| class name | count |
|---|---|
| Magnoliophyta | 47 |
| eudicotyledons | 38 |
| rosids | 7 |
| asterids | 1 |
| Liliopsida | 1 |
| class name | count |
|---|---|
| Annonaceae | 27 |
| Lauraceae | 17 |
| Papaveraceae | 16 |
| Menispermaceae | 10 |
| Berberidaceae | 8 |
| Ranunculaceae | 3 |
| Celastraceae | 2 |
| Rhamnaceae | 2 |
| Euphorbiaceae | 2 |
| Hernandiaceae | 2 |
| Loganiaceae | 1 |
| Siparunaceae | 1 |
| Nelumbonaceae | 1 |
| Fabaceae | 1 |
| Colchicaceae | 1 |
| br08003 Category | # of metabolite |
|---|---|
| Isoquinoline alkaloids | 3 |
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|---|---|
| Isoquinoline alkaloids | C09555 | C00001875 |
| Isoquinoline alkaloids | C09558 | C00001876 |
| Isoquinoline alkaloids | C17592 | C00028453 |
| Isoquinoline alkaloids | C09558 | C00028454 |
| 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 |
|---|---|---|---|---|---|---|
|
C00001810
|
Armepavine
/ (-)-Armepavine / (R)-(-)-Armepavine |
CHEMBL451722
CHEMBL1186477 CHEMBL1186510 |
7 / 5 / 3 |
|
||
|
C00001875
|
Tritopin
/ Tritopine / Laudanidine / (-)-Laudanidine |
CHEMBL251625
CHEMBL1425007 |
2 / 0 / 0 |
|
||
|
C00001876
|
Laudanosine
/ L-Laudanosine / O-Methylcodamine / L-(+)-Laudanosine |
CHEMBL1407
CHEMBL519894 CHEMBL1613 |
C001522
|
18 / 26 / 21 | 0 / 1 |
|
|
C00001910
|
Reticuline
/ (+)-Reticuline |
CHEMBL235212
CHEMBL401501 CHEMBL464734 |
C003298
|
1 / 0 / 0 |
|
|
|
C00025654
|
Codamine
/ (+)-Codamine / L-(+)-Codamine / (S)-(+)-Codamine |
CHEMBL251624
|
|
|||
|
C00025666
|
(S)-Laudanine
/ (+)-Laudanidine / L-(+)-Laudanidine |
CHEMBL251625
CHEMBL1425007 |
2 / 0 / 0 |
|
||
|
C00026017
|
Protosinomenine
/ (S)-Protosinomenine |
|
||||
|
C00026113
|
Canadaline
/ (+)-Canadaline |
CHEMBL1968299
|
|
|||
|
C00027523
|
Bernumicine
/ (+)-Bernumicine / (R)-Bernumicine |
|
||||
|
C00027524
|
Bernumine
/ (+)-Bernumine |
|
||||
|
C00027866
|
Anicanine
|
|
||||
|
C00028078
|
Colchiethine
|
|
||||
|
C00028453
|
Laudanine
|
CHEMBL251625
CHEMBL1425007 |
2 / 0 / 0 |
|
||
|
C00028454
|
Laudanosine
|
CHEMBL1407
CHEMBL519894 CHEMBL1613 |
18 / 26 / 21 |
|
||
|
C00028871
|
Pseudolaudanine
|
|
||||
|
C00028938
|
Roefractine
|
|
||||
|
C00034987
|
(+)-Parvinine
|
CHEMBL452500
|
|
|||
|
C00040992
|
Heterocarpine
|
|
||||
|
C00046196
|
N-Demethylphyllocryptine
|
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001810 C00001875 C00001876 C00025666 C00028453 C00028454 | 0 / 0 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001810 C00001876 C00028454 | 3 / 3 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001810 C00001876 C00028454 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00001810 C00001876 C00028454 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00001875 C00025666 C00028453 | 0 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00001876 C00028454 | 0 / 0 |
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001876 C00028454 | 1 / 0 |
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00001876 C00028454 | 2 / 2 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00001876 C00028454 | 7 / 3 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001876 C00028454 | 0 / 0 |
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00001876 C00028454 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00001876 C00028454 | 0 / 0 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001876 C00028454 | 0 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001876 C00028454 | 0 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001876 C00028454 | 0 / 1 |
| P02545 | Prelamin-A/C | Unclassified protein | C00001876 C00028454 | 11 / 10 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001876 C00028454 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001876 C00028454 | 1 / 1 |
| P22303 | Acetylcholinesterase | Hydrolase | C00001876 C00028454 | 1 / 0 |
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00001810 | 0 / 0 |
| P35372 | Mu-type opioid receptor | Opioid receptor | C00001910 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00001810 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00001810 | 2 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #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
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #112100 | Yt blood group antigen |
P22303
|
| KEGG | name | UniProt |
|---|---|---|
| H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
| H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
| H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
| H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
| H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
| H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
| H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
| H00663 | Restrictive dermopathy |
P02545
(related)
|
| H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
| H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
| H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|