This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
1re3
From Proteopedia
(Difference between revisions)
| Line 1: | Line 1: | ||
| - | {{Seed}} | ||
[[Image:1re3.png|left|200px]] | [[Image:1re3.png|left|200px]] | ||
| Line 18: | Line 17: | ||
--> | --> | ||
{{ABSTRACT_PUBMED_14992584}} | {{ABSTRACT_PUBMED_14992584}} | ||
| - | |||
| - | ==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]], 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]] | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1re3]] is a 8 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=1RE3 OCA]. | |
| + | |||
| + | ==See Also== | ||
| + | *[[Fibrinogen]] | ||
==Reference== | ==Reference== | ||
| Line 34: | Line 33: | ||
[[Category: Bbetad398a fibrinogen]] | [[Category: Bbetad398a fibrinogen]] | ||
[[Category: Bbetad398a fibrinogen with ghrpam]] | [[Category: Bbetad398a fibrinogen with ghrpam]] | ||
| + | [[Category: Blood clotting]] | ||
[[Category: Ghrpam]] | [[Category: Ghrpam]] | ||
[[Category: Mutant fibrinogen]] | [[Category: Mutant fibrinogen]] | ||
| Line 39: | Line 39: | ||
[[Category: Recombinant fibrinogen fragment d]] | [[Category: Recombinant fibrinogen fragment d]] | ||
[[Category: Variant fibrinogen]] | [[Category: Variant fibrinogen]] | ||
| - | |||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 23:41:17 2009'' | ||
Revision as of 22:36, 26 December 2010
Contents |
Crystal Structure of Fragment D of BbetaD398A Fibrinogen with the Peptide Ligand Gly-His-Arg-Pro-Amide
Template:ABSTRACT PUBMED 14992584
About this Structure
1re3 is a 8 chain structure of Fibrinogen with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Kostelansky MS, Bolliger-Stucki B, Betts L, Gorkun OV, Lord ST. B beta Glu397 and B beta Asp398 but not B beta Asp432 are required for "B:b" interactions. Biochemistry. 2004 Mar 9;43(9):2465-74. PMID:14992584 doi:10.1021/bi035996f
