|
|
| Line 1: |
Line 1: |
| {{Seed}}
| |
| [[Image:1rf0.png|left|200px]] | | [[Image:1rf0.png|left|200px]] |
|
| |
|
| <!--
| |
| The line below this paragraph, containing "STRUCTURE_1rf0", 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_1rf0| PDB=1rf0 | SCENE= }} | | {{STRUCTURE_1rf0| PDB=1rf0 | SCENE= }} |
|
| |
|
| ===Crystal Structure of Fragment D of gammaE132A Fibrinogen=== | | ===Crystal Structure of Fragment D of gammaE132A Fibrinogen=== |
|
| |
|
|
| |
| <!--
| |
| The line below this paragraph, {{ABSTRACT_PUBMED_14992585}}, adds the Publication Abstract to the page
| |
| (as it appears on PubMed at http://www.pubmed.gov), where 14992585 is the PubMed ID number.
| |
| -->
| |
| {{ABSTRACT_PUBMED_14992585}} | | {{ABSTRACT_PUBMED_14992585}} |
|
| |
|
| ==Disease== | | ==About this Structure== |
| 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]]
| | [[1rf0]] is a 6 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=1RF0 OCA]. |
|
| |
|
| ==About this Structure== | | ==See Also== |
| 1RF0 is a 6 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=1RF0 OCA].
| | *[[Fibrinogen|Fibrinogen]] |
|
| |
|
| ==Reference== | | ==Reference== |
| <ref group="xtra">PMID:14992585</ref><references group="xtra"/> | | <ref group="xtra">PMID:014992585</ref><references group="xtra"/> |
| [[Category: Homo sapiens]] | | [[Category: Homo sapiens]] |
| [[Category: Gorkun, O V.]] | | [[Category: Gorkun, O V.]] |
| [[Category: Kostelansky, M S.]] | | [[Category: Kostelansky, M S.]] |
| [[Category: Lord, S T.]] | | [[Category: Lord, S T.]] |
| | [[Category: Blood clotting]] |
| [[Category: Blood coagulation]] | | [[Category: Blood coagulation]] |
| [[Category: Fibrinogen]] | | [[Category: Fibrinogen]] |
| Line 37: |
Line 26: |
| [[Category: Recombinant fibrinogen fragment d]] | | [[Category: Recombinant fibrinogen fragment d]] |
| [[Category: Recombinant fibrinogen gammae132a]] | | [[Category: Recombinant fibrinogen gammae132a]] |
|
| |
| ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 14:24:36 2009''
| |
