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MECP2_e1 S144F [nucleoplasm]
Stable Identifier
R-HSA-9022507
Type
Genes and Transcripts [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
nucleoplasm
Synonyms
MECP2B S144F
Icon
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Disorders of Developmental Biology (Homo sapiens)
Disorders of Nervous System Development (Homo sapiens)
Pervasive developmental disorders (Homo sapiens)
Loss of function of MECP2 in Rett syndrome (Homo sapiens)
Loss of MECP2 binding ability to 5hmC-DNA (Homo sapiens)
MECP2 mutants R133C ,D121G, R133H and S134F do not bind 5hmC-DNA (Homo sapiens)
MECP2 R133C,MECP2 D121G,MECP2 R133H,MECP2 S134F [nucleoplasm] (Homo sapiens)
MECP2 R106W, MECP2 D121G,MECP2 R133H,MECP2S134F,MECP2 T158M/A [nucleoplasm] (Homo sapiens)
MECP2 S134F [nucleoplasm] (Homo sapiens)
MECP2_e1 S144F [nucleoplasm] (Homo sapiens)
Loss of MECP2 binding ability to 5mC-DNA (Homo sapiens)
MECP2 mutants R106W, D121G, R133H, S134F, T158M and T158A do not bind to 5mC-DNA (Homo sapiens)
MECP2 R106W, MECP2 D121G,MECP2 R133H,MECP2S134F,MECP2 T158M/A [nucleoplasm] (Homo sapiens)
MECP2 S134F [nucleoplasm] (Homo sapiens)
MECP2_e1 S144F [nucleoplasm] (Homo sapiens)
External Reference Information
External Reference
UniProt:P51608-2 MECP2
Gene Names
MECP2
Participates
as a candidate of
MECP2 S134F [nucleoplasm] (Homo sapiens)
Other forms of this molecule
MECP2_e1 [nucleoplasm]
p-S92-MECP2_e1 [nucleoplasm]
p-T320-MeCP2_e1 [nucleoplasm]
p-S435-MECP2_e1 [nucleoplasm]
MeCP2_e1 R318H [nucleoplasm]
MeCP2_e1 R318C [nucleoplasm]
MeCP2_e1 K316E [nucleoplasm]
MeCP2_e1 P314R [nucleoplasm]
MeCP2_e1 K317R [nucleoplasm]
MECP2_e1 T170M [nucleoplasm]
MECP2_e1 T170A [nucleoplasm]
MECP2_e1 R118W [nucleoplasm]
MECP2_e1 R145H [nucleoplasm]
MECP2_e1 D133G [nucleoplasm]
MECP2_e1 R145C [nucleoplasm]
Modified Residues
Name
L-serine 144 replaced with L-phenylalanine
Coordinate
144
PsiMod
L-phenylalanine residue [MOD:00023]
A protein modification that effectively converts a source amino acid residue to L-phenylalanine.
L-serine removal [MOD:01646]
A protein modification that effectively removes or replaces an L-serine.
Disease
Name
Identifier
Synonyms
Rett syndrome
DOID:1206
Rett's disorder, cerebroatrophic hyperammonemia
Cross References
RefSeq
NP_004983.1
,
XP_054183066.1
,
XP_054183067.1
,
XP_047298071.1
,
XP_047298072.1
,
NP_001104262.1
,
NP_001303266.1
OpenTargets
ENSG00000169057
ENSEMBL
ENST00000630151
,
ENSG00000169057
,
ENSP00000301948
,
ENSP00000395535
,
ENST00000453960
,
ENSP00000486089
,
ENST00000303391
Mondo
0010726
GeneCards
MECP2
HPA
ENSG00000169057-MECP2
PRO
P51608
Pharos - Targets
P51608
GlyGen
P51608
Orphanet
MECP2
PDB
6YWW
,
8AJR
,
3C2I
,
8ALQ
,
6OGJ
,
1QK9
,
6OGK
,
5BT2
,
6C1Y
Interactors (32)
Accession
#Entities
Entities
Confidence Score
Evidence (IntAct)
UniProt:Q60974 Ncor1
3
Ncor1 [cytosol]
(R-MMU-1253324)
Ncor1 [nucleoplasm]
(R-MMU-442459)
Ncor1 [nucleoplasm]
(R-MMU-442501)
0.591
4
UniProt:Q9QXE7 Tbl1x
2
Tbl1x [nucleoplasm]
(R-MMU-2064253)
Tbl1x [nucleoplasm]
(R-MMU-351644)
0.591
3
UniProt:Q9QZR5
3
Hipk2 [nucleoplasm]
(R-MMU-4090405)
phospho-Hipk2 [nucleoplasm]
(R-MMU-6799375)
Hipk2 [nucleoplasm]
(R-MMU-3215222)
0.581
3
UniProt:P63165 SUMO1
11
lysyl-G97-SUMO1 [nucleoplasm]
(R-HSA-9761562)
SUMO1(2-101) [nucleoplasm]
(R-HSA-2990831)
SUMO1 [nucleoplasm]
(R-HSA-877304)
UBA2-G97-SUMO1 [nucleoplasm]
(R-HSA-3730616)
UBE2I-G97-SUMO1 [nucleoplasm]
(R-HSA-3730622)
lysyl-G97-SUMO1 [cytosol]
(R-HSA-9762266)
lysyl-G97-SUMO1 [endoplasmic reticulum-Golgi intermediate compartment membrane]
(R-HSA-9762380)
UBE2I-G97-SUMO1 [cytosol]
(R-HSA-4656941)
lysyl-G97-SUMO1 [viral capsid]
(R-HSA-9762386)
lysyl-G97-SUMO1 [nucleolus]
(R-HSA-9762385)
lysyl-G97-SUMO1 [plasma membrane]
(R-HSA-9762382)
0.564
2
UniProt:P35222 CTNNB1
20
CTNNB1 S45A [cytosol]
(R-HSA-9663982)
CTNNB1 S45F [cytosol]
(R-HSA-4791268)
CTNNB1 S45C [cytosol]
(R-HSA-9663983)
CTNNB1 S45Y [cytosol]
(R-HSA-9663975)
CTNNB1 S45N [cytosol]
(R-HSA-9663984)
CTNNB1 S45P [cytosol]
(R-HSA-4791272)
pT41,S45-CTNNB1 S37P [cytosol]
(R-HSA-9663981)
pT41,S45-CTNNB1 S37F [cytosol]
(R-HSA-4839621)
CTNNB1 [nucleoplasm]
(R-HSA-3451168)
CTNNB1 [cytosol]
(R-HSA-448839)
CTNNB1(1-115) [cytosol]
(R-HSA-202930)
CTNNB1(116-376) [cytosol]
(R-HSA-202950)
CTNNB1 [plasma membrane]
(R-HSA-9038440)
p-S33,S37,T41,S45 CTNNB1 [cytosol]
(R-HSA-8942374)
p-S37,T41,S45, CTNNB1 [cytosol]
(R-HSA-8942369)
p-T41,S45 CTNNB1 [cytosol]
(R-HSA-8942367)
p-S45 CTNNB1 [cytosol]
(R-HSA-8942363)
p-Y-CTNNB1 [cytosol]
(R-HSA-8876940)
p-S552-CTNNB1 [cytosol]
(R-HSA-3134933)
p-S552-CTNNB1 [nucleoplasm]
(R-HSA-3134926)
0.556
3
UniProt:Q12824 SMARCB1
1
SMARCB1 [nucleoplasm]
(R-HSA-389261)
0.556
3
UniProt:P10599 TXN
4
TXN [cytosol]
(R-HSA-66000)
2xHC-TXN [cytosol]
(R-HSA-73668)
TXN [nucleoplasm]
(R-HSA-9617732)
2xHC-TXN [nucleoplasm]
(R-HSA-9617733)
0.556
3
UniProt:P07948 LYN
7
LYN [cytosol]
(R-HSA-354251)
MyrG2-PalmC3-LYN [plasma membrane]
(R-HSA-9606875)
p-Y397-LYN [plasma membrane]
(R-HSA-2454229)
p-Y397-LYN [cytosol]
(R-HSA-8942608)
LYN [plasma membrane]
(R-HSA-197943)
MyrG2-PalmC3-LYN [lysosomal membrane]
(R-HSA-9707903)
MyrG2-PalmC3-LYN [endocytic vesicle membrane]
(R-HSA-9705728)
0.556
3
UniProt:P07196 NEFL
1
NEFL [cytosol]
(R-HSA-432284)
0.556
3
UniProt:P04792 HSPB1
3
HSPB1 [cytosol]
(R-HSA-450563)
p-S15,S78,S82-HSP27 [cytosol]
(R-HSA-5218697)
p-S78,S82 HSPB1 [cytosol]
(R-HSA-5687009)
0.556
3
UniProt:P42858 HTT
1
HTT [nucleoplasm]
(R-HSA-9023590)
0.556
18
UniProt:Q96CV9 OPTN
6
p-S177,S473,S513-OPTN [cytosol]
(R-HSA-9687840)
OPTN [cytosol]
(R-HSA-9687907)
OPTN [Golgi membrane]
(R-HSA-2161111)
p-S177-OPTN [cytosol]
(R-HSA-2562525)
p-S177-OPTN [nucleoplasm]
(R-HSA-2562595)
OPTN [recycling endosome membrane]
(R-HSA-8854141)
0.556
3
UniProt:O75925 PIAS1
1
PIAS1 [nucleoplasm]
(R-HSA-877307)
0.556
3
UniProt:O76024 WFS1
3
WFS1 [endoplasmic reticulum lumen]
(R-HSA-8956747)
p-WFS1 [endoplasmic reticulum lumen]
(R-HSA-8956998)
WFS1 [endoplasmic reticulum membrane]
(R-HSA-535474)
0.556
3
UniProt:Q9NW13 RBM28
1
RBM28 [nucleoplasm]
(R-HSA-6791192)
0.527
3
UniProt:Q9Y3T9 NOC2L
1
NOC2L [nucleoplasm]
(R-HSA-3222129)
0.527
3
UniProt:O43159 RRP8
1
RRP8 [nucleoplasm]
(R-HSA-427524)
0.527
3
UniProt:Q96RR1 TWNK
1
TWNK [mitochondrial matrix]
(R-HSA-1592222)
0.527
3
UniProt:Q9H5J8 TAF1D
1
TAF1D [nucleoplasm]
(R-HSA-5138533)
0.527
2
UniProt:Q9HD42 CHMP1A
1
CHMP1A [cytosol]
(R-HSA-917721)
0.527
2
UniProt:P54132 BLM
2
BLM [nucleoplasm]
(R-HSA-174881)
4SUMO2,3-BLM [nucleoplasm]
(R-HSA-4568883)
0.527
2
UniProt:Q8WVM0 TFB1M
1
TFB1M [mitochondrial matrix]
(R-HSA-1592207)
0.527
2
UniProt:O15379 HDAC3
2
HDAC3 [nucleoplasm]
(R-HSA-442464)
Unfolded HDAC3 [cytosol]
(R-HSA-6813777)
0.527
3
UniProt:P62241 RPS8
2
RPS8 [cytosol]
(R-HSA-72385)
RPS8 [nucleoplasm]
(R-HSA-6791203)
0.527
3
UniProt:P19525 EIF2AK2
5
EIF2AK2 [cytosol]
(R-HSA-168699)
p-EIF2AK2 [cytosol]
(R-HSA-9833834)
ISG15-EIF2AK2 [cytosol]
(R-HSA-9833968)
SUMO-EIF2AK2 [cytosol]
(R-HSA-9834829)
p-EIF2AK2 [nucleoplasm]
(R-HSA-9836332)
0.527
2
UniProt:Q9BZK7 TBL1XR1
1
TBL1XR1 [nucleoplasm]
(R-HSA-351643)
0.527
3
UniProt:P62917 RPL8
3
RPL8 [cytosol]
(R-HSA-72490)
RPL8 [nucleoplasm]
(R-HSA-9630985)
3OHH216-RPL8 [nucleoplasm]
(R-HSA-9630976)
0.527
3
UniProt:Q07020 RPL18
1
RPL18 [cytosol]
(R-HSA-72420)
0.527
3
UniProt:Q8BHJ5 Tbl1xr1
1
Tbl1xr1 [nucleoplasm]
(R-MMU-2064254)
0.525
4
UniProt:Q9WU42 Ncor2
3
monoSumo1-K668-Ncor2 [nucleoplasm]
(R-MMU-3927907)
Ncor2 [nucleoplasm]
(R-MMU-442511)
Ncor2 [nucleoplasm]
(R-MMU-442469)
0.525
4
UniProt:P51531 SMARCA2
1
SMARCA2 [nucleoplasm]
(R-HSA-389256)
0.524
4
UniProt:Q96ST3 SIN3A
2
SIN3A [nucleoplasm]
(R-HSA-351657)
monoSUMO1-SIN3A [nucleoplasm]
(R-HSA-4086071)
0.499
2
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