1z76: Difference between revisions

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New page: left|200px<br /><applet load="1z76" size="450" color="white" frame="true" align="right" spinBox="true" caption="1z76, resolution 1.85Å" /> '''Crystal structure of...
 
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[[Image:1z76.gif|left|200px]]<br /><applet load="1z76" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1z76.gif|left|200px]]<br /><applet load="1z76" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1z76, resolution 1.85&Aring;" />
caption="1z76, resolution 1.85&Aring;" />
'''Crystal structure of an acidic phospholipase A2 (BthA-I) from Bothrops jararacussu venom complexed with p-bromophenacyl bromide'''<br />
'''Crystal structure of an acidic phospholipase A2 (BthA-I) from Bothrops jararacussu venom complexed with p-bromophenacyl bromide'''<br />


==Overview==
==Overview==
The crystal structure of an acidic phospholipase A(2) isolated from, Bothrops jararacussu venom (BthA-I) chemically modified with, p-bromophenacyl bromide (BPB) has been determined at 1.85 Angstroms, resolution. The catalytic, platelet-aggregation inhibition, anticoagulant, and hypotensive activities of BthA-I are abolished by ligand binding., Electron-density maps permitted unambiguous identification of inhibitor, covalently bound to His48 in the substrate-binding cleft. The BthA-I-BPB, complex contains three structural regions that are modified after, inhibitor binding: the Ca(2+)-binding loop, beta-wing and C-terminal, regions. Comparison of BthA-I-BPB with two other BPB-inhibited PLA(2), structures suggests that in the absence of Na(+) ions at the, Ca(2+)-binding loop, this loop and other regions of the PLA(2)s undergo, structural changes. The BthA-I-BPB structure reveals a novel oligomeric, conformation. This conformation is more energetically and conformationally, stable than the native structure and the abolition of pharmacological, activities by the ligand may be related to the oligomeric structural, changes. A residue of the ;pancreatic' loop (Lys69), which is usually, attributed as providing the anticoagulant effect, is in the dimeric, interface of BthA-I-BPB, leading to a new hypothesis regarding the, abolition of this activity by BPB.
The crystal structure of an acidic phospholipase A(2) isolated from Bothrops jararacussu venom (BthA-I) chemically modified with p-bromophenacyl bromide (BPB) has been determined at 1.85 Angstroms resolution. The catalytic, platelet-aggregation inhibition, anticoagulant and hypotensive activities of BthA-I are abolished by ligand binding. Electron-density maps permitted unambiguous identification of inhibitor covalently bound to His48 in the substrate-binding cleft. The BthA-I-BPB complex contains three structural regions that are modified after inhibitor binding: the Ca(2+)-binding loop, beta-wing and C-terminal regions. Comparison of BthA-I-BPB with two other BPB-inhibited PLA(2) structures suggests that in the absence of Na(+) ions at the Ca(2+)-binding loop, this loop and other regions of the PLA(2)s undergo structural changes. The BthA-I-BPB structure reveals a novel oligomeric conformation. This conformation is more energetically and conformationally stable than the native structure and the abolition of pharmacological activities by the ligand may be related to the oligomeric structural changes. A residue of the ;pancreatic' loop (Lys69), which is usually attributed as providing the anticoagulant effect, is in the dimeric interface of BthA-I-BPB, leading to a new hypothesis regarding the abolition of this activity by BPB.


==About this Structure==
==About this Structure==
1Z76 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bothrops_jararacussu Bothrops jararacussu] with PBP as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Phospholipase_A(2) Phospholipase A(2)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.4 3.1.1.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Z76 OCA].  
1Z76 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bothrops_jararacussu Bothrops jararacussu] with <scene name='pdbligand=PBP:'>PBP</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Phospholipase_A(2) Phospholipase A(2)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.1.4 3.1.1.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Z76 OCA].  


==Reference==
==Reference==
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[[Category: Phospholipase A(2)]]
[[Category: Phospholipase A(2)]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Fontes, M.R.]]
[[Category: Fontes, M R.]]
[[Category: Magro, A.J.]]
[[Category: Magro, A J.]]
[[Category: Soares, A.M.]]
[[Category: Soares, A M.]]
[[Category: Takeda, A.A.]]
[[Category: Takeda, A A.]]
[[Category: PBP]]
[[Category: PBP]]
[[Category: acidic phospholipase a2]]
[[Category: acidic phospholipase a2]]
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[[Category: x-ray crystallography]]
[[Category: x-ray crystallography]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:12:45 2008''