Species

KNApSAcK Entry

Organism name Salvia compressa
Genus Salvia
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Salvia
Linked NCBI taxonomy ID 21880
Linked level genus

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (1)

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
C00004632 External link 512 Quercetin 3-methyl ether
/ Quercetin 3-O-methyl ether
CHEMBL163316
32 / 21 / 21 No. 3 No. 15

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00004632 0 / 0
Q99700 Ataxin-2 Unclassified protein C00004632 1 / 1
P06746 DNA polymerase beta Enzyme C00004632 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00004632 1 / 1
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00004632 0 / 1
P04792 Heat shock protein beta-1 Unclassified protein C00004632 2 / 1
P54132 Bloom syndrome protein Enzyme C00004632 1 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00004632 1 / 0
P39748 Flap endonuclease 1 Enzyme C00004632 0 / 0
P42858 Huntingtin Unclassified protein C00004632 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00004632 2 / 0
O75496 Geminin Unclassified protein C00004632 0 / 0
P15121 Aldose reductase Enzyme C00004632 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00004632 1 / 1
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00004632 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00004632 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00004632 3 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00004632 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00004632 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00004632 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00004632 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00004632 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00004632 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00004632 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004632 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00004632 0 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00004632 0 / 0
O00255 Menin Unclassified protein C00004632 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00004632 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00004632 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00004632 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00004632 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (21)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#210900 Bloom syndrome; blm P54132
#606595 Charcot-marie-tooth disease, axonal, type 2f; cmt2f P04792
#114500 Colorectal cancer; crc P84022
Q14191
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#143100 Huntington disease; hd P42858
#145000 Hyperparathyroidism 1; hrpt1 O00255
#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
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#608634 Neuronopathy, distal hereditary motor, type iib; hmn2b P04792
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (21)

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)
H00856 Distal hereditary motor neuropathies (dHMN) P04792 (related)
H00079 Asthma P07550 (related)
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)
H00059 Huntington's disease (HD) P42858 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (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) 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)