Organism name | Meconopsis robusta |
---|---|
Genus | Meconopsis |
Family | Papaveraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Meconopsis |
---|---|
Linked NCBI taxonomy ID | 72195 |
Linked level | genus |
Family in NCBI taxonomy | Papaveraceae |
---|---|
ID | 3465 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | eudicotyledons |
---|---|
ID | 71240 |
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 |
---|---|---|---|---|---|---|---|---|
C00025655
![]() |
Corytuberine
/ (+)-Corytuberine |
CHEMBL227965
|
C013896
|
1 / 0 / 0 | No. 20 | No. 4 |
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|
C00026118
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Corysamine
|
No. 155 | No. 4 |
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||||
C00024668
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YHL II
/ Coptisine |
CHEMBL362071
|
C034384
|
No. 155 | No. 4 |
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||
C00001885
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Escholin
/ Escholine / Thalictrin / Thalictrine / Magnoflorine / (+)-Magnoflorine |
CHEMBL235428
|
C001670
|
No. 286 | No. 4 |
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||
C00025459
![]() |
Papaverrubine C
/ Epiporphyroxine / 14-Epiporphyroxine |
No. 305 |
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|||||
C00001911
![]() |
Rhoeadine
|
C019078
|
No. 305 |
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||||
C00025460
![]() |
Porphyroxine
/ Papaverrubine D |
No. 305 |
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|||||
C00025461
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Papaverrubine E
|
No. 305 |
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|||||
C00001799
![]() |
Thalictrimine
/ Allocryptopine / alpha-Fagarine / beta-Homochelidonine / alpha-Allocryptopine |
CHEMBL520043
|
C109505
|
3 / 2 / 3 | 2 / 0 | No. 820 | No. 4 |
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C00001906
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Fumarin
/ Biflorine / Protopine / Fumarine / Corydinine |
CHEMBL453019
|
C009093
|
5 / 5 / 4 | 2 / 0 | No. 820 | No. 4 |
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C00027332
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Cryptopin
/ Cryptopine / Kryptopine / Kryptocavin / Cryptocavine |
CHEMBL1339015
|
C007159
|
6 / 5 / 8 | No. 820 | No. 4 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001906 C00027332 | 1 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001906 C00027332 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001799 C00027332 | 1 / 2 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001906 C00027332 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00027332 | 0 / 0 |
P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00025655 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001906 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00001799 | 0 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00001906 | 3 / 2 |
O00255 | Menin | Unclassified protein | C00027332 | 2 / 5 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00001799 | 1 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00001799
C00001906
|
1544 | CYP1A2, CP12, P3-450, P450(PA) | cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) |
C00001799
C00001906
|
OMIM | preferred title | UniProt |
---|---|---|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|