1mss: Difference between revisions

New page: left|200px<br /><applet load="1mss" size="450" color="white" frame="true" align="right" spinBox="true" caption="1mss, resolution 2.4Å" /> '''LARGE SCALE STRUCTURA...
 
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caption="1mss, resolution 2.4&Aring;" />
caption="1mss, resolution 2.4&Aring;" />
'''LARGE SCALE STRUCTURAL REARRANGEMENTS OF THE FRONT LOOPS IN MONOMERISED TRIOSEPHOSPHATE ISOMERASE, AS DEDUCED FROM THE COMPARISON OF THE STRUCTURAL PROPERTIES OF MONOTIM AND ITS POINT MUTATION VARIANT MONOSS'''<br />
'''LARGE SCALE STRUCTURAL REARRANGEMENTS OF THE FRONT LOOPS IN MONOMERISED TRIOSEPHOSPHATE ISOMERASE, AS DEDUCED FROM THE COMPARISON OF THE STRUCTURAL PROPERTIES OF MONOTIM AND ITS POINT MUTATION VARIANT MONOSS'''<br />


==Overview==
==Overview==
BACKGROUND: Wild-type triosephosphate isomerase (TIM) is a very stable, dimeric enzyme. This dimer can be converted into a stable monomeric, protein (monoTIM) by replacing the 15-residue interface loop (loop-3) by a, shorter, 8-residue, loop. The crystal structure of monoTIM shows that two, active-site loops (loop-1 and loop-4), which are at the dimer interface in, wild-type TIM, have acquired rather different structural properties., Nevertheless, monoTIM has residual catalytic activity. RESULTS: Three new, structures of variants of monoTIM are presented, a double-point mutant, crystallized in the presence and absence of bound inhibitor, and a, single-point mutant in the presence of a different inhibitor. These new, structures show large structural variability for the active-site loops, loop-1, loop-4 and loop-8. In the structures with inhibitor bound, the, catalytic lysine (Lys13 in loop-1) and the catalytic histidine (His95 in, loop-4) adopt conformations similar to those observed in wild-type TIM, but very different from the monoTIM structure. CONCLUSIONS: The residual, catalytic activity of monoTIM can now be rationalized. In the presence of, substrate analogues the active-site loops, loop-1, loop-4 and loop-8, as, well as the catalytic residues, adopt conformations similar to those seen, in the wild-type protein. These loops lack conformational flexibility in, wild-type TIM. The data suggest that the rigidity of these loops in, wild-type TIM, resulting from subunit-subunit contacts at the dimer, interface, is important for optimal catalysis.
BACKGROUND: Wild-type triosephosphate isomerase (TIM) is a very stable dimeric enzyme. This dimer can be converted into a stable monomeric protein (monoTIM) by replacing the 15-residue interface loop (loop-3) by a shorter, 8-residue, loop. The crystal structure of monoTIM shows that two active-site loops (loop-1 and loop-4), which are at the dimer interface in wild-type TIM, have acquired rather different structural properties. Nevertheless, monoTIM has residual catalytic activity. RESULTS: Three new structures of variants of monoTIM are presented, a double-point mutant crystallized in the presence and absence of bound inhibitor, and a single-point mutant in the presence of a different inhibitor. These new structures show large structural variability for the active-site loops, loop-1, loop-4 and loop-8. In the structures with inhibitor bound, the catalytic lysine (Lys13 in loop-1) and the catalytic histidine (His95 in loop-4) adopt conformations similar to those observed in wild-type TIM, but very different from the monoTIM structure. CONCLUSIONS: The residual catalytic activity of monoTIM can now be rationalized. In the presence of substrate analogues the active-site loops, loop-1, loop-4 and loop-8, as well as the catalytic residues, adopt conformations similar to those seen in the wild-type protein. These loops lack conformational flexibility in wild-type TIM. The data suggest that the rigidity of these loops in wild-type TIM, resulting from subunit-subunit contacts at the dimer interface, is important for optimal catalysis.


==About this Structure==
==About this Structure==
1MSS 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]. 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=1MSS OCA].  
1MSS 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]. 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=1MSS OCA].  


==Reference==
==Reference==
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[[Category: Triose-phosphate isomerase]]
[[Category: Triose-phosphate isomerase]]
[[Category: Trypanosoma brucei brucei]]
[[Category: Trypanosoma brucei brucei]]
[[Category: Kishan, K.V.Radha.]]
[[Category: Kishan, K V.Radha.]]
[[Category: Wierenga, R.K.]]
[[Category: Wierenga, R K.]]
[[Category: isomerase(intramolecular oxidoreductase)]]
[[Category: isomerase(intramolecular oxidoreductase)]]


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