2iqc
From Proteopedia
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==Crystal structure of Human FancF Protein that Functions in the Assembly of a DNA Damage Signaling Complex==  | ==Crystal structure of Human FancF Protein that Functions in the Assembly of a DNA Damage Signaling Complex==  | ||
| - | <StructureSection load='2iqc' size='340' side='right' caption='[[2iqc]], [[Resolution|resolution]] 2.40Å' scene=''>  | + | <StructureSection load='2iqc' size='340' side='right'caption='[[2iqc]], [[Resolution|resolution]] 2.40Å' scene=''>  | 
== Structural highlights ==  | == Structural highlights ==  | ||
| - | <table><tr><td colspan='2'>[[2iqc]] is a 1 chain structure with sequence from [  | + | <table><tr><td colspan='2'>[[2iqc]] 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=2IQC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2IQC FirstGlance]. <br>  | 
| - | </td></tr><tr id='  | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.4Å</td></tr>  | 
| - | <tr id='  | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=HG:MERCURY+(II)+ION'>HG</scene></td></tr>  | 
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[  | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2iqc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2iqc OCA], [https://pdbe.org/2iqc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2iqc RCSB], [https://www.ebi.ac.uk/pdbsum/2iqc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2iqc ProSAT]</span></td></tr>  | 
</table>  | </table>  | ||
== Disease ==  | == Disease ==  | ||
| - | [  | + | [https://www.uniprot.org/uniprot/FANCF_HUMAN FANCF_HUMAN] Defects in FANCF are the cause of Fanconi anemia complementation group F (FANCF) [MIM:[https://omim.org/entry/603467 603467]. A disorder affecting all bone marrow elements and resulting in anemia, leukopenia and thrombopenia. It is associated with cardiac, renal and limb malformations, dermal pigmentary changes, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage) and defective DNA repair.<ref>PMID:10615118</ref>   | 
== Function ==  | == Function ==  | ||
| - | [  | + | [https://www.uniprot.org/uniprot/FANCF_HUMAN FANCF_HUMAN] DNA repair protein that may operate in a postreplication repair or a cell cycle checkpoint function. May be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability (By similarity).  | 
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== References ==  | == References ==  | ||
<references/>  | <references/>  | ||
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</StructureSection>  | </StructureSection>  | ||
[[Category: Homo sapiens]]  | [[Category: Homo sapiens]]  | ||
| - | [[Category: Andrea  | + | [[Category: Large Structures]]  | 
| - | [[Category: Ellenberger  | + | [[Category: D'Andrea A]]  | 
| - | [[Category: Gurtan  | + | [[Category: Ellenberger TE]]  | 
| - | [[Category: Kowal  | + | [[Category: Gurtan AM]]  | 
| - | [[Category: Lehmann  | + | [[Category: Kowal P]]  | 
| - | [[Category: Stuckert  | + | [[Category: Lehmann C]]  | 
| - | + | [[Category: Stuckert P]]  | |
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Current revision
Crystal structure of Human FancF Protein that Functions in the Assembly of a DNA Damage Signaling Complex
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