1cqs: Difference between revisions
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New page: left|200px<br /><applet load="1cqs" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cqs, resolution 1.90Å" /> '''CRYSTAL STRUCTURE OF... |
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[[Image:1cqs.gif|left|200px]]<br /><applet load="1cqs" size=" | [[Image:1cqs.gif|left|200px]]<br /><applet load="1cqs" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1cqs, resolution 1.90Å" /> | caption="1cqs, resolution 1.90Å" /> | ||
'''CRYSTAL STRUCTURE OF D103E MUTANT WITH EQUILENINEOF KSI IN PSEUDOMONAS PUTIDA'''<br /> | '''CRYSTAL STRUCTURE OF D103E MUTANT WITH EQUILENINEOF KSI IN PSEUDOMONAS PUTIDA'''<br /> | ||
==Overview== | ==Overview== | ||
Delta 5-3-ketosteroid isomerase (KSI) catalyzes the allylic isomerization | Delta 5-3-ketosteroid isomerase (KSI) catalyzes the allylic isomerization of Delta 5-3-ketosteroids at a rate approaching the diffusion limit by an intramolecular transfer of a proton. Despite the extensive studies on the catalytic mechanism, it still remains controversial whether the catalytic residue Asp-99 donates a hydrogen bond to the steroid or to Tyr-14. To clarify the role of Asp-99 in the catalysis, two single mutants of D99E and D99L and three double mutants of Y14F/D99E, Y14F/D99N, and Y14F/D99L have been prepared by site-directed mutagenesis. The D99E mutant whose side chain at position 99 is longer by an additional methylene group exhibits nearly the same kcat as the wild-type while the D99L mutant exhibits ca. 125-fold lower kcat than that of the wild-type. The mutations made at positions 14 and 99 exert synergistic or partially additive effect on kcat in the double mutants, which is inconsistent with the mechanism based on the hydrogen-bonded catalytic dyad, Asp-99 COOH...Tyr-14 OH...C3-O of the steroid. The crystal structure of D99E/D38N complexed with equilenin, an intermediate analogue, at 1.9 A resolution reveals that the distance between Tyr-14 O eta and Glu-99 O epsilon is ca. 4.2 A, which is beyond the range for a hydrogen bond, and that the distance between Glu-99 O epsilon and C3-O of the steroid is maintained to be ca. 2.4 A, short enough for a hydrogen bond to be formed. Taken together, these results strongly support the idea that Asp-99 contributes to the catalysis by donating a hydrogen bond directly to the intermediate. | ||
==About this Structure== | ==About this Structure== | ||
1CQS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pseudomonas_putida Pseudomonas putida] with EQU as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Steroid_Delta-isomerase Steroid Delta-isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.3.1 5.3.3.1] Full crystallographic information is available from [http:// | 1CQS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Pseudomonas_putida Pseudomonas putida] with <scene name='pdbligand=EQU:'>EQU</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Steroid_Delta-isomerase Steroid Delta-isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.3.1 5.3.3.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CQS OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Steroid Delta-isomerase]] | [[Category: Steroid Delta-isomerase]] | ||
[[Category: Choi, G.]] | [[Category: Choi, G.]] | ||
[[Category: Choi, K | [[Category: Choi, K Y.]] | ||
[[Category: Ha, N | [[Category: Ha, N C.]] | ||
[[Category: Kim, D | [[Category: Kim, D H.]] | ||
[[Category: Kim, S | [[Category: Kim, S W.]] | ||
[[Category: Oh, B | [[Category: Oh, B H.]] | ||
[[Category: Park, S.]] | [[Category: Park, S.]] | ||
[[Category: EQU]] | [[Category: EQU]] | ||
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[[Category: putida lbhb]] | [[Category: putida lbhb]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:08:46 2008'' | ||