Difference between revisions of "Arachidonate 5-lipoxygenase"

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===Protein Function ===
 
===Protein Function ===
Lipoxygenases are a family of iron-containing enzymes that catalyze the dioxygenation of polyunsaturated fatty acids in lipids containing a cis,cis-1,4-pentadiene structure. It catalyses the following reaction:  
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Lipoxygenases are a family of iron-containing enzymes that catalyze the dioxygenation of polyunsaturated fatty acids in lipids containing a cis,cis-1,4-pentadiene structure. It catalyses the following reaction: <br/>
'''fatty acid + O2 = fatty acid hydroperoxide'''
+
'''fatty acid + O2 = fatty acid hydroperoxide'''<br/>
These enzymes are most common in plants where they may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. In mammals a number of lipoxygenases isozymes are involved in the metabolism of eicosanoids (such as prostaglandins, leu*[https://www.genome.jp/kegg-bin/show_pathway?kotrienes and nonclassic eicosanoids). (From Wikipedia)
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These enzymes are most common in plants where they may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. In mammals a number of lipoxygenases isozymes are involved in the metabolism of eicosanoids (such as prostaglandins, leukotrienes and nonclassic eicosanoids). (From Wikipedia)<br/>
5-Lipoxygenase (5-LO) is the key enzyme in the biosynthesis of leu*[https://www.genome.jp/kegg-bin/show_pathway?kotrienes (LTs) which are mediators involved in the development of atherosclerosis, inflammatory diseases and cancer. 5-LO metabolizes arachidonic acid to leu*[https://www.genome.jp/kegg-bin/show_pathway?kotriene A4 in a two step reaction by incorporation of molecular oxygen. (PMID: 22137889)
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5-Lipoxygenase (5-LO) is the key enzyme in the biosynthesis of leukotrienes (LTs) which are mediators involved in the development of atherosclerosis, inflammatory diseases and cancer. 5-LO metabolizes arachidonic acid to leukotriene A4 in a two step reaction by incorporation of molecular oxygen. (PMID: 22137889)<br/>
<br/>
 
  
 
===Cys Function & Property===
 
===Cys Function & Property===
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==Reference==
 
==Reference==
# Hörnig M, Mar*[https://www.genome.jp/kegg-bin/show_pathway?koutsa S, Häfner A K, et al. '''Inhibition of 5-lipoxygenase by U73122 is due to covalent binding to cysteine 416[J].''' Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids, 2012, 1821(2): 279-286. [https://www.ncbi.nlm.nih.gov/pubmed/?term=22137889 22137889]<br/>
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# Hörnig M, Markoutsa S, Häfner A K, et al. '''Inhibition of 5-lipoxygenase by U73122 is due to covalent binding to cysteine 416[J].''' Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids, 2012, 1821(2): 279-286. [https://www.ncbi.nlm.nih.gov/pubmed/?term=22137889 22137889]<br/>
  
[[Category:Targets|Targets]]
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[[Category:Targets]]
[[Category:Homo sapiens|Homo sapiens]]
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[[Category:Homo sapiens]]
[[Category:Metabolic enzyme|Metabolic enzyme]]
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[[Category:Metabolic enzyme]]
[[Category:Lipoxygenase family|Lipoxygenase family]]
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[[Category:Lipoxygenase family]]
[[Category:Arachidonic acid metabolism|Arachidonic acid metabolism]]
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[[Category:Arachidonic acid metabolism]]
[[Category:Metabolic pathways|Metabolic pathways]]
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[[Category:Metabolic pathways]]
[[Category:Serotonergic synapse|Serotonergic synapse]]
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[[Category:Serotonergic synapse]]
[[Category:Ovarian steroidogenesis|Ovarian steroidogenesis]]
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[[Category:Ovarian steroidogenesis]]
[[Category:Toxoplasmosis|Toxoplasmosis]]
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[[Category:Toxoplasmosis]]

Latest revision as of 21:37, 19 August 2019

Basic Information
Short Name 5-LO, ALOX5
UNP ID P09917
Organism Homo sapiens
Cys Site Cys417
Family/Domain Lipoxygenase family
Known Ligand Ligand list
Function Type Metabolic enzyme

Summary

Protein Function

Lipoxygenases are a family of iron-containing enzymes that catalyze the dioxygenation of polyunsaturated fatty acids in lipids containing a cis,cis-1,4-pentadiene structure. It catalyses the following reaction:
fatty acid + O2 = fatty acid hydroperoxide
These enzymes are most common in plants where they may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. In mammals a number of lipoxygenases isozymes are involved in the metabolism of eicosanoids (such as prostaglandins, leukotrienes and nonclassic eicosanoids). (From Wikipedia)
5-Lipoxygenase (5-LO) is the key enzyme in the biosynthesis of leukotrienes (LTs) which are mediators involved in the development of atherosclerosis, inflammatory diseases and cancer. 5-LO metabolizes arachidonic acid to leukotriene A4 in a two step reaction by incorporation of molecular oxygen. (PMID: 22137889)

Cys Function & Property

Cys417 is close to the active site and the Fe cation in space.

  • Hydrophobic property:
529-hydro.png
  • SASA:
Cys417: 26.389 A^2

Protein Sequence

MPSYTVTVAT GSQWFAGTDD YIYLSLVGSA GCSEKHLLDK PFYNDFERGA
VDSYDVTVDE ELGEIQLVRI EKRKYWLNDD WYLKYITLKT PHGDYIEFPC
YRWITGDVEV VLRDGRAKLA RDDQIHILKQ HRRKELETRQ KQYRWMEWNP
GFPLSIDAKC HKDLPRDIQF DSEKGVDFVL NYSKAMENLF INRFMHMFQS
SWNDFADFEK IFVKISNTIS ERVMNHWQED LMFGYQFLNG CNPVLIRRCT
ELPEKLPVTT EMVECSLERQ LSLEQEVQQG NIFIVDFELL DGIDANKTDP
CTLQFLAAPI CLLYKNLANK IVPIAIQLNQ IPGDENPIFL PSDAKYDWLL
AKIWVRSSDF HVHQTITHLL RTHLVSEVFG IAMYRQLPAV HPIFKLLVAH
VRFTIAINTK AREQLICECG LFDKANATGG GGHVQMVQRA MKDLTYASLC
FPEAIKARGM ESKEDIPYYF YRDDGLLVWE AIRTFTAEVV DIYYEGDQVV
EEDPELQDFV NDVYVYGMRG RKSSGFPKSV KSREQLSEYL TVVIFTASAQ
HAAVNFGQYD WCSWIPNAPP TMRAPPPTAK GVVTIEQIVD TLPDRGRSCW
HLGAVWALSQ FQENELFLGM YPEEHFIEKP VKEAMARFRK NLEAIVSVIA
ERNKKKQLPY YYLSPDRIPN SVAI

Structural Information

  • Known structures with covalent ligands:
Unknown
  • Protein structure:
529.png

Related Pathway

Experimental Evidence

Cys-directed Mutation, MALDI-MS

Reference

  1. Hörnig M, Markoutsa S, Häfner A K, et al. Inhibition of 5-lipoxygenase by U73122 is due to covalent binding to cysteine 416[J]. Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids, 2012, 1821(2): 279-286. 22137889