5qrb: Difference between revisions
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==PanDDA analysis group deposition -- Crystal Structure of human ALAS2A in complex with Z2856434868== | |||
<StructureSection load='5qrb' size='340' side='right'caption='[[5qrb]], [[Resolution|resolution]] 1.72Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[5qrb]] is a 2 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=5QRB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5QRB FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.72Å</td></tr> | |||
[[Category: | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NVY:1-ethyl-N-(2-fluorophenyl)piperidin-4-amine'>NVY</scene>, <scene name='pdbligand=PLP:PYRIDOXAL-5-PHOSPHATE'>PLP</scene></td></tr> | ||
[[Category: Foster | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5qrb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5qrb OCA], [https://pdbe.org/5qrb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5qrb RCSB], [https://www.ebi.ac.uk/pdbsum/5qrb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5qrb ProSAT]</span></td></tr> | ||
</table> | |||
== Disease == | |||
[https://www.uniprot.org/uniprot/HEM0_HUMAN HEM0_HUMAN] X-linked sideroblastic anemia;Erythropoietic protoporphyria. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Gain of function mutations in ALS2 are responsible for XLDPT, but they can also be a possible aggravating factor in congenital erythropoietic porphyria and other erythropoietic disorders caused by mutations in other genes (PubMed:21309041).<ref>PMID:21309041</ref> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/HEM0_HUMAN HEM0_HUMAN] | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Arrowsmith CH]] | |||
[[Category: Bailey H]] | |||
[[Category: Bezerra GA]] | |||
[[Category: Bountra C]] | |||
[[Category: Brandao-Neto J]] | |||
[[Category: Brennan PE]] | |||
[[Category: Douangamath A]] | |||
[[Category: Edwards A]] | |||
[[Category: Foster W]] | |||
[[Category: Krojer T]] | |||
[[Category: Nicola BB]] | |||
[[Category: Shrestha L]] | [[Category: Shrestha L]] | ||
[[Category: Talon R]] | |||
[[Category: Yue WW]] | |||
[[Category: Talon | [[Category: Von Delft F]] | ||
[[Category: Yue | |||
[[Category: Von Delft | |||
Latest revision as of 14:25, 21 February 2024
PanDDA analysis group deposition -- Crystal Structure of human ALAS2A in complex with Z2856434868PanDDA analysis group deposition -- Crystal Structure of human ALAS2A in complex with Z2856434868
Structural highlights
DiseaseHEM0_HUMAN X-linked sideroblastic anemia;Erythropoietic protoporphyria. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Gain of function mutations in ALS2 are responsible for XLDPT, but they can also be a possible aggravating factor in congenital erythropoietic porphyria and other erythropoietic disorders caused by mutations in other genes (PubMed:21309041).[1] FunctionReferences
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