(GlTIM) as a target for rational drug design against giardiasis, one of the most common parasitic infections in humans. Since the enzyme exists in the parasite and the host, selective inhibition is a major challenge because essential regions that could be considered molecular targets are highly conserved. Previous biochemical evidence showed that chemical modification of the non-conserved non-catalytic cysteine 222 (C222) inactivates specifically GlTIM. The inactivation correlates with the physicochemical properties of the modifying agent: addition of a non-polar, small chemical group at C222 reduces the enzyme activity by one half, whereas negatively charged, large chemical groups cause full inactivation.In this work we used mutagenesis t...
Cys126 is a completely conserved residue in triosephosphate isomerase that is proximal to the active...
This thesis discusses the structure-function studies on triosephosphate isomerase (TIM) from Plasmod...
Human triosephosphate isomerase (hTIM), a dimeric enzyme, was altered by site-directed mutagenesis i...
(GlTIM) as a target for rational drug design against giardiasis, one of the most common parasitic i...
<div><p>Background</p><p>We have previously proposed triosephosphate isomerase of <i>Giardia lamblia...
AbstractBackground: Many studies that attempt to design species-specific drugs focus on differences ...
The active site of triosephosphate isomerase (TIM, EC: 5.3.1.1), a dimeric enzyme, lies very close t...
All the members of the triosephosphate isomerase (TIM) family possess a cystein residue (Cys126) loc...
Conserved residues in protein are crucial for maintaining structure and function, either by direct i...
Highly conserved residues in enzymes are often found to be clustered close to active sites, suggesti...
It is well known that enzymes differ from small-molecule catalysts by use of non-covalent interactio...
Plasmodium falciparum triose-phosphate isomerase, a homodimeric enzyme, contains four cysteine resid...
Triosephosphate isomerase (TIM), a central enzyme in the glycolytic pathway, has been the subject of...
The role of inter-subunit interactions in maintaining optimal catalytic activity in triosephosphate ...
The importance of the fully conserved active site proline, Pro168, for the reaction mechanism of tri...
Cys126 is a completely conserved residue in triosephosphate isomerase that is proximal to the active...
This thesis discusses the structure-function studies on triosephosphate isomerase (TIM) from Plasmod...
Human triosephosphate isomerase (hTIM), a dimeric enzyme, was altered by site-directed mutagenesis i...
(GlTIM) as a target for rational drug design against giardiasis, one of the most common parasitic i...
<div><p>Background</p><p>We have previously proposed triosephosphate isomerase of <i>Giardia lamblia...
AbstractBackground: Many studies that attempt to design species-specific drugs focus on differences ...
The active site of triosephosphate isomerase (TIM, EC: 5.3.1.1), a dimeric enzyme, lies very close t...
All the members of the triosephosphate isomerase (TIM) family possess a cystein residue (Cys126) loc...
Conserved residues in protein are crucial for maintaining structure and function, either by direct i...
Highly conserved residues in enzymes are often found to be clustered close to active sites, suggesti...
It is well known that enzymes differ from small-molecule catalysts by use of non-covalent interactio...
Plasmodium falciparum triose-phosphate isomerase, a homodimeric enzyme, contains four cysteine resid...
Triosephosphate isomerase (TIM), a central enzyme in the glycolytic pathway, has been the subject of...
The role of inter-subunit interactions in maintaining optimal catalytic activity in triosephosphate ...
The importance of the fully conserved active site proline, Pro168, for the reaction mechanism of tri...
Cys126 is a completely conserved residue in triosephosphate isomerase that is proximal to the active...
This thesis discusses the structure-function studies on triosephosphate isomerase (TIM) from Plasmod...
Human triosephosphate isomerase (hTIM), a dimeric enzyme, was altered by site-directed mutagenesis i...