2gz5: Difference between revisions

New page: left|200px<br /> <applet load="2gz5" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gz5, resolution 1.10Å" /> '''Human Type 1 methio...
 
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[[Image:2gz5.gif|left|200px]]<br />
[[Image:2gz5.gif|left|200px]]<br /><applet load="2gz5" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2gz5" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2gz5, resolution 1.10&Aring;" />
caption="2gz5, resolution 1.10&Aring;" />
'''Human Type 1 methionine aminopeptidase in complex with ovalicin at 1.1 Ang'''<br />
'''Human Type 1 methionine aminopeptidase in complex with ovalicin at 1.1 Ang'''<br />


==Overview==
==Overview==
Methionine aminopeptidases (MetAPs) remove the initiator methionine during, protein biosynthesis. They exist in two isoforms, MetAP1 and MetAP2. The, anti-angiogenic compound fumagillin binds tightly to the Type 2 MetAPs but, only weakly to Type 1. High-affinity complexes of fumagillin and its, relative ovalicin with Type 2 human MetAP have been reported. Here we, describe the crystallographic structure of the low-affinity complex, between ovalicin and Type 1 human MetAP at 1.1 A resolution. This provides, the first opportunity to compare the structures of ovalicin or fumagillin, bound to a Type 1 and a Type 2 MetAP. For both Type 1 and Type 2 human, MetAPs the inhibitor makes a covalent adduct with a corresponding, histidine. At the same time there are significant differences in the, alignment of the inhibitors within the respective active sites. It has, been argued that the lower affinity of ovalicin and fumagillin for the, Type 1 MetAPs is due to the smaller size of their active sites relative to, the Type 2 enzymes. Comparison with the uncomplexed structure of human, Type 1 MetAP indicates that there is some truth to this. Several active, site residues have to move "outward" by 0.5 Angstroms or so to accommodate, the inhibitor. Other residues move "inward." There are, however, other, factors that come into play. In particular, the side chain of His310, rotates by 134 degrees into a different position where (together with, Glu128 and Tyr195) it coordinates a metal ion not seen at this site in the, native enzyme.
Methionine aminopeptidases (MetAPs) remove the initiator methionine during protein biosynthesis. They exist in two isoforms, MetAP1 and MetAP2. The anti-angiogenic compound fumagillin binds tightly to the Type 2 MetAPs but only weakly to Type 1. High-affinity complexes of fumagillin and its relative ovalicin with Type 2 human MetAP have been reported. Here we describe the crystallographic structure of the low-affinity complex between ovalicin and Type 1 human MetAP at 1.1 A resolution. This provides the first opportunity to compare the structures of ovalicin or fumagillin bound to a Type 1 and a Type 2 MetAP. For both Type 1 and Type 2 human MetAPs the inhibitor makes a covalent adduct with a corresponding histidine. At the same time there are significant differences in the alignment of the inhibitors within the respective active sites. It has been argued that the lower affinity of ovalicin and fumagillin for the Type 1 MetAPs is due to the smaller size of their active sites relative to the Type 2 enzymes. Comparison with the uncomplexed structure of human Type 1 MetAP indicates that there is some truth to this. Several active site residues have to move "outward" by 0.5 Angstroms or so to accommodate the inhibitor. Other residues move "inward." There are, however, other factors that come into play. In particular, the side chain of His310 rotates by 134 degrees into a different position where (together with Glu128 and Tyr195) it coordinates a metal ion not seen at this site in the native enzyme.


==About this Structure==
==About this Structure==
2GZ5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with CO, K, OVA and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Methionyl_aminopeptidase Methionyl aminopeptidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.11.18 3.4.11.18] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2GZ5 OCA].  
2GZ5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=CO:'>CO</scene>, <scene name='pdbligand=K:'>K</scene>, <scene name='pdbligand=OVA:'>OVA</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Methionyl_aminopeptidase Methionyl aminopeptidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.11.18 3.4.11.18] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GZ5 OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Addlagatta, A.]]
[[Category: Addlagatta, A.]]
[[Category: Matthews, B.W.]]
[[Category: Matthews, B W.]]
[[Category: CO]]
[[Category: CO]]
[[Category: GOL]]
[[Category: GOL]]
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[[Category: pita-bread fold]]
[[Category: pita-bread fold]]


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