3hus: Difference between revisions

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~~'''Unreleased structure'''~~

[[Image:3hus.jpg|left|200px]]

The ~~entry~~ 3hus ~~is ON HOLD~~ ~~until Paper Publication~~

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~~Authors: Lord, S.T., Bowley, S.R., Okumura, N.~~

===Crystal structure of recombinant gamma N308K fibrinogen fragment D with the peptide ligand Gly-Pro-Arg-Pro-amide===

~~Description: Crystal structure of recombinant gamma N308K fibrinogen fragment D with the peptide ligand Gly-Pro-Arg-Pro-amide~~

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug ~~5 09~~:45:41 2009''

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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==

3HUS 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=3HUS OCA].

==Reference==

[[Category: Homo sapiens]]

[[Category: Bowley, S R.]]

[[Category: Lord, S T.]]

[[Category: Okumura, N.]]

[[Category: Alternative splicing]]

[[Category: Amyloid]]

[[Category: Amyloidosis]]

[[Category: Blood clotting]]

[[Category: Blood coagulation]]

[[Category: Calcium]]

[[Category: Coiled coil]]

[[Category: Disease mutation]]

[[Category: Disulfide bond]]

[[Category: Fibrinogen fragment d]]

[[Category: Glycoprotein]]

[[Category: Isopeptide bond]]

[[Category: Phosphoprotein]]

[[Category: Polymorphism]]

[[Category: Pyrrolidone carboxylic acid]]

[[Category: Secreted]]

[[Category: Sulfation]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 19 13:14:58 2009''

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+{{Seed}}
+[[Image:3hus.jpg|left|200px]]
-The entry 3hus is ON HOLD  until Paper Publication
+<!--
+The line below this paragraph, containing "STRUCTURE_3hus", 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_3hus|  PDB=3hus  |  SCENE=  }}
-Authors: Lord, S.T., Bowley, S.R., Okumura, N.
+===Crystal structure of recombinant gamma N308K fibrinogen fragment D with the peptide ligand Gly-Pro-Arg-Pro-amide===
-Description: Crystal structure of recombinant gamma N308K fibrinogen fragment D with the peptide ligand Gly-Pro-Arg-Pro-amide
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug  5 09:45:41 2009''
+<!--
+The line below this paragraph, {{ABSTRACT_PUBMED_19650644}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 19650644 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_19650644}}
+==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==
+HUS 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=3HUS OCA].
+==Reference==
+<ref group="xtra">PMID:19650644</ref><references group="xtra"/>
+[[Category: Homo sapiens]]
+[[Category: Bowley, S R.]]
+[[Category: Lord, S T.]]
+[[Category: Okumura, N.]]
+[[Category: Alternative splicing]]
+[[Category: Amyloid]]
+[[Category: Amyloidosis]]
+[[Category: Blood clotting]]
+[[Category: Blood coagulation]]
+[[Category: Calcium]]
+[[Category: Coiled coil]]
+[[Category: Disease mutation]]
+[[Category: Disulfide bond]]
+[[Category: Fibrinogen fragment d]]
+[[Category: Glycoprotein]]
+[[Category: Isopeptide bond]]
+[[Category: Phosphoprotein]]
+[[Category: Polymorphism]]
+[[Category: Pyrrolidone carboxylic acid]]
+[[Category: Secreted]]
+[[Category: Sulfation]]
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 19 13:14:58 2009''