class name | count |
---|
class name | count |
---|---|
Pleosporaceae | 6 |
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 |
---|---|---|---|---|---|---|
C00016655
![]() |
Radicinin
/ Stemphylone |
CHEMBL1894884
CHEMBL1994984 |
10 / 6 / 7 |
![]() |
||
C00034923
![]() |
4-Epiradicinol
/ (-)-4-Epiradicinol |
![]() |
||||
C00049695
![]() |
3-Epiradicinol
|
![]() |
||||
C00049696
![]() |
3-Methoxy-3-epiradicinol
/ (-)-3-Methoxy-3-epiradicinol |
![]() |
||||
C00049742
![]() |
Radicinol
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00016655 | 1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00016655 | 0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00016655 | 2 / 2 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00016655 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00016655 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00016655 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00016655 | 1 / 1 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00016655 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00016655 | 0 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00016655 | 0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#114500 | Colorectal cancer; crc |
P84022
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|