Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Micromonosporaceae 5
Streptomycetaceae 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
C00017607 External link 512 6108A1
/ Antibiotic 6108A1
C066089
C00017608 External link 512 6108B
/ Antibiotic 6108B
C066090
C00017609 External link 512 6108C
/ Antibiotic 6108C
C066091
C00017610 External link 512 Antibiotic 6108D
C066088
C00018762 External link 512 NSC 246129
/ Cirramycin A1
/ Antibiotic B 58941B
CHEMBL1976094
C059005
C00018851 External link 512 M 4365A2
/ Rosamicin
/ Sch 14947
/ NSC 175150
/ Rosaramicin
/ Juvenimicin A3
/ Antibiotic 67-694
/ Antibiotic T 1124C
/ Antibiotic M 4365A2
/ 4'-Deoxycirramycin A1
CHEMBL8965
CHEMBL26194
CHEMBL1546091
CHEMBL1966403
CHEMBL2357105
C060286
4 / 5 / 7

Human Protein / Gene in interactions

4 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00018851 1 / 4
O75496 Geminin Unclassified protein C00018851 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00018851 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00018851 4 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#208900 Ataxia-telangiectasia; at Q13315
#600274 Frontotemporal dementia; ftd P10636
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (7)

KEGG name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)