1iy7: Difference between revisions

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New page: left|200px<br /><applet load="1iy7" size="450" color="white" frame="true" align="right" spinBox="true" caption="1iy7, resolution 2.00Å" /> '''Crystal Structure of...
 
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[[Image:1iy7.gif|left|200px]]<br /><applet load="1iy7" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1iy7.gif|left|200px]]<br /><applet load="1iy7" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1iy7, resolution 2.00&Aring;" />
caption="1iy7, resolution 2.00&Aring;" />
'''Crystal Structure of CPA and sulfamide-based inhibitor complex'''<br />
'''Crystal Structure of CPA and sulfamide-based inhibitor complex'''<br />


==Overview==
==Overview==
N-Sulfamoylphenylalanine and its derivatives having varied alkyl groups on, the terminal amino group were designed rationally as transition state, analogue inhibitors for carboxypeptidase A (CPA) and synthesized. In CPA, inhibitory assays the parent compound having the (S)-configuration, i.e., (S)-1a, showed potent inhibitory activity with the K(i) value of 0.64, microM. Its enantiomer was shown to be much less potent (K(i) = 470, microM). Introduction of an alkyl group such as methyl or isopropyl group, on the terminal amino group of (S)-1a lowered the inhibitory potency, drastically. Introduction of a methyl group on the internal amino group of, (S)-1a also caused a drastic reduction of the inhibitory activity. The, structure of the CPA x(S)-1a complex determined by single-crystal X-ray, diffraction reveals that the sulfamoyl moiety interacts with the zinc ion, and functional groups at the active site of CPA, which is reminiscent of, the postulated stabilization mode of a tetrahedral transition state in the, CPA-catalyzed hydrolysis of a peptide substrate. On the basis of the, design rationale and the binding mode of (S)-1a to CPA shown by X-ray, crystallographic analysis, the present inhibitors are inferred to be a, novel type of transition state analogue inhibitor for CPA.
N-Sulfamoylphenylalanine and its derivatives having varied alkyl groups on the terminal amino group were designed rationally as transition state analogue inhibitors for carboxypeptidase A (CPA) and synthesized. In CPA inhibitory assays the parent compound having the (S)-configuration, i.e., (S)-1a, showed potent inhibitory activity with the K(i) value of 0.64 microM. Its enantiomer was shown to be much less potent (K(i) = 470 microM). Introduction of an alkyl group such as methyl or isopropyl group on the terminal amino group of (S)-1a lowered the inhibitory potency drastically. Introduction of a methyl group on the internal amino group of (S)-1a also caused a drastic reduction of the inhibitory activity. The structure of the CPA x(S)-1a complex determined by single-crystal X-ray diffraction reveals that the sulfamoyl moiety interacts with the zinc ion and functional groups at the active site of CPA, which is reminiscent of the postulated stabilization mode of a tetrahedral transition state in the CPA-catalyzed hydrolysis of a peptide substrate. On the basis of the design rationale and the binding mode of (S)-1a to CPA shown by X-ray crystallographic analysis, the present inhibitors are inferred to be a novel type of transition state analogue inhibitor for CPA.


==About this Structure==
==About this Structure==
1IY7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with ZN and CXA as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Carboxypeptidase_A Carboxypeptidase A], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.17.1 3.4.17.1] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1IY7 OCA].  
1IY7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=CXA:'>CXA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Carboxypeptidase_A Carboxypeptidase A], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.17.1 3.4.17.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1IY7 OCA].  


==Reference==
==Reference==
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[[Category: Carboxypeptidase A]]
[[Category: Carboxypeptidase A]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Kim, D.H.]]
[[Category: Kim, D H.]]
[[Category: Kim, S.J.]]
[[Category: Kim, S J.]]
[[Category: Park, J.D.]]
[[Category: Park, J D.]]
[[Category: Ryu, S.E.]]
[[Category: Ryu, S E.]]
[[Category: Woo, J.R.]]
[[Category: Woo, J R.]]
[[Category: CXA]]
[[Category: CXA]]
[[Category: ZN]]
[[Category: ZN]]
[[Category: protein-inhibitor complex]]
[[Category: protein-inhibitor complex]]


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