Organism name | Caesalpinia violacea |
---|---|
Genus | Caesalpinia |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Caesalpinia violacea |
---|---|
Linked NCBI taxonomy ID | 508994 |
Linked level | species |
Family in NCBI taxonomy | Fabaceae |
---|---|
ID | 3803 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
---|---|---|---|---|---|---|---|---|
C00010268
![]() |
Brazilin
|
CHEMBL598951
CHEMBL1370456 |
C044362
|
32 / 25 / 25 | No. 1670 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00010268 | 1 / 1 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00010268 | 2 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00010268 | 0 / 0 |
P14735 | Insulin-degrading enzyme | Enzyme | C00010268 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00010268 | 3 / 1 |
P11473 | Vitamin D3 receptor | NR1I1 | C00010268 | 2 / 3 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00010268 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00010268 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00010268 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00010268 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00010268 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00010268 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00010268 | 1 / 1 |
P11308 | Transcriptional regulator ERG | Unclassified protein | C00010268 | 1 / 2 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00010268 | 0 / 0 |
P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00010268 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00010268 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00010268 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00010268 | 3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00010268 | 2 / 2 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00010268 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00010268 | 0 / 1 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00010268 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00010268 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00010268 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00010268 | 0 / 0 |
Q14145 | Kelch-like ECH-associated protein 1 | Unclassified protein | C00010268 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00010268 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00010268 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00010268 | 1 / 2 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00010268 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00010268 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#119900 | Digital clubbing, isolated congenital |
P15428
|
#612219 | Ewing sarcoma; es |
P11308
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00024 | Prostate cancer |
P11308
(related)
|
H00035 | Ewing's sarcoma |
P11308
(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)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|