1cfi: Difference between revisions
New page: left|200px<br /> <applet load="1cfi" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cfi" /> '''NMR STRUCTURE OF CALCIUM ION-BOUND GAMMA-CA... |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:1cfi. | [[Image:1cfi.jpg|left|200px]]<br /><applet load="1cfi" size="350" color="white" frame="true" align="right" spinBox="true" | ||
<applet load="1cfi" size=" | |||
caption="1cfi" /> | caption="1cfi" /> | ||
'''NMR STRUCTURE OF CALCIUM ION-BOUND GAMMA-CARBOXY-GLUTAMIC ACID-RICH DOMAIN OF FACTOR IX'''<br /> | '''NMR STRUCTURE OF CALCIUM ION-BOUND GAMMA-CARBOXY-GLUTAMIC ACID-RICH DOMAIN OF FACTOR IX'''<br /> | ||
| Line 11: | Line 10: | ||
==About this Structure== | ==About this Structure== | ||
1CFI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Coagulation_factor_IXa Coagulation factor IXa], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.22 3.4.21.22] Full crystallographic information is available from [http:// | 1CFI is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Active as [http://en.wikipedia.org/wiki/Coagulation_factor_IXa Coagulation factor IXa], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.22 3.4.21.22] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CFI OCA]. | ||
==Reference== | ==Reference== | ||
| Line 28: | Line 27: | ||
[[Category: serine protease]] | [[Category: serine protease]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 15:35:34 2008'' | ||
Revision as of 16:35, 15 February 2008
|
NMR STRUCTURE OF CALCIUM ION-BOUND GAMMA-CARBOXY-GLUTAMIC ACID-RICH DOMAIN OF FACTOR IX
OverviewOverview
We have determined the Ca(II)-bound structure of factor IX, residues 1-47, by nuclear magnetic resonance (NMR) spectroscopy. The amino-terminal 47, residues include the gamma-carboxyglutamic acid-rich and aromatic amino, acid stack domains, and this region is responsible for Ca(II)-dependent, phospholipid binding in factor IX. Protons in the 1-47 amino acid sequence, were assigned using standard two-dimensional homonuclear NMR experiments., A total of 851 distance restraints and 57 torsion angle restraints were, used to generate 17 final structures by distance geometry and simulated, annealing methods. The backbone RMSD to the geometric average is 0.6 +/-, 0.1 A. The Ca(II)-bound structure is substantially more ordered with, increased helical content compared to the apo-factor IX (1-47) structure., The global fold is similar to the crystal structure of the Ca(II)-bound, Gla domain of prothrombin fragment I from residues 12 to 47 (RMSD, approximately 1.3 A), but the backbone conformation differs in the first, 11 residues, particularly between residues 3 and 6. The amino-terminal, nine Gla residues are oriented to the interior of the protein and suggest, an internal Ca(II) binding pocket. The carboxyl-terminal three Gla, residues are exposed to solvent. The majority of hydrophobic residues are, required to stabilize a globular core in the carboxyl-terminal, three-quarters of the molecule. However, a hydrophobic surface patch in, the amino-terminal region may represent a phospholipid binding site in, factor IX.
DiseaseDisease
Known diseases associated with this structure: Hemophilia B OMIM:[306900], Warfarin sensitivity OMIM:[306900]
About this StructureAbout this Structure
1CFI is a Single protein structure of sequence from Homo sapiens. Active as Coagulation factor IXa, with EC number 3.4.21.22 Full crystallographic information is available from OCA.
ReferenceReference
Structure of the calcium ion-bound gamma-carboxyglutamic acid-rich domain of factor IX., Freedman SJ, Furie BC, Furie B, Baleja JD, Biochemistry. 1995 Sep 26;34(38):12126-37. PMID:7547952
Page seeded by OCA on Fri Feb 15 15:35:34 2008