5tei
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 5tei is ON HOLD Authors: Morgan, C.A., Hurley, T.D. Description: Structure of human ALDH1A1 with inhibitor CM039 [[Category: Unreleased Structures]...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Structure of human ALDH1A1 with inhibitor CM039== | |
| + | <StructureSection load='5tei' size='340' side='right'caption='[[5tei]], [[Resolution|resolution]] 2.10Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[5tei]] 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=5TEI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5TEI 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]] 2.1Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=M39:6-{[(3-fluorophenyl)methyl]sulfanyl}-5-(2-methylphenyl)-2,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one'>M39</scene>, <scene name='pdbligand=NAI:1,4-DIHYDRONICOTINAMIDE+ADENINE+DINUCLEOTIDE'>NAI</scene>, <scene name='pdbligand=YB:YTTERBIUM+(III)+ION'>YB</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=5tei FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5tei OCA], [https://pdbe.org/5tei PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5tei RCSB], [https://www.ebi.ac.uk/pdbsum/5tei PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5tei ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/AL1A1_HUMAN AL1A1_HUMAN] Binds free retinal and cellular retinol-binding protein-bound retinal. Can convert/oxidize retinaldehyde to retinoic acid (By similarity). | ||
| - | + | ==See Also== | |
| - | + | *[[Aldehyde dehydrogenase 3D structures|Aldehyde dehydrogenase 3D structures]] | |
| - | + | __TOC__ | |
| - | [[Category: | + | </StructureSection> |
| - | [[Category: Hurley | + | [[Category: Homo sapiens]] |
| - | [[Category: Morgan | + | [[Category: Large Structures]] |
| + | [[Category: Hurley TD]] | ||
| + | [[Category: Morgan CA]] | ||
Current revision
Structure of human ALDH1A1 with inhibitor CM039
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