2gbf: Difference between revisions
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New page: left|200px<br /><applet load="2gbf" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gbf, resolution 3.100Å" /> '''rat dpp-IV with alk... |
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[[Image:2gbf.gif|left|200px]]<br /><applet load="2gbf" size=" | [[Image:2gbf.gif|left|200px]]<br /><applet load="2gbf" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="2gbf, resolution 3.100Å" /> | caption="2gbf, resolution 3.100Å" /> | ||
'''rat dpp-IV with alkynyl cyanopyrrolidine #1'''<br /> | '''rat dpp-IV with alkynyl cyanopyrrolidine #1'''<br /> | ||
==Overview== | ==Overview== | ||
Dipeptidyl peptidase IV (DPP-IV) belongs to a family of serine peptidases, and due to its indirect regulatory role in plasma glucose modulation, DPP-IV has become an attractive pharmaceutical target for diabetes | Dipeptidyl peptidase IV (DPP-IV) belongs to a family of serine peptidases, and due to its indirect regulatory role in plasma glucose modulation, DPP-IV has become an attractive pharmaceutical target for diabetes therapy. DPP-IV inactivates the glucagon-like peptide (GLP-1) and several other naturally produced bioactive peptides that contain preferentially a proline or alanine residue in the second amino acid sequence position by cleaving the N-terminal dipeptide. To elucidate the details of the active site for structure-based drug design, we crystallized a natural source preparation of DPP-IV isolated from rat kidney and determined its three-dimensional structure using X-ray diffraction techniques. With a high degree of similarity to structures of human DPP-IV, the active site architecture provides important details for the design of inhibitory compounds, and structures of inhibitor-protein complexes offer detailed insight into three-dimensional structure-activity relationships that include a conformational change of Tyr548. Such accommodation is exemplified by the response to chemical substitution on 2-cyanopyrrolidine inhibitors at the 5 position, which conveys inhibitory selectivity for DPP-IV over closely related homologues. A similar conformational change is also observed in the complex with an unrelated synthetic inhibitor containing a xanthine core that is also selective for DPP-IV. These results suggest the conformational flexibility of Tyr548 is unique among protein family members and may be utilized in drug design to achieve peptidase selectivity. | ||
==About this Structure== | ==About this Structure== | ||
2GBF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with AIA as [http://en.wikipedia.org/wiki/ligand ligand]. 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:// | 2GBF is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with <scene name='pdbligand=AIA:'>AIA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. 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=2GBF OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Rattus norvegicus]] | [[Category: Rattus norvegicus]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Fry, E | [[Category: Fry, E H.]] | ||
[[Category: Jakob, C | [[Category: Jakob, C G.]] | ||
[[Category: Longenecker, K | [[Category: Longenecker, K L.]] | ||
[[Category: Wilk, S.]] | [[Category: Wilk, S.]] | ||
[[Category: AIA]] | [[Category: AIA]] | ||
[[Category: serine peptidase beta propeller]] | [[Category: serine peptidase beta propeller]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:30:00 2008'' | ||