Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Aspergillaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (1)

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
C00046868 External link 512 Pyrophen
CHEMBL1334926
CHEMBL1983219
C067225
15 / 11 / 13

Human Protein / Gene in interactions

15 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 C00046868 0 / 0
P06746 DNA polymerase beta Enzyme C00046868 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00046868 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00046868 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00046868 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00046868 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00046868 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00046868 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00046868 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00046868 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00046868 1 / 1
O00255 Menin Unclassified protein C00046868 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00046868 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00046868 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00046868 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc Q14191
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (13)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)
H00296 Defects in RecQ helicases Q14191 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)