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K313_Y338del Lipo-K105-DBT [mitochondrial matrix]
Stable Identifier
R-HSA-9865051
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
mitochondrial matrix
Synonyms
dihydrolipoamide branched chain transacylase E2, DBT
Icon
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of branched-chain amino acid catabolism (Homo sapiens)
Maple Syrup Urine Disease (Homo sapiens)
Loss-of-function mutations in DBT cause MSUD2 (Homo sapiens)
DBT loss-of-function mutants don't synthesize BCAA-CoA (Homo sapiens)
DBT mutant-BCKDH [mitochondrial matrix] (Homo sapiens)
DBT mutants [mitochondrial matrix] (Homo sapiens)
K313_Y338del Lipo-K105-DBT [mitochondrial matrix] (Homo sapiens)
DBT mutants [mitochondrial matrix] (Homo sapiens)
K313_Y338del Lipo-K105-DBT [mitochondrial matrix] (Homo sapiens)
Literature References
PubMed ID
Title
Journal
Year
2010537
Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5'-splice donor site of an intron of the E2 gene disrupts the consensus sequence in this region
Nobukuni, Y
,
Indo, Y
,
Matsuda, I
,
Mitsubuchi, H
,
Akaboshi, I
,
Endo, F
J Clin Invest
1991
External Reference Information
External Reference
UniProt:P11182 DBT
Gene Names
DBT, BCATE2, BCKDHE2
Chain
transit peptide:1-61, chain:62-482
Reference Genes
BioGPS Gene:1629 DBT
COSMIC (genes):DBT DBT
CTD Gene:1629 DBT
dbSNP Gene:1629 DBT
ENSEMBL:ENSG00000137992 DBT
HGNC:2698 DBT
KEGG:hsa:1629 DBT
Monarch:1629 DBT
NCBI Gene:1629 DBT
OMIM:248610 DBT
UCSC:P11182 DBT
Reference Transcript
RefSeq:NM_001918.5 DBT
RefSeq:NM_001918.3 DBT
Other Identifiers
11731509_x_at
11731510_at
11731511_s_at
11751182_a_at
11752357_a_at
11762117_at
1629
16690103
205369_3p_x_at
205369_PM_x_at
205369_x_at
205370_PM_x_at
205370_x_at
205371_PM_s_at
205371_s_at
211196_3p_at
211196_PM_at
211196_at
231919_PM_at
231919_at
2425203
2425205
2425207
2425209
2425210
2425211
2425213
2425214
2425215
2425216
2425217
2425218
2425219
2425220
2425221
2425222
2425226
2425231
2425233
2425234
2425237
2425238
2425239
2425240
2425241
2425242
2425243
244687_PM_at
244687_at
37862_at
51919_at
7918008
86425_at
A_23_P74022
A_24_P28524
A_32_P50005
A_33_P3291594
A_33_P3308949
GE59930
GE85471
GO:0003824
GO:0005515
GO:0005737
GO:0005739
GO:0005759
GO:0005829
GO:0005856
GO:0006520
GO:0008289
GO:0009083
GO:0015630
GO:0016407
GO:0016491
GO:0016740
GO:0016746
GO:0016747
GO:0031405
GO:0031625
GO:0042645
GO:0043226
GO:0043754
GO:0045252
GO:0047101
GO:0160157
GO:1990204
HMNXSV003008442
HMNXSV003021704
Hs.199210.0.A1_3p_at
Hs.257043.0.S1_3p_at
ILMN_1714990
ILMN_1887403
M19301_at
M27093_s_at
PH_hs_0013509
PH_hs_0021360
PH_hs_0027858
TC01002918.hg
X66785_at
g179353_3p_a_at
g179353_3p_x_at
g186635_3p_a_at
g186635_3p_at
g186635_3p_x_at
g4503264_3p_at
g736674_3p_a_at
Participates
as a candidate of
DBT mutants [mitochondrial matrix] (Homo sapiens)
Other forms of this molecule
Lipo-K105-DBT [mitochondrial matrix]
Isobutyryl-lipoH2-K105-DBT [mitochondrial matrix]
Isovaleryl-lipoH2-K105-DBT [mitochondrial matrix]
2-Methylbutyryl-lipoH2-K105-DBT [mitochondrial matrix]
LipoH2-K105-DBT [mitochondrial matrix]
DBT [mitochondrial matrix]
P276C Lipo-K105-DBT [mitochondrial matrix]
S399C Lipo-K105-DBT [mitochondrial matrix]
I98M Lipo-K105-DBT [mitochondrial matrix]
DBT [cytosol]
Modified Residues
Name
N6-lipoyl-L-lysine at 105
Coordinate
105
PsiMod Name
N6-lipoyl-L-lysine [MOD:00127]
PsiMod Definition
A protein modification that effectively converts an L-lysine residue to N6-lipoyl-L-lysine.
Name
Deletion of residues 313 to 338
Disease
Name
Identifier
Synonyms
maple syrup urine disease
DOID:9269
dihydrolipoamide dehydrogenase deficiency
Cross References
RefSeq
NP_001909.3
,
NP_001909.4
ClinGen
CA212932
OpenTargets
ENSG00000137992
ENSEMBL
ENST00000370132
,
ENSG00000137992
,
ENSP00000359151
GeneCards
DBT
HPA
ENSG00000137992-DBT
PRO
P11182
Pharos - Targets
P11182
GlyGen
P11182
Orphanet
DBT
HMDB Protein
HMDBP03078
PDB
1K8O
,
1K8M
,
2COO
,
3RNM
,
1ZWV
Interactors (26)
Accession
#Entities
Entities
Confidence Score
Evidence (IntAct)
UniProt:Q8N3J5 PPM1K
2
H139Hfs13* PPM1K [mitochondrial matrix]
(R-HSA-9912515)
PPM1K [mitochondrial matrix]
(R-HSA-5693145)
0.788
8
UniProt:Q8TAA5 GRPEL2
1
GRPEL2 [mitochondrial inner membrane]
(R-HSA-1252076)
0.708
4
UniProt:P20333 TNFRSF1B
3
TNFRSF1B(27-?) [plasma membrane]
(R-HSA-6785037)
TNFRSF1B [specific granule membrane]
(R-HSA-6806149)
TNFRSF1B [plasma membrane]
(R-HSA-5661484)
0.669
3
UniProt:Q9BVS5 TRMT61B
1
TRMT61B [mitochondrial matrix]
(R-HSA-6787512)
0.643
3
UniProt:Q9H845 ACAD9
1
ACAD9 [mitochondrial inner membrane]
(R-HSA-5689049)
0.643
3
UniProt:Q8N4Q0 PTGR3
0.643
4
UniProt:Q96E11 MRRF
1
MRRF [mitochondrial matrix]
(R-HSA-5419265)
0.623
3
UniProt:Q96EY8 MMAB
4
MMAB E193K [mitochondrial matrix]
(R-HSA-3322150)
MMAB R191W [mitochondrial matrix]
(R-HSA-3322112)
MMAB R186W [mitochondrial matrix]
(R-HSA-3322128)
MMAB [mitochondrial matrix]
(R-HSA-2980970)
0.623
4
UniProt:P13073 COX4I1
2
COX4I1 [mitochondrial inner membrane]
(R-HSA-164305)
COX4I1 [mitochondrial intermembrane space]
(R-HSA-9865413)
0.564
2
UniProt:Q9Y2D0 CA5B
1
CA5B [mitochondrial matrix]
(R-HSA-1237023)
0.564
2
UniProt:Q9Y234 LIPT1
1
LIPT1 [mitochondrial matrix]
(R-HSA-6792623)
0.527
3
UniProt:Q96PE7 MCEE
1
MCEE [mitochondrial matrix]
(R-HSA-71012)
0.527
3
UniProt:Q16878 CDO1
1
CDO1 [cytosol]
(R-HSA-1614586)
0.527
2
UniProt:P35914 HMGCL
3
HMGCL(1-325) [peroxisomal matrix]
(R-HSA-9033125)
HMGCL(1-325) [cytosol]
(R-HSA-9033112)
HMGCL [mitochondrial matrix]
(R-HSA-74172)
0.527
2
UniProt:Q8TEB1 DCAF11
1
DCAF11 [nucleoplasm]
(R-HSA-8863251)
0.527
2
UniProt:Q96GK7 FAH2A
0.527
2
UniProt:P30084 ECHS1
17
ECHS1 [mitochondrial matrix]
(R-HSA-54125)
A2V ECHS1 [mitochondrial matrix]
(R-HSA-9916688)
T180A ECHS1 [mitochondrial matrix]
(R-HSA-9916687)
A238V ECHS1 [mitochondrial matrix]
(R-HSA-9916686)
A132T ECHS1 [mitochondrial matrix]
(R-HSA-9916665)
G195S ECHS1 [mitochondrial matrix]
(R-HSA-9916681)
K273E ECHS1 [mitochondrial matrix]
(R-HSA-9916680)
R54H ECHS1 [mitochondrial matrix]
(R-HSA-9916676)
I66T ECHS1 [mitochondrial matrix]
(R-HSA-9916659)
D150G ECHS1 [mitochondrial matrix]
(R-HSA-9916674)
A158D ECHS1 [mitochondrial matrix]
(R-HSA-9916689)
C225R ECHS1 [mitochondrial matrix]
(R-HSA-9916672)
N59S ECHS1 [mitochondrial matrix]
(R-HSA-9916684)
A138V ECHS1 [mitochondrial matrix]
(R-HSA-9916683)
E77Q ECHS1 [mitochondrial matrix]
(R-HSA-9916667)
F33S ECHS1 [mitochondrial matrix]
(R-HSA-9916682)
Q159R ECHS1 [mitochondrial matrix]
(R-HSA-9916666)
0.527
3
UniProt:Q8NI37 PPTC7
0.527
2
UniProt:Q9UK39 NOCT
1
CCRN4L [nucleoplasm]
(R-HSA-508391)
0.527
2
UniProt:P09622 DLD
8
DLD [mitochondrial matrix]
(R-HSA-69978)
M361V DLD [mitochondrial matrix]
(R-HSA-9907714)
I393T DLD [mitochondrial matrix]
(R-HSA-9907713)
E375K DLD [mitochondrial matrix]
(R-HSA-9907711)
R495G DLD [mitochondrial matrix]
(R-HSA-9907710)
G229C DLD [mitochondrial matrix]
(R-HSA-9907709)
D479V DLD [mitochondrial matrix]
(R-HSA-9907708)
I47T DLD [mitochondrial matrix]
(R-HSA-9907707)
0.527
2
UniProt:Q9UBN7 HDAC6
4
HDAC6 [lysosomal lumen]
(R-HSA-9660002)
HDAC6 [cytosol]
(R-HSA-5324660)
HDAC6 [late endosome lumen]
(R-HSA-9659980)
HDAC6 [nucleoplasm]
(R-HSA-351589)
0.527
2
UniProt:P21953 BCKDHB
8
BCKDHB [mitochondrial matrix]
(R-HSA-70015)
p-S342-BCKDHB [mitochondrial matrix]
(R-HSA-5693124)
Q346R BCKDHB [mitochondrial matrix]
(R-HSA-9865060)
R183P BCKDHB [mitochondrial matrix]
(R-HSA-9865041)
R170H BCKDHB [mitochondrial matrix]
(R-HSA-9865071)
G278S BCKDHB [mitochondrial matrix]
(R-HSA-9865069)
N176Y BCKDHB [mitochondrial matrix]
(R-HSA-9865063)
H206R BCKDHB [mitochondrial matrix]
(R-HSA-9865047)
0.527
2
UniProt:Q5T1C6 THEM4
3
THEM4 [mitochondrial matrix]
(R-HSA-162408)
THEM4 [cytosol]
(R-HSA-6809345)
THEM4 [plasma membrane]
(R-HSA-199437)
0.527
2
UniProt:P10606 COX5B
1
COX5B [mitochondrial inner membrane]
(R-HSA-164307)
0.527
2
UniProt:P11234 RALB
1
RALB [cytosol]
(R-HSA-171015)
0.527
2
UniProt:Q6IN84 MRM1
1
MRM1 [mitochondrial matrix]
(R-HSA-6793088)
0.527
3
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