Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Streptomycetaceae 2
Pseudomonadaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (3)

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
C00018609 External link 512 Phenacein
C043271
C00018654 External link 512 Hemipyocyanin
CHEMBL1416045
C050093
19 / 22 / 12
C00018678 External link 512 Gutolactone
/ 1,6-Dihydroxyphenazine
CHEMBL2071426
1 / 1 / 0

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00018654 0 / 0
Q99700 Ataxin-2 Unclassified protein C00018654 1 / 1
P10253 Lysosomal alpha-glucosidase Hydrolase C00018654 1 / 1
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00018654 0 / 0
P37840 Alpha-synuclein Unclassified protein C00018654 4 / 2
P00352 Retinal dehydrogenase 1 Enzyme C00018654 0 / 0
P39748 Flap endonuclease 1 Enzyme C00018654 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00018654 2 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00018654 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00018654 7 / 3
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00018654 1 / 2
Q8NER1 Transient receptor potential cation channel subfamily V member 1 TRPV (Vanilloid) C00018654 0 / 0
P22303 Acetylcholinesterase Hydrolase C00018678 1 / 0
Q9UNA4 DNA polymerase iota Enzyme C00018654 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00018654 1 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00018654 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00018654 4 / 3
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00018654 0 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00018654 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00018654 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (23)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#114500 Colorectal cancer; crc P84022
#127750 Dementia, lewy body; dlb P37840
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#112100 Yt blood group antigen P22303

KEGG DISEASE (12)

KEGG name UniProt
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)