KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (5)

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
C00030222 External link 512 Progallin A
/ Ethyl gallate
CHEMBL453196
C048734
C00030754 External link 512 Methyl gallate
/ Methyl 3,4,5-trihydroxybenzoate
CHEMBL65675
C052082
16 / 15 / 13
C00031089 External link 512 Protocatechuic acid methyl ester
CHEMBL486027
7 / 3 / 5
C00032950 External link 512 Ethyl protocatechuate
/ Ethyl 3,4-dihydroxybenzoate
CHEMBL486216
C018063
7 / 3 / 5
C00044447 External link 512 3-Bromo-4,5-dihydroxybenzoic acid methyl ester

Human Protein / Gene in interactions

23 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9ULX7 Carbonic anhydrase 14 Lyase C00031089 C00032950 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00031089 C00032950 0 / 1
P00915 Carbonic anhydrase 1 Lyase C00031089 C00032950 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00031089 C00032950 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00031089 C00032950 1 / 2
P00918 Carbonic anhydrase 2 Lyase C00031089 C00032950 1 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00030754 C00031089 1 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00030754 0 / 0
P02545 Prelamin-A/C Unclassified protein C00030754 11 / 10
P02768 Serum albumin Secreted protein C00030754 0 / 0
Q9GZT9 Egl nine homolog 1 Enzyme C00032950 1 / 1
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00030754 1 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00030754 0 / 0
P39748 Flap endonuclease 1 Enzyme C00030754 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00030754 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00030754 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00030754 0 / 0
P06746 DNA polymerase beta Enzyme C00030754 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00030754 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00030754 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00030754 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00030754 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00030754 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#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
#232300 Glycogen storage disease ii P10253
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#143860 Hyperchlorhidrosis, isolated O43570
#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
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#275210 Restrictive dermopathy, lethal P02545
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#278300 Xanthinuria, type i P47989

KEGG DISEASE (18)

KEGG name UniProt
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
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)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00192 Xanthinuria P47989 (related)
H00236 Congenital polycythemia Q9GZT9 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)