4l02: Difference between revisions
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{{STRUCTURE_4l02| PDB=4l02 | SCENE= }} | |||
===Crystal Structure of SphK1 with inhibitor=== | |||
{{ABSTRACT_PUBMED_23845219}} | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/SPHK1_HUMAN SPHK1_HUMAN]] Catalyzes the phosphorylation of sphingosine to form sphingosine 1-phosphate (SPP), a lipid mediator with both intra- and extracellular functions. Also acts on D-erythro-sphingosine and to a lesser extent sphinganine, but not other lipids, such as D,L-threo-dihydrosphingosine, N,N-dimethylsphingosine, diacylglycerol, ceramide, or phosphatidylinositol.<ref>PMID:20577214</ref> | |||
==About this Structure== | |||
[[4l02]] is a 3 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4L02 OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:023845219</ref><references group="xtra"/><references/> | |||
[[Category: Homo sapiens]] | |||
[[Category: Sphinganine kinase]] | |||
[[Category: Min, X.]] | |||
[[Category: Walker, N.]] | |||
[[Category: Wang, Z.]] | |||
[[Category: Lipid kinase]] | |||
[[Category: Transferase-transferase inhibitor complex]] | |||