Organism name | Torreya nucifera |
---|---|
Genus | Torreya |
Family | Taxaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Torreya nucifera |
---|---|
Linked NCBI taxonomy ID | 50189 |
Linked level | species |
Family in NCBI taxonomy | Taxaceae |
---|---|
ID | 25623 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Spermatophyta |
---|---|
ID | 58024 |
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
---|---|---|---|---|---|---|---|---|
C00022520
![]() |
Kayadiol
/ 4-Epiagathadiol / 8(17),13E-Labdadien-15,18-diol |
CHEMBL1277840
|
No. 165 |
![]() |
||||
C00000609
![]() |
(-)-Arctigenin
|
CHEMBL369142
CHEMBL435734 CHEMBL1966556 |
C071942
|
13 / 7 / 6 | No. 223 | No. 21 |
![]() |
|
C00022717
![]() |
Torreferol
|
CHEMBL596905
CHEMBL1521278 |
3 / 15 / 12 | No. 256 | No. 46 |
![]() |
||
C00022718
![]() |
13-Epitorreferol
|
CHEMBL596905
CHEMBL1521278 |
3 / 15 / 12 | No. 256 | No. 46 |
![]() |
||
C00011623
![]() |
(+-)-Nuciferol
/ (+-)-(E)-Nuciferol |
No. 456 | No. 38 |
![]() |
||||
C00011624
![]() |
(+)-Nuciferal
/ (E)-Nuciferal / (E,S)-(+)-Nuciferal |
No. 456 | No. 38 |
![]() |
||||
C00011489
![]() |
Neotorreyol
|
No. 4152 | No. 38 |
![]() |
||||
C00011445
![]() |
Dendrolasin
|
C454810
|
No. 4152 | No. 38 |
![]() |
|||
C00011490
![]() |
Torreyal
|
No. 4152 | No. 38 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00000609 C00022717 C00022718 | 0 / 1 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00022717 C00022718 | 4 / 1 |
P02545 | Prelamin-A/C | Unclassified protein | C00022717 C00022718 | 11 / 10 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00000609 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00000609 | 1 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00000609 | 0 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000609 | 2 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00000609 | 1 / 1 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00000609 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00000609 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00000609 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00000609 | 1 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00000609 | 1 / 1 |
Q02750 | Dual specificity mitogen-activated protein kinase kinase 1 | Ste7 | C00000609 | 1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00000609 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#615279 | Cardiofaciocutaneous syndrome 3; cfc3 |
Q02750
|
#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
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
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)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00523 | Noonan syndrome and related disorders |
Q02750
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|