7bhx
From Proteopedia
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==Crystal structure of MAT2a bound to allosteric inhibitor (compound 31)== | ==Crystal structure of MAT2a bound to allosteric inhibitor (compound 31)== | ||
| - | <StructureSection load='7bhx' size='340' side='right'caption='[[7bhx]]' scene=''> | + | <StructureSection load='7bhx' size='340' side='right'caption='[[7bhx]], [[Resolution|resolution]] 1.08Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7BHX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7BHX FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7bhx]] 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=7BHX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7BHX FirstGlance]. <br> |
| - | </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=7bhx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bhx OCA], [https://pdbe.org/7bhx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7bhx RCSB], [https://www.ebi.ac.uk/pdbsum/7bhx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7bhx ProSAT]</span></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.08Å</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=DMS:DIMETHYL+SULFOXIDE'>DMS</scene>, <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene>, <scene name='pdbligand=TO5:7-chloranyl-4-(dimethylamino)-1-pyridin-3-yl-quinazolin-2-one'>TO5</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=7bhx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bhx OCA], [https://pdbe.org/7bhx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7bhx RCSB], [https://www.ebi.ac.uk/pdbsum/7bhx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7bhx ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/METK2_HUMAN METK2_HUMAN] Catalyzes the formation of S-adenosylmethionine from methionine and ATP. | ||
| + | |||
| + | ==See Also== | ||
| + | *[[S-adenosylmethionine synthetase 3D structures|S-adenosylmethionine synthetase 3D structures]] | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Argyrou A]] | [[Category: Argyrou A]] | ||
Current revision
Crystal structure of MAT2a bound to allosteric inhibitor (compound 31)
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Categories: Homo sapiens | Large Structures | Argyrou A | Bagal S | Borjesson U | Cheung T | Chiarparin E | Collie I | De Fusco C | Evans L | Grondine M | Narasimhan P | Robb G | Schimpl M | Scott JS | Stubbs C | Tentarelli S | Underwood E | Vazquez-Chantada M | Wagner DJ
