1bsk: Difference between revisions
New page: left|200px<br /><applet load="1bsk" size="450" color="white" frame="true" align="right" spinBox="true" caption="1bsk, resolution 3.0Å" /> '''ZINC DEFORMYLASE INHI... |
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[[Image:1bsk.gif|left|200px]]<br /><applet load="1bsk" size=" | [[Image:1bsk.gif|left|200px]]<br /><applet load="1bsk" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1bsk, resolution 3.0Å" /> | caption="1bsk, resolution 3.0Å" /> | ||
'''ZINC DEFORMYLASE INHIBITOR COMPLEX FROM E.COLI'''<br /> | '''ZINC DEFORMYLASE INHIBITOR COMPLEX FROM E.COLI'''<br /> | ||
==Overview== | ==Overview== | ||
While protein synthesis in bacteria begins with a formylated methionine, the formyl group of the nascent polypeptide is removed by peptide | While protein synthesis in bacteria begins with a formylated methionine, the formyl group of the nascent polypeptide is removed by peptide deformylase. Since eukaryotic protein synthesis does not involve formylation and deformylation at the N-terminus, there has been increasing interest in peptide deformylase as a potential target for antibacterial chemotherapy. Toward this end and to aid in the design of effective antibiotics targeting peptide deformylase, the structures of the protein-inhibitor complexes of both the cobalt and the zinc containing Escherichia coli peptide deformylase bound to the transition-state analogue, (S)-2-O-(H-phosphonoxy)-L-caproyl-L-leucyl-p-nitroanilide (PCLNA), have been determined. The proteins for both deformylase-inhibitor complexes show basically the same fold as for the native enzyme. The PCLNA inhibitor adopts an extended conformation and fits nicely into a hydrophobic cavity located near the metal site. On the basis of these structures, guidelines for the design of high-affinity deformylase inhibitors are suggested. As our results show that the protein residues which interact with the PCLNA inhibitor are conserved over a wide variety of species, we suggest that antibiotics targeting deformylase could have wide applicability. | ||
==About this Structure== | ==About this Structure== | ||
1BSK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with ZN, PO4 and MLN as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/N-formylmethionylaminoacyl-tRNA_deformylase N-formylmethionylaminoacyl-tRNA deformylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.1.27 3.5.1.27] Full crystallographic information is available from [http:// | 1BSK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=PO4:'>PO4</scene> and <scene name='pdbligand=MLN:'>MLN</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/N-formylmethionylaminoacyl-tRNA_deformylase N-formylmethionylaminoacyl-tRNA deformylase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.1.27 3.5.1.27] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1BSK OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: N-formylmethionylaminoacyl-tRNA deformylase]] | [[Category: N-formylmethionylaminoacyl-tRNA deformylase]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Chan, M | [[Category: Chan, M K.]] | ||
[[Category: Gong, W.]] | [[Category: Gong, W.]] | ||
[[Category: Hao, B.]] | [[Category: Hao, B.]] | ||
[[Category: Hu, Y.]] | [[Category: Hu, Y.]] | ||
[[Category: Pei, D.]] | [[Category: Pei, D.]] | ||
[[Category: Rajagopalan, P | [[Category: Rajagopalan, P T.]] | ||
[[Category: MLN]] | [[Category: MLN]] | ||
[[Category: PO4]] | [[Category: PO4]] | ||
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[[Category: metalloproteinase]] | [[Category: metalloproteinase]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:58:48 2008'' |