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2ffd

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[[Image:2ffd.gif|left|200px]]
[[Image:2ffd.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 2ffd |SIZE=350|CAPTION= <scene name='initialview01'>2ffd</scene>, resolution 2.890&Aring;
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The line below this paragraph, containing "STRUCTURE_2ffd", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=FUC:ALPHA-L-FUCOSE'>FUC</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY=
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or leave the SCENE parameter empty for the default display.
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|GENE= FGA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), FGB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), FGG ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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-->
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|DOMAIN=
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{{STRUCTURE_2ffd| PDB=2ffd | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ffd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ffd OCA], [http://www.ebi.ac.uk/pdbsum/2ffd PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ffd RCSB]</span>
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}}
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'''Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE'''
'''Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE'''
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Betts, L.]]
[[Category: Betts, L.]]
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[[Category: complex of fibrinogen with a site mimic gprvve in both a and b site]]
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[[Category: Complex of fibrinogen with a site mimic gprvve in both a and b site]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 03:49:53 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:02:04 2008''
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Revision as of 00:49, 4 May 2008

Image:2ffd.gif

Template:STRUCTURE 2ffd

Fibrinogen Fragment D with "A" knob peptide mimic GPRVVE


Disease

Known disease associated with this structure: Afibrinogenemia, congenital OMIM:[134820], Amyloidosis, hereditary renal OMIM:[134820], Dysfibrinogenemia, alpha type, causing bleeding diathesis OMIM:[134820], Dysfibrinogenemia, alpha type, causing recurrent thrombosis OMIM:[134820], Afibrinogenemia, congenital OMIM:[134830], Dysfibrinogenemia, beta type OMIM:[134830], Thrombophilia, dysfibrinogenemic OMIM:[134830], Dysfibrinogenemia, gamma type OMIM:[134850], Hypofibrinogenemia, gamma type OMIM:[134850], Thrombophilia, dysfibrinogenemic OMIM:[134850]

About this Structure

2FFD is a Protein complex structure of sequences from Homo sapiens. 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 Sun May 4 03:49:53 2008

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OCA

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