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)
|