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.


2oyh

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
{{Seed}}
 
[[Image:2oyh.png|left|200px]]
[[Image:2oyh.png|left|200px]]
Line 18: Line 17:
-->
-->
{{ABSTRACT_PUBMED_17411074}}
{{ABSTRACT_PUBMED_17411074}}
- 
-
==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==
-
2OYH 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=2OYH OCA].
+
[[2oyh]] 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=2OYH OCA].
 +
 
 +
==See Also==
 +
*[[Fibrinogen]]
==Reference==
==Reference==
Line 31: Line 30:
[[Category: Kostelansky, M S.]]
[[Category: Kostelansky, M S.]]
[[Category: Lord, S T.]]
[[Category: Lord, S T.]]
 +
[[Category: 301a fibrinogen]]
[[Category: Blood clotting]]
[[Category: Blood clotting]]
[[Category: Fibrinogen]]
[[Category: Fibrinogen]]
[[Category: Fibrinogen fragment d]]
[[Category: Fibrinogen fragment d]]
-
[[Category: Gammad298,301a fibrinogen]]
+
[[Category: Gammad298]]
[[Category: Variant fibrinogen]]
[[Category: Variant fibrinogen]]
- 
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 17:57:08 2009''
 

Revision as of 01:25, 27 December 2010

Template:STRUCTURE 2oyh

Contents

Crystal Structure of Fragment D of gammaD298,301A Fibrinogen with the Peptide Ligand Gly-His-Arg-Pro-Amide

Template:ABSTRACT PUBMED 17411074

About this Structure

2oyh is a 10 chain structure of Fibrinogen with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Kostelansky MS, Lounes KC, Ping LF, Dickerson SK, Gorkun OV, Lord ST. Probing the gamma2 calcium-binding site: studies with gammaD298,301A fibrinogen reveal changes in the gamma294-301 loop that alter the integrity of the "a" polymerization site. Biochemistry. 2007 May 1;46(17):5114-23. Epub 2007 Apr 6. PMID:17411074 doi:10.1021/bi602607a

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools