Journal:Acta Cryst F:S2053230X18018083

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<b>Molecular Tour</b><br>
<b>Molecular Tour</b><br>
Further refinement of three methylenetetrahydrofolate dehydrogenase/cyclohydrolase antifolate inhibitor complexes in the Protein Data Bank has produced models that allow for a critical reassessment of ligand placement.
Further refinement of three methylenetetrahydrofolate dehydrogenase/cyclohydrolase antifolate inhibitor complexes in the Protein Data Bank has produced models that allow for a critical reassessment of ligand placement.
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One complex has a well-ordered ligand in a catalytic site and the model provides an improved description of enzyme-inhibitor interactions ([[1dib]]: <scene name='80/804503/Cv/2'>L34</scene>). One ligand may adopt two conformations in the binding site rather than the single one previously described ([[1dia]]: <scene name='80/804503/Cv/3'>L24</scene>; 1st conformation is colored in wheat and 2nd conformation is in magenta). There is no evidence to support incorporation of the third compound in the model ([[1dig]]:L37). Our interpretation of the data supports a correlation between the models and inhibition activity for two of the compounds. In the case of the third, inconsistencies are noted that would need to be addressed by further work.
One complex has a well-ordered ligand in a catalytic site and the model provides an improved description of enzyme-inhibitor interactions ([[1dib]]: <scene name='80/804503/Cv/2'>L34</scene>). One ligand may adopt two conformations in the binding site rather than the single one previously described ([[1dia]]: <scene name='80/804503/Cv/3'>L24</scene>; 1st conformation is colored in wheat and 2nd conformation is in magenta). There is no evidence to support incorporation of the third compound in the model ([[1dig]]:L37). Our interpretation of the data supports a correlation between the models and inhibition activity for two of the compounds. In the case of the third, inconsistencies are noted that would need to be addressed by further work.

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