A138V ECHS1 [mitochondrial matrix]

Stable Identifier
R-HSA-9916683
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Enoyl-CoA hydratase, mitochondrial precursor , Short chain enoyl-CoA hydratase, Enoyl-CoA hydratase 1
A138V ECHS1 [mitochondrial matrix] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
26251176 Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion

Shimomura, Y, Yamaguchi, S, Nomura, N, Yamada, K, Kondo, Y, Pitt, J, Murayama, K, Aiba, K, Wakamatsu, N, Nakamura, Y, Fukushi, D, Yokochi, K, Kitaura, Y

J. Med. Genet. 2015
External Reference Information
External Reference
Gene Names
ECHS1
Chain
transit peptide:1-27, chain:28-290
Reference Transcript
Other Identifiers
11757606_s_at
16719892
1892
201135_PM_at
201135_at
3315232
3315233
3315234
3315238
3315242
3315245
3315247
3315248
3315250
3315252
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:0016836
GO:0016853
GO:0043226
GO:0043956
GO:0120092
HMNXSV003046503
ILMN_1718132
PH_hs_0004410
TC10001790.hg
g12707569_3p_at
Participates
Other forms of this molecule
Modified Residues
Name
L-alanine 138 replaced with L-valine
Coordinate
138
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-valine.
A protein modification that effectively removes or replaces an L-alanine.
Cross References
RefSeq
ClinGen
OpenTargets
GeneCards
PRO
Pharos - Targets
GlyGen
Orphanet
PDB
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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