class name | count |
---|
class name | count |
---|---|
Micromonosporaceae | 5 |
Streptomycetaceae | 1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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
![]() |
6108A1
/ Antibiotic 6108A1 |
C066089
|
![]() |
|||
C00017608
![]() |
6108B
/ Antibiotic 6108B |
C066090
|
![]() |
|||
C00017609
![]() |
6108C
/ Antibiotic 6108C |
C066091
|
![]() |
|||
C00017610
![]() |
Antibiotic 6108D
|
C066088
|
![]() |
|||
C00018762
![]() |
NSC 246129
/ Cirramycin A1 / Antibiotic B 58941B |
CHEMBL1976094
|
C059005
|
![]() |
||
C00018851
![]() |
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 |
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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 |
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 | 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)
|