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A2V ECHS1 [mitochondrial matrix]
Stable Identifier
R-HSA-9916688
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
mitochondrial matrix
Synonyms
Enoyl-CoA hydratase, mitochondrial precursor , Short chain enoyl-CoA hydratase, Enoyl-CoA hydratase 1
Icon
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of branched-chain amino acid catabolism (Homo sapiens)
Mitochondrial short-chain enoyl-CoA hydratase deficiency 1 (Homo sapiens)
ECHS1 mutants don't synthesize beta-hydroxyisobutyryl-CoA (Homo sapiens)
ECHS1 mutant hexamer [mitochondrial matrix] (Homo sapiens)
ECHS1 mutants [mitochondrial matrix] (Homo sapiens)
A2V ECHS1 [mitochondrial matrix] (Homo sapiens)
ECHS1 mutants [mitochondrial matrix] (Homo sapiens)
A2V ECHS1 [mitochondrial matrix] (Homo sapiens)
Literature References
PubMed ID
Title
Journal
Year
25393721
ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome
Sakai, C
,
Yamaguchi, S
,
Sasaki, M
,
Miyamoto, Y
,
Matsushima, Y
,
Goto, Y
Hum Mutat
2015
External Reference Information
External Reference
UniProt:P30084 ECHS1
Gene Names
ECHS1
Chain
transit peptide:1-27, chain:28-290
Reference Genes
BioGPS Gene:1892 ECHS1
COSMIC (genes):ECHS1 ECHS1
CTD Gene:1892 ECHS1
dbSNP Gene:1892 ECHS1
ENSEMBL:ENSG00000127884 ECHS1
HGNC:3151 ECHS1
KEGG:hsa:1892 ECHS1
Monarch:1892 ECHS1
NCBI Gene:1892 ECHS1
OMIM:602292 ECHS1
UCSC:P30084 ECHS1
Reference Transcript
RefSeq:NM_004092.3 ECHS1
Other Identifiers
11757606_s_at
16719892
16719903
1892
201135_PM_at
201135_at
3315232
3315233
3315234
3315238
3315242
3315245
3315247
3315248
3315250
3315251
3315252
3315253
37016_at
7937217
A_23_P104362
D13900_at
GE548043
GO:0003824
GO:0004165
GO:0004300
GO:0005515
GO:0005739
GO:0005759
GO:0006520
GO:0006629
GO:0006631
GO:0006635
GO:0009083
GO:0016829
GO:0016853
GO:0018812
GO:0043956
GO:0120092
HMNXSV003032605
HMNXSV003046503
ILMN_1718132
PH_hs_0004410
TC10001790.hg
TC10001791.hg
g12707569_3p_at
Participates
as a candidate of
ECHS1 mutants [mitochondrial matrix] (Homo sapiens)
Other forms of this molecule
ECHS1 [mitochondrial matrix]
T180A ECHS1 [mitochondrial matrix]
A238V ECHS1 [mitochondrial matrix]
A132T ECHS1 [mitochondrial matrix]
G195S ECHS1 [mitochondrial matrix]
K273E ECHS1 [mitochondrial matrix]
R54H ECHS1 [mitochondrial matrix]
I66T ECHS1 [mitochondrial matrix]
D150G ECHS1 [mitochondrial matrix]
A158D ECHS1 [mitochondrial matrix]
C225R ECHS1 [mitochondrial matrix]
N59S ECHS1 [mitochondrial matrix]
A138V ECHS1 [mitochondrial matrix]
E77Q ECHS1 [mitochondrial matrix]
F33S ECHS1 [mitochondrial matrix]
Q159R ECHS1 [mitochondrial matrix]
Modified Residues
Name
L-alanine 2 replaced with L-valine
Coordinate
2
PsiMod
L-valine residue [MOD:00029]
A protein modification that effectively converts a source amino acid residue to an L-valine.
L-alanine removal [MOD:01631]
A protein modification that effectively removes or replaces an L-alanine.
Disease
Name
Identifier
Synonyms
mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
DOID:0070540
ECHS1D
Cross References
RefSeq
NP_004083.3
ClinGen
CA214806
OpenTargets
ENSG00000127884
ENSEMBL
ENST00000368547
,
ENSP00000357535
,
ENSG00000127884
Mondo
0014563
PRO
P30084
GlyGen
P30084
PDB
2HW5
GeneCards
ECHS1
HPA
ENSG00000127884-ECHS1
Pharos - Targets
P30084
Orphanet
ECHS1
HMDB Protein
HMDBP00388
Interactors (4)
Accession
#Entities
Entities
Confidence Score
Evidence (IntAct)
UniProt:Q5S007 LRRK2
1
LRRK2 [cytosol]
(R-HSA-5661173)
0.713
4
UniProt:P11182 DBT
11
Lipo-K105-DBT [mitochondrial matrix]
(R-HSA-70017)
Isobutyryl-lipoH2-K105-DBT [mitochondrial matrix]
(R-HSA-9859151)
Isovaleryl-lipoH2-K105-DBT [mitochondrial matrix]
(R-HSA-9859144)
2-Methylbutyryl-lipoH2-K105-DBT [mitochondrial matrix]
(R-HSA-9859145)
LipoH2-K105-DBT [mitochondrial matrix]
(R-HSA-9859167)
DBT [mitochondrial matrix]
(R-HSA-6792584)
P276C Lipo-K105-DBT [mitochondrial matrix]
(R-HSA-9865046)
S399C Lipo-K105-DBT [mitochondrial matrix]
(R-HSA-9865036)
K313_Y338del Lipo-K105-DBT [mitochondrial matrix]
(R-HSA-9865051)
I98M Lipo-K105-DBT [mitochondrial matrix]
(R-HSA-9865057)
DBT [cytosol]
(R-HSA-9714663)
0.527
3
UniProt:P42227 Stat3
13
phospho-Stat3 [nucleoplasm]
(R-MMU-1112554)
phospho-Stat3 [cytosol]
(R-MMU-914048)
Stat3 [cytosol]
(R-MMU-539044)
phospho-Stat3 [cytosol]
(R-MMU-8983130)
Stat3 [cytosol]
(R-MMU-914084)
p-Y705-Stat3 [cytosol]
(R-MMU-914034)
p(Y705)-Stat3 [nucleoplasm]
(R-MMU-2730582)
phospho-Stat3 [nucleoplasm]
(R-MMU-9027589)
phospho-Stat3 [nucleoplasm]
(R-MMU-9701429)
phospho-Stat3 [cytosol]
(R-MMU-8982823)
phospho-Stat3 [cytosol]
(R-MMU-539048)
phospho-Stat3 [nucleoplasm]
(R-MMU-9701435)
phospho-Stat3 [nucleoplasm]
(R-MMU-8983188)
0.524
3
UniProt:P40763 STAT3
12
p-Y705-STAT3 [nucleoplasm]
(R-HSA-1112554)
p-Y705-STAT3 [cytosol]
(R-HSA-914048)
STAT3 [cytosol]
(R-HSA-539044)
p-Y705-STAT3 [cytosol]
(R-HSA-8983130)
p-Y705-STAT3 [nucleoplasm]
(R-HSA-9027589)
p-Y705,S727-STAT3 [nucleoplasm]
(R-HSA-9701429)
p-STAT3 [cytosol]
(R-HSA-8982823)
p-Y705,S727-STAT3 [cytosol]
(R-HSA-539048)
p-S727-STAT3 [cytosol]
(R-HSA-198705)
AcK685- p-Y705,S727-STAT3 [nucleoplasm]
(R-HSA-9701435)
p-STAT3 [nucleoplasm]
(R-HSA-8983188)
Unfolded STAT3 [cytosol]
(R-HSA-6813811)
0.508
3
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