Organism name | Haplopappus bailahuen |
---|---|
Genus | Haplopappus |
Family | Asteraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Haplopappus |
---|---|
Linked NCBI taxonomy ID | 71051 |
Linked level | genus |
Family in NCBI taxonomy | Asteraceae |
---|---|
ID | 4210 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
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 |
---|---|---|---|---|---|---|---|---|
C00005730
![]() |
Myricitrin
/ Myricetin 3-O-rhamnoside / Myricetin 3-O-alpha-L-rhamnoside / Myricetin 3-O-alpha-L-rhamnopyranoside |
CHEMBL454576
CHEMBL522983 CHEMBL1599224 |
C008577
|
25 / 11 / 11 | No. 2 | No. 15 |
![]() |
|
C00005728
![]() |
Myricetin 3-galactoside
/ Myricetin 3-O-galactoside |
CHEMBL462244
CHEMBL1221722 |
No. 2 | No. 15 |
![]() |
|||
C00004635
![]() |
Isorhamnetin
/ 3'-O-Methylquercetin / 3,4',5,7-Tetrahydroxy-3'-methoxyflavone / 3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one |
CHEMBL379064
|
C047368
|
12 / 10 / 13 | 10 / 0 | No. 3 | No. 15 |
![]() |
C00003867
![]() |
Velutin
/ Flavoyadorigenin B / Luteolin 7,3'-dimethyl ether / 5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one |
CHEMBL508292
|
No. 3 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P39748 | Flap endonuclease 1 | Enzyme | C00004635 C00005730 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00004635 C00005730 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00004635 C00005730 | 0 / 0 |
P04745 | Alpha-amylase 1 | Enzyme | C00004635 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00005730 | 1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005730 | 0 / 0 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00004635 | 1 / 1 |
P04798 | Cytochrome P450 1A1 | Cytochrome P450 1A1 | C00004635 | 0 / 0 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005730 | 0 / 0 |
P04792 | Heat shock protein beta-1 | Unclassified protein | C00004635 | 2 / 1 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00005730 | 1 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00005730 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00005730 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00005730 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00005730 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00005730 | 0 / 0 |
Q16678 | Cytochrome P450 1B1 | Cytochrome P450 1B1 | C00004635 | 4 / 4 |
P06746 | DNA polymerase beta | Enzyme | C00005730 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00004635 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00005730 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00005730 | 0 / 0 |
P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00004635 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00005730 | 4 / 3 |
P34949 | Mannose-6-phosphate isomerase | Enzyme | C00005730 | 1 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00005730 | 1 / 1 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00005730 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00005730 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00005730 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00005730 | 1 / 1 |
O00255 | Menin | Unclassified protein | C00004635 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00004635 | 1 / 2 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00005730 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00005730 | 1 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00005730 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
5243 | ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 | ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) |
C00004635
|
4363 | ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 | ATP-binding cassette, sub-family C (CFTR/MRP), member 1 |
C00004635
|
196 | AHR, bHLHe76 | aryl hydrocarbon receptor |
C00004635
|
1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00004635
|
1545 | CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 | cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) |
C00004635
|
2099 | ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 | estrogen receptor 1 |
C00004635
|
2100 | ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 | estrogen receptor 2 (ER beta) |
C00004635
|
4846 | NOS3, ECNOS, eNOS | nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) |
C00004635
|
4973 | OLR1, CLEC8A, LOX1, LOXIN, SCARE1, SLOX1 | oxidized low density lipoprotein (lectin-like) receptor 1 |
C00004635
|
7031 | TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 | trefoil factor 1 |
C00004635
|
OMIM | preferred title | UniProt |
---|---|---|
#606595 | Charcot-marie-tooth disease, axonal, type 2f; cmt2f |
P04792
|
#602579 | Congenital disorder of glycosylation, type ib; cdg1b |
P34949
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137750 | Glaucoma 1, open angle, a; glc1a |
Q16678
|
#231300 | Glaucoma 3, primary congenital, a; glc3a |
Q16678
|
#137760 | Glaucoma, primary open angle; poag |
Q16678
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#608634 | Neuronopathy, distal hereditary motor, type iib; hmn2b |
P04792
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#604229 | Peters anomaly |
Q16678
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#278300 | Xanthinuria, type i |
P47989
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
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)
|
H00856 | Distal hereditary motor neuropathies (dHMN) |
P04792
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00118 | Congenital disorders of glycosylation (CDG) type I |
P34949
(related)
|
H00192 | Xanthinuria |
P47989
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00612 | Primary open angle glaucoma |
Q16678
(related)
|
H01075 | Peters anomaly |
Q16678
(related)
|
H01159 | Anterior segment dysgenesis (ASD) |
Q16678
(related)
|
H01203 | Primary congenital glaucoma (PCG) |
Q16678
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|