Organism name | Aristolochia yunnanensis |
---|---|
Genus | Aristolochia |
Family | Aristolochiaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Aristolochia |
---|---|
Linked NCBI taxonomy ID | 12947 |
Linked level | genus |
Family in NCBI taxonomy | Aristolochiaceae |
---|---|
ID | 16727 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Magnoliophyta |
---|---|
ID | 3398 |
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 |
---|---|---|---|---|---|---|---|---|
C00012170
![]() |
Melampolide
|
CHEMBL86416
CHEMBL190377 CHEMBL1575037 |
10 / 7 / 15 | No. 107 | No. 38 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00012170 | 0 / 3 |
P11473 | Vitamin D3 receptor | NR1I1 | C00012170 | 2 / 3 |
Q04206 | Transcription factor p65 | Transcription Factor | C00012170 | 0 / 0 |
P03372 | Estrogen receptor | NR3A1 | C00012170 | 1 / 1 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00012170 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00012170 | 1 / 1 |
O00255 | Menin | Unclassified protein | C00012170 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00012170 | 1 / 2 |
Q00653 | Nuclear factor NF-kappa-B p100 subunit | Transcription Factor | C00012170 | 0 / 0 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00012170 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#615363 | Estrogen resistance; estrr |
P03372
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
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)
|
H00026 | Endometrial Cancer |
P03372
(marker)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(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)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|