2ffd: Difference between revisions
New page: left|200px<br /> <applet load="2ffd" size="450" color="white" frame="true" align="right" spinBox="true" caption="2ffd, resolution 2.890Å" /> '''Fibrinogen Fragmen... |
No edit summary |
||
| Line 1: | Line 1: | ||
[[Image:2ffd.gif|left|200px]]<br /> | [[Image:2ffd.gif|left|200px]]<br /><applet load="2ffd" size="350" color="white" frame="true" align="right" spinBox="true" | ||
<applet load="2ffd" size=" | |||
caption="2ffd, resolution 2.890Å" /> | caption="2ffd, resolution 2.890Å" /> | ||
'''Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE'''<br /> | '''Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE'''<br /> | ||
| Line 8: | Line 7: | ||
==About this Structure== | ==About this Structure== | ||
2FFD 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 CA as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http:// | 2FFD 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=CA:'>CA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FFD OCA]. | ||
==Reference== | ==Reference== | ||
| Line 18: | Line 17: | ||
[[Category: complex of fibrinogen with "a" site mimic gprvve in both "a" and "b" sites]] | [[Category: complex of fibrinogen with "a" site mimic gprvve in both "a" and "b" sites]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:20:52 2008'' | ||
Revision as of 15:20, 21 February 2008
|
Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE
Disease
Known diseases associated with this structure: Afibrinogenemia, congenital OMIM:[134820], Afibrinogenemia, congenital OMIM:[134830], Amyloidosis, hereditary renal OMIM:[134820], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[134820], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[134820], Dysfibrinogenemia, beta type OMIM:[134830], Dysfibrinogenemia, gamma type OMIM:[134850], Hypofibrinogenemia, gamma type OMIM:[134850], Thrombophilia, dysfibrinogenemic OMIM:[134830], Thrombophilia, dysfibrinogenemic OMIM:[134850]
About this Structure
2FFD is a Protein complex structure of sequences from Homo sapiens with CA as ligand. Full crystallographic information is available from OCA.
Reference
The structure of fibrinogen fragment D with the 'A' knob peptide GPRVVE., Betts L, Merenbloom BK, Lord ST, J Thromb Haemost. 2006 May;4(5):1139-41. PMID:16689770
Page seeded by OCA on Thu Feb 21 17:20:52 2008
