4cr9: Difference between revisions

<StructureSection load='4cr9' size='340' side='right'caption='[[4cr9]], [[Resolution|resolution]] 1.70&Aring;' scene=''>

<table><tr><td colspan='2'>[[4cr9]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CR9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4CR9 FirstGlance]. <br>

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=OTW:4-METHYLQUINOLINE-2,6-DIAMINE'>OTW</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>

<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4cr9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4cr9 OCA], [https://pdbe.org/4cr9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4cr9 RCSB], [https://www.ebi.ac.uk/pdbsum/4cr9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4cr9 ProSAT]</span></td></tr>

[[https://www.uniprot.org/uniprot/FA11_HUMAN FA11_HUMAN]] Defects in F11 are the cause of factor XI deficiency (FA11D) [MIM:[https://omim.org/entry/612416 612416]]; also known as plasma thromboplastin antecedent deficiency or Rosenthal syndrome. It is a hemorrhagic disease characterized by reduced levels and activity of factor XI resulting in moderate bleeding symptoms, usually occurring after trauma or surgery. Patients usually do not present spontaneous bleeding but women can present with menorrhagia. Hemorrhages are usually moderate.<ref>PMID:2813350</ref> <ref>PMID:1547342</ref> <ref>PMID:7888672</ref> <ref>PMID:7669672</ref> <ref>PMID:9401068</ref> <ref>PMID:9787168</ref> <ref>PMID:10027710</ref> <ref>PMID:10606881</ref> <ref>PMID:11895778</ref> <ref>PMID:15026311</ref> <ref>PMID:15180874</ref> <ref>PMID:15953011</ref> <ref>PMID:16607084</ref> <ref>PMID:18005151</ref> <ref>PMID:21668437</ref> <ref>PMID:21457405</ref> <ref>PMID:22016685</ref> <ref>PMID:22322133</ref> <ref>PMID:21999818</ref> <ref>PMID:22159456</ref>  

[[https://www.uniprot.org/uniprot/FA11_HUMAN FA11_HUMAN]] Factor XI triggers the middle phase of the intrinsic pathway of blood coagulation by activating factor IX.

[[Category: Homo sapiens]]

[[Category: Large Structures]]

[[Category: Akkaya S]]

[[Category: Beisel HG]]

[[Category: Eriksson PO]]

[[Category: Erixon K]]

[[Category: Fjellstrom O]]

[[Category: Gustafsson D]]

[[Category: Jurva U]]

[[Category: Kang D]]

[[Category: Karis D]]

[[Category: Knecht W]]

[[Category: Nerme V]]

[[Category: Nilsson I]]

[[Category: Olsson T]]

[[Category: Oster L]]

[[Category: Redzic A]]

[[Category: Roth R]]

[[Category: Sandmark J]]

[[Category: Tigerstrom A]]