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="450" color="white" frame="true" align="right" spinBox="true"  
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caption="1bsk, resolution 3.0&Aring;" />
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'''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, 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.
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://ispc.weizmann.ac.il/oca-bin/ocashort?id=1BSK OCA].  
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.K.]]
[[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.T.]]
[[Category: Rajagopalan, P T.]]
[[Category: MLN]]
[[Category: MLN]]
[[Category: PO4]]
[[Category: PO4]]
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[[Category: metalloproteinase]]
[[Category: metalloproteinase]]


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