| 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)
|