KEGG   ENZYME: 2.1.1.17Help
Entry
EC 2.1.1.17                 Enzyme                                 

Name
phosphatidylethanolamine N-methyltransferase;
PEMT;
LMTase;
lipid methyl transferase;
phosphatidylethanolamine methyltransferase;
phosphatidylethanolamine-N-methylase;
phosphatidylethanolamine-S-adenosylmethionine methyltransferase
Class
Transferases;
Transferring one-carbon groups;
Methyltransferases
BRITE hierarchy
Sysname
S-adenosyl-L-methionine:phosphatidylethanolamine N-methyltransferase
Reaction(IUBMB)
S-adenosyl-L-methionine + phosphatidylethanolamine = S-adenosyl-L-homocysteine + phosphatidyl-N-methylethanolamine [RN:R02056]
Reaction(KEGG)
Substrate
S-adenosyl-L-methionine [CPD:C00019];
phosphatidylethanolamine [CPD:C00350]
Product
S-adenosyl-L-homocysteine [CPD:C00021];
phosphatidyl-N-methylethanolamine [CPD:C01241]
History
EC 2.1.1.17 created 1972
Pathway
ec00564  Glycerophospholipid metabolism
ec01100  Metabolic pathways
ec01110  Biosynthesis of secondary metabolites
Orthology
K00551  phosphatidylethanolamine/phosphatidyl-N-methylethanolamine N-methyltransferase
K00570  phosphatidylethanolamine/phosphatidyl-N-methylethanolamine N-methyltransferase
K16369  phosphatidylethanolamine N-methyltransferase
Genes
HSA: 10400(PEMT)
PTR: 454478(PEMT)
PPS: 100972213(PEMT)
GGO: 101129284(PEMT)
PON: 100435357(PEMT)
NLE: 100590379(PEMT)
MCC: 699083(PEMT)
MCF: 102139053(PEMT)
CSAB: 103242475(PEMT)
RRO: 104666746(PEMT)
RBB: 108544482(PEMT)
CJC: 100408388(PEMT)
SBQ: 101027664(PEMT)
MMU: 18618(Pemt)
RNO: 25511(Pemt)
CGE: 100767954(Pemt)
NGI: 103724843(Pemt)
HGL: 101706125(Pemt)
CCAN: 109696976(Pemt)
OCU: 100342505(PEMT)
TUP: 102468555(PEMT)
CFA: 479526(PEMT)
AML: 100471478
UMR: 103658492(PEMT)
ORO: 101374319(PEMT)
FCA: 101088035(PEMT)
PTG: 102954031(PEMT)
AJU: 106981385(PEMT)
BTA: 360197(PEMT)
BOM: 106700740(PEMT)
PHD: 102343028(PEMT)
CHX: 102170908(PEMT)
OAS: 101112913(PEMT)
SSC: 397654(PEMT)
CFR: 102522081(PEMT)
CDK: 105100583(PEMT)
BACU: 103012191(PEMT)
LVE: 103070967(PEMT)
OOR: 101278054(PEMT)
ECB: 100050945(PEMT)
EPZ: 103562583(PEMT)
EAI: 106840619(PEMT)
MYB: 102263113(PEMT)
MYD: 102761259(PEMT)
HAI: 109390350(PEMT)
RSS: 109436860(PEMT)
PALE: 102891834(PEMT)
LAV: 100677591(PEMT)
TMU: 101353252
MDO: 100010012(PEMT)
SHR: 100934849(PEMT)
OAA: 100079865(PEMT)
GGA: 416508(PEMT)
MGP: 100543379
CJO: 107320620(PEMT)
APLA: 101800672(PEMT)
ACYG: 106032105(PEMT)
TGU: 100230786(PEMT)
GFR: 102041578(PEMT)
FAB: 101822001(PEMT)
PHI: 102111635(PEMT)
PMAJ: 107211297(PEMT)
CCW: 104684776(PEMT)
FPG: 101915767(PEMT)
FCH: 102054382(PEMT)
CLV: 102098836(PEMT)
EGZ: 104123099(PEMT)
AAM: 106487305(PEMT) 106500318
ASN: 102369991(PEMT)
AMJ: 102561567(PEMT)
PSS: 102447762(PEMT)
CMY: 102941958(PEMT)
CPIC: 101953495(PEMT)
ACS: 100567746(pemt)
PVT: 110090327(PEMT)
PBI: 103063432(PEMT)
GJA: 107124237(PEMT)
XLA: 447155(pemt.L)
XTR: 448594(pemt)
NPR: 108788740(PEMT)
DRE: 393127(pemt)
SRX: 107719881 107726260(pemt)
SANH: 107653979(pemt)
SGH: 107595637(pemt)
CCAR: 109078719(pemt)
IPU: 100528737(pemt)
AMEX: 103037752(pemt)
TRU: 101076246(pemt)
LCO: 104929229(pemt)
MZE: 101474773(pemt)
XMA: 102221066(pemt)
PRET: 103482052(pemt)
NFU: 107388266(pemt)
CSEM: 103382052(pemt)
LCF: 108889178(pemt)
HCQ: 109512037(pemt)
BPEC: 110173691(pemt)
SASA: 100196273(pemt)
ELS: 105005625(pemt)
SFM: 108930166(pemt)
LCM: 102347713(PEMT)
CMK: 103190670(pemt)
SPU: 581512
APLC: 110986061
SKO: 102807297
PRAP: 110991784
CRG: 105326242
MYI: 110462610
ADF: 107332339
BVG: 104886016
SCE: YGR157W(CHO2) YJR073C(OPI3)
KMX: KLMA_30035(OPI3) KLMA_40103(CHO2)
NCS: NCAS_0A12330(NCAS0A12330) NCAS_0C05650(NCAS0C05650)
NDI: NDAI_0A03900(NDAI0A03900) NDAI_0H00470(NDAI0H00470)
TPF: TPHA_0F00460(TPHA0F00460) TPHA_0F03600(TPHA0F03600) TPHA_0K01880(TPHA0K01880)
TBL: TBLA_0B09830(TBLA0B09830) TBLA_0D03630(TBLA0D03630)
TDL: TDEL_0F00350(TDEL0F00350) TDEL_0F02880(TDEL0F02880)
KAF: KAFR_0I01250(KAFR0I01250) KAFR_0K02560(KAFR0K02560)
PIC: PICST_56448(OPI3) PICST_57055(CHO2)
SLB: AWJ20_2161(OPI3) AWJ20_3111(CHO2)
NCR: NCU04699 NCU08045(chol-1)
NTE: NEUTE1DRAFT124377(NEUTE1DRAFT_124377) NEUTE1DRAFT145535(NEUTE1DRAFT_145535)
ANG: ANI_1_64074(An08g00560) ANI_1_854134(An15g06310)
PNO: SNOG_06783(SNOG_06782) SNOG_13932
SPO: SPBC26H8.03(cho2) SPBC337.16(cho1)
ABP: AGABI1DRAFT109452(AGABI1DRAFT_109452) AGABI1DRAFT76829(AGABI1DRAFT_76829)
ABV: AGABI2DRAFT121645(AGABI2DRAFT_121645) AGABI2DRAFT211112(AGABI2DRAFT_211112)
DFA: DFA_01140(pemtB) DFA_01224 DFA_05291(pemtA)
LPN: lpg2158(pmtA)
LPH: LPV_2409
LPO: LPO_2222
LPM: LP6_2181(pmtA)
LPF: lpl2086
LPP: lpp2097
LPA: lpa_03098
LPE: lp12_2150
LLO: LLO_3400
LFA: LFA_0551
LOK: Loa_02535
MCA: MCA3065
NOC: Noc_0914
NHL: Nhal_1108
NWA: Nwat_0780
TEE: Tel_09350
NTT: TAO_1398
HHA: Hhal_0826
TKM: TK90_0730
TVR: TVD_03700
SLIM: SCL_1104
SVA: SVA_2165
CBAA: SRAA_1512
CBAB: SMCB_0498
EBA: ebA6680(pemT)
MLO: mll4753
MES: Meso_0681
PLA: Plav_2189
SME: SMc00414
SMX: SM11_chr3811(pmtA)
SMEL: SM2011_c00414(pmtA)
SMER: DU99_01800
SMD: Smed_3542
EAD: OV14_1225
ATU: Atu0300
ARA: Arad_0541
AVI: Avi_0349
AGR: AGROH133_03436(pmtA)
RLE: RL0333(pmtA) RL1338(pmtA)
RHL: LPU83_0386(pmtA)
RHT: NT26_4281
SHZ: shn_22230
BME: BMEI2000
BMEL: DK63_1491
BMEE: DK62_1457
BMF: BAB1_2131
BMB: BruAb1_2102(pmtA)
BABO: DK55_2061
BABR: DO74_1915
BABT: DK49_1817
BABB: DK48_58
BABU: DK53_2045
BABS: DK51_1498
BABC: DO78_1964
BMS: BR2127(pmtA)
BSI: BS1330_I2121(pmtA)
BSF: BSS2_I2061(pmtA)
BSZ: DK67_243
BSV: BSVBI22_A2123(pmtA)
BOV: BOV_2043(pmtA)
BOL: BCOUA_I2127(pmtA)
BCAR: DK60_58
BCAS: DA85_10235
BMR: BMI_I2149(pmtA)
BPP: BPI_I2185(pmtA)
BPV: DK65_1412
BVL: BF3285c1_0816(pmtA)
OAN: Oant_0788
OAH: DR92_325
BJA: bll6634(pmtA) bll6994 blr0681(pmtA)
BRS: S23_01550(pmtA) S23_13110(pmtX1) S23_16750(pmtA)
OCG: OCA5_c01120 OCA5_c26320(pmtA1) OCA5_c27610(pmtA2)
OCO: OCA4_c01120 OCA4_c26310(pmtA1) OCA4_c27600(pmtA2)
MDI: METDI3731(pmtA) METDI5092
HDN: Hden_2491
RVA: Rvan_3372
MCG: GL4_2815
HDI: HDIA_4168(ubiE_1) HDIA_4815
SIL: SPOA0294(pmtA)
RSP: RSP_0721(PmtA)
RCP: RCAP_rcc00559(pmtA)
PDE: Pden_4690
DSH: Dshi_2712
PSF: PSE_0487
PGA: PGA1_c29610(pmtA)
PGL: PGA2_c27520(pmtA)
PGD: Gal_00470
PHP: PhaeoP97_00543(pmtA_1)
PPIC: PhaeoP14_02731(pmtA)
MALG: MALG_03931
GOX: GOX1862
GOH: B932_0129
GOY: GLS_c19790(pmtA)
ACR: Acry_2168
AMV: ACMV_24160(pmtA)
GDI: GDI2102(pmtA)
GDJ: Gdia_0321
GXY: GLX_26190
GXL: H845_564
KEU: S101446_02953(pmtA)
APK: APA386B_612(pmtA)
ASZ: ASN_3042(pmtA)
TMO: TMO_1929
PHM: PSMK_14180(pmtA)
ABAC: LuPra_03024(ubiE_5)
NDE: NIDE0511(pmtA)
NMV: NITMOv2_0425(pmtA)
NIO: NITINOP_1227(pmtA)
NJA: NSJP_1550(pmtA)
MOX: DAMO_1446(pmtA)
 » show all
Taxonomy
Reference
1  [PMID:25437]
  Authors
Hirata F, Viveros OH, Diliberto EJ Jr, Axelrod J.
  Title
Identification and properties of two methyltransferases in conversion of phosphatidylethanolamine to phosphatidylcholine.
  Journal
Proc. Natl. Acad. Sci. U. S. A. 75 (1978) 1718-21.
Reference
2  [PMID:5773456]
  Authors
Morgan TE.
  Title
Isolation and characterization of lipid N-methylrtansferase from dog lung.
  Journal
Biochim. Biophys. Acta. 178 (1969) 21-34.
Reference
3  [PMID:438165]
  Authors
Schneider WJ, Vance DE.
  Title
Conversion of phosphatidylethanolamine to phosphatidylcholine in rat liver. Partial purification and characterization of the enzymatic activities.
  Journal
J. Biol. Chem. 254 (1979) 3886-91.
Other DBs
ExplorEnz - The Enzyme Database: 2.1.1.17
IUBMB Enzyme Nomenclature: 2.1.1.17
ExPASy - ENZYME nomenclature database: 2.1.1.17
BRENDA, the Enzyme Database: 2.1.1.17
CAS: 37256-91-0

KEGG   ENZYME: 2.1.1.71Help
Entry
EC 2.1.1.71                 Enzyme                                 

Name
phosphatidyl-N-methylethanolamine N-methyltransferase;
phosphatidylmonomethylethanolamine methyltransferase;
methyltransferase II;
phospholipid methyltransferase;
PLMT;
phosphatidyl-N-methylethanolamine methyltransferase;
phosphatidyl-N-monomethylethanolamine methyltransferase;
phosphatidylethanolamine methyltransferase I;
phosphatidylmonomethylethanolamine methyltransferase
Class
Transferases;
Transferring one-carbon groups;
Methyltransferases
BRITE hierarchy
Sysname
S-adenosyl-L-methionine:phosphatidyl-N-methylethanolamine N-methyltransferase
Reaction(IUBMB)
S-adenosyl-L-methionine + phosphatidyl-N-methylethanolamine = S-adenosyl-L-homocysteine + phosphatidyl-N-dimethylethanolamine [RN:R03424]
Reaction(KEGG)
R03424;
(other) R01320
Show
Substrate
S-adenosyl-L-methionine [CPD:C00019];
phosphatidyl-N-methylethanolamine [CPD:C01241]
Product
S-adenosyl-L-homocysteine [CPD:C00021];
phosphatidyl-N-dimethylethanolamine [CPD:C04308]
Comment
The enzyme also catalyses the transfer of a further methyl group, producing phosphatidylcholine.
History
EC 2.1.1.71 created 1984
Pathway
ec00564  Glycerophospholipid metabolism
ec01100  Metabolic pathways
ec01110  Biosynthesis of secondary metabolites
Orthology
K00550  phosphatidyl-N-methylethanolamine N-methyltransferase
K00551  phosphatidylethanolamine/phosphatidyl-N-methylethanolamine N-methyltransferase
K00570  phosphatidylethanolamine/phosphatidyl-N-methylethanolamine N-methyltransferase
Genes
HSA: 10400(PEMT)
PTR: 454478(PEMT)
PPS: 100972213(PEMT)
GGO: 101129284(PEMT)
PON: 100435357(PEMT)
NLE: 100590379(PEMT)
MCC: 699083(PEMT)
MCF: 102139053(PEMT)
CSAB: 103242475(PEMT)
RRO: 104666746(PEMT)
RBB: 108544482(PEMT)
CJC: 100408388(PEMT)
SBQ: 101027664(PEMT)
MMU: 18618(Pemt)
RNO: 25511(Pemt)
CGE: 100767954(Pemt)
NGI: 103724843(Pemt)
HGL: 101706125(Pemt)
CCAN: 109696976(Pemt)
OCU: 100342505(PEMT)
TUP: 102468555(PEMT)
CFA: 479526(PEMT)
AML: 100471478
UMR: 103658492(PEMT)
ORO: 101374319(PEMT)
FCA: 101088035(PEMT)
PTG: 102954031(PEMT)
AJU: 106981385(PEMT)
BTA: 360197(PEMT)
BOM: 106700740(PEMT)
PHD: 102343028(PEMT)
CHX: 102170908(PEMT)
OAS: 101112913(PEMT)
SSC: 397654(PEMT)
CFR: 102522081(PEMT)
CDK: 105100583(PEMT)
BACU: 103012191(PEMT)
LVE: 103070967(PEMT)
OOR: 101278054(PEMT)
ECB: 100050945(PEMT)
EPZ: 103562583(PEMT)
EAI: 106840619(PEMT)
MYB: 102263113(PEMT)
MYD: 102761259(PEMT)
HAI: 109390350(PEMT)
RSS: 109436860(PEMT)
PALE: 102891834(PEMT)
LAV: 100677591(PEMT)
TMU: 101353252
MDO: 100010012(PEMT)
SHR: 100934849(PEMT)
OAA: 100079865(PEMT)
GGA: 416508(PEMT)
MGP: 100543379
CJO: 107320620(PEMT)
APLA: 101800672(PEMT)
ACYG: 106032105(PEMT)
TGU: 100230786(PEMT)
GFR: 102041578(PEMT)
FAB: 101822001(PEMT)
PHI: 102111635(PEMT)
PMAJ: 107211297(PEMT)
CCW: 104684776(PEMT)
FPG: 101915767(PEMT)
FCH: 102054382(PEMT)
CLV: 102098836(PEMT)
EGZ: 104123099(PEMT)
AAM: 106487305(PEMT) 106500318
ASN: 102369991(PEMT)
AMJ: 102561567(PEMT)
PSS: 102447762(PEMT)
CMY: 102941958(PEMT)
CPIC: 101953495(PEMT)
ACS: 100567746(pemt)
PVT: 110090327(PEMT)
PBI: 103063432(PEMT)
GJA: 107124237(PEMT)
XLA: 447155(pemt.L)
XTR: 448594(pemt)
NPR: 108788740(PEMT)
DRE: 393127(pemt)
SRX: 107719881 107726260(pemt)
SANH: 107653979(pemt)
SGH: 107595637(pemt)
CCAR: 109078719(pemt)
IPU: 100528737(pemt)
AMEX: 103037752(pemt)
TRU: 101076246(pemt)
LCO: 104929229(pemt)
MZE: 101474773(pemt)
XMA: 102221066(pemt)
PRET: 103482052(pemt)
NFU: 107388266(pemt)
CSEM: 103382052(pemt)
LCF: 108889178(pemt)
HCQ: 109512037(pemt)
BPEC: 110173691(pemt)
SASA: 100196273(pemt)
ELS: 105005625(pemt)
SFM: 108930166(pemt)
LCM: 102347713(PEMT)
CMK: 103190670(pemt)
SPU: 581512
APLC: 110986061
SKO: 102807297
PRAP: 110991784
CRG: 105326242
MYI: 110462610
ADF: 107332339
ATH: AT1G80860(PLMT)
CRB: 17894426
BRP: 103853212
BOE: 106327895
THJ: 104812409
CPAP: 110821171
CIT: 102616857
TCC: 18595435
GRA: 105774093
DZI: 111318507
EGR: 104450625
GMX: 100301902(PLMT) 100527804
VRA: 106774076
VAR: 108320589
CCAJ: 109808823
CAM: 101511698
ADU: 107472168
AIP: 107618472
LJA: Lj0g3v0319119.1(Lj0g3v0319119.1) Lj0g3v0319129.1(Lj0g3v0319129.1)
LANG: 109355783
FVE: 101301023
PPER: 18782047
PMUM: 103328177
PAVI: 110763381
MDM: 103405574
CSV: 101218126
CMO: 103502819
MCHA: 111020909
CMAX: 111492722
CMOS: 111452701
CPEP: 111787888
RCU: 8280240
JCU: 105630312
HBR: 110640774
JRE: 108979108
VVI: 100258621
SLY: 101257780
SPEN: 107023731
SOT: 102581223
CANN: 107876013
NSY: 104216461
NTO: 104118378
SIND: 105166825
OEU: 111391802
HAN: 110941605
LSV: 111914861
DCR: 108227898
BVG: 104904873
SOE: 110805011
NNU: 104610753
OSA: 4329961
DOSA: Os02t0612100-01(Os02g0612100)
OBR: 102705597
BDI: 100822772
ATS: 109736193(LOC109736193)
SBI: 8072454
ZMA: 100276493
SITA: 101782590
PDA: 103717195
EGU: 105060175
MUS: 103983929
DCT: 110093093
AOF: 109843522
ATR: 18447075
PPP: 112283098
MNG: MNEG_4975
APRO: F751_5940
SCE: YJR073C(OPI3)
ERC: Ecym_3611
KMX: KLMA_30035(OPI3)
NCS: NCAS_0A12330(NCAS0A12330)
NDI: NDAI_0A03900(NDAI0A03900)
TPF: TPHA_0F03600(TPHA0F03600)
TBL: TBLA_0D03630(TBLA0D03630)
TDL: TDEL_0F00350(TDEL0F00350)
KAF: KAFR_0K02560(KAFR0K02560)
PIC: PICST_56448(OPI3)
CAL: CAALFM_C306570CA(OPI3)
CAUR: QG37_05964
SLB: AWJ20_2161(OPI3)
NCR: NCU04699
NTE: NEUTE1DRAFT124377(NEUTE1DRAFT_124377)
MGR: MGG_01295
MAW: MAC_03502
MAJ: MAA_02204
CMT: CCM_04620
MBE: MBM_06023
ANI: AN1376.2
ANG: ANI_1_64074(An08g00560)
ABE: ARB_08040
TVE: TRV_04355
PNO: SNOG_06783(SNOG_06782)
PTE: PTT_09357
SPO: SPBC337.16(cho1)
CNE: CND06200
CNB: CNBD0210
ABP: AGABI1DRAFT76829(AGABI1DRAFT_76829)
ABV: AGABI2DRAFT211112(AGABI2DRAFT_211112)
MGL: MGL_0956
DDI: DDB_G0282527(pemtA) DDB_G0289645(pemtB)
DFA: DFA_01140(pemtB) DFA_05291(pemtA)
NGR: NAEGRDRAFT_4009(AM15)
LPN: lpg2158(pmtA)
LPH: LPV_2409
LPO: LPO_2222
LPM: LP6_2181(pmtA)
LPF: lpl2086
LPP: lpp2097
LPA: lpa_03098
LPE: lp12_2150
LLO: LLO_3400
LFA: LFA_0551
LOK: Loa_02535
MCA: MCA3065
NOC: Noc_0914
NHL: Nhal_1108
NWA: Nwat_0780
TEE: Tel_09350
NTT: TAO_1398
HHA: Hhal_0826
TKM: TK90_0730
TVR: TVD_03700
SLIM: SCL_1104
SVA: SVA_2165
CBAA: SRAA_1512
CBAB: SMCB_0498
EBA: ebA6680(pemT)
MLO: mll4753
MES: Meso_0681
PLA: Plav_2189
SME: SMc00414
SMX: SM11_chr3811(pmtA)
SMEL: SM2011_c00414(pmtA)
SMER: DU99_01800
SMD: Smed_3542
EAD: OV14_1225
ATU: Atu0300
ARA: Arad_0541
AVI: Avi_0349
AGR: AGROH133_03436(pmtA)
RLE: RL0333(pmtA) RL1338(pmtA)
RHL: LPU83_0386(pmtA)
RHT: NT26_4281
SHZ: shn_22230
BME: BMEI2000
BMEL: DK63_1491
BMEE: DK62_1457
BMF: BAB1_2131
BMB: BruAb1_2102(pmtA)
BABO: DK55_2061
BABR: DO74_1915
BABT: DK49_1817
BABB: DK48_58
BABU: DK53_2045
BABS: DK51_1498
BABC: DO78_1964
BMS: BR2127(pmtA)
BSI: BS1330_I2121(pmtA)
BSF: BSS2_I2061(pmtA)
BSZ: DK67_243
BSV: BSVBI22_A2123(pmtA)
BOV: BOV_2043(pmtA)
BOL: BCOUA_I2127(pmtA)
BCAR: DK60_58
BCAS: DA85_10235
BMR: BMI_I2149(pmtA)
BPP: BPI_I2185(pmtA)
BPV: DK65_1412
BVL: BF3285c1_0816(pmtA)
OAN: Oant_0788
OAH: DR92_325
BJA: bll6634(pmtA) bll6994 blr0681(pmtA)
BRS: S23_01550(pmtA) S23_13110(pmtX1) S23_16750(pmtA)
OCG: OCA5_c01120 OCA5_c26320(pmtA1) OCA5_c27610(pmtA2)
OCO: OCA4_c01120 OCA4_c26310(pmtA1) OCA4_c27600(pmtA2)
MDI: METDI3731(pmtA) METDI5092
HDN: Hden_2491
RVA: Rvan_3372
MCG: GL4_2815
HDI: HDIA_4168(ubiE_1) HDIA_4815
SIL: SPOA0294(pmtA)
RSP: RSP_0721(PmtA)
RCP: RCAP_rcc00559(pmtA)
PDE: Pden_4690
DSH: Dshi_2712
PSF: PSE_0487
PGA: PGA1_c29610(pmtA)
PGL: PGA2_c27520(pmtA)
PGD: Gal_00470
PHP: PhaeoP97_00543(pmtA_1)
PPIC: PhaeoP14_02731(pmtA)
MALG: MALG_03931
GOX: GOX1862
GOH: B932_0129
GOY: GLS_c19790(pmtA)
ACR: Acry_2168
AMV: ACMV_24160(pmtA)
GDI: GDI2102(pmtA)
GDJ: Gdia_0321
GXY: GLX_26190
GXL: H845_564
KEU: S101446_02953(pmtA)
APK: APA386B_612(pmtA)
ASZ: ASN_3042(pmtA)
TMO: TMO_1929
PHM: PSMK_14180(pmtA)
ABAC: LuPra_03024(ubiE_5)
NDE: NIDE0511(pmtA)
NMV: NITMOv2_0425(pmtA)
NIO: NITINOP_1227(pmtA)
NJA: NSJP_1550(pmtA)
MOX: DAMO_1446(pmtA)
 » show all
Taxonomy
Reference
1  [PMID:25437]
  Authors
Hirata F, Viveros OH, Diliberto EJ Jr, Axelrod J.
  Title
Identification and properties of two methyltransferases in conversion of phosphatidylethanolamine to phosphatidylcholine.
  Journal
Proc. Natl. Acad. Sci. U. S. A. 75 (1978) 1718-21.
Reference
2  [PMID:438165]
  Authors
Schneider WJ, Vance DE.
  Title
Conversion of phosphatidylethanolamine to phosphatidylcholine in rat liver. Partial purification and characterization of the enzymatic activities.
  Journal
J. Biol. Chem. 254 (1979) 3886-91.
Other DBs
ExplorEnz - The Enzyme Database: 2.1.1.71
IUBMB Enzyme Nomenclature: 2.1.1.71
ExPASy - ENZYME nomenclature database: 2.1.1.71
BRENDA, the Enzyme Database: 2.1.1.71
CAS: 67167-73-1

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