|
|
| Line 1: |
Line 1: |
| {{Seed}}
| |
| [[Image:2ffd.png|left|200px]] | | [[Image:2ffd.png|left|200px]] |
|
| |
|
| <!--
| |
| The line below this paragraph, containing "STRUCTURE_2ffd", creates the "Structure Box" on the page.
| |
| You may change the PDB parameter (which sets the PDB file loaded into the applet)
| |
| or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
| |
| or leave the SCENE parameter empty for the default display.
| |
| -->
| |
| {{STRUCTURE_2ffd| PDB=2ffd | SCENE= }} | | {{STRUCTURE_2ffd| PDB=2ffd | SCENE= }} |
|
| |
|
| Line 13: |
Line 6: |
|
| |
|
|
| |
|
| ==Disease== | | ==About this Structure== |
| Known disease associated with this structure: Afibrinogenemia, congenital OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Amyloidosis, hereditary renal OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820 134820]], Afibrinogenemia, congenital OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134830 134830]], Dysfibrinogenemia, beta type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134830 134830]], Thrombophilia, dysfibrinogenemic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134830 134830]], Dysfibrinogenemia, gamma type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134850 134850]], Hypofibrinogenemia, gamma type OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134850 134850]], Thrombophilia, dysfibrinogenemic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134850 134850]]
| | [[2ffd]] is a 10 chain structure of [[Fibrinogen]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FFD OCA]. |
|
| |
|
| ==About this Structure== | | ==See Also== |
| 2FFD is a 10 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FFD OCA].
| | *[[Fibrinogen|Fibrinogen]] |
|
| |
|
| ==Reference== | | ==Reference== |
| <ref group="xtra">PMID:16689770</ref><references group="xtra"/> | | <ref group="xtra">PMID:016689770</ref><references group="xtra"/> |
| [[Category: Homo sapiens]] | | [[Category: Homo sapiens]] |
| [[Category: Betts, L.]] | | [[Category: Betts, L.]] |
| | [[Category: Blood clotting]] |
| [[Category: Complex of fibrinogen with a site mimic gprvve in both a and b site]] | | [[Category: Complex of fibrinogen with a site mimic gprvve in both a and b site]] |
|
| |
| ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 09:04:36 2009''
| |
