Entry
Name
soluble epoxide hydrolase;
epoxide hydrase (ambiguous);
epoxide hydratase (ambiguous);
arene-oxide hydratase (ambiguous);
aryl epoxide hydrase (ambiguous);
trans-stilbene oxide hydrolase;
sEH;
cytosolic epoxide hydrolase
Class
Hydrolases;
Acting on ether bonds;
Ether hydrolases
BRITE hierarchy
Sysname
epoxide hydrolase
Reaction(IUBMB)
an epoxide + H2O = a glycol [RN:
R02822 ]
Reaction(KEGG)
Substrate
Product
Comment
Catalyses the hydrolysis of trans-substituted epoxides, such as trans-stilbene oxide, as well as various aliphatic epoxides derived from fatty-acid metabolism [7]. It is involved in the metabolism of arachidonic epoxides (epoxyicosatrienoic acids; EETs) and linoleic acid epoxides. The EETs, which are endogenous chemical mediators, act at the vascular, renal and cardiac levels to regulate blood pressure [4,5]. The enzyme from mammals is a bifunctional enzyme: the C-terminal domain exhibits epoxide-hydrolase activity and the N-terminal domain has the activity of EC
3.1.3.76 , lipid-phosphate phosphatase [1,2]. Like EC
3.3.2.9 , microsomal epoxide hydrolase, it is probable that the reaction involves the formation of an hydroxyalkyl---enzyme intermediate [4,6]. The enzyme can also use leukotriene A4, the substrate of EC
3.3.2.6 , leukotriene-A4 hydrolase, but it forms 5,6-dihydroxy-7,9,11,14-icosatetraenoic acid rather than leukotriene B4 as the product [9,10]. In vertebrates, five epoxide-hydrolase enzymes have been identified to date: EC
3.3.2.6 (leukotriene-A4 hydrolase), EC
3.3.2.7 (hepoxilin-epoxide hydrolase), EC
3.3.2.9 (microsomal epoxide hydrolase), EC
3.3.2.10 (soluble epoxide hydrolase) and EC
3.3.2.11 (cholesterol 5,6-oxide hydrolase) [7].
History
EC 3.3.2.10 created 2006 (EC 3.3.2.3 created 1978, part incorporated 2006)
Pathway
ec00590 Arachidonic acid metabolism
ec00625 Chloroalkane and chloroalkene degradation
ec01120 Microbial metabolism in diverse environments
Orthology
K08726 soluble epoxide hydrolase / lipid-phosphate phosphatase
Genes
HSA : 2053(EPHX2) 79852(EPHX3)
PTR : 455793(EPHX3) 464074(EPHX2)
PPS : 100983619(EPHX3) 100990932(EPHX2)
GGO : 101136750(EPHX2) 129528921(EPHX3)
PON : 100172736(EPHX2) 100455128(EPHX3)
PPYG : 129021013(EPHX3) 129043151(EPHX2)
NLE : 100585861(EPHX2) 100592370(EPHX3)
HMH : 116461991(EPHX2) 116478615(EPHX3)
SSYN : 129459174(EPHX3) 129491435(EPHX2)
MCC : 712926(EPHX2) 718176(EPHX3)
MCF : 102124136(EPHX3) 102134633(EPHX2)
MTHB : 126942283 126961771
MNI : 105482015(EPHX2) 105495717(EPHX3)
CSAB : 103215526(EPHX2) 103234067(EPHX3)
CATY : 105579174(EPHX2) 105601607(EPHX3)
PANU : 101003613(EPHX3) 101025043(EPHX2)
TGE : 112613109(EPHX3) 112629928(EPHX2)
MLEU : 105540090(EPHX3) 105542346(EPHX2)
RRO : 104661024(EPHX3) 104673945(EPHX2)
RBB : 108523071(EPHX3) 108537568(EPHX2)
TFN : 117075567(EPHX3) 117093881(EPHX2)
PTEH : 111545735(EPHX2) 111554367(EPHX3)
CANG : 105513660(EPHX2) 105519765(EPHX3)
CJC : 100402999(EPHX2) 100405833(EPHX3)
SBQ : 101033420(EPHX2) 101039796(EPHX3)
CIMI : 108296599(EPHX3) 108312475(EPHX2)
ANAN : 105705326(EPHX2) 105720962(EPHX3)
CSYR : 103250514(EPHX2) 103260731(EPHX3)
MMUR : 105867940(EPHX3) 105877163(EPHX2)
LCAT : 123626651(EPHX2) 123636835(EPHX3)
PCOQ : 105825075(EPHX3) 105825288(EPHX2)
OGA : 100958729(EPHX2) 100966277(EPHX3)
MMU : 13850(Ephx2) 71932(Ephx3)
MCAL : 110284324(Ephx3) 110309184(Ephx2)
MPAH : 110325104(Ephx2) 110335924(Ephx3)
RNO : 366836(Ephx3) 65030(Ephx2)
MCOC : 116076366(Ephx3) 116084507(Ephx2)
ANU : 117696538(Ephx3) 117696731 117706330(Ephx2)
MUN : 110548893(Ephx3) 110559220(Ephx2)
CGE : 100753937(Ephx3) 100757328(Ephx2)
MAUA : 101825518(Ephx3) 101836372(Ephx2)
PROB : 127216684(Ephx3) 127230245(Ephx2)
PLEU : 114686142(Ephx3) 114707310(Ephx2)
MORG : 121432503(Ephx3) 121459865(Ephx2)
MFOT : 126504071 126507630
AAMP : 119800184(Ephx2) 119807284(Ephx3)
NGI : 103730002(Ephx2) 103731623(Ephx3)
HGL : 101715352(Ephx2) 101722570(Ephx3)
CPOC : 100732055(Ephx3) 100734490(Ephx2)
CCAN : 109681381(Ephx3) 109683973
DORD : 105991601(Ephx2) 105994648(Ephx3)
DSP : 122100322(Ephx3) 122123504(Ephx2)
PLOP : 125339453(Ephx2) 125348870(Ephx3)
NCAR : 124969473 124982494
MMMA : 107145290(Ephx3) 107153899(Ephx2)
OPI : 101526632(EPHX2) 101532806(EPHX3)
TUP : 102480725(EPHX2) 102499982(EPHX3)
GVR : 103593419(EPHX3) 103606837(EPHX2)
CFA : 100684177(EPHX3) 477373(EPHX2)
CLUD : 112666659(EPHX3) 112669696(EPHX2)
VVP : 112913147(EPHX3) 112926786(EPHX2)
VLG : 121496009(EPHX3) 121496796(EPHX2)
NPO : 129521794(EPHX3) 129523302(EPHX2)
AML : 100483292(EPHX3) 100483572(EPHX2)
UMR : 103675990(EPHX2) 103677203
UAH : 113248703(EPHX3) 113269956(EPHX2)
UAR : 123777357(EPHX2) 123780013(EPHX3)
MPUF : 101673413(EPHX3) 101689697(EPHX2)
MNP : 131999722(EPHX2) 132009729(EPHX3)
MLK : 131823675(EPHX3) 131833301(EPHX2)
NVS : 122889650(EPHX2) 122910723(EPHX3)
ORO : 101373863(EPHX2) 101374433(EPHX3)
EJU : 114202202(EPHX3) 114217531(EPHX2)
ZCA : 113916260(EPHX3) 113924682(EPHX2)
MLX : 118005711(EPHX3) 118022112(EPHX2)
NSU : 110574575(EPHX3) 110588489(EPHX2)
FCA : 101092355(EPHX2) 101099782(EPHX3)
PYU : 121010927(EPHX3) 121022524(EPHX2)
PCOO : 112852998(EPHX3) 112858307(EPHX2)
PBG : 122473878(EPHX2) 122487028(EPHX3)
PVIV : 125161037(EPHX3) 125164153(EPHX2)
LRUF : 124520826 124524599
PTG : 102954012(EPHX3) 102957184(EPHX2)
PPAD : 109247513 109262341(EPHX2)
HHV : 120220308(EPHX2) 120239254(EPHX3)
BTA : 511716(EPHX2) 617882(EPHX3)
BOM : 102265452(EPHX3) 102267808(EPHX2)
BIU : 109561482(EPHX3) 109563159(EPHX2)
BBUB : 102390473(EPHX3) 102411270(EPHX2)
BBIS : 104984309(EPHX3) 104988717(EPHX2)
CHX : 102184515(EPHX3) 102185835(EPHX2)
OAS : 101106654(EPHX2) 101120077(EPHX3)
BTAX : 128050903(EPHX3) 128052164(EPHX2)
ODA : 120860355 120864150(EPHX3) 120866098
CCAD : 122431866(EPHX2) 122440643(EPHX3)
MBEZ : 129556921(EPHX2) 129559117(EPHX3)
SSC : 100625866(EPHX3) 414425(EPHX2)
CFR : 102517269(EPHX2) 102521591(EPHX3)
CBAI : 105063866(EPHX2) 105074550(EPHX3)
CDK : 105102229(EPHX2) 105105142(EPHX3)
VPC : 102525763(EPHX3) 102535491(EPHX2)
BACU : 102998957(EPHX3) 103015729(EPHX2)
BMUS : 118891890(EPHX3) 118896989(EPHX2)
LVE : 103082628(EPHX2) 103086935(EPHX3)
OOR : 101277852(EPHX3) 101282222(EPHX2)
DLE : 111166730(EPHX3) 111185405(EPHX2)
PCAD : 102974927(EPHX3) 102997018(EPHX2)
NASI : 112414931(EPHX3) 112415002(EPHX2)
ECB : 100060414(EPHX2) 100063124(EPHX3)
EPZ : 103550424(EPHX2) 103563921(EPHX3)
EAI : 106832514(EPHX2) 106839070(EPHX3)
MYB : 102255588(EPHX2) 102264163(EPHX3)
MYD : 102755564(EPHX2) 102768225(EPHX3)
MMYO : 118652586(EPHX3) 118659062(EPHX2)
MLF : 102426648(EPHX2) 102431711(EPHX3)
MDT : 132234893(EPHX3) 132235327 132235331
PKL : 118706562(EPHX3) 118710951(EPHX2)
EFUS : 103294334(EPHX2) 103300912(EPHX3)
MNA : 107534291(EPHX3) 107538569(EPHX2)
DRO : 112305266(EPHX3) 112312409(EPHX2)
SHON : 118984357(EPHX2) 118993394(EPHX3)
AJM : 119044629 119061772(EPHX3)
PDIC : 114503007(EPHX2) 114503326(EPHX3)
PHAS : 123813726(EPHX2) 123828373(EPHX3)
PPAM : 129072532(EPHX2) 129074801(EPHX3)
HAI : 109376078(EPHX3) 109379561(EPHX2)
RFQ : 117037789(EPHX2) 117037837(EPHX3)
PALE : 102886924(EPHX2) 102895797(EPHX3)
PGIG : 120606481(EPHX3) 120613418(EPHX2)
PVP : 105292223(EPHX2) 105308250(EPHX3)
RAY : 107507539(EPHX2) 107517222(EPHX3)
MJV : 108394328(EPHX2) 108408748(EPHX3)
TOD : 119240022(EPHX3) 119258012(EPHX2)
SARA : 101543845(EPHX3) 101555407(EPHX2)
SETR : 126006093(EPHX2) 126031014(EPHX3)
LAV : 100658579(EPHX2) 100672531(EPHX3)
ETF : 101648782(EPHX2) 101662622(EPHX3)
MDO : 100012757(EPHX3) 100030580(EPHX2)
GAS : 123232178(EPHX3) 123233526(EPHX2)
SHR : 100927232(EPHX3) 100931196 100931457 100931720
AFZ : 127545027 127548796 127548797
PCW : 110196222(EPHX3) 110206532(EPHX2)
TVP : 118834656(EPHX3) 118843890(EPHX2)
OAA : 100093187(EPHX2) 100093585(EPHX3)
ZLE : 135441653 135445122(EPHX2)
RTD : 128901374(EPHX3) 128907632(EPHX2)
ASN : 102380849 102382847(EPHX2)
AMJ : 102558789(EPHX2) 102571865(EPHX3)
DCC : 119853551(EPHX2) 122458349(EPHX3)
CABI : 116822698 116830887 116837371
MRV : 120391208(EPHX3) 120401417 120402424
ACS : 100564154(ephx2) 100568091(ephx3)
PVT : 110080425(EPHX3) 110089501(EPHX2)
CTIG : 120309116(EPHX2) 120315342(EPHX3)
PGUT : 117659547(EPHX3) 117667686(EPHX2)
APRI : 131189006(EPHX2) 131192182(EPHX3)
PTEX : 113433589(EPHX3) 113446324(EPHX2)
NSS : 113414578(EPHX2) 113418204
VKO : 123033639(EPHX2) 123035578(EPHX3)
PRAF : 128407644 128411464(EPHX2)
ZVI : 118079953 118082948(EPHX2)
HCG : 128324683(EPHX2) 128344379(EPHX3)
GJA : 107118053(EPHX2) 107118743
EMC : 129328430 129335898(EPHX2)
XLA : 108712668(ephx3.S) 447032(ephx2.L)
XTR : 448759(ephx2) 779884(ephx3)
NPR : 108797013 108798538(EPHX2)
RTEM : 120933201(EPHX3) 120936048(EPHX2)
BBUF : 120986251 120997151(EPHX2)
BGAR : 122929435 122934206(EPHX2)
MUO : 115466133(EPHX3) 115467028(EPHX2)
GSH : 117350922(EPHX3) 117357611(EPHX2)
SRX : 107717245(ephx2) 107733988
SANH : 107653762 107692411
SGH : 107552031 107594076(ephx2)
CAUA : 113060837 113117731
CGIB : 127976311 128031809
RKG : 130088847 130088950(ephx2)
MSAM : 119892822 119901244 119901687 119901935 119903463 119915610
ALAT : 119015231 119015235
CSAI : 133429860(ephx2) 133439060
SASA : 106604359(HYES) 106611412(HYES)
STRU : 115161918 115172954
OTW : 112239012 112239182 112256950
OMY : 110498218(ephx2) 110504256
OGO : 124001944(ephx2) 124046757
OKE : 118380841 127913538(ephx2)
CCLU : 121539061(ephx2) 121544563
SCLV : 120337441 120337631
SPU : 590472(EH1) 752510(eh2)
LPIC : 129260275 129261305 129261533
APLC : 110985936 110985937
TAD : TRIADDRAFT_30313 TRIADDRAFT_59995 TRIADDRAFT_60010 TRIADDRAFT_60079 TRIADDRAFT_64238
YLI : 2909628(YALI2_B00303g) 2911786(YALI2_E00402g)
NTE : NEUTE1DRAFT119163(NEUTE1DRAFT_119163)
SMP : 10801551(SMAC4_06471) 10809559(SMAC4_12126)
PAN : PODANSg2586 PODANSg4881
MGR : MGG_05175 MGG_05826 MGG_07954 MGG_09603 MGG_13875
FGR : FGSG_06744 FGSG_11196
FPU : FPSE_02822 FPSE_09090
FOX : FOXG_08935 FOXG_10109 FOXG_13323 FOXG_14841 FOXG_19442 FOXG_22390
NHE : NECHADRAFT_30431 NECHADRAFT_38604 NECHADRAFT_51532 NECHADRAFT_98121
TRE : TRIREDRAFT_53220 TRIREDRAFT_57045
TRR : M419DRAFT_69084 M419DRAFT_72359
MAW : 19248035(J3458_007240)
PLJ : 28892531(PLICBS_006442)
VAL : VDBG_05347 VDBG_08907
VDA : VDAG_06569 VDAG_06997
CFJ : CFIO01_01948 CFIO01_02421 CFIO01_04356 CFIO01_06499 CFIO01_11995
CHIG : CH63R_09605 CH63R_12939
CDET : 87940481(CDEST_03978) 87940721(CDEST_04218) 87945553(CDEST_09050) 87950015(CDEST_13515)
ELA : UCREL1_10468 UCREL1_2213 UCREL1_3351 UCREL1_9854
PFY : PFICI_03331 PFICI_05569 PFICI_08381 PFICI_14790
SSL : SS1G_08093 SS1G_13652
BFU : BCIN_10g01840 BCIN_13g00770 BCIN_15g00230
PSCO : LY89DRAFT_507394 LY89DRAFT_594279 LY89DRAFT_662388 LY89DRAFT_683181 LY89DRAFT_702826 LY89DRAFT_785580
GLZ : GLAREA_02712 GLAREA_04148 GLAREA_09895 GLAREA_12612
TRG : TRUGW13939_04437 TRUGW13939_05195 TRUGW13939_08349
AJE : HCAG_03262 HCAG_06274
PNO : SNOG_12792 SNOG_13782(SNOG_13781) SNOG_14994
PTRR : 6345755(PtrM4_038700)
BZE : COCCADRAFT_10479 COCCADRAFT_23112 COCCADRAFT_24314
BSC : COCSADRAFT_329080 COCSADRAFT_37209
BOR : COCMIDRAFT_26566 COCMIDRAFT_3129 COCMIDRAFT_97004
AALT : CC77DRAFT_1020259 CC77DRAFT_1067778 CC77DRAFT_23691 CC77DRAFT_924398 CC77DRAFT_933869 CC77DRAFT_991934
ZTR : MYCGRDRAFT_101398 MYCGRDRAFT_45185 MYCGRDRAFT_67922 MYCGRDRAFT_69862 MYCGRDRAFT_74004
PFJ : MYCFIDRAFT_186960 MYCFIDRAFT_202874 MYCFIDRAFT_31012 MYCFIDRAFT_35544 MYCFIDRAFT_63852
NPA : UCRNP2_1253 UCRNP2_2402 UCRNP2_2781 UCRNP2_536 UCRNP2_578 UCRNP2_7692 UCRNP2_9159
TVS : TRAVEDRAFT_114934 TRAVEDRAFT_116461 TRAVEDRAFT_121619 TRAVEDRAFT_163026 TRAVEDRAFT_171945 TRAVEDRAFT_42938 TRAVEDRAFT_42939 TRAVEDRAFT_42940 TRAVEDRAFT_42941 TRAVEDRAFT_42942 TRAVEDRAFT_60092 TRAVEDRAFT_72850 TRAVEDRAFT_94256
DSQ : DICSQDRAFT_101446 DICSQDRAFT_104823 DICSQDRAFT_61223
PCO : PHACADRAFT_104575 PHACADRAFT_118086 PHACADRAFT_151144 PHACADRAFT_191247 PHACADRAFT_194943 PHACADRAFT_198096 PHACADRAFT_207661 PHACADRAFT_208465 PHACADRAFT_255121 PHACADRAFT_260148 PHACADRAFT_91351 PHACADRAFT_93100
SHS : STEHIDRAFT_106361 STEHIDRAFT_122857 STEHIDRAFT_61089 STEHIDRAFT_80676 STEHIDRAFT_81610
HIR : HETIRDRAFT_148090 HETIRDRAFT_155125 HETIRDRAFT_156748 HETIRDRAFT_156749 HETIRDRAFT_174637 HETIRDRAFT_63479
PSQ : PUNSTDRAFT_112781 PUNSTDRAFT_116520 PUNSTDRAFT_139547 PUNSTDRAFT_98990
ADL : AURDEDRAFT_110586 AURDEDRAFT_117379 AURDEDRAFT_117569 AURDEDRAFT_117572 AURDEDRAFT_152313 AURDEDRAFT_175477 AURDEDRAFT_80706
FME : FOMMEDRAFT_106649 FOMMEDRAFT_127219 FOMMEDRAFT_135095
GTR : GLOTRDRAFT_45684 GLOTRDRAFT_68350
RSX : RhiXN_03509 RhiXN_04225 RhiXN_05233 RhiXN_07686
LBC : LACBIDRAFT_303899 LACBIDRAFT_311540(LbEPHX1)
CCI : CC1G_00644 CC1G_00645 CC1G_14690
ABP : AGABI1DRAFT110229(AGABI1DRAFT_110229) AGABI1DRAFT38499(AGABI1DRAFT_38499) AGABI1DRAFT70817(AGABI1DRAFT_70817)
ABV : AGABI2DRAFT184905(AGABI2DRAFT_184905) AGABI2DRAFT189875(AGABI2DRAFT_189875) AGABI2DRAFT78715(AGABI2DRAFT_78715)
MPR : MPER_04928 MPER_09275 MPER_11089
MRR : Moror_11208 Moror_13472 Moror_13512 Moror_13860 Moror_14385 Moror_14388 Moror_16097 Moror_2330 Moror_2947 Moror_4070 Moror_6712 Moror_8127
MORE : E1B28_004695 E1B28_008290
SCM : SCHCO_01159789(SCHCODRAFT_01159789) SCHCO_02625205(SCHCODRAFT_02625205) SCHCO_02645722(SCHCODRAFT_02645722) SCHCO_02666784(SCHCODRAFT_02666784)
CPUT : CONPUDRAFT_122227 CONPUDRAFT_93019
SLA : SERLADRAFT_354546 SERLADRAFT_448219 SERLADRAFT_479064 SERLADRAFT_479070 SERLADRAFT_480679
PGR : PGTG_00491 PGTG_05962 PGTG_05973
MLR : MELLADRAFT_102079 MELLADRAFT_115158 MELLADRAFT_123933
RIE : OCT59_002948 OCT59_015702 OCT59_017452
PIF : PITG_11920 PITG_11921 PITG_11922 PITG_15955 PITG_15956
PSOJ : PHYSODRAFT_314147 PHYSODRAFT_318677 PHYSODRAFT_525117 PHYSODRAFT_558062 PHYSODRAFT_564652
SPAR : SPRG_06039 SPRG_06040 SPRG_06041
» show all
Taxonomy
Reference
Authors
Newman JW, Morisseau C, Harris TR, Hammock BD
Title
The soluble epoxide hydrolase encoded by EPXH2 is a bifunctional enzyme with novel lipid phosphate phosphatase activity.
Journal
Sequence
Reference
Authors
Cronin A, Mowbray S, Durk H, Homburg S, Fleming I, Fisslthaler B, Oesch F, Arand M.
Title
The N-terminal domain of mammalian soluble epoxide hydrolase is a phosphatase.
Journal
Sequence
Reference
Authors
Oesch F.
Title
Mammalian epoxide hydrases: inducible enzymes catalysing the inactivation of carcinogenic and cytotoxic metabolites derived from aromatic and olefinic compounds.
Journal
Reference
Authors
Morisseau C, Hammock BD.
Title
Epoxide hydrolases: mechanisms, inhibitor designs, and biological roles.
Journal
Reference
Authors
Yu Z, Xu F, Huse LM, Morisseau C, Draper AJ, Newman JW, Parker C, Graham L, Engler MM, Hammock BD, Zeldin DC, Kroetz DL.
Title
Soluble epoxide hydrolase regulates hydrolysis of vasoactive epoxyeicosatrienoic acids.
Journal
Reference
6
Authors
Lacourciere GM, Armstrong RN.
Title
The catalytic mechanism of microsomal epoxide hydrolase involves an ester intermediate.
Journal
J Am Chem Soc 115:10466-10456 (1993)
Reference
Authors
Fretland AJ, Omiecinski CJ.
Title
Epoxide hydrolases: biochemistry and molecular biology.
Journal
Reference
Authors
Zeldin DC, Wei S, Falck JR, Hammock BD, Snapper JR, Capdevila JH.
Title
Metabolism of epoxyeicosatrienoic acids by cytosolic epoxide hydrolase: substrate structural determinants of asymmetric catalysis.
Journal
Reference
Authors
Haeggstrom J, Meijer J, Radmark O.
Title
Leukotriene A4. Enzymatic conversion into 5,6-dihydroxy-7,9,11,14-eicosatetraenoic acid by mouse liver cytosolic epoxide hydrolase.
Journal
J Biol Chem 261:6332-7 (1986)
Reference
Authors
Newman JW, Morisseau C, Hammock BD.
Title
Epoxide hydrolases: their roles and interactions with lipid metabolism.
Journal
Other DBs
ExplorEnz - The Enzyme Database: 3.3.2.10
ExPASy - ENZYME nomenclature database: 3.3.2.10
UM-BBD (Biocatalysis/Biodegradation Database): 3.3.2.10
LinkDB
All DBs