Organism name | Luma chequen |
---|---|
Genus | Luma |
Family | Myrtaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Luma chequen |
---|---|
Linked NCBI taxonomy ID | 375239 |
Linked level | species |
Family in NCBI taxonomy | Myrtaceae |
---|---|
ID | 3931 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
Species | Activity |
---|---|
Luma chequen (Molina) A. Gray. | Antibacterial |
Luma chequen (Molina) A. Gray. | Antihypertensive |
Luma chequen (Molina) A. Gray. | Astringent |
Luma chequen (Molina) A. Gray. | Astringent |
Luma chequen (Molina) A. Gray. | Bactericide |
Luma chequen (Molina) A. Gray. | Digestive |
Luma chequen (Molina) A. Gray. | Digestive |
Luma chequen (Molina) A. Gray. | Diuretic |
Luma chequen (Molina) A. Gray. | Diuretic |
Luma chequen (Molina) A. Gray. | Expectorant |
Luma chequen (Molina) A. Gray. | Expectorant |
Luma chequen (Molina) A. Gray. | Fungicide |
Luma chequen (Molina) A. Gray. | Fungicide |
Luma chequen (Molina) A. Gray. | Hypotensive |
Luma chequen (Molina) A. Gray. | Tonic |
Luma chequen (Molina) A. Gray. | Tonic |
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 |
---|---|---|---|---|---|---|---|---|
C00005728
![]() |
Myricetin 3-galactoside
/ Myricetin 3-O-galactoside |
CHEMBL462244
CHEMBL1221722 |
No. 2 | No. 15 |
![]() |
|||
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 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00005730 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00005730 | 1 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00005730 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00005730 | 1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005730 | 0 / 0 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005730 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00005730 | 1 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00005730 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | 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 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00005730 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00005730 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005730 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00005730 | 4 / 3 |
P34949 | Mannose-6-phosphate isomerase | Enzyme | C00005730 | 1 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00005730 | 0 / 0 |
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 |
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 |
OMIM | preferred title | UniProt |
---|---|---|
#602579 | Congenital disorder of glycosylation, type ib; cdg1b |
P34949
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#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
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
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)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|