1dkw: Difference between revisions

New page: left|200px<br /><applet load="1dkw" size="450" color="white" frame="true" align="right" spinBox="true" caption="1dkw, resolution 2.65Å" /> '''CRYSTAL STRUCTURE OF...
 
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[[Image:1dkw.jpg|left|200px]]<br /><applet load="1dkw" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1dkw.jpg|left|200px]]<br /><applet load="1dkw" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1dkw, resolution 2.65&Aring;" />
caption="1dkw, resolution 2.65&Aring;" />
'''CRYSTAL STRUCTURE OF TRIOSE-PHOSPHATE ISOMERASE WITH MODIFIED SUBSTRATE BINDING SITE'''<br />
'''CRYSTAL STRUCTURE OF TRIOSE-PHOSPHATE ISOMERASE WITH MODIFIED SUBSTRATE BINDING SITE'''<br />


==Overview==
==Overview==
Loop 8 (residues 232-242) in triosephosphate isomerase (TIM) is a highly, conserved loop that forms a tight binding pocket for the phosphate moiety, of the substrate. Its sequence includes the fully conserved, solvent-exposed Leu238. The tight phosphate-binding pocket explains the, high substrate specificity of TIM being limited to the in vivo substrates, dihydroxyacetone-phosphate and D-glyceraldehyde-3-phosphate. Here we use, the monomeric variant of trypanosomal TIM for exploring the structural, consequences of shortening this loop. The mutagenesis, guided by extensive, modeling calculations and followed up by crystallographic, characterization, is aimed at widening the phosphate-binding pocket and, consequently, changing the substrate specificity. Two new variants were, characterized. The crystal structures of these variants indicate that in, monomeric forms of TIM, the Leu238 side-chain is nicely buried in a, hydrophobic cluster. Monomeric forms of wild-type dimeric TIM are known to, exist transiently as folding intermediates; our structural analysis, suggests that in this monomeric form, Leu238 of loop 8 also adopts this, completely buried conformation, which explains its full conservation, across the evolution. The much wider phosphate-binding pocket of the new, variant allows for the development of a new TIM variant with a different, substrate specificity.
Loop 8 (residues 232-242) in triosephosphate isomerase (TIM) is a highly conserved loop that forms a tight binding pocket for the phosphate moiety of the substrate. Its sequence includes the fully conserved, solvent-exposed Leu238. The tight phosphate-binding pocket explains the high substrate specificity of TIM being limited to the in vivo substrates dihydroxyacetone-phosphate and D-glyceraldehyde-3-phosphate. Here we use the monomeric variant of trypanosomal TIM for exploring the structural consequences of shortening this loop. The mutagenesis, guided by extensive modeling calculations and followed up by crystallographic characterization, is aimed at widening the phosphate-binding pocket and, consequently, changing the substrate specificity. Two new variants were characterized. The crystal structures of these variants indicate that in monomeric forms of TIM, the Leu238 side-chain is nicely buried in a hydrophobic cluster. Monomeric forms of wild-type dimeric TIM are known to exist transiently as folding intermediates; our structural analysis suggests that in this monomeric form, Leu238 of loop 8 also adopts this completely buried conformation, which explains its full conservation across the evolution. The much wider phosphate-binding pocket of the new variant allows for the development of a new TIM variant with a different substrate specificity.


==About this Structure==
==About this Structure==
1DKW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Trypanosoma_brucei_brucei Trypanosoma brucei brucei] with TBU as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Triose-phosphate_isomerase Triose-phosphate isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.1.1 5.3.1.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1DKW OCA].  
1DKW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Trypanosoma_brucei_brucei Trypanosoma brucei brucei] with <scene name='pdbligand=TBU:'>TBU</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Triose-phosphate_isomerase Triose-phosphate isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.1.1 5.3.1.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DKW OCA].  


==Reference==
==Reference==
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[[Category: Triose-phosphate isomerase]]
[[Category: Triose-phosphate isomerase]]
[[Category: Trypanosoma brucei brucei]]
[[Category: Trypanosoma brucei brucei]]
[[Category: Abagyan, R.A.]]
[[Category: Abagyan, R A.]]
[[Category: Fernandez, A.M.]]
[[Category: Fernandez, A M.]]
[[Category: Filimonov, V.V.]]
[[Category: Filimonov, V V.]]
[[Category: Lambeir, A.M.]]
[[Category: Lambeir, A M.]]
[[Category: Norledge, B.V.]]
[[Category: Norledge, B V.]]
[[Category: Peter, M.G.]]
[[Category: Peter, M G.]]
[[Category: Rottman, A.]]
[[Category: Rottman, A.]]
[[Category: Wierenga, R.K.]]
[[Category: Wierenga, R K.]]
[[Category: TBU]]
[[Category: TBU]]
[[Category: isomerase]]
[[Category: isomerase]]
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[[Category: tim barrel]]
[[Category: tim barrel]]


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