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4j7y
From Proteopedia
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==Human LTC4 synthase in complex with product analogs - implications for enzyme catalysis== | ==Human LTC4 synthase in complex with product analogs - implications for enzyme catalysis== | ||
| - | <StructureSection load='4j7y' size='340' side='right' caption='[[4j7y]], [[Resolution|resolution]] 2.90Å' scene=''> | + | <StructureSection load='4j7y' size='340' side='right'caption='[[4j7y]], [[Resolution|resolution]] 2.90Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[4j7y]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4j7y]] 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=4J7Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4J7Y FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=1JP:D-GAMMA-GLUTAMYL-(Z)-N-(CARBOXYMETHYLIDENE)-S-[(2R)-2-HYDROXY-4-PHENYLBUTYL]-L-CYSTEINAMIDE'>1JP</scene>, <scene name='pdbligand=NI:NICKEL+(II)+ION'>NI</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.901Å</td></tr> |
| - | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=1JP:D-GAMMA-GLUTAMYL-(Z)-N-(CARBOXYMETHYLIDENE)-S-[(2R)-2-HYDROXY-4-PHENYLBUTYL]-L-CYSTEINAMIDE'>1JP</scene>, <scene name='pdbligand=NI:NICKEL+(II)+ION'>NI</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</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=4j7y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4j7y OCA], [https://pdbe.org/4j7y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4j7y RCSB], [https://www.ebi.ac.uk/pdbsum/4j7y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4j7y ProSAT]</span></td></tr> | |
| - | + | ||
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/LTC4S_HUMAN LTC4S_HUMAN] Defects in LTC4S are the cause of leukotriene C4 synthase deficiency (LTC4 synthase deficiency) [MIM:[https://omim.org/entry/246530 246530]. LTC4 synthase deficiency is a fatal neurometabolic developmental disorder. It is associated with muscular hypotonia, psychomotor retardation, failure to thrive, and microcephaly. |
== Function == | == Function == | ||
| - | [ | + | [https://www.uniprot.org/uniprot/LTC4S_HUMAN LTC4S_HUMAN] Catalyzes the conjugation of leukotriene A4 with reduced glutathione to form leukotriene C4. |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
| + | <div class="pdbe-citations 4j7y" style="background-color:#fffaf0;"></div> | ||
==See Also== | ==See Also== | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | [[Category: Haeggstrom | + | [[Category: Large Structures]] |
| - | [[Category: Niegowski | + | [[Category: Haeggstrom JZ]] |
| - | [[Category: Rinaldo-Matthis | + | [[Category: Niegowski D]] |
| - | + | [[Category: Rinaldo-Matthis A]] | |
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Current revision
Human LTC4 synthase in complex with product analogs - implications for enzyme catalysis
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