Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Chaetomiaceae 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
C00038728 External link 512 Chaetochromin A
CHEMBL162783
CHEMBL1099258
CHEMBL1096606
C032678
41 / 23 / 13

Human Protein / Gene in interactions

41 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00038728 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00038728 0 / 0
Q99700 Ataxin-2 Unclassified protein C00038728 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00038728 2 / 0
P06746 DNA polymerase beta Enzyme C00038728 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00038728 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00038728 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00038728 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00038728 3 / 1
P11473 Vitamin D3 receptor NR1I1 C00038728 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00038728 0 / 0
P39748 Flap endonuclease 1 Enzyme C00038728 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00038728 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00038728 2 / 0
O75496 Geminin Unclassified protein C00038728 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00038728 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00038728 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00038728 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00038728 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00038728 0 / 0
P98073 Enteropeptidase Enzyme C00038728 1 / 1
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00038728 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00038728 0 / 0
P16298 Serine/threonine-protein phosphatase 2B catalytic subunit beta isoform Ser_Thr C00038728 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00038728 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00038728 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00038728 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00038728 1 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00038728 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00038728 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00038728 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00038728 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00038728 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00038728 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00038728 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00038728 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00038728 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00038728 1 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00038728 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00038728 2 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00038728 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (23)

OMIM preferred title UniProt
#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
Q14191
#226200 Enterokinase deficiency P98073
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257220 Niemann-pick disease, type c1; npc1 O15118
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (13)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
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)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00988 Enterokinase deficiency P98073 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)