Organism name | Vinca minor |
---|---|
Genus | Vinca |
Family | Apocynaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Vinca minor |
---|---|
Linked NCBI taxonomy ID | 60093 |
Linked level | species |
Family in NCBI taxonomy | Apocynaceae |
---|---|
ID | 4056 |
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 |
---|---|---|---|---|---|---|---|---|
C00005747
![]() |
Myricetin 3-robinobioside-7-rhamnoside
|
No. 5 | No. 15 |
![]() |
||||
C00005461
![]() |
Clovin
/ Quercetin 3-robinobioside-7-rhamnoside |
No. 5 | No. 15 |
![]() |
||||
C00002631
![]() |
(+)-Lirioresinol B
/ (+)-Syringaresinol |
CHEMBL361362
CHEMBL402653 |
C042192
|
1 / 0 / 0 | No. 38 | No. 21 |
![]() |
|
C00024482
![]() |
11-Methoxyvincadifformine
/ 6,7-Dihydro-11-methoxytabersonine |
No. 61 | No. 4 |
![]() |
||||
C00025069
![]() |
Vincareine
/ (+)-Vincaminine |
No. 452 | No. 4 |
![]() |
||||
C00025042
![]() |
(-)-16-Epivincamine
/ (-)-cis-Epivincamine |
CHEMBL1165342
CHEMBL1361052 CHEMBL1592905 CHEMBL1604925 CHEMBL1728279 |
27 / 24 / 25 | No. 452 | No. 4 |
![]() |
||
C00025070
![]() |
(+)-Vincinine
|
No. 452 | No. 4 |
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||||
C00025041
![]() |
(-)-11-Methoxyeburnamonine
|
No. 502 | No. 4 |
![]() |
||||
C00001714
![]() |
Eburnamonine
|
CHEMBL1318553
CHEMBL1553441 CHEMBL1733074 CHEMBL1892145 |
14 / 20 / 16 | No. 502 | No. 4 |
![]() |
||
C00025061
![]() |
(+)-Eburnamenine
|
CHEMBL1097688
|
No. 502 | No. 4 |
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|||
C00025062
![]() |
(+)-Isoeburnamine
|
CHEMBL2104946
|
No. 502 | No. 4 |
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|||
C00024291
![]() |
21-Deoxyvomilenine
|
No. 523 | No. 4 |
![]() |
||||
C00024313
![]() |
Vinorine
/ (-)-Vinorine / 21-Deoxyvomilenine |
No. 523 | No. 4 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001714 C00025042 | 1 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00001714 C00025042 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001714 C00025042 | 0 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001714 C00025042 | 1 / 1 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001714 C00025042 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001714 C00025042 | 0 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00025042 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00001714 | 11 / 10 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00025042 | 1 / 0 |
P11387 | DNA topoisomerase 1 | Isomerase | C00002631 | 0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00025042 | 2 / 3 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00025042 | 2 / 2 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00025042 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00025042 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00001714 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00001714 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00001714 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00025042 | 7 / 3 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00001714 | 3 / 2 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00001714 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00025042 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00025042 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00025042 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00025042 | 1 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00001714 | 1 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00025042 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00025042 | 4 / 3 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00025042 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00025042 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001714 | 1 / 0 |
Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00025042 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00025042 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00025042 | 1 / 2 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00025042 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00025042 | 1 / 4 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00025042 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#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)
|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (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)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(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)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|