| class name | count |
|---|---|
| asterids | 28 |
| rosids | 3 |
| eudicotyledons | 1 |
| class name | count |
|---|---|
| Apiaceae | 28 |
| Rutaceae | 2 |
| Crassulaceae | 1 |
| Moraceae | 1 |
| br08003 Category | # of metabolite |
|---|---|
| Furanocoumarins | 2 |
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|---|---|
| Furanocoumarins | C09279 | C00002486 |
| Furanocoumarins | C09309 | C00002496 |
| 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 |
|---|---|---|---|---|---|---|
|
C00002486
|
Nodakenin
|
CHEMBL459825
|
C471579
|
11 / 8 / 6 |
|
|
|
C00002496
|
Rutarin
|
|
||||
|
C00019822
|
Columbianetin-beta-D-glucopyranoside
|
C062747
|
|
|||
|
C00019919
|
(2R)-2'-Hydroxymarmesin 2'-O-beta-D-glucopyranoside
|
|
||||
|
C00020008
|
Praeroside II
/ (-)-Praeroside II |
|
||||
|
C00020009
|
Praeroside III
|
|
||||
|
C00020010
|
Praeroside IV
|
CHEMBL1159445
|
2 / 0 / 0 |
|
||
|
C00020028
|
Tortuoside
|
|
||||
|
C00020036
|
Praeroside V
|
|
||||
|
C00029680
|
Ammajin
/ Marmesinin / (-)-Marmesinin |
CHEMBL459825
|
11 / 8 / 6 |
|
||
|
C00031440
|
Yunngnoside A
/ (+)-Yunngnoside A |
|
||||
|
C00031441
|
Yunngnoside B
/ (+)-Yunngnoside B |
CHEMBL1335374
|
4 / 9 / 5 |
|
||
|
C00031472
|
(R)-Peucedanol 7-O-beta-D-glucopyranoside
|
CHEMBL1159420
|
2 / 0 / 0 |
|
||
|
C00031604
|
Apterin
|
CHEMBL1335374
|
4 / 9 / 5 |
|
||
|
C00035164
|
Turbinatocoumarin
|
|
||||
|
C00037263
|
Heraclenol 3'-O-beta-D-glucopyranoside
/ (+)-Heraclenol 3'-O-beta-D-glucopyranoside |
|
||||
|
C00037589
|
Oxypeucedanin hydrate 3'-O-beta-glucopyranoside
|
|
||||
|
C00042467
|
Devenyoside A
/ (-)-Devenyoside A |
|
||||
|
C00042468
|
Devenyoside B
/ (-)-Devenyoside B |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00002486 C00029680 C00031441 C00031604 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00002486 C00020010 C00029680 C00031472 | 0 / 0 |
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002486 C00029680 C00031441 C00031604 | 2 / 2 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00002486 C00029680 C00031472 | 0 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | C00002486 C00029680 | 1 / 1 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00031441 C00031604 | 7 / 3 |
| Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00002486 C00029680 | 0 / 0 |
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00002486 C00029680 | 2 / 2 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002486 C00029680 | 1 / 1 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00031441 C00031604 | 0 / 0 |
| P22303 | Acetylcholinesterase | Hydrolase | C00002486 C00029680 | 1 / 0 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002486 C00029680 | 1 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002486 C00029680 | 0 / 0 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00020010 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #119900 | Digital clubbing, isolated congenital |
P15428
|
| #301500 | Fabry disease |
P06280
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #257200 | Niemann-pick disease, type a |
P17405
|
| #607616 | Niemann-pick disease, type b |
P17405
|
| #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
|
| #112100 | Yt blood group antigen |
P22303
|
| KEGG | name | UniProt |
|---|---|---|
| H00125 | Fabry disease |
P06280
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
| H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
| H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
| H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|