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3e1i
From Proteopedia
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| + | [[Image:3e1i.jpg|left|200px]] | ||
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| + | {{STRUCTURE_3e1i| PDB=3e1i | SCENE= }} | ||
| - | + | ===Crystal Structure of BbetaD432A Variant Fibrinogen Fragment D with the Peptide Ligand Gly-His-Arg-Pro-amide=== | |
| - | Description: Crystal Structure of BbetaD432A Variant Fibrinogen Fragment D with the Peptide Ligand Gly-His-Arg-Pro-amide | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19075185}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19075185 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19075185}} | ||
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| + | ==Disease== | ||
| + | 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]] | ||
| + | |||
| + | ==About this Structure== | ||
| + | 3E1I is a 8 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=3E1I OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | Fibrinogen variant B{beta}D432A has normal polymerization but does not bind knob "B", Bowley SR, Lord ST, Blood. 2008 Dec 15. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/19075185 19075185] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Bowley, S R.]] | ||
| + | [[Category: Lord, S T.]] | ||
| + | [[Category: Alternative splicing]] | ||
| + | [[Category: Blood clotting]] | ||
| + | [[Category: Blood coagulation]] | ||
| + | [[Category: Calcium]] | ||
| + | [[Category: Coiled coil]] | ||
| + | [[Category: Disease mutation]] | ||
| + | [[Category: Glycoprotein]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Pyrrolidone carboxylic acid]] | ||
| + | [[Category: Secreted]] | ||
| + | [[Category: Sulfation]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 14 13:04:42 2009'' | ||
Revision as of 11:04, 14 January 2009
Contents |
Crystal Structure of BbetaD432A Variant Fibrinogen Fragment D with the Peptide Ligand Gly-His-Arg-Pro-amide
Template:ABSTRACT PUBMED 19075185
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]
About this Structure
3E1I is a 8 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Fibrinogen variant B{beta}D432A has normal polymerization but does not bind knob "B", Bowley SR, Lord ST, Blood. 2008 Dec 15. PMID:19075185
Page seeded by OCA on Wed Jan 14 13:04:42 2009
