7bhv: Difference between revisions
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==Crystal structure of MAT2a bound to allosteric inhibitor and in vivo tool compound 28== | ==Crystal structure of MAT2a bound to allosteric inhibitor and in vivo tool compound 28== | ||
<StructureSection load='7bhv' size='340' side='right'caption='[[7bhv]]' scene=''> | <StructureSection load='7bhv' size='340' side='right'caption='[[7bhv]], [[Resolution|resolution]] 1.16Å' 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=7BHV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7BHV FirstGlance]. <br> | <table><tr><td colspan='2'>[[7bhv]] 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=7BHV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7BHV 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=7bhv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bhv OCA], [https://pdbe.org/7bhv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7bhv RCSB], [https://www.ebi.ac.uk/pdbsum/7bhv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7bhv 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]] 1.16Å</td></tr> | ||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene>, <scene name='pdbligand=TQB:7-chloranyl-4-(dimethylamino)-1-phenyl-quinazolin-2-one'>TQB</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=7bhv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7bhv OCA], [https://pdbe.org/7bhv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7bhv RCSB], [https://www.ebi.ac.uk/pdbsum/7bhv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7bhv 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]] | ||
Latest revision as of 07:48, 1 May 2024
Crystal structure of MAT2a bound to allosteric inhibitor and in vivo tool compound 28
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