Organism name | Veratrum nigrum |
---|---|
Genus | Veratrum |
Family | Melanthiaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Veratrum nigrum |
---|---|
Linked NCBI taxonomy ID | 203100 |
Linked level | species |
Family in NCBI taxonomy | Melanthiaceae |
---|---|
ID | 50362 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Liliopsida |
---|---|
ID | 4447 |
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 |
---|---|---|---|---|---|---|---|---|
C00029205
![]() |
Verazine
|
CHEMBL458682
CHEMBL457588 |
C052979
|
No. 265 | No. 11 |
![]() |
||
C00028412
![]() |
Isorubijervine
|
No. 265 | No. 11 |
![]() |
||||
C00028946
![]() |
Rubijervine
|
CHEMBL1512978
CHEMBL1993702 |
5 / 2 / 3 | No. 265 | No. 11 |
![]() |
||
C00028667
![]() |
Neogermbudine
|
C052980
|
No. 321 | No. 11 |
![]() |
|||
C00029204
![]() |
Veratroylzygadenine
|
No. 321 | No. 11 |
![]() |
||||
C00002253
![]() |
Jervine
|
CHEMBL186779
CHEMBL1402135 CHEMBL1717145 CHEMBL1742371 |
C010206
|
11 / 15 / 12 | No. 587 | No. 11 |
![]() |
|
C00002270
![]() |
Veratramine
|
CHEMBL464724
CHEMBL1398335 |
C009649
|
7 / 2 / 3 | No. 1681 | No. 11 |
![]() |
|
C00029196
![]() |
Veramine
|
No. 1844 | No. 11 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002253 C00002270 C00028946 | 1 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002253 C00002270 C00028946 | 0 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002253 C00002270 C00028946 | 0 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002253 C00002270 C00028946 | 1 / 1 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002253 C00002270 C00028946 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00002253 | 7 / 3 |
Q99720 | Sigma non-opioid intracellular receptor 1 | Membrane receptor | C00002253 | 1 / 0 |
P06276 | Cholinesterase | Hydrolase | C00002270 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002253 | 0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002270 | 0 / 0 |
Q15465 | Sonic hedgehog protein | Unclassified protein | C00002253 | 4 / 5 |
Q15125 | 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase | Enzyme | C00002253 | 1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002253 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#614373 | Amyotrophic lateral sclerosis 16, juvenile; als16 |
Q99720
|
#302960 | Chondrodysplasia punctata 2, x-linked dominant; cdpx2 |
Q15125
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#142945 | Holoprosencephaly 3; hpe3 |
Q15465
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#611638 | Microphthalmia, isolated, with coloboma 5; mcopcb5 |
Q15465
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#174500 | Polydactyly, preaxial ii; ppd2 |
Q15465
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#147250 | Solitary median maxillary central incisor; smmci |
Q15465
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(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)
|
H01194 | X-linked chondrodysplasia punctata |
Q15125
(related)
|
H00039 | Basal cell carcinoma |
Q15465
(related)
|
H00267 | Holoprosencephaly (HPE) |
Q15465
(related)
|
H00652 | Solitary median maxillary central incisor syndrome |
Q15465
(related)
|
H01027 | Anophthalmia and microphthalmia (A/M) |
Q15465
(related)
|
H01160 | Schizencephaly |
Q15465
(related)
|