1e3v: Difference between revisions

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New page: left|200px<br /><applet load="1e3v" size="450" color="white" frame="true" align="right" spinBox="true" caption="1e3v, resolution 2.0Å" /> '''CRYSTAL STRUCTURE OF ...
 
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[[Image:1e3v.jpg|left|200px]]<br /><applet load="1e3v" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1e3v.jpg|left|200px]]<br /><applet load="1e3v" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1e3v, resolution 2.0&Aring;" />
caption="1e3v, resolution 2.0&Aring;" />
'''CRYSTAL STRUCTURE OF KETOSTEROID ISOMERASE FROM PSEDOMONAS PUTIDA COMPLEXED WITH DEOXYCHOLATE'''<br />
'''CRYSTAL STRUCTURE OF KETOSTEROID ISOMERASE FROM PSEDOMONAS PUTIDA COMPLEXED WITH DEOXYCHOLATE'''<br />


==Overview==
==Overview==
Delta(5)-3-Ketosteroid isomerase catalyzes cleavage and formation of a C-H, bond at a diffusion-controlled limit. By determining the crystal, structures of the enzyme in complex with each of three different, inhibitors and by nuclear magnetic resonance (NMR) spectroscopic, investigation, we evidenced the ionization of a hydroxyl group (pK(a), approximately 16.5) of an inhibitor, which forms a low barrier hydrogen, bond (LBHB) with a catalytic residue Tyr(14) (pK(a) approximately 11.5), and the protonation of the catalytic residue Asp(38) with pK(a) of, approximately 4.5 at pH 6.7 in the interaction with a carboxylate group of, an inhibitor. The perturbation of the pK(a) values in both cases arises, from the formation of favorable interactions between inhibitors and, catalytic residues. The results indicate that the pK(a) difference between, catalytic residue and substrate can be significantly reduced in the active, site environment as a result of the formation of energetically favorable, interactions during the course of enzyme reactions. The reduction in the, pK(a) difference should facilitate the abstraction of a proton and thereby, eliminate a large fraction of activation energy in general acid/base, enzyme reactions. The pK(a) perturbation provides a mechanistic ground for, the fast reactivity of many enzymes and for the understanding of how some, enzymes are able to extract a proton from a C-H group with a pK(a) value, as high as approximately 30.
Delta(5)-3-Ketosteroid isomerase catalyzes cleavage and formation of a C-H bond at a diffusion-controlled limit. By determining the crystal structures of the enzyme in complex with each of three different inhibitors and by nuclear magnetic resonance (NMR) spectroscopic investigation, we evidenced the ionization of a hydroxyl group (pK(a) approximately 16.5) of an inhibitor, which forms a low barrier hydrogen bond (LBHB) with a catalytic residue Tyr(14) (pK(a) approximately 11.5), and the protonation of the catalytic residue Asp(38) with pK(a) of approximately 4.5 at pH 6.7 in the interaction with a carboxylate group of an inhibitor. The perturbation of the pK(a) values in both cases arises from the formation of favorable interactions between inhibitors and catalytic residues. The results indicate that the pK(a) difference between catalytic residue and substrate can be significantly reduced in the active site environment as a result of the formation of energetically favorable interactions during the course of enzyme reactions. The reduction in the pK(a) difference should facilitate the abstraction of a proton and thereby eliminate a large fraction of activation energy in general acid/base enzyme reactions. The pK(a) perturbation provides a mechanistic ground for the fast reactivity of many enzymes and for the understanding of how some enzymes are able to extract a proton from a C-H group with a pK(a) value as high as approximately 30.


==About this Structure==
==About this Structure==
1E3V 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 DXC as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1E3V OCA].  
1E3V 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=DXC:'>DXC</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1E3V OCA].  


==Reference==
==Reference==
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[[Category: Pseudomonas putida]]
[[Category: Pseudomonas putida]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Ha, N.C.]]
[[Category: Ha, N C.]]
[[Category: Kim, J.S.]]
[[Category: Kim, J S.]]
[[Category: Kim, M.S.]]
[[Category: Kim, M S.]]
[[Category: Oh, B.H.]]
[[Category: Oh, B H.]]
[[Category: DXC]]
[[Category: DXC]]
[[Category: deoxychlate]]
[[Category: deoxychlate]]
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[[Category: reverse binding]]
[[Category: reverse binding]]


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