KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (2)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00001193 External link 512 Malonic acid
CHEMBL7942
C030290
6 / 1 / 5 1 / 2
C00001205 External link 512 Succinic acid
CHEMBL576
D019802
6 / 13 / 17 1 / 3

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16798 NADP-dependent malic enzyme, mitochondrial Enzyme C00001193 C00001205 0 / 0
Q8TCC7 Solute carrier family 22 member 8 Antiporter C00001205 0 / 0
P02545 Prelamin-A/C Unclassified protein C00001205 11 / 10
P14920 D-amino-acid oxidase Enzyme C00001193 0 / 0
Q9GZT9 Egl nine homolog 1 Enzyme C00001205 1 / 1
Q99489 D-aspartate oxidase Enzyme C00001193 0 / 0
Q9GZT4 Serine racemase Enzyme C00001193 0 / 0
P00338 L-lactate dehydrogenase A chain Enzyme C00001193 1 / 5
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00001193 0 / 0
Q7Z4W1 L-xylulose reductase Enzyme C00001205 0 / 1
Q00987 E3 ubiquitin-protein ligase Mdm2 Other nuclear protein C00001205 1 / 5

2 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00001193
64849 SLC13A3, NADC3, SDCT2 solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 C00001205

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#614401 Accelerated tumor formation, susceptibility to; actfs Q00987
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#609820 Erythrocytosis, familial, 3; ecyt3 Q9GZT9
#612933 Glycogen storage disease xi; gsd11 P00338
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (22)

KEGG name UniProt
H00069 Glycogen storage diseases (GSD) P00338 (related)
H00010 Multiple myeloma P00338 (marker)
H00023 Testicular cancer P00338 (marker)
H00035 Ewing's sarcoma P00338 (marker)
H00043 Neuroblastoma P00338 (marker)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00025 Penile cancer Q00987 (related)
H00028 Choriocarcinoma Q00987 (related)
H00036 Osteosarcoma Q00987 (related)
H00037 Alveolar rhabdomyosarcoma Q00987 (related)
H00042 Glioma Q00987 (related)
H01065 Pentosuria Q7Z4W1 (related)
H00236 Congenital polycythemia Q9GZT9 (related)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D001930 Brain Injuries C00001193
D020258 Neurotoxicity Syndromes C00001193
D003128 COMA C00001205
D062787 Drug Overdose C00001205
D007035 Hypothermia C00001205