2014-05-06
|
R-HSA-5263616
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MeSeO2H is reduced to MeSeOH by TXNRD1
|
BibTex
|
2014-05-06
|
R-HSA-5333612
|
MeSebGalNac is oxidatively cleaved to MeSeO2H and 2-acetamidoglucal
|
BibTex
|
2014-05-06
|
R-HSA-5333608
|
GSSebGalNac is reduced and methylated to MeSebGalNac
|
BibTex
|
2014-05-06
|
R-HSA-5333607
|
GSSeH combines with bGalNAc derivative to form GSSebGalNac
|
BibTex
|
2014-05-06
|
R-HSA-2408542
|
GSSeSG is reduced to GSSeH and GSH by GSR
|
BibTex
|
2014-05-06
|
R-HSA-2408556
|
SeO3(2-) combines with GSH to form GSSeSG and GSSG
|
BibTex
|
2014-05-06
|
R-HSA-2408548
|
PAPSe is reduced to SeO3(2-) by PAPSe reductase
|
BibTex
|
2014-05-06
|
R-HSA-2408540
|
APSe is phosphorylated to PAPSe by PAPSS1,2
|
BibTex
|
2014-05-06
|
R-HSA-2408525
|
H2SeO4 is converted to APSe by PAPSS1,2
|
BibTex
|
2014-05-06
|
R-RNO-2408504
|
H2SeO4 is converted to APSe by PAPSS1,2
|
BibTex
|
2014-05-06
|
R-PCH-2408503
|
APSe is phosphorylated to PAPSe by Kaps
|
BibTex
|
2014-05-06
|
R-SCE-2408518
|
PAPSe is reduced to SeO3(2-) by MET16
|
BibTex
|
2014-05-06
|
R-RNO-2408553
|
SeO3(2-) combines with GSH to form GSSeSG and GSSG
|
BibTex
|
2014-05-06
|
R-RNO-2408514
|
GSSeSG is reduced to GSSeH and GSH by Gsr
|
BibTex
|
2014-05-06
|
R-RNO-5333617
|
GSSeH combines with bGalNAc derivative to form GSSebGalNac
|
BibTex
|
2014-05-06
|
R-RNO-5333614
|
GSSebGalNac is reduced and methylated to MeSebGalNac
|
BibTex
|
2014-05-06
|
R-RNO-5333613
|
MeSebGalNac is oxidatively cleaved to MeSeO2H and 2-acetamidoglucal
|
BibTex
|
2014-05-06
|
R-HSA-5263614
|
MeSeOH is reduced to MeSeH by TXNRD1
|
BibTex
|
2014-05-06
|
R-HSA-2408500
|
GSSeH condenses with GSH to form H2Se and GSSG
|
BibTex
|
2014-05-06
|
R-RNO-2408520
|
GSSeH condenses with GSH to form H2Se and GSSG
|
BibTex
|
2014-05-06
|
R-HSA-2408558
|
SeO3(2-) is reduced to H2Se by TXNRD1
|
BibTex
|
2014-05-06
|
R-BTA-2408527
|
SeO3(2-) is reduced to H2Se by TXNRD1
|
BibTex
|
2014-05-06
|
R-HSA-2408546
|
tRNA(Met) is selenomethionylated to SeMet-tRNA(Met) by multisynthetase complex
|
BibTex
|
2014-05-06
|
R-TAE-2408513
|
tRNA(Met) is selenomethionylated to SeMet-tRNA(Met) by Mars
|
BibTex
|
2014-05-06
|
R-VRA-2408510
|
tRNA(Met) is selenomethionylated to SeMet-tRNA(Met) by Mars
|
BibTex
|
2014-05-06
|
R-HSA-5333609
|
MeSebGalNac is hydrolysed to MeSeH and bGalNac
|
BibTex
|
2014-05-06
|
R-RNO-5333611
|
MeSebGalNac is hydrolysed to MeSeH and bGalNac
|
BibTex
|
2014-05-06
|
R-HSA-2408532
|
AdeSeHCys is hydrolysed to SeHCys by AHCY
|
BibTex
|
2014-05-06
|
R-HSA-2408544
|
AdoSeMet is converted to AdeSeHCys by MetTrans(1)
|
BibTex
|
2014-05-06
|
R-HSA-2408551
|
SeMet is converted to AdoSeMet by MAT
|
BibTex
|
2014-05-06
|
R-RNO-2408545
|
AdoSeMet is converted to AdeSeHCys by MetTrans(2)
|
BibTex
|
2014-05-06
|
R-RNO-2408512
|
AdeSeHCys is hydrolysed to SeHCys by Ahcy
|
BibTex
|
2014-05-06
|
R-HSA-2408530
|
MeSeH is hydrolysed to H2Se by methylselenol demethylase
|
BibTex
|
2014-05-06
|
R-HSA-2408536
|
H2Se is methylated to MeSeH by H2Se methyltransferase
|
BibTex
|
2014-05-06
|
R-HSA-2408524
|
Sec is reduced to H2Se by PXLP-K259-SCLY dimer
|
BibTex
|
2014-05-06
|
R-HSA-2408543
|
SeCysta is hydrolysed to Sec by PXLP-K212-CTH
|
BibTex
|
2014-05-06
|
R-HSA-2408559
|
SeHCys and Ser are dehydrated into SeCysta by CBS
|
BibTex
|
2014-05-06
|
R-RNO-2408533
|
SeHCys and Ser are dehydrated into SeCysta by Cbs
|
BibTex
|
2014-05-06
|
R-RNO-2408502
|
SeCysta is hydrolysed to Sec by PXLP-K211-Cth
|
BibTex
|
2014-05-06
|
R-RNO-2408511
|
H2Se is methylated to MeSeH by H2Se methyltransferase
|
BibTex
|
2014-05-06
|
R-HSA-2408537
|
Excess SeMet is cleaved into MeSeH by PXLP-K212-CTH
|
BibTex
|
2014-05-06
|
R-MMU-2408528
|
Excess SeMet is cleaved into MeSeH by PXLP-K211-Cth
|
BibTex
|
2014-05-06
|
R-HSA-2408539
|
MeSec is hydrolysed to MeSeH by PXLP-K212-CTH
|
BibTex
|
2014-05-06
|
R-RNO-2408538
|
MeSec is hydrolysed to MeSeH by PXLP-K211-Cth
|
BibTex
|
2014-05-06
|
R-RNO-2408521
|
MeSeH is hydrolysed to H2Se by methylselenol demethylase
|
BibTex
|
2014-05-06
|
R-HSA-2408529
|
Sec-tRNA(Sec):EEFSEC:GTP binds to 80S Ribosome
|
BibTex
|
2014-05-06
|
R-HSA-2408509
|
Sec-tRNA(Sec) binds to EEFSEC:GTP
|
BibTex
|
2014-05-06
|
R-HSA-2408555
|
Sep-tRNA(Sec) is converted to Sec-tRNA(Sec) by PXLP-K284-SEPSECS tetramer
|
BibTex
|
2014-05-06
|
R-HSA-2408507
|
Ser-tRNA(Sec) is phosphorylated to Sep-tRNA(Sec) by PSTK
|
BibTex
|
2014-05-06
|
R-HSA-2408526
|
tRNA(Sec) is serylated to Ser-tRNA(Sec) by SARS dimer
|
BibTex
|
2014-05-06
|
R-MMU-2408505
|
Ser-tRNA(Sec) is phosphorylated to Sep-tRNA(Sec) by Pstk
|
BibTex
|
2014-05-06
|
R-MMU-2408515
|
Sec-tRNA(Sec) binds to Eefsec:GTP
|
BibTex
|
2014-05-06
|
R-RNO-2408535
|
Sec-tRNA(Sec):Eefsec:GTP binds to Rpl30
|
BibTex
|
2014-05-06
|
R-HSA-5333615
|
80S:Met-tRNAi:mRNA:SECISBP2:Sec-tRNA(Sec):EEFSEC:GTP is hydrolysed to 80S:Met-tRNAi:mRNA:SECISBP2:Sec and EEFSEC:GDP by EEFSEC
|
BibTex
|
2014-05-06
|
R-RNO-5333610
|
Rpl30:Met-tRNAi:mRNA:Secisbp2:Sec-tRNA(Sec):Eefsec:GTP is hydrolysed to Rpl30:Met-tRNAi:mRNA:Secisbp2:Sec and Eefsec:GDP by Eefsec
|
BibTex
|
2014-05-06
|
R-HSA-2408541
|
MeSeH is methylated to Me2Se by MeSeH methyltransferase
|
BibTex
|
2014-05-06
|
R-RNO-2408501
|
MeSeH is methylated to Me2Se by MeSeH methyltransferase
|
BibTex
|
2014-05-06
|
R-HSA-2408554
|
Me2Se is methylated to Me3Se+ by INMT
|
BibTex
|
2014-05-06
|
R-MMU-2408549
|
Me2Se is methylated to Me3Se+ by Inmt
|
BibTex
|
2012-03-19
|
R-HSA-2162253
|
PDSS1,2 ligates FPP to IPPP
|
BibTex
|
2012-03-19
|
R-HSA-2162192
|
COQ2 ligates all-E-10PrP2 to PHB
|
BibTex
|
2012-03-19
|
R-HSA-2162188
|
COQ5 methylates MDMQ10H2
|
BibTex
|
2012-03-19
|
R-HSA-2162191
|
Unknown enzyme hydroxylates DMPhOH
|
BibTex
|
2012-03-19
|
R-HSA-2162195
|
Unknown enzyme decarboxylates MHDB
|
BibTex
|
2012-03-19
|
R-HSA-2162193
|
COQ3 methylates DHDB
|
BibTex
|
2012-03-19
|
R-HSA-2162187
|
COQ6 hydroxylates DHB
|
BibTex
|
2012-03-19
|
R-SCE-2162292
|
HHB is hydroxylated to DHHB by Coq6
|
BibTex
|
2012-03-19
|
R-SCE-2164816
|
MHHB is decarboxylated to HMPhOH by MHHB decarboxylase
|
BibTex
|
2012-03-19
|
R-SCE-2164813
|
HMPhOH is hydroxylated to MDMQ6H2 by HMPhOH monooxygenase
|
BibTex
|
2012-03-19
|
R-HSA-2162194
|
COQ7:COQ9 octamer hydroxylates DMQ10H2
|
BibTex
|
2012-03-19
|
R-HSA-2162186
|
COQ3 methylates DeMQ10H2
|
BibTex
|
2012-02-24
|
R-HSA-2161917
|
ALOX5 oxidises 15S-HpETE to LXA4/B4
|
BibTex
|
2012-02-24
|
R-HSA-2162002
|
Arachidonic acid is oxidised to 15S-HpETE by ALOX15/15B
|
BibTex
|
2012-02-24
|
R-HSA-2161949
|
HXA3/B3 is hydrolysed to TrXA3/B3 by HXEH
|
BibTex
|
2012-02-24
|
R-HSA-2161794
|
Arachidonic acid is converted to HXA3/B3 by ALOX12
|
BibTex
|
2012-02-24
|
R-HSA-2161701
|
PGH2 is isomerised to PGD2 by HPGDS
|
BibTex
|
2012-02-24
|
R-HSA-2161651
|
PGE2 is converted to PGF2a by CBR1
|
BibTex
|
2012-02-24
|
R-HSA-2161588
|
Delta12-PGJ2 is dehydrated to 15d-PGJ2
|
BibTex
|
2012-02-24
|
R-HSA-2161563
|
PGJ2 is isomerised to delta12-PGJ2
|
BibTex
|
2012-02-24
|
R-HSA-2161733
|
PGD2 is dehydrated to PGJ2
|
BibTex
|
2012-02-24
|
R-HSA-2161620
|
PGH2 is isomerised to PGD2 by PTGDS
|
BibTex
|
2012-02-24
|
R-HSA-2161659
|
PGE2 is dehydrated to PGA2
|
BibTex
|
2012-02-24
|
R-HSA-2161660
|
PGH2 is isomerised to PGE2 by PTGES
|
BibTex
|
2012-02-24
|
R-HSA-2161662
|
PGD2/E2/F2a is oxidised to 15k-PGD2/E2/F2a by HPGD
|
BibTex
|
2012-02-24
|
R-OCU-2161568
|
PGD2/E2/F2a is oxidised to 15k-PGD2/E2/F2a by HPGD
|
BibTex
|
2012-02-24
|
R-HSA-2161666
|
PGA2 is isomerised to PGC2
|
BibTex
|
2012-02-24
|
R-HSA-2161668
|
PGA2 is dehydrated to 15d-PGA2
|
BibTex
|
2012-02-24
|
R-MMU-2161646
|
PGA2 is dehydrated to 15d-PGA2
|
BibTex
|
2012-02-24
|
R-HSA-2161732
|
TXB2 is converted to 11dh-TXB2 by TXDH
|
BibTex
|
2012-02-24
|
R-HSA-443894
|
TXA2 is hydrolysed to TXB2
|
BibTex
|
2012-02-24
|
R-HSA-2161735
|
PGC2 is isomerised to PGB2
|
BibTex
|
2012-02-24
|
R-HSA-2161673
|
PGD2 is dehydrated to 15d-PGD2
|
BibTex
|
2012-02-24
|
R-HSA-2161612
|
PGH2 is reduced to PGF2a by FAM213B
|
BibTex
|
2012-02-24
|
R-MMU-2161718
|
PGH2 is reduced to PGF2a by Fam213b
|
BibTex
|
2012-02-24
|
R-HSA-2161549
|
PGH2 is reduced to PGF2a by AKR1C3
|
BibTex
|
2012-02-24
|
R-HSA-2161613
|
PGH2 is degraded to 12S-HHT and MDA by TBXAS1
|
BibTex
|
2012-02-24
|
R-HSA-2161614
|
PGD2 is reduced to 11-epi-PGF2a by AKRIC3
|
BibTex
|
2012-02-24
|
R-HSA-2161619
|
PGI2 is hydrolysed to 6k-PGF1a
|
BibTex
|
2012-02-24
|
R-HSA-2161692
|
15k-PGE2/F2a is reduced to dhk-PGE2/F2a by PTGR1
|
BibTex
|
2012-02-24
|
R-MMU-2161638
|
15k-PGE2/F2a is reduced to dhk-PGE2/F2a by Ptgr2
|
BibTex
|
2012-02-24
|
R-HSA-2161776
|
5S-HETE is oxidised to 5-oxoETE by 5-HEDH
|
BibTex
|
2012-02-24
|
R-HSA-2161946
|
5S-HpETE is reduced to 5S-HETE by GPX1/2/4
|
BibTex
|
2012-02-24
|
R-OCU-2161896
|
5S-HpETE is reduced to 5S-HETE by GPX1
|
BibTex
|
2012-02-24
|
R-HSA-2161795
|
Arachidonic acid is hydroxylated to 16/17/18-HETE by CYP(1)
|
BibTex
|
2012-02-24
|
R-HSA-2161940
|
Arachidonic acid is hydroxylated to 20-HETE by CYP(3)
|
BibTex
|
2012-02-24
|
R-HSA-2161814
|
Arachidonic acid is hydroxylated to 19-HETE by CYP(2)
|
BibTex
|
2012-02-24
|
R-HSA-2161792
|
20cho-LTB4 is oxidised to 20cooh-LTB4 by CYP4F2/4F3
|
BibTex
|
2012-02-24
|
R-HSA-2161745
|
20oh-LTB4 is oxidised to 20cho-LTB4 by CYP4F2/4F3
|
BibTex
|
2012-02-24
|
R-HSA-2162019
|
LTA4 is converted to EXA4 by ALOX15
|
BibTex
|
2012-02-24
|
R-HSA-2161768
|
EXA4 is converted to EXC4 by LTC4S
|
BibTex
|
2012-02-24
|
R-HSA-2161962
|
LTA4 is hydrolysed to 6t-/6t,12epi-LTB4
|
BibTex
|
2012-02-24
|
R-HSA-2161868
|
EXD4 is converted to EXE4 by DPEP
|
BibTex
|
2012-02-24
|
R-HSA-2161945
|
EXC4 is converted to EXD4 by GGT
|
BibTex
|
2012-02-24
|
R-HSA-2161979
|
20cho-LTB4 is oxidised to 20cooh-LTB4 by ALDH
|
BibTex
|
2012-02-24
|
R-HSA-2161790
|
20cooh-LTB4 is converted to 18cooh-LTB4
|
BibTex
|
2012-02-24
|
R-HSA-2161567
|
LTB4 is oxidised to 12-oxoLTB4 by PTGR1
|
BibTex
|
2012-02-24
|
R-SSC-2161617
|
LTB4 is oxidised to 12-oxoLTB4 by PTGR1
|
BibTex
|
2012-02-24
|
R-HSA-2161890
|
Arachidonic acid is epoxidated to 5,6-EET by CYP(4)
|
BibTex
|
2012-02-24
|
R-HSA-2161961
|
EET(1) is hydrolysed to DHET(1) by EPHX2
|
BibTex
|
2012-02-24
|
R-HSA-2161899
|
Arachidonic acid is epoxidated to 8,9/11,12/14,15-EET by CYP(5)
|
BibTex
|
2012-02-24
|
R-HSA-2161789
|
15S-HETE is oxidised to 15-oxoETE by 15-HEDH
|
BibTex
|
2012-02-24
|
R-HSA-2161791
|
15S-HpETE is reduced to 15S-HETE by GPX1/2/4
|
BibTex
|
2012-02-24
|
R-HSA-2161951
|
Arachidonic acid is oxidised to 15R-HETE by Acetyl-PTGS2
|
BibTex
|
2012-02-24
|
R-HSA-2161959
|
12R-HpETE is reduced to 12R-HETE by GPX1/2/4
|
BibTex
|
2012-02-24
|
R-HSA-2161950
|
Arachidonic acid is oxidised to 12R-HpETE by ALOX12B
|
BibTex
|
2012-02-24
|
R-HSA-2161964
|
Arachidonic acid is oxidised to 12S-HpETE by ALOX12/15
|
BibTex
|
2012-02-24
|
R-HSA-2161948
|
Arachidonic acid is converted to 12-oxoETE by ALOX12
|
BibTex
|
2012-02-24
|
R-HSA-2161999
|
12S-HpETE is reduced to 12S-HETE by GPX1/2/4
|
BibTex
|
2012-02-24
|
R-HSA-2161907
|
ALOX5 oxidises 15R-HETE to 15epi-LXA4/B4
|
BibTex
|
2012-02-24
|
R-HSA-2161779
|
LXA4 is oxidised to 15k-LXA4 by HPGD
|
BibTex
|
2012-02-24
|
R-HSA-2161775
|
ALOX12 oxidises LTA4 to LXA4/B4
|
BibTex
|
2012-02-24
|
R-HSA-2161844
|
15k-LXA4 is reduced to dhk-LXA4 by PTGR1
|
BibTex
|
2012-02-24
|
R-SSC-2161847
|
15k-LXA4 is reduced to dhk-LXA4 by PTGR1
|
BibTex
|
2011-10-28
|
R-HSA-1855214
|
PL(C)D4:3xCa2+ hydrolse PI(4,5)P2 to I(1,4,5)P3 and DAG at the ER membrane
|
BibTex
|
2011-10-28
|
R-HSA-1855177
|
PI(4,5)P2 is hydrolysed to I(1,4,5)P3 and DAG by cytosolic PLC[2] at the plasma membrane
|
BibTex
|
2011-10-28
|
R-HSA-1855221
|
PI(4,5)P2 is hydrolysed to I(1,4,5)P3 and DAG by tethered PLC[1] at the plasma membrane
|
BibTex
|
2011-10-28
|
R-HSA-1855205
|
I(1,3,4,5)P4 is dephosphorylated to I(1,4,5)P3 by PTEN in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855172
|
I(1,3,4)P3 is phosphorylated to I(1,3,4,5)P4 by ITPK1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855213
|
I(1,3,4,5)P4 is dephosphorylated to I(1,3,4)P3 by INPP5B at the plasma membrane
|
BibTex
|
2011-10-28
|
R-HSA-1855153
|
I(1,4,5)P3 is phosphorylated to I(1,3,4,5)P4 by ITPKA/B/C in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855217
|
I(1,4,5)P3 transports from the ER lumen to the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855200
|
I(1,3,4,5)P4 is dephosphorylated to I(1,4,5)P3 by MINPP1 in the ER lumen
|
BibTex
|
2011-10-28
|
R-HSA-1855186
|
I(1,3,4,5)P4 transports from the cytosol to the ER lumen
|
BibTex
|
2011-10-28
|
R-HSA-1855218
|
I(1,3,4,5)P4 is dephosphorylated to I(1,3,4)P3 by INPP5[3]/ITPK1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855197
|
I(1,3,4)P3 is phosphorylated to I(1,3,4,6)P4 by ITPK1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855171
|
I(1,3,4,6)P4 is dephosphorylated to I(1,3,4)P3 by ITPK1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855169
|
I(3,4,6)P3 is phosphorylated to I(1,3,4,6)P4 by ITPK1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855159
|
I(1,3,4,6)P4 is dephosphorylated to I(3,4,6)P3 by ITPK1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855162
|
I(3,4,5,6)P4 is phosphorylated to I(1,3,4,5,6)P5 by ITPK1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855219
|
I(1,3,4,5,6)P5 is dephosphorylated to I(3,4,5,6)P4 by ITPK1 in the cytosol
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BibTex
|
2011-10-28
|
R-HSA-1855166
|
PP-IP4 is dephosphorylated to I(1,3,4,5,6)P5 by NUDT4 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855173
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5-PP-IP4 transports from the nucleus to the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855181
|
I(1,3,4,5,6)P5 is phosphorylated to 5-PP-IP4 by IP6K1/2 in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855228
|
I(1,3,4,6)P4 is phosphorylated to I(1,3,4,5,6)P5 by IPMK in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855201
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I(1,3,4,6)P4 transports from the cytosol to the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855160
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I(1,3,4,5,6)P5 transports from the ER lumen to the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855225
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IP6 is dephosphorylated to I(1,2,4,5,6)P5 by MINPP1 in the ER lumen
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BibTex
|
2011-10-28
|
R-HSA-1855164
|
IP6 transports from the cytosol to the ER lumen
|
BibTex
|
2011-10-28
|
R-HSA-1855198
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5-PP-IP5 is dephosphorylated to IP6 by NUDT(1) in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855165
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(PP)2-IP4 is dephosphorylated to 5-PP-IP5 by NUDT(1) in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855182
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5-PP-IP5 is phosphorylated to 1,5-(PP)2-IP4 by PPIP5K1/2 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855227
|
IP6 is phosphorylated to 5-PP-IP5 by IP6K1/3 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855179
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I(1,3,4,5,6)P5 is phosphorylated to IP6 by IPPK in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855161
|
I(1,3,4,5,6)P5 transports from the nucleus to the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855206
|
I(1,3,4,5)P4 is phosphorylated to I(1,3,4,5,6)P5 by IPMK in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855168
|
I(1,3,4,5)P4 transports from the cytosol to the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855233
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I(1,4,5)P3 is phosphorylated to I(1,3,4,5)P4 by IPMK in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855190
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I(1,4,5)P3 transports from the cytosol to the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855185
|
I(1,4,5,6)P4 is phosphorylated to I(1,3,4,5,6)P5 by IPMK in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855189
|
I(1,4,5,6)P4 transports from the ER lumen to the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855163
|
I(1,3,4,5,6)P5 is dephosphorylated to I(1,4,5,6)P4 by MINPP1 in the ER lumen
|
BibTex
|
2011-10-28
|
R-HSA-1855195
|
I(1,3,4,5,6)P5 transports from the cytosol to the ER lumen
|
BibTex
|
2011-10-28
|
R-HSA-1855155
|
I(1,3,4,5,6)P5 transports from the ER lumen to the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855223
|
I(1,3,4,5,6)P5 is phosphorylated to 5-PP-IP4 by IP6K1/3 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-2023971
|
1/3 PP-IP5 is dephosphorylated to IP6 by NUDT(1) in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-2023973
|
(PP)2-IP4 is dephosphorylated to 1/3-PP-IP5 by NUDT(1) in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855194
|
1-PP-IP5 is phosphorylated to 1,5-(PP)2-IP4 by IP6K1/3 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855216
|
IP6 is phosphorylated to 1-PP-IP5 by PPIP5K1/2 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855220
|
(PP)2-IP4 transports from the nucleus to the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855157
|
1-PP-IP5 is phosphorylated to 1,5-(PP)2-IP4 by IP6K1/2 in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855212
|
1/3-PP-IP5 transports from the cytosol to the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855203
|
5-PP-IP5 transports from the nucleus to the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855207
|
IP6 is phosphorylated to 5-PP-IP5 by IP6K1/2 in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855176
|
I(1,3,4,5,6)P5 is phosphorylated to IP6 by IPPK (IP5-2K) in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855188
|
IP6 transports from the cytosol to the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855187
|
IP6 transports from the nucleus to the ER lumen
|
BibTex
|
2011-10-28
|
R-HSA-1855193
|
1-PP-IP4 is phosphorylated to 1,5-(PP)2-IP3 by IP6K1/3 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855158
|
5-PP-IP5 is phosphorylated to 5-PPP-IP5 by IP6K1/3 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855210
|
I3P is dephosphorylated to Ins by IMPA1/2 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855178
|
Glc6P is isomerised to I3P by ISYNA1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855202
|
I(3,4)P2 is dephosphorylated to I3P by INPP4A/B in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855232
|
I(1,3,4)P3 is dephosphorylated to I(3,4)P2 by INPP1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855222
|
I(1,4,5)P3 is dephosphorylated to I(1,4)P2 by INPP5A/B at the plasma membrane
|
BibTex
|
2011-10-28
|
R-HSA-1855154
|
I1P is dephosphorylated to Ins by IMPA1/2 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855180
|
I(1,3,4)P3 is dephosphorylated to I(1,3)P2 by INPP4A/B in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855208
|
I(1,4)P2 is dephosphorylated to I4P by INPP1 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855174
|
I(1,4,5)P3 is dephosphorylated to I(1,4)P2 by INPP5(4) in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855211
|
I4P is dephosphorylated to Ins by IMPA1/2 in the cytosol
|
BibTex
|
2011-10-28
|
R-HSA-1855230
|
5-PP-IP4 is phosphorylated to 1,5-(PP)2-IP3 by IP6K1/2 in the nucleus
|
BibTex
|
2011-10-28
|
R-HSA-1855224
|
5-PP-IP5 is phosphorylated to 5-PPP-IP5 by IP6K1/2 in the nucleus
|
BibTex
|
2011-10-18
|
R-HSA-1676082
|
PI4P is phosphorylated to PI(4,5)P2 by PIP5K1A-C at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676177
|
PI(4,5)P2 is dephosphorylated to PI4P by SYNJ/INPP5[1] at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675776
|
PI5P is phosphorylated to PI(4,5)P2 by PIP4K2 dimers at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676203
|
PI(3,5)P2 is dephosphorylated to PI5P by SYNJ/MTMs at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676134
|
PI3P is phosphorylated to PI(3,5)P2 by PIP5K1A/B at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675836
|
PI(3,5)P2 is dephosphorylated to PI3P by SYNJ at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676145
|
PI3P is phosphorylated to PI(3,4)P2 by PIP4K2/5K1 at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676164
|
PI(3,4)P2 is dephosphorylated to PI3P by INPP4A/B at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675949
|
PI(3,4,5)P3 is dephosphorylated to PI(3,4)P2 by INPP5[2] at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675773
|
PI(3,4)P2 is phosphorylated to PI(3,4,5)P3 by PIP5K1A-C at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676109
|
PI4P is phosphorylated to PI(3,4)P2 by PI3K3C[2] at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676149
|
PI(3,4)P2 is dephosphorylated to PI4P by PTEN at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675994
|
PI3P is dephosphorylated to PI by SYNJ/MTMs at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675780
|
PI is phosphorylated to PI4P by PI4K2A/B at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675988
|
PI4P is dephosphorylated to PI by SYNJ at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675815
|
PI4P transports from the Golgi membrane to the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676185
|
PI is phosphorylated to PI4P by PI4KA/2A/2B at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1483087
|
PI is exchanged with PC by PITPNB
|
BibTex
|
2011-10-18
|
R-HSA-1483229
|
PI:PITPNB is transported from the ER membrane to the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1483219
|
PC is exchanged with PI by PITPNB
|
BibTex
|
2011-10-18
|
R-HSA-1676124
|
PI4P is dephosphorylated to PI by SACM1L at the ER membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675813
|
PI is phosphorylated to PI4P by PI4KA/2B at the ER membrane
|
BibTex
|
2011-10-18
|
R-HSA-1483211
|
PC:PITPNB is transported from the Golgi membrane to the ER membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676114
|
PI3P is dephosphorylated to PI by SACM1L at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675961
|
PI is phosphorylated to PI3P by PIK3C2A/3 at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676133
|
PI4P is dephosphorylated to PI by SACM1L at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675883
|
PI is phosphorylated to PI4P by PI4KB at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676152
|
PI4KB binds to ARF1/3:GTP at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675824
|
PI(4,5)P2 is dephosphorylated to PI4P by OCRL/INPP5E at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675928
|
PI4P is phosphorylated to PI(3,4)P2 by PIK3C2A/G at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676204
|
PI(3,4)P2 is dephosphorylated to PI4P by TPTE2 at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676005
|
PI(3,5)P2 is dephosphorylated to PI3P by FIG4 at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675896
|
PI(3,5)P2 transports from the early endosome membrane to the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676168
|
PI3P is phosphorylated to PI(3,5)P2 by PIKFYVE at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676174
|
PI(3,5)P2 is dephosphorylated to PI3P by FIG4 at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675939
|
PI is phosphorylated to PI3P by PIK3C2A/3 at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676141
|
PI3P is dephosphorylated to PI by MTM proteins at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676162
|
PI(3,4)P2 is dephosphorylated to PI3P by INPP4A/B at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675834
|
PI(3,4)P2 is transported from the plasma membrane to the early endosome membrane
|
BibTex
|
2011-10-18
|
R-MMU-1676139
|
PI(3,4)P2 is transported from the plasma membrane to the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676206
|
PI4P is phosphorylated to PI(3,4)P2 by PIK3C2A at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675974
|
PI is phosphorylated to PI4P by PI4K2A/B at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-NUL-1675886
|
PI3P is phosphorylated to PI(3,5)P2 by Pikfyve at the early endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675921
|
PI3P is phosphorylated to PI(3,5)P2 by PIKFYVE at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-NUL-1675982
|
PI3P is phosphorylated to PI(3,5)P2 by Pikfyve at the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676161
|
PI(3,5)P2 transports from the late endosome membrane to the Golgi membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676041
|
Presence of PI(3,5)P2 stimulates the maturation of the early endosome into the late endosome
|
BibTex
|
2011-10-18
|
R-HSA-1675910
|
PI3P is phosphorylated to PI(3,5)P2 by PIKFYVE at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676024
|
PI is phosphorylated to PI3P by PIK3C2A/3 at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675795
|
PI3P is dephosphorylated to PI by MTM proteins at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676020
|
PI(3,5)P2 is dephosphorylated to PI3P by FIG4 at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-NUL-1675925
|
PI3P is phosphorylated to PI(3,5)P2 by Pikfyve at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675810
|
PI is phosphorylated to PI5P by PIP5K1A/B at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676048
|
PI(4,5)P2 is phosphorylated to PI(3,4,5)P3 by PIK3C[1] at the plasma membrane
|
BibTex
|
2011-10-18
|
R-HSA-1675866
|
PI is phosphorylated to PI5P by PIKFYVE at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-NUL-1676051
|
PI is phosphorylated to PI5P by Pikfyve at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676065
|
PI(3,5)P2 is dephosphorylated to PI5P by MTM proteins at the late endosome membrane
|
BibTex
|
2011-10-18
|
R-HSA-1676105
|
PI(3,5)P2 is dephosphorylated to PI5P by MTM proteins at the early endosome membrane
|
BibTex
|
2011-09-14
|
R-HSA-1482598
|
1-acyl LPI is acylated to PI by MBOAT7
|
BibTex
|
2011-09-14
|
R-HSA-1482868
|
PI is hydrolyzed to 1-acyl LPI by PLA2[12]
|
BibTex
|
2011-09-14
|
R-HSA-1482626
|
2-acyl LPI is acylated to PI by MBOAT7
|
BibTex
|
2011-09-14
|
R-HSA-1482932
|
PI is hydrolyzed to 2-acyl LPI by PLA2[13]
|
BibTex
|
2011-09-14
|
R-HSA-1482976
|
CDP-DAG is converted to PI by CDIPT
|
BibTex
|
2011-09-14
|
R-HSA-1483121
|
PA is converted to CDP-DAG by CDS1
|
BibTex
|
2011-09-14
|
R-HSA-1483182
|
PC is hydrolyzed to PA and choline by PLD1/2
|
BibTex
|
2011-09-14
|
R-HSA-1482533
|
2-acyl LPC is acylated to PC by LPCAT
|
BibTex
|
2011-09-14
|
R-HSA-1482862
|
PC is hydrolysed to 2-acyl LPC by PLA2[7]
|
BibTex
|
2011-09-14
|
R-HSA-1482547
|
1-acyl LPC is acylated to PC by LPCAT
|
BibTex
|
2011-09-14
|
R-HSA-1482816
|
PC is hydrolyzed to 1-acyl LPC by PLA2[6]
|
BibTex
|
2011-09-14
|
R-HSA-1482961
|
CDP-Cho and DAG are converted to PC by CEPT1 at the ER membrane
|
BibTex
|
2011-09-14
|
R-HSA-1483203
|
PA is dephosphorylated to DAG by LPIN
|
BibTex
|
2011-09-14
|
R-HSA-1483107
|
GPETA is hydrolyzed to ETA and G3P by GPCPD1
|
BibTex
|
2011-09-14
|
R-HSA-1482545
|
2-acyl LPE is hydrolyzed to GPETA by PLA2G4C
|
BibTex
|
2011-09-14
|
R-HSA-1482828
|
PE is hydrolyzed to 2-acyl LPE by PLA2[4]
|
BibTex
|
2011-09-14
|
R-HSA-1482646
|
2-acyl LPE is acylated to PE by LPEAT
|
BibTex
|
2011-09-14
|
R-HSA-1482892
|
PE is hydrolyzed to 2-acyl LPE by PLA2G4C
|
BibTex
|
2011-09-14
|
R-HSA-1483077
|
PE transports from the mitochondrial membrane to the ER
|
BibTex
|
2011-09-14
|
R-HSA-1482894
|
CL and 1-acyl LPE are converted to MLCL and PE by TAZ (IM) (Reversible)
|
BibTex
|
2011-09-14
|
R-HSA-1482850
|
MLCL and PE are converted to CL and 1-acyl LPE by TAZ (IM) (Reversible)
|
BibTex
|
2011-09-14
|
R-HSA-1483212
|
PS is decarboxylated to PE by PISD
|
BibTex
|
2011-09-14
|
R-HSA-1483170
|
PS transports from the ER membrane to the IM membrane
|
BibTex
|
2011-09-14
|
R-HSA-1483186
|
PC is converted to PS by PTDSS1
|
BibTex
|
2011-09-14
|
R-HSA-1482889
|
DAG is acylated to TAG by DGAT1/2
|
BibTex
|
2011-09-14
|
R-HSA-1482654
|
2-MAG is transacylated to DAG by PNPLA2/3
|
BibTex
|
2011-09-14
|
R-HSA-1482811
|
DAG is hydrolyzed to 2-MAG by PNPLA2/3
|
BibTex
|
2011-09-14
|
R-HSA-1482777
|
TAG is hydrolyzed to DAG by PNPLA2/3
|
BibTex
|
2011-09-14
|
R-HSA-1482647
|
2-MAG and DAG are transacylated to TAG by PNPLA2/3
|
BibTex
|
2011-09-14
|
R-HSA-1483159
|
PCho is dephosphorylated to Cho by PHOSPHO1
|
BibTex
|
2011-09-14
|
R-HSA-1483004
|
Cho is phosphorylated to PCho by CHK dimer
|
BibTex
|
2011-09-14
|
R-HSA-1483116
|
GPCho is hydrolyzed to Cho and G3P by GPCPD1
|
BibTex
|
2011-09-14
|
R-HSA-1482612
|
2-acyl LPC is hydrolyzed to GPCho by PLA2[8]
|
BibTex
|
2011-09-14
|
R-HSA-1482827
|
PC is hydrolyzed to 2-acyl LPC by PLA2G4C
|
BibTex
|
2011-09-14
|
R-HSA-1482679
|
PA is hydrolysed to 1-acyl LPA by PLA2G2A
|
BibTex
|
2011-09-14
|
R-HSA-1483081
|
PCho and CTP are condensed to CDP-Cho by PCYT1 dimer
|
BibTex
|
2011-09-14
|
R-HSA-1482656
|
PA is hydrolysed to 1-acyl LPA by PLA2[1]
|
BibTex
|
2011-09-14
|
R-HSA-1482973
|
CDP-Cho and DAG are converted to PC by CHPT1 at the Golgi membrane
|
BibTex
|
2011-09-14
|
R-HSA-1482825
|
PI is hydrolyzed to 1-acyl LPI by PLA2[11]
|
BibTex
|
2011-09-14
|
R-HSA-1482856
|
PC is hydrolyzed to 1-acyl LPC by PLA2[5]
|
BibTex
|
2011-09-14
|
R-HSA-1482629
|
2-acyl LPC is hydrolyzed to GPCho by PLA2G4C
|
BibTex
|
2011-09-14
|
R-HSA-1482685
|
1-acyl LPC is hydrolyzed to GPCho by PLA2[8]
|
BibTex
|
2011-09-14
|
R-HSA-1482696
|
1-acyl LPC is hydrolyzed to GPCho by PLA2G4C
|
BibTex
|
2011-09-14
|
R-MMU-1483112
|
GPCho is hydrolyzed to Cho and G3P by Gpcpd1
|
BibTex
|
2011-09-14
|
R-HSA-1482691
|
2-acyl LPS is acylated to PS by LPSAT
|
BibTex
|
2011-09-14
|
R-HSA-1482897
|
PS is hydrolyzed to 2-acyl LPS by PLA2[10]
|
BibTex
|
2011-09-14
|
R-HSA-1483089
|
PE is converted to PS by PTDSS2
|
BibTex
|
2011-09-14
|
R-HSA-1482962
|
CDP-ETA and DAG are converted to PE by CEPT1/EPT1
|
BibTex
|
2011-09-14
|
R-HSA-1483190
|
PETA and CTP are condensed to CDP-ETA by PCY2
|
BibTex
|
2011-09-14
|
R-HSA-1483222
|
ETA is phosphorylated to PETA by CHK/ETNK
|
BibTex
|
2011-09-14
|
R-HSA-1483096
|
PETA is dephosphorylated to ETA by PHOSPHO1
|
BibTex
|
2011-09-14
|
R-HSA-1482667
|
1-acyl LPE is acylated to PE by LPEAT
|
BibTex
|
2011-09-14
|
R-HSA-1482887
|
PE is hydrolyzed to 1-acyl LPE by PLA2[3]
|
BibTex
|
2011-09-14
|
R-HSA-1482884
|
PE is hydrolyzed to 1-acyl LPE by PLA2[2]
|
BibTex
|
2011-09-14
|
R-HSA-1482636
|
1-acyl LPS is acylated to PS by LPSAT
|
BibTex
|
2011-09-14
|
R-HSA-1482771
|
PS is hydrolyzed to 1-acyl LPS by PLA2[9]
|
BibTex
|
2011-09-14
|
R-HSA-1482776
|
PS is hydrolyzed to 1-acyl LPS by PLA2G2A
|
BibTex
|
2011-09-14
|
R-RNO-1483078
|
PS transports from the ER membrane to the IM membrane
|
BibTex
|
2011-09-14
|
R-RNO-1483118
|
PS is decarboxylated to PE by Pisd
|
BibTex
|
2011-09-14
|
R-HSA-1482778
|
CL is hydrolyzed to MLCL by PLA2G6 (IM)
|
BibTex
|
2011-09-14
|
R-HSA-1483063
|
PG and CDP-DAG are converted to CL by CRLS1
|
BibTex
|
2011-09-14
|
R-HSA-1483197
|
PTPMT1 dephosphorylates PGP to PG
|
BibTex
|
2011-09-14
|
R-HSA-1482939
|
CDP-DAG is converted to PGP by PGS1
|
BibTex
|
2011-09-14
|
R-HSA-1483165
|
PA is converted to CDP-DAG by CDS2
|
BibTex
|
2011-09-14
|
R-HSA-1483099
|
PA translocates from the outer to the inner mitochondrial membrane
|
BibTex
|
2011-09-14
|
R-HSA-1482548
|
1-acyl LPA is acylated to PA by AGPAT5 (OM)
|
BibTex
|
2011-09-14
|
R-HSA-1482695
|
G3P is acylated to 1-acyl LPA by GPAM/GPAT2 (OM)
|
BibTex
|
2011-09-14
|
R-HSA-1482604
|
PA is hydrolyzed to 1-acyl LPA by PLA2[1] (OM)
|
BibTex
|
2011-09-14
|
R-RNO-1483154
|
PA transports from the outer to the inner mitochondrial membrane
|
BibTex
|
2011-09-14
|
R-RNO-1482978
|
CDP-DAG is converted to PGP by Pgs1
|
BibTex
|
2011-09-14
|
R-HSA-1482775
|
MLCL is acylated to CL by HADH (IM)
|
BibTex
|
2011-09-14
|
R-HSA-1482794
|
CL and 1-acyl LPC are converted to MLCL and PC by TAZ (IM) (Reversible)
|
BibTex
|
2011-09-14
|
R-HSA-1482781
|
MLCL and PC are converted to CL and 1-acyl LPC by TAZ (IM) (Reversible)
|
BibTex
|
2011-09-14
|
R-HSA-1482857
|
CL transports from the ER to the IM
|
BibTex
|
2011-09-14
|
R-HSA-1482861
|
MLCL is acylated to CL by LCLAT1 (ER)
|
BibTex
|
2011-09-14
|
R-HSA-1482773
|
MLCL transports from the IM to the ER
|
BibTex
|
2011-09-14
|
R-HSA-1482867
|
DLCL is acylated to MLCL by LCLAT1 (ER)
|
BibTex
|
2011-09-14
|
R-HSA-1482860
|
DLCL transports from the IM to the ER
|
BibTex
|
2011-09-14
|
R-HSA-1482759
|
MLCL is hydrolyzed to DLCL by PLA2G4A (IM)
|
BibTex
|
2011-09-14
|
R-RNO-1482836
|
CL is hydrolyzed to MLCL by Pla2g6 (IM)
|
BibTex
|
2011-09-14
|
R-RNO-1483065
|
PE transports from the mitochondrial membrane to the ER
|
BibTex
|
2011-09-14
|
R-HSA-1482571
|
1-acyl LPE is hydrolyzed to GPETA by PLA2G4C
|
BibTex
|
2011-09-14
|
R-MMU-1483231
|
GPETA is hydrolyzed to ETA and G3P by Gpcpd1
|
BibTex
|
2011-09-14
|
R-HSA-1602398
|
PE is hydrolyzed to 1-acyl LPE by PLA2[16]
|
BibTex
|
2011-09-14
|
R-HSA-1483174
|
PE is methylated to PC by PEMT
|
BibTex
|
2011-09-14
|
R-HSA-1602374
|
PS is hydrolyzed to 1-acyl LPS by PLA2[15]
|
BibTex
|
2011-09-14
|
R-HSA-1483002
|
DHAP is converted to 1-acyl GO3P by GNPAT
|
BibTex
|
2011-09-14
|
R-HSA-1602446
|
PA is hydrolyzed to 1-acyl LPA by PLA2[15]
|
BibTex
|
2011-09-14
|
R-HSA-1602399
|
PC is hydrolyzed to 1-acyl LPC by PLB1
|
BibTex
|
2011-09-14
|
R-HSA-1602417
|
PC is hydrolyzed to 1-acyl LPC by PLA2[16]
|
BibTex
|
2011-09-14
|
R-HSA-1482543
|
2-MAG is hydrolyzed to fatty acid and glycerol by MGLL
|
BibTex
|
2011-09-14
|
R-HSA-1483218
|
PG transports from the ER membrane to the late endosome membrane
|
BibTex
|
2011-09-14
|
R-HSA-1483142
|
PC is transphosphatidylated to PG by PLD1-4/6
|
BibTex
|
2011-09-14
|
R-MMU-1483172
|
PC is transphosphatidylated to PG by Pld1-4/6
|
BibTex
|
2011-09-14
|
R-HSA-1482539
|
1-acyl LPG is acylated to PG by LPGAT
|
BibTex
|
2011-09-14
|
R-HSA-1482900
|
PG is hydrolyzed to 1-acyl LPG by PLA2[1]
|
BibTex
|
2011-09-14
|
R-HSA-1482635
|
2-acyl LPG is acylated to PG by LPGAT
|
BibTex
|
2011-09-14
|
R-HSA-1482920
|
PG is hydrolyzed to 2-acyl LPG by PLA2[14]
|
BibTex
|
2011-09-14
|
R-HSA-1482907
|
PG is hydrolyzed to 1-acyl LPG by PLA2G2A
|
BibTex
|
2011-09-14
|
R-HSA-1483209
|
PG is converted to BMP
|
BibTex
|
2011-09-14
|
R-HSA-1482546
|
2-acyl LPG is acylated to PG by CRLS1 (IM)
|
BibTex
|
2011-09-14
|
R-HSA-1482847
|
PG is hydrolysed to 2-acyl LPG by PLA2G4B (IM)
|
BibTex
|
2011-09-14
|
R-HSA-1482689
|
1-acyl LPG is acylated to PG by CRLS1 (IM)
|
BibTex
|
2011-09-14
|
R-HSA-1482745
|
PG is hydrolyzed to 1-acyl LPG by PLA2G4B (IM)
|
BibTex
|
2011-09-14
|
R-HSA-1602368
|
PG is hydrolyzed to 1-acyl LPG by PLA2[16]
|
BibTex
|
2011-09-14
|
R-HSA-1602377
|
PI is hydrolyzed to 1-acyl LPI by PLA2[15]
|
BibTex
|
2010-08-17
|
R-HSA-934604
|
Phosphorylated SPRY2 is ubiquitinated by CBL
|
BibTex
|
2010-08-17
|
R-HSA-934559
|
SPRY2 is phosphorylated by phosphorylated MNK1
|
BibTex
|
2010-06-28
|
R-DME-881988
|
CRY is phosphorylated by SGG
|
BibTex
|
2010-06-08
|
R-HSA-870437
|
USP9X (FAM) deubiquitinates SMAD4
|
BibTex
|
2010-06-08
|
R-HSA-870479
|
USP9X (FAM) binds to ubiquitinated SMAD4
|
BibTex
|
2010-06-08
|
R-HSA-870477
|
Ubiquitinated SMAD4 translocates from the nucleus to the cytosol
|
BibTex
|
2010-06-08
|
R-HSA-870449
|
TRIM33 monoubiquitinates SMAD4
|
BibTex
|
2010-06-08
|
R-HSA-870538
|
TRIM33 (Ectodermin) binds SMAD heterotrimer in the nucleus
|
BibTex
|
2010-03-08
|
R-DME-538904
|
Phosphorylated PER binds to CLK
|
BibTex
|
2010-03-08
|
R-DME-538900
|
Phosphorylated PER rebinds to phosphorylated TIM
|
BibTex
|
2010-03-08
|
R-DME-538835
|
PER binds to DCO
|
BibTex
|
2010-03-08
|
R-DME-538891
|
CLK:CYC heterodimer dissociates from per, tim, vri, and Pdp1 genes
|
BibTex
|
2010-03-08
|
R-DME-538822
|
Cytosolic PP2A dephosphorylates phosphorylated PER complexed with TIM and DCO
|
BibTex
|
2010-03-08
|
R-DME-538824
|
PP1 binds to phosphorylated TIM in complex with PER
|
BibTex
|
2010-03-08
|
R-DME-538832
|
PP1 dephosphorylates phosphorylated TIM in the complex with PER and DCO
|
BibTex
|
2010-01-14
|
R-DME-451846
|
LFT binds to FT and DS
|
BibTex
|
2010-01-14
|
R-DME-451856
|
FT is phosphorylated by DCO
|
BibTex
|
2010-01-14
|
R-DME-451839
|
DCO binds to FT
|
BibTex
|
2010-01-14
|
R-DME-451858
|
YKI binds to HPO homodimer
|
BibTex
|
2010-01-14
|
R-DME-451826
|
YKI binds to EX
|
BibTex
|
2010-01-14
|
R-DME-451811
|
YKI binds to WTS
|
BibTex
|
2010-01-14
|
R-DME-451819
|
YKI binds to HTH and TSH and activates transcription
|
BibTex
|
2009-12-11
|
R-DME-450723
|
RAC1:GTP and MSN activate HEP
|
BibTex
|
2009-12-11
|
R-DME-450802
|
FZ and VANG bind to STAN homodimer
|
BibTex
|
2009-12-11
|
R-DME-450741
|
VANG, IN, FY, and FRTZ colocalise at the plasma membrane
|
BibTex
|
2009-12-11
|
R-DME-450770
|
MWH binds to RHO1:GTP and is activated
|
BibTex
|
2009-08-13
|
R-DME-432642
|
Phosphorylated TIM transports from the cytosol to the nucleus
|
BibTex
|
2009-08-13
|
R-DME-432544
|
Phosphorylated PER transports from the cytosol to the nucleus
|
BibTex
|
2009-08-13
|
R-DME-432464
|
Phosphorylated TIM:PER heterodimer dissociate
|
BibTex
|
2009-08-13
|
R-DME-432535
|
TIM is phosphorylated by CK2
|
BibTex
|
2009-08-13
|
R-DME-432590
|
Phosphorylated PER is phosphorylated by CK2
|
BibTex
|
2009-08-13
|
R-DME-432647
|
Phosphorylated PER binds to TIM
|
BibTex
|
2009-08-13
|
R-DME-432559
|
PER is phosphorylated by DCO
|
BibTex
|
2009-08-13
|
R-DME-432556
|
Cytosolic PP2A dephosphorylates phosphorylated PER complexed with DCO
|
BibTex
|
2009-08-13
|
R-DME-432607
|
VRI replaces PDP1 as binder to Clk and cry genes
|
BibTex
|
2009-08-13
|
R-DME-432436
|
CLK:CYC heterodimer binds to per, tim, vri, and Pdp1 genes
|
BibTex
|
2009-08-13
|
R-DME-432516
|
CLK and CYC bind to form a heterodimer
|
BibTex
|
2009-08-13
|
R-DME-432510
|
CLK is degraded by the 26S proteasome
|
BibTex
|
2009-08-13
|
R-DME-432455
|
Nuclear PER is degraded by the 26S proteasome
|
BibTex
|
2009-08-13
|
R-DME-432483
|
SLMB binds phosphorylated nuclear PER, facilitating its ubiquitination
|
BibTex
|
2009-08-13
|
R-DME-432371
|
CRY is activated by light and binds to phosphorylated nuclear TIM
|
BibTex
|
2009-08-13
|
R-DME-432513
|
CLK is phosphorylated by DCO
|
BibTex
|
2009-08-13
|
R-DME-432381
|
PDP1 replaces VRI as binder to Clk and cry genes
|
BibTex
|
2009-08-13
|
R-DME-432424
|
JET binds phosphorylated nuclear TIM, facilitating its ubiquitination
|
BibTex
|
2009-08-13
|
R-DME-432652
|
Nuclear CRY is degraded by the 26S proteasome
|
BibTex
|
2009-08-13
|
R-DME-432378
|
Nuclear JET binds CRY, facilitating its ubiquitination
|
BibTex
|
2009-08-13
|
R-DME-432521
|
Nuclear TIM is degraded by the 26S proteasome
|
BibTex
|
2009-08-13
|
R-DME-432361
|
Cytosolic PER is degraded by the 26S proteasome
|
BibTex
|
2009-08-13
|
R-DME-432411
|
SLMB binds phosphorylated cytosolic PER, facilitating its ubiquitination
|
BibTex
|
2009-08-13
|
R-DME-432401
|
JET binds cytosolic TIM, facilitating its ubiquitination
|
BibTex
|
2009-08-13
|
R-DME-432428
|
Cytosolic CRY is degraded by the 26S proteasome
|
BibTex
|
2009-08-13
|
R-DME-432593
|
Cytosolic JET binds to CRY, facilitating its ubiquitination
|
BibTex
|
2009-08-13
|
R-DME-432507
|
Cytosolic TIM is degraded by the 26S proteasome
|
BibTex
|
2009-08-13
|
R-DME-432426
|
CRY is activated by light and binds to cytosolic TIM
|
BibTex
|
2009-08-13
|
R-DME-432527
|
Nuclear PP2A dephosphorylates phosphorylated PER
|
BibTex
|
2009-08-13
|
R-DME-432533
|
PP1 binds to phosphorylated TIM
|
BibTex
|
2009-08-13
|
R-DME-432427
|
PP1 dephosphorylates phosphorylated TIM
|
BibTex
|
2009-08-13
|
R-DME-432487
|
CWO binds to cwo gene and represses transcription
|
BibTex
|
2009-08-13
|
R-DME-432520
|
CLK:CYC heterodimer binds to cwo gene and activates transcription
|
BibTex
|
2009-08-13
|
R-DME-432537
|
PP2A dephosphorylates phosphorylated CLK
|
BibTex
|
2009-01-23
|
R-DME-390116
|
Phospho FT reduces D accumulation at the plasma membrane
|
BibTex
|
2009-01-23
|
R-DME-390061
|
YKI binds to phosphorylated WTS
|
BibTex
|
2009-01-23
|
R-DME-390044
|
YKI is phosphorylated by and then dissociates from phosphorylated WTS
|
BibTex
|
2009-01-23
|
R-DME-390025
|
Phosphorylated WTS autophosphorylates
|
BibTex
|
2009-01-23
|
R-DME-390154
|
MATS is phosphorylated by HPO dimer and binds to phosphorylated WTS
|
BibTex
|
2009-01-23
|
R-DME-390112
|
Phosphorylated HPO dimer phosphorylates WTS
|
BibTex
|
2009-01-23
|
R-DME-390145
|
Phosphorylated HPO dimer phosphorylates SAV
|
BibTex
|
2009-01-23
|
R-DME-390035
|
HPO dimer autophosphorylates
|
BibTex
|
2009-01-23
|
R-DME-390124
|
MATS binds to HPO dimer
|
BibTex
|
2009-01-23
|
R-DME-390087
|
WTS binds to SAV
|
BibTex
|
2009-01-23
|
R-DME-390011
|
HPO dimer binds to SAV
|
BibTex
|
2009-01-23
|
R-DME-390078
|
14-3-3 dimer binds to phosphorylated YKI
|
BibTex
|
2009-01-23
|
R-DME-390120
|
Phosphorylated HPO dimer phosphorylates TH
|
BibTex
|
2009-01-23
|
R-DME-390059
|
HPO dimer binds to RASSF
|
BibTex
|
2009-01-23
|
R-DME-390133
|
YKI transports from the cytosol to the nucleus
|
BibTex
|
2009-01-23
|
R-DME-390184
|
YKI binds to SD and activates transcription
|
BibTex
|
2009-01-23
|
R-DME-390141
|
D inhibits WTS
|
BibTex
|
2008-09-08
|
R-HSA-74716
|
Insulin binds the insulin receptor
|
BibTex
|
2008-05-20
|
R-DME-350385
|
DSH binds to RAC1:GTP
|
BibTex
|
2008-05-20
|
R-DME-350436
|
DGO binds to DSH
|
BibTex
|
2008-05-20
|
R-DME-350408
|
PK binds to VANG at the plasma membrane
|
BibTex
|
2008-05-20
|
R-DME-350486
|
DSH binds to FZ at the plasma membrane
|
BibTex
|
2008-05-20
|
R-DME-350377
|
Extracellular domains of STAN bind to each other in adjacent cells
|
BibTex
|
2008-05-20
|
R-NUL-350365
|
Dvl2 binds to Rac1:GTP
|
BibTex
|
2008-05-20
|
R-DME-350400
|
PK binds to DSH
|
BibTex
|
2008-05-20
|
R-DME-350403
|
DGO binds to PK
|
BibTex
|
2008-05-20
|
R-DME-350467
|
GUG binds to FT
|
BibTex
|
2008-05-20
|
R-DME-350405
|
RHOGEF2 binds to RHO1:GDP complex at the plasma membrane
|
BibTex
|
2008-05-20
|
R-DME-350359
|
RHO1:GDP complex dissociates from RHOGDI and binds to the plasma membrane
|
BibTex
|
2008-05-20
|
R-DME-350395
|
RHOGDI binds to and sequesters RHO1:GDP complex to the cytosol
|
BibTex
|
2008-05-20
|
R-DME-350410
|
RHO1:GDP complex dissociates from RHOGAPP190
|
BibTex
|
2008-05-20
|
R-DME-350458
|
RHOGAPP190 activates GTP hydrolysis by RHO1:GTP
|
BibTex
|
2008-05-20
|
R-DME-350453
|
RHOGAPP190 binds to RHO1:GTP complex at the plasma membrane
|
BibTex
|
2008-05-20
|
R-DME-350450
|
RHO1:GTP complex dissociates from RHOGEF2
|
BibTex
|
2008-05-20
|
R-DME-350477
|
RHOGEF2 stimulates nucleotide exchange of RHO1:GDP complex
|
BibTex
|
2008-05-20
|
R-DME-350388
|
ROK binds to activated RHO1:GTP
|
BibTex
|
2008-05-20
|
R-DME-350391
|
RHO1:GTP binds to activated DAAM
|
BibTex
|
2008-05-20
|
R-DME-350396
|
DSH binds to DAAM
|
BibTex
|
2008-05-20
|
R-NUL-350375
|
Dvl2 binds to Daam1
|
BibTex
|
2008-05-20
|
R-NUL-350485
|
RhoA:GTP binds to activated Daam1
|
BibTex
|
2008-05-20
|
R-DME-350444
|
ROK phosphorylates SQH
|
BibTex
|
2008-05-20
|
R-DME-350441
|
FLW:MYPT-75D complex dephosphorylates SQH
|
BibTex
|
2008-05-20
|
R-DME-350475
|
FLW:MBS complex dephosphorylates SQH
|
BibTex
|
2008-05-20
|
R-DME-350443
|
PP1-87B:MBS complex dephosphorylates SQH
|
BibTex
|
2008-05-20
|
R-DME-350362
|
ROK phosphorylates MBS
|
BibTex
|
2008-05-19
|
R-DME-350440
|
FT binds to DS in an adjacent cell
|
BibTex
|
2007-07-11
|
R-HSA-83650
|
FasL:Fas binds FADD
|
BibTex
|
2007-07-11
|
R-DME-354273
|
AP-1 transcription factor forms a complex with STAT92E and DSP1 which displaces REL-68 from its target gene
|
BibTex
|
2007-07-11
|
R-DME-209257
|
Phosphorylated REL-68 forms a complex with PCAF at its target gene and activates transcription
|
BibTex
|
2007-07-11
|
R-DME-209309
|
Phosphorylated REL-68 transports from the cytosol to the nucleus
|
BibTex
|
2007-07-11
|
R-DME-214393
|
Phosphorylated REL is cleaved by and dissociates from DREDD in the monomeric PGN:PGRP-LE oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214398
|
Activated Phospho IRD5:KEY dimer phosphorylates REL in the monomeric PGN:PGRP-LE oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214418
|
REL binds to monomeric PGN:PGRP-LE oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214405
|
Assembly of the monomeric PGN:PGRP-LE oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214395
|
Monomeric PGN bound PGRP-LE oligomerises in the cytosol
|
BibTex
|
2007-07-11
|
R-DME-214410
|
Monomeric PGN binds to PGRP-LE in the cytosol
|
BibTex
|
2007-07-11
|
R-DME-209240
|
Activated phosphorylated TAK1 kinase phosphorylates and activates IRD5
|
BibTex
|
2007-07-11
|
R-DME-209320
|
Activated TAK1 kinase is autophosphorylated
|
BibTex
|
2007-07-11
|
R-DME-209289
|
TAB2 binds to ubiquitinated IAP2:BEN:UEV1A E3 ligase complex and activates TAK1 kinase
|
BibTex
|
2007-07-11
|
R-DME-209188
|
TAK1-binding protein TAB2 binds to TAK1 kinase
|
BibTex
|
2007-07-11
|
R-DME-209179
|
IAP2:BEN:UEV1A E3 ligase complex auto-ubiquitinates
|
BibTex
|
2007-07-11
|
R-DME-209167
|
Phosphorylated REL is cleaved by and dissociates from DREDD in the PGN:PGRP-LC oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-209227
|
Activated Phospho IRD5:KEY dimer phosphorylates REL in the PGN:PGRP-LC oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-209244
|
REL binds to DREDD in the PGN:PGRP-LC oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-209221
|
Assembly of the PGN:PGRP-LC oligomer receptor 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-209185
|
Monomeric PGN bound PGRP-LCx heterodimerises with PGRP-LCa at the plasma membrane
|
BibTex
|
2007-07-11
|
R-DME-209355
|
Monomeric PGN binds to PGRP-LCx at the plasma membrane
|
BibTex
|
2007-07-11
|
R-DME-209158
|
Polymeric PGN bound PGRP-LCx multimerises at the plasma membrane
|
BibTex
|
2007-07-11
|
R-DME-209377
|
Polymeric PGN binds to PGRP-LCx at the plasma membrane
|
BibTex
|
2007-07-11
|
R-DME-354289
|
AP-1:DSP1:STAT92E complex recruits RPD3 and represses transcription of the REL-68 target gene
|
BibTex
|
2007-07-11
|
R-DME-209200
|
HEP is phosphorylated and activated by Phospho TAK1:TAB2 kinase complex
|
BibTex
|
2007-07-11
|
R-MMU-209329
|
Murine MKK4 kinase is phosphorylated and activated by Phospho TAK1:Phospho TAB1:Phospho TAB2 kinase complex
|
BibTex
|
2007-07-11
|
R-DME-209235
|
Phosphorylated BSK kinase transports from the cytosol to the nucleus
|
BibTex
|
2007-07-11
|
R-DME-209302
|
Phosphorylated BSK kinase dissociates from CKA scaffolding protein
|
BibTex
|
2007-07-11
|
R-DME-209199
|
CKA is phosphorylated by phosphorylated BSK kinase
|
BibTex
|
2007-07-11
|
R-DME-209298
|
BSK is phosphorylated and activated by phosphorylated HEP kinase
|
BibTex
|
2007-07-11
|
R-DME-209183
|
Scaffolding protein CKA binds BSK and phosphorylated HEP kinases
|
BibTex
|
2007-07-11
|
R-DME-209157
|
Phosphorylated BSK kinase is dephosphorylated and deactivated by PUC phosphatase
|
BibTex
|
2007-07-11
|
R-RNO-209184
|
Rat JNK1 kinase transports from the cytosol to the nucleus
|
BibTex
|
2007-07-11
|
R-DME-209330
|
Phosphorylated BSK kinase and the AP-1 transcription factor, JRA:KAY, bind to CKA scaffolding protein in the nucleus
|
BibTex
|
2007-07-11
|
R-DME-209381
|
AP-1 transcription factor, JRA:KAY, is phosphorylated by phosphorylated BSK kinase
|
BibTex
|
2007-07-11
|
R-DME-209193
|
Phosphorylated AP-1, Phospho JRA:Phospho KAY dissociates from CKA
|
BibTex
|
2007-07-11
|
R-DME-209358
|
Phosphorylated AP-1, Phospho JRA:Phospho KAY binds to a target gene and activates transcription
|
BibTex
|
2007-07-11
|
R-DME-209376
|
SPN27A binds to and inhibits EA protease activity
|
BibTex
|
2007-07-11
|
R-DME-209130
|
Full-length SPZ dimer is cleaved by EA/SPE serine protease
|
BibTex
|
2007-07-11
|
R-DME-214956
|
Full-length EA is cleaved by SNK serine protease
|
BibTex
|
2007-07-11
|
R-DME-214953
|
Full-length SNK is cleaved by GD serine protease
|
BibTex
|
2007-07-11
|
R-DME-214891
|
Full-length GD is cleaved by an unknown protease
|
BibTex
|
2007-07-11
|
R-DME-209141
|
ProSPZ:SPZ dimer binds to TL receptor at the plasma membrane
|
BibTex
|
2007-07-11
|
R-DME-209076
|
SPZ dimer bound TL dimerises at the plasma membrane
|
BibTex
|
2007-07-11
|
R-DME-209156
|
MYD88 binds to TUB
|
BibTex
|
2007-07-11
|
R-DME-209072
|
PLL kinase binds to TL:MYD88:TUB 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-209100
|
MYD88:TUB binds to TL receptor
|
BibTex
|
2007-07-11
|
R-DME-214878
|
PLL kinase binds to TL:WEK:MYD88:TUB 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214853
|
WEK and MYD88:TUB bind to the TL receptor
|
BibTex
|
2007-07-11
|
R-DME-209218
|
Phosphorylated DL/DIF dimer activates transcription
|
BibTex
|
2007-07-11
|
R-DME-209295
|
Phosphorylated DL/DIF dimer transports from the cytosol to the nucleus
|
BibTex
|
2007-07-11
|
R-DME-214871
|
Phosphorylated CACT is degraded in the cytosol
|
BibTex
|
2007-07-11
|
R-DME-214864
|
Phosphorylated CACT and DL/DIF dimer dissociate from the TL:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214860
|
CACT and DL/DIF dimer are phosphorylated in TL:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214857
|
DL/DIF dimer binds to TUB and phosphorylated PLL in TL:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-209057
|
Activated PLL kinase is autophosphorylated in TL:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214847
|
Phosphorylated CACT and DL dimer dissociate from the TL:WEK:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214845
|
CACT and DL dimer are phosphorylated in TL:WEK:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214880
|
DL dimer binds to TUB and phosphorylated PLL in TL:WEK:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-07-11
|
R-DME-214859
|
Activated PLL kinase is autophosphorylated in TL:WEK:MYD88:TUB:PLL 'signalling complex'
|
BibTex
|
2007-03-22
|
R-HSA-209055
|
PPM1A dephosphorylates nuclear SMAD2/3
|
BibTex
|
2006-12-07
|
R-DME-209224
|
SLMB binds to and ubiquitinates phosphorylated CI
|
BibTex
|
2006-12-07
|
R-DME-209187
|
Further phosphorylation of CI by CKIalphaepsilon
|
BibTex
|
2006-12-07
|
R-DME-209172
|
Phosphorylation of CI by SGG
|
BibTex
|
2006-12-07
|
R-DME-209293
|
Phosphorylation of CI by CKIalphaepsilon (CKIalpha/DCO)
|
BibTex
|
2006-12-07
|
R-DME-209196
|
Phosphorylation of CI by PKA-C1
|
BibTex
|
2006-12-07
|
R-DME-209331
|
Formation of the 'scaffold complex'
|
BibTex
|
2006-12-07
|
R-DME-209278
|
Ubiquitinated and phosphorylated CI is partially degraded by the proteasome complex
|
BibTex
|
2006-12-07
|
R-DME-216136
|
Formation of the CI:SU(FU) complex
|
BibTex
|
2006-12-07
|
R-DME-209252
|
CI75 inhibits transcription
|
BibTex
|
2006-12-07
|
R-DME-209370
|
CI75 transports from the cytosol to the nucleus
|
BibTex
|
2006-12-07
|
R-DME-209313
|
Autocleavage of HH
|
BibTex
|
2006-12-07
|
R-DME-209271
|
N-HH moves from the cytosol to the extracellular region
|
BibTex
|
2006-12-07
|
R-DME-209357
|
N-HH is palmitoylated by RASP
|
BibTex
|
2006-12-07
|
R-DME-209272
|
N-HH binds to the transmembrane HSPG proteins
|
BibTex
|
2006-12-07
|
R-DME-216133
|
Dissociation of CI from COS
|
BibTex
|
2006-12-07
|
R-DME-209253
|
Autophosphorylated FU phosphorylates COS
|
BibTex
|
2006-12-07
|
R-DME-216202
|
Phosphorylated SMO changes conformation and is activated
|
BibTex
|
2006-12-07
|
R-DME-209168
|
Phosphorylation of SMO by CKIalpha
|
BibTex
|
2006-12-07
|
R-DME-209341
|
Phosphorylation of SMO by PKA-C1
|
BibTex
|
2006-12-07
|
R-DME-209178
|
N-HH binds to PTC receptor complex
|
BibTex
|
2006-12-07
|
R-DME-216222
|
COS binds to SMO
|
BibTex
|
2006-12-07
|
R-DME-209220
|
Liberation of CI from SU(FU) repression
|
BibTex
|
2006-12-07
|
R-DME-209163
|
CI transports from the cytosol to the nucleus
|
BibTex
|
2006-12-07
|
R-DME-209215
|
CI activates transcription
|
BibTex
|
2006-12-07
|
R-DME-216283
|
RDX binds to and ubiquitinates CI
|
BibTex
|
2006-12-07
|
R-DME-216282
|
Ubiquitinated CI is degraded by the proteasome complex
|
BibTex
|
2006-11-02
|
R-DME-210662
|
Phosphorylated HOP is dephosphorylated by PTP61F isoform 1
|
BibTex
|
2006-11-02
|
R-DME-209336
|
Activated HOP is autophosphorylated and/or transphosphorylated
|
BibTex
|
2006-11-02
|
R-DME-209255
|
UPD ligand binds to the HOP:DOME:DOME:HOP complex and activates HOP
|
BibTex
|
2006-11-02
|
R-DME-209231
|
DOME:HOP complex forms a dimer at the plasma membrane
|
BibTex
|
2006-11-02
|
R-DME-209245
|
Tyrosine kinase Hopscotch (HOP) binds to the transmembrane cytokine receptor Domeless (DOME) to form the HOP:DOME complex
|
BibTex
|
2006-11-02
|
R-MMU-209310
|
Murine JAK2 binds to the Erythropoietin receptor, EpoR
|
BibTex
|
2006-11-02
|
R-DME-210646
|
Phosphorylated STAT92E dimer is dephosphorylated by PTP61F isoform 1
|
BibTex
|
2006-11-02
|
R-DME-209321
|
Phosphorylated STAT92E dissociates from HOP and DOME and dimerises
|
BibTex
|
2006-11-02
|
R-DME-209210
|
STAT92E is phosphorylated by phosphorylated HOP
|
BibTex
|
2006-11-02
|
R-DME-209361
|
STAT92E binds to phosphorylated HOP and phosphorylated DOME
|
BibTex
|
2006-11-02
|
R-DME-209160
|
Phosphorylated HOP phosphorylates DOME
|
BibTex
|
2006-11-02
|
R-MMU-210644
|
Phosphorylated STAT5A dimer is dephosphorylated by PTP1B
|
BibTex
|
2006-11-02
|
R-DME-210694
|
Phosphorylated STAT92E dimer is dephosphorylated by PTP61F isoform 2
|
BibTex
|
2006-11-02
|
R-DME-209365
|
Phosphorylated STAT92E dimer transports from the cytosol to the nucleus
|
BibTex
|
2006-11-02
|
R-DME-209307
|
Phosphorylated STAT92E dimer activates transcription
|
BibTex
|
2006-11-02
|
R-DME-209296
|
SU(VAR)2-10 binds to the phosphorylated STAT92E dimer and inhibits transcription
|
BibTex
|
2006-11-02
|
R-DME-210700
|
KEN dimer represses transcription
|
BibTex
|
2006-09-21
|
R-DME-209226
|
DL/SER is ubiquitinated by E3 ubiquitination ligases (NEUR/MIB1)
|
BibTex
|
2006-09-21
|
R-NUL-209162
|
Murine ADAM10 cleaves Notch at the S2 site producing transmembrane spanning NEXT and ligand-bound NECD
|
BibTex
|
2006-09-21
|
R-MMU-209285
|
The transmembrane complex Murine gamma-secretase cleaves Murine NEXT at the S3 site leaving NTM and releasing NICD into the cytoplasm
|
BibTex
|
2006-07-26
|
R-MMU-209096
|
Murine Axin1 is dephosphorylated by PP2A leading to reduced binding affinity with beta-catenin
|
BibTex
|
2006-07-26
|
R-DME-209107
|
Further phosphorylation of APC by DCO
|
BibTex
|
2006-07-26
|
R-DME-209049
|
Phosphorylation of AXN and APC by SGG
|
BibTex
|
2006-07-26
|
R-DME-209143
|
Phosphorylation of AXN and APC by DCO
|
BibTex
|
2006-07-26
|
R-DME-209133
|
Formation of the 'destruction complex'
|
BibTex
|
2006-07-26
|
R-DME-209081
|
Disassembly of the destabilised 'destruction complex'
|
BibTex
|
2006-07-26
|
R-DME-209075
|
Destabilisation and degradation of AXN in the 'destruction complex'
|
BibTex
|
2006-07-26
|
R-DME-209112
|
Inhibition of SGG results in the dephosphorylation of the 'destruction complex' by PP2A and release of ARM
|
BibTex
|
2006-07-26
|
R-DME-209120
|
Membrane recruitment of DSH to FZ and AXN to phosphorylated ARR
|
BibTex
|
2006-07-26
|
R-DME-209109
|
Further phosphorylation of ARM by SGG
|
BibTex
|
2006-07-26
|
R-DME-209134
|
Phosphorylation of ARM by CKIalpha
|
BibTex
|
2006-07-26
|
R-DME-209097
|
ARM binds to APC and AXN in the 'destruction complex'
|
BibTex
|
2006-07-26
|
R-DME-209094
|
Dissociation of free ubiquitinated and phosphorylated ARM from SLMB and the 'destruction complex'
|
BibTex
|
2006-07-26
|
R-DME-209102
|
SLMB binds to phosphorylated ARM to form the 'destruction complex'
|
BibTex
|
2006-07-26
|
R-DME-209082
|
Further phosphorylation of APC by SGG
|
BibTex
|
2006-07-26
|
R-NUL-209144
|
Human APC is finally phosphorylated by Murine GSK3beta
|
BibTex
|
2006-07-26
|
R-DME-209135
|
GISH further phosphorylates ARR in the receptor complex
|
BibTex
|
2006-07-26
|
R-DME-209118
|
Membrane localised SGG phosphorylates ARR
|
BibTex
|
2006-07-26
|
R-DME-209108
|
Membrane-bound GISH binds to ARR receptor complex
|
BibTex
|
2006-07-26
|
R-DME-209074
|
WG, FZ and ARR bind to each other
|
BibTex
|
2006-07-26
|
R-NUL-209104
|
Frog CKIgamma further phosphorylates Human LRP6 in the receptor complex
|
BibTex
|
2006-07-26
|
R-MMU-209059
|
Murine CKIepsilon binds to Murine Axin1
|
BibTex
|
2006-07-26
|
R-MMU-209148
|
Murine CKIalpha binds to Murine Axin1
|
BibTex
|
2006-07-26
|
R-NUL-209132
|
Human APC is initially phosphorylated by Murine CKIepsilon
|
BibTex
|
2006-07-26
|
R-NUL-209060
|
Human APC is further phosphorylated by Murine GSK3beta
|
BibTex
|
2006-07-26
|
R-NUL-209146
|
Murine Axin1 is further phosphorylated by Human GSK3beta
|
BibTex
|
2006-07-26
|
R-NUL-209065
|
Human APC is further phosphorylated by Murine CKIepsilon
|
BibTex
|
2006-07-26
|
R-DME-209129
|
Ubiquitinated and phosphorylated ARM binds to and is degraded by the proteasome complex
|
BibTex
|
2006-07-26
|
R-DME-209322
|
In the absence of ARM, GRO binds to PAN and inhibits transcription
|
BibTex
|
2006-07-26
|
R-DME-209303
|
LGS transports from the nucleus to the cytosol
|
BibTex
|
2006-07-26
|
R-DME-209332
|
LGS dissociates from the PYGO complex
|
BibTex
|
2006-07-26
|
R-DME-209371
|
LGS binds to ARM
|
BibTex
|
2006-07-26
|
R-DME-209177
|
LGS:ARM complex transports from the cytosol to the nucleus
|
BibTex
|
2006-07-26
|
R-DME-209297
|
PYGO binds to the LGS:ARM complex
|
BibTex
|
2006-07-26
|
R-DME-209181
|
ARM displaces GRO and binds to PAN which activates transcription
|
BibTex
|