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3hus

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3hus.jpg|left|200px]]
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The entry 3hus is ON HOLD until Paper Publication
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{{STRUCTURE_3hus| PDB=3hus | SCENE= }}
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Authors: Lord, S.T., Bowley, S.R., Okumura, N.
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===Crystal structure of recombinant gamma N308K fibrinogen fragment D with the peptide ligand Gly-Pro-Arg-Pro-amide===
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Description: Crystal structure of recombinant gamma N308K fibrinogen fragment D with the peptide ligand Gly-Pro-Arg-Pro-amide
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 5 09:45:41 2009''
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{{ABSTRACT_PUBMED_19650644}}
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==Disease==
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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]]
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==About this Structure==
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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].
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==Reference==
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<ref group="xtra">PMID:19650644</ref><references group="xtra"/>
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[[Category: Homo sapiens]]
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[[Category: Bowley, S R.]]
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[[Category: Lord, S T.]]
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[[Category: Okumura, N.]]
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[[Category: Alternative splicing]]
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[[Category: Amyloid]]
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[[Category: Amyloidosis]]
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[[Category: Blood clotting]]
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[[Category: Blood coagulation]]
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[[Category: Calcium]]
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[[Category: Coiled coil]]
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[[Category: Disease mutation]]
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[[Category: Disulfide bond]]
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[[Category: Fibrinogen fragment d]]
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[[Category: Glycoprotein]]
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[[Category: Isopeptide bond]]
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[[Category: Phosphoprotein]]
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[[Category: Polymorphism]]
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[[Category: Pyrrolidone carboxylic acid]]
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[[Category: Secreted]]
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[[Category: Sulfation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 19 13:14:58 2009''

Revision as of 10:15, 19 August 2009

Image:3hus.jpg

Template:STRUCTURE 3hus

Contents

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

Template:ABSTRACT PUBMED 19650644

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

3HUS is a 10 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Bowley SR, Okumura N, Lord ST. Impaired protofibril formation in fibrinogen N308K is due to altered D:D and A:a interactions. Biochemistry. 2009 Aug 3. PMID:19650644 doi:10.1021/bi900239b

Page seeded by OCA on Wed Aug 19 13:14:58 2009

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