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=" | [[Image:1iy7.gif|left|200px]]<br /><applet load="1iy7" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1iy7, resolution 2.00Å" /> | caption="1iy7, resolution 2.00Å" /> | ||
'''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 | 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:// | 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 | [[Category: Kim, D H.]] | ||
[[Category: Kim, S | [[Category: Kim, S J.]] | ||
[[Category: Park, J | [[Category: Park, J D.]] | ||
[[Category: Ryu, S | [[Category: Ryu, S E.]] | ||
[[Category: Woo, J | [[Category: Woo, J R.]] | ||
[[Category: CXA]] | [[Category: CXA]] | ||
[[Category: ZN]] | [[Category: ZN]] | ||
[[Category: protein-inhibitor complex]] | [[Category: protein-inhibitor complex]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:16:58 2008'' | ||