A158D ECHS1 [mitochondrial matrix]

Stable Identifier
R-HSA-9916689
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Enoyl-CoA hydratase, mitochondrial precursor , Short chain enoyl-CoA hydratase, Enoyl-CoA hydratase 1
A158D ECHS1 [mitochondrial matrix] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
25125611 ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism

Peters, H, Buck, N, Wanders, R, Ruiter, J, Waterham, H, Koster, J, Yaplito-Lee, J, Ferdinandusse, S, Pitt, J

Brain 2014
External Reference Information
External Reference
Gene Names
ECHS1
Chain
transit peptide:1-27, chain:28-290
Reference Transcript
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
Other forms of this molecule
Modified Residues
Name
L-alanine 158 replaced with L-aspartic acid
Coordinate
158
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-aspartic acid.
A protein modification that effectively removes or replaces an L-alanine.
Cross References
RefSeq
ClinGen
OpenTargets
Mondo
PRO
GlyGen
PDB
GeneCards
Pharos - Targets
Orphanet
HMDB Protein
Interactors (4)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:Q5S007 LRRK2  1 0.713 4
 UniProt:P11182 DBT  11 0.527 3
 UniProt:P42227 Stat3  13 0.524 3
 UniProt:P40763 STAT3  12 0.508 3
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