbstractWe have employed 15N NMR to characterize the conformations of Escherichia coli dihydrofolate...
Redox proteins functions in many biological processes, such as metabolism, photosynthesis, respirati...
R67 dihydrofolate reductase (DHFR) is a homotetramer with a single active site pore and no sequence ...
Neutron crystallography enables direct observation of hydrogen atoms which play crucial roles in the...
Protein neutron crystallography is a powerful technique to determine the positions of hydrogen atoms...
Crystal diffraction data of heart fatty acid binding protein (H-FABP) in complex with oleic acid wer...
International audienceBackgroundHydrogen atoms represent about half of the total number of atoms in ...
AbstractThe structure of the complex between E. coli (RT500) form I dihydrofolate reductase, the ant...
A crystal of Escherichia coli dihydrofolate reductase (ecDHFR) complexed with folate and NADP+ of 4 ...
Dihydrofolate Reductases (DHFRs) have been identified in nearly every proteome and are essential for...
Dihydrofolate reductase from Pneumocystis carinii has been crystallized in a form suitable for high ...
Many redox proteins possess cofactors, such as heme, FAD, and Fe-S cluster and the cofactors are inv...
Neutron crystallography is a powerful technique to obtain accurate positions of hydrogen atoms in pr...
Hydrogen atoms and hydration water molecules in proteins are essential for many biochemical processe...
Information about hydrogen atoms and valence electrons is important to understand functions of elect...
AbstractWe have employed 15N NMR to characterize the conformations of Escherichia coli dihydrofolate...
Redox proteins functions in many biological processes, such as metabolism, photosynthesis, respirati...
R67 dihydrofolate reductase (DHFR) is a homotetramer with a single active site pore and no sequence ...
Neutron crystallography enables direct observation of hydrogen atoms which play crucial roles in the...
Protein neutron crystallography is a powerful technique to determine the positions of hydrogen atoms...
Crystal diffraction data of heart fatty acid binding protein (H-FABP) in complex with oleic acid wer...
International audienceBackgroundHydrogen atoms represent about half of the total number of atoms in ...
AbstractThe structure of the complex between E. coli (RT500) form I dihydrofolate reductase, the ant...