3hkk
From Proteopedia
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| - | [[Image:3hkk.png|left|200px]] | ||
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{{STRUCTURE_3hkk| PDB=3hkk | SCENE= }} | {{STRUCTURE_3hkk| PDB=3hkk | SCENE= }} | ||
| + | ===Structure of human Leukotriene C4 synthase in complex with glutathione sulfonate=== | ||
| + | {{ABSTRACT_PUBMED_022217203}} | ||
| - | === | + | ==Disease== |
| + | [[http://www.uniprot.org/uniprot/LTC4S_HUMAN LTC4S_HUMAN]] Defects in LTC4S are the cause of leukotriene C4 synthase deficiency (LTC4 synthase deficiency) [MIM:[http://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== | ||
| + | [[http://www.uniprot.org/uniprot/LTC4S_HUMAN LTC4S_HUMAN]] Catalyzes the conjugation of leukotriene A4 with reduced glutathione to form leukotriene C4. | ||
==About this Structure== | ==About this Structure== | ||
Revision as of 09:16, 24 March 2013
Contents |
Structure of human Leukotriene C4 synthase in complex with glutathione sulfonate
Template:ABSTRACT PUBMED 022217203
Disease
[LTC4S_HUMAN] Defects in LTC4S are the cause of leukotriene C4 synthase deficiency (LTC4 synthase deficiency) [MIM:246530]. LTC4 synthase deficiency is a fatal neurometabolic developmental disorder. It is associated with muscular hypotonia, psychomotor retardation, failure to thrive, and microcephaly.
Function
[LTC4S_HUMAN] Catalyzes the conjugation of leukotriene A4 with reduced glutathione to form leukotriene C4.
About this Structure
3hkk is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
