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New page: left|200px<br /><applet load="1orv" size="450" color="white" frame="true" align="right" spinBox="true" caption="1orv, resolution 1.80Å" /> '''Crystal Structure of...
 
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[[Image:1orv.jpg|left|200px]]<br /><applet load="1orv" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1orv.jpg|left|200px]]<br /><applet load="1orv" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1orv, resolution 1.80&Aring;" />
caption="1orv, resolution 1.80&Aring;" />
'''Crystal Structure of Porcine Dipeptidyl Peptidase IV (CD26)'''<br />
'''Crystal Structure of Porcine Dipeptidyl Peptidase IV (CD26)'''<br />


==Overview==
==Overview==
The membrane-bound glycoprotein dipeptidyl peptidase IV (DP IV, CD26) is a, unique multifunctional protein, acting as receptor, binding and, proteolytic molecule. We have determined the sequence and 1.8 A crystal, structure of native DP IV prepared from porcine kidney. The crystal, structure reveals a 2-2-2 symmetric tetrameric assembly which depends on, the natively glycosylated beta-propeller blade IV. The crystal structure, indicates that tetramerization of DP IV is a key mechanism to regulate its, interaction with other components. Each subunit comprises two structural, domains, the N-terminal eight-bladed beta-propeller with open Velcro, topology and the C-terminal alpha/beta-hydrolase domain. Analogy with the, structurally related POP and tricorn protease suggests that substrates, access the buried active site through the beta-propeller tunnel while, products leave the active site through a separate side exit. A dipeptide, mimicking inhibitor complexed to the active site discloses key, determinants for substrate recognition, including a Glu-Glu motif that, distinguishes DP IV as an aminopeptidase and an oxyanion trap that binds, and activates the P(2)-carbonyl oxygen necessary for efficient postproline, cleavage. We discuss active and nonactive site-directed inhibition, strategies of this pharmaceutical target protein.
The membrane-bound glycoprotein dipeptidyl peptidase IV (DP IV, CD26) is a unique multifunctional protein, acting as receptor, binding and proteolytic molecule. We have determined the sequence and 1.8 A crystal structure of native DP IV prepared from porcine kidney. The crystal structure reveals a 2-2-2 symmetric tetrameric assembly which depends on the natively glycosylated beta-propeller blade IV. The crystal structure indicates that tetramerization of DP IV is a key mechanism to regulate its interaction with other components. Each subunit comprises two structural domains, the N-terminal eight-bladed beta-propeller with open Velcro topology and the C-terminal alpha/beta-hydrolase domain. Analogy with the structurally related POP and tricorn protease suggests that substrates access the buried active site through the beta-propeller tunnel while products leave the active site through a separate side exit. A dipeptide mimicking inhibitor complexed to the active site discloses key determinants for substrate recognition, including a Glu-Glu motif that distinguishes DP IV as an aminopeptidase and an oxyanion trap that binds and activates the P(2)-carbonyl oxygen necessary for efficient postproline cleavage. We discuss active and nonactive site-directed inhibition strategies of this pharmaceutical target protein.


==About this Structure==
==About this Structure==
1ORV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa] with NAG and SO4 as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Dipeptidyl-peptidase_IV Dipeptidyl-peptidase IV], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.14.5 3.4.14.5] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ORV OCA].  
1ORV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Sus_scrofa Sus scrofa] with <scene name='pdbligand=NAG:'>NAG</scene> and <scene name='pdbligand=SO4:'>SO4</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Dipeptidyl-peptidase_IV Dipeptidyl-peptidase IV], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.14.5 3.4.14.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ORV OCA].  


==Reference==
==Reference==
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[[Category: Bode, W.]]
[[Category: Bode, W.]]
[[Category: Brandstetter, H.]]
[[Category: Brandstetter, H.]]
[[Category: Demuth, H.U.]]
[[Category: Demuth, H U.]]
[[Category: Engel, M.]]
[[Category: Engel, M.]]
[[Category: Heiser, U.]]
[[Category: Heiser, U.]]
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[[Category: substrate channeling]]
[[Category: substrate channeling]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:20:53 2008''