Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Streptomycetaceae 3
Thermomonosporaceae 2
Pseudonocardiaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (6)

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
C00014944 External link 512 Chandrananimycin A
CHEMBL2322651
1 / 0 / 0
C00014945 External link 512 Chandrananimycin B
C00016208 External link 512 4-Demethoxymichigazone
C00017063 External link 512 Exfoliazone
/ Antibiotic BT 38
CHEMBL2311997
C067081
1 / 0 / 0
C00018683 External link 512 NSC 94945
/ AV Toxin C
/ Questiomycin A
/ 2-Aminophenoxazone
/ 2-Amino-3-phenoxazone
/ Acrospermum viticola toxin C
CHEMBL146710
C005512
32 / 18 / 20
C00027921 External link 512 BE-39907B

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme C00014944 C00017063 C00018683 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00018683 0 / 0
P06746 DNA polymerase beta Enzyme C00018683 0 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00018683 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00018683 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00018683 1 / 0
P11473 Vitamin D3 receptor NR1I1 C00018683 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00018683 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00018683 0 / 0
P39748 Flap endonuclease 1 Enzyme C00018683 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00018683 2 / 0
O75496 Geminin Unclassified protein C00018683 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00018683 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00018683 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00018683 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00018683 3 / 1
Q99700 Ataxin-2 Unclassified protein C00018683 1 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00018683 1 / 2
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00018683 0 / 0
P10696 Alkaline phosphatase, placental-like Enzyme C00018683 0 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00018683 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00018683 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00018683 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00018683 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00018683 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00018683 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00018683 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00018683 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00018683 1 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00018683 0 / 0
O00255 Menin Unclassified protein C00018683 2 / 5
P01215 Glycoprotein hormones alpha chain Unclassified protein C00018683 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (20)

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)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00213 Hypophosphatasia P05186 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00023 Testicular cancer P10696 (marker)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)