Organism name | Morinda citrifolia L., |
---|---|
Genus | Morinda |
Family | Rubiaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Morinda citrifolia |
---|---|
Linked NCBI taxonomy ID | 43522 |
Linked level | species |
Family in NCBI taxonomy | Rubiaceae |
---|---|
ID | 24966 |
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 |
---|---|---|---|---|---|---|---|---|
C00019420
![]() |
Physcion
/ 1,8-Dihydroxy-3-methyl-6-methoxyanthraquinone |
CHEMBL42624
|
C008905
|
18 / 20 / 14 | 1 / 0 | No. 41 | No. 62 |
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C00035974
![]() |
7-Hydroxy-8-methoxy-2-methylanthraquinone
|
No. 41 | No. 62 |
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||||
C00032078
![]() |
Nordamnacanthal
|
No. 41 | No. 62 |
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||||
C00031601
![]() |
Anthragallol 2-methyl ether
|
CHEMBL227588
|
No. 41 | No. 62 |
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|||
C00031233
![]() |
Rubiadin-1-methyl ether
|
C079172
|
No. 41 | No. 62 |
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|||
C00031591
![]() |
Alizarin 1-methyl ether
|
CHEMBL446748
|
C035010
|
No. 41 | No. 62 |
![]() |
||
C00031600
![]() |
Anthragallol 1,3-dimethyl ether
|
No. 41 | No. 62 |
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||||
C00029570
![]() |
6alpha-Hydroxyadoxoside
|
No. 56 | No. 36 |
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||||
C00029749
![]() |
Asperulosidic acid
|
CHEMBL389958
|
No. 100 | No. 36 |
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|||
C00030093
![]() |
Deacetylasperulosidic acid
|
CHEMBL459415
|
No. 100 | No. 36 |
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|||
C00031679
![]() |
Citrifolinin A
|
CHEMBL446254
|
No. 774 |
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||||
C00031680
![]() |
Yopaaoside A
/ (-)-Yopaaoside A |
No. 774 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P08246 | Neutrophil elastase | S1A | C00019420 | 2 / 1 |
P11473 | Vitamin D3 receptor | NR1I1 | C00019420 | 2 / 3 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00019420 | 0 / 0 |
P08311 | Cathepsin G | S1A | C00019420 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00019420 | 0 / 0 |
Q9H244 | P2Y purinoceptor 12 | Purine receptor | C00019420 | 1 / 1 |
P06280 | Alpha-galactosidase A | Enzyme | C00019420 | 1 / 1 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00019420 | 2 / 2 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00019420 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00019420 | 4 / 3 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00019420 | 0 / 0 |
P06239 | Tyrosine-protein kinase Lck | Src | C00019420 | 0 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00019420 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00019420 | 0 / 0 |
Q92731 | Estrogen receptor beta | NR3A2 | C00019420 | 0 / 1 |
P03372 | Estrogen receptor | NR3A1 | C00019420 | 1 / 1 |
P09619 | Platelet-derived growth factor receptor beta | Pdgfr | C00019420 | 5 / 1 |
P16234 | Platelet-derived growth factor receptor alpha | Pdgfr | C00019420 | 2 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
581 | BAX, BCL2L4 | BCL2-associated X protein |
C00019420
|
OMIM | preferred title | UniProt |
---|---|---|
#615007 | Basal ganglia calcification, idiopathic, 4; ibgc4 |
P09619
|
#609821 | Bleeding disorder, platelet-type, 8; bdplt8 |
Q9H244
|
#162800 | Cyclic neutropenia |
P08246
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#615363 | Estrogen resistance; estrr |
P03372
|
#301500 | Fabry disease |
P06280
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#606764 | Gastrointestinal stromal tumor; gist |
P16234
|
#607685 | Hypereosinophilic syndrome, idiopathic; hes |
P16234
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#607785 | Juvenile myelomonocytic leukemia; jmml |
P09619
|
#601626 | Leukemia, acute myeloid; aml |
P09619
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#131440 | Myeloproliferative disorder, chronic, with eosinophilia |
P09619
|
#228550 | Myofibromatosis, infantile, 1; imf1 |
P09619
|
#202700 | Neutropenia, severe congenital, 1, autosomal dominant; scn1 |
P08246
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG | name | UniProt |
---|---|---|
H00026 | Endometrial Cancer |
P03372
(marker)
Q92731 (marker) |
H00093 | Combined immunodeficiencies (CIDs) |
P06239
(related)
|
H00125 | Fabry disease |
P06280
(related)
|
H00100 | Neutropenic disorders |
P08246
(related)
|
H00042 | Glioma |
P09619
(related)
P16234 (related) |
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H01235 | Bleeding disorder platelet-type |
Q9H244
(related)
|