Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Streptomycetaceae 5

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
C00015930 External link 512 Aclidinomycin A
C00015931 External link 512 Aclidinomycin B
/ (+)-Aclidinomycin B
C00016428 External link 512 31F508b1
/ Bioxalomycin beta1
/ Antibiotic 31F508b1
C00016429 External link 512 31F508b2
/ Bioxalomycin beta2
/ Antibiotic 31F508b2
/ Naphthyridinomycin A
C00018432 External link 512 NSC 349644
/ Cyanocycline A
/ (+)-Cyanocycline A
/ Cyanonaphthyridinomycin
CHEMBL520550
CHEMBL1727019
C035070
9 / 12 / 7

Human Protein / Gene in interactions

9 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00018432 1 / 1
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00018432 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00018432 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00018432 2 / 0
O75496 Geminin Unclassified protein C00018432 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00018432 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00018432 7 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00018432 0 / 0
Q06710 Paired box protein Pax-8 Unclassified protein C00018432 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (12)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#300615 Brunner syndrome P21397
#114500 Colorectal cancer; crc P84022
#218700 Hypothyroidism, congenital, nongoitrous, 2; chng2 Q06710
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#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

KEGG DISEASE (7)

KEGG name UniProt
H00548 Brunner syndrome P21397 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00032 Thyroid cancer Q06710 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) Q06710 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)