8it9

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Current revision (07:19, 14 February 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8it9 is ON HOLD until Paper Publication
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==Co-crystal structure of FTO bound to 22==
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<StructureSection load='8it9' size='340' side='right'caption='[[8it9]], [[Resolution|resolution]] 2.14&Aring;' scene=''>
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Authors: Yang, C.-G., Gan, J.H.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8it9]] 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=8IT9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8IT9 FirstGlance]. <br>
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Description: Co-crystal structure of FTO bound to 22
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.14&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AKG:2-OXOGLUTARIC+ACID'>AKG</scene>, <scene name='pdbligand=ZL6:2-[(2,6-diethyl-4-pyridin-4-yl-phenyl)amino]-6-(1,4-oxazepan-4-ylmethyl)benzoic+acid'>ZL6</scene></td></tr>
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[[Category: Gan, J.H]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8it9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8it9 OCA], [https://pdbe.org/8it9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8it9 RCSB], [https://www.ebi.ac.uk/pdbsum/8it9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8it9 ProSAT]</span></td></tr>
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[[Category: Yang, C.-G]]
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/FTO_HUMAN FTO_HUMAN] Defects in FTO are the cause of growth retardation developmental delay coarse facies and early death (GDFD) [MIM:[https://omim.org/entry/612938 612938]. A severe polymalformation syndrome characterized by postnatal growth retardation, microcephaly, severe psychomotor delay, functional brain deficits and characteristic facial dysmorphism. In some patients, structural brain malformations, cardiac defects, genital anomalies, and cleft palate are observed. Early death occurs by the age of 3 years.<ref>PMID:19559399</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/FTO_HUMAN FTO_HUMAN] Dioxygenase that repairs alkylated DNA and RNA by oxidative demethylation. Has highest activity towards single-stranded RNA containing 3-methyluracil, followed by single-stranded DNA containing 3-methylthymine. Has low demethylase activity towards single-stranded DNA containing 1-methyladenine or 3-methylcytosine. Has no activity towards 1-methylguanine. Has no detectable activity towards double-stranded DNA. Requires molecular oxygen, alpha-ketoglutarate and iron. Contributes to the regulation of the global metabolic rate, energy expenditure and energy homeostasis. Contributes to the regulation of body size and body fat accumulation.<ref>PMID:18775698</ref> <ref>PMID:20376003</ref>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Gan JH]]
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[[Category: Yang C-G]]

Current revision

Co-crystal structure of FTO bound to 22

PDB ID 8it9

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