3bef
From Proteopedia
(New page: 200px<br /><applet load="3bef" size="350" color="white" frame="true" align="right" spinBox="true" caption="3bef, resolution 2.20Å" /> '''Crystal structure of...) |
|||
Line 7: | Line 7: | ||
==About this Structure== | ==About this Structure== | ||
- | 3BEF is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NAG:'>NAG</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Thrombin Thrombin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.5 3.4.21.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3BEF OCA]. | + | 3BEF is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NAG:'>NAG</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Thrombin Thrombin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.5 3.4.21.5] Known structural/functional Site: <scene name='pdbsite=AC1:Nag Binding Site For Residue E 302'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3BEF OCA]. |
==Reference== | ==Reference== | ||
Line 40: | Line 40: | ||
[[Category: zymogen]] | [[Category: zymogen]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Jan 31 11:02:23 2008'' |
Revision as of 09:02, 31 January 2008
|
Crystal structure of thrombin bound to the extracellular fragment of PAR1
Overview
Na(+) binding near the primary specificity pocket of thrombin promotes the, procoagulant, prothrombotic, and signaling functions of the enzyme. The, effect is mediated allosterically by a communication between the Na(+), site and regions involved in substrate recognition. Using a panel of 78, Ala mutants of thrombin, we have mapped the allosteric core of residues, that are energetically linked to Na(+) binding. These residues are, Asp-189, Glu-217, Asp-222, and Tyr-225, all in close proximity to the, bound Na(+). Among these residues, Asp-189 shares with Asp-221 the, important function of transducing Na(+) binding into enhanced catalytic, activity. None of the residues of exosite I, exosite II, or the 60-loop, plays a significant role in Na(+) binding and allosteric transduction., X-ray crystal structures of the Na(+)-free (slow) and Na(+)-bound (fast), forms of thrombin, free or bound to the active site inhibitor, H-d-Phe-Pro-Arg-chloromethyl-ketone, document the conformational changes, induced by Na(+) binding. The slow --> fast transition results in, formation of the Arg-187:Asp-222 ion pair, optimal orientation of Asp-189, and Ser-195 for substrate binding, and a significant shift of the side, chain of Glu-192 linked to a rearrangement of the network of water, molecules that connect the bound Na(+) to Ser-195 in the active site. The, changes in the water network and the allosteric core explain the, thermodynamic signatures linked to Na(+) binding and the mechanism of, thrombin activation by Na(+). The role of the water network uncovered in, this study establishes a new paradigm for the allosteric regulation of, thrombin and other Na(+)-activated enzymes involved in blood coagulation, and the immune response.
About this Structure
3BEF is a Protein complex structure of sequences from Homo sapiens with as ligand. Active as Thrombin, with EC number 3.4.21.5 Known structural/functional Site: . Full crystallographic information is available from OCA.
Reference
Molecular dissection of Na+ binding to thrombin., Pineda AO, Carrell CJ, Bush LA, Prasad S, Caccia S, Chen ZW, Mathews FS, Di Cera E, J Biol Chem. 2004 Jul 23;279(30):31842-53. Epub 2004 May 19. PMID:15152000
Page seeded by OCA on Thu Jan 31 11:02:23 2008
Categories: Homo sapiens | Protein complex | Thrombin | Bah, A. | Cera, E.Di. | Chen, Z. | Gandhi, P.S. | Mathews, F.S. | NAG | Acute phase | Blood coagulation | Calcium | Cleavage on pair of basic residues | Disease mutation | G-protein coupled receptor | Gamma-carboxyglutamic acid | Glycoprotein | Hydrolase | Kringle | Membrane | Phosphoprotein | Polymorphism | Receptor | Secreted | Serine protease | Transducer | Transmembrane | Zymogen