Species

KNApSAcK Entry

Organism name Salvia carnosa
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
C00003410 External link 512 Carnosol
CHEMBL218693
CHEMBL1514916
C068623
17 / 17 / 17 12 / 0 No. 734 No. 40

Human Protein / Gene in interactions

17 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00003410 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003410 2 / 0
Q9Y5X4 Photoreceptor-specific nuclear receptor NR2E3 C00003410 2 / 2
P37840 Alpha-synuclein Unclassified protein C00003410 4 / 2
P11473 Vitamin D3 receptor NR1I1 C00003410 2 / 3
P39748 Flap endonuclease 1 Enzyme C00003410 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00003410 0 / 0
P11413 Glucose-6-phosphate 1-dehydrogenase Enzyme C00003410 1 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00003410 2 / 0
O75496 Geminin Unclassified protein C00003410 0 / 0
P16233 Pancreatic triacylglycerol lipase Hydrolase C00003410 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00003410 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00003410 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00003410 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00003410 0 / 0
O00255 Menin Unclassified protein C00003410 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003410 1 / 2

12 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
196 AHR, bHLHe76 aryl hydrocarbon receptor C00003410
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00003410
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00003410
2729 GCLC, GCL, GCS, GLCL, GLCLC glutamate-cysteine ligase, catalytic subunit (EC:6.3.2.2) C00003410
2730 GCLM, GLCLR glutamate-cysteine ligase, modifier subunit (EC:6.3.2.2) C00003410
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00003410
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00003410
3551 IKBKB, IKK-beta, IKK2, IKKB, NFKBIKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta (EC:2.7.11.10) C00003410
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00003410
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00003410
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00003410
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00003410

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

OMIM preferred title UniProt
#300908 Anemia, nonspherocytic hemolytic, due to g6pd deficiency P11413
#114500 Colorectal cancer; crc P84022
#127750 Dementia, lewy body; dlb P37840
#268100 Enhanced s-cone syndrome; escs Q9Y5X4
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#611131 Retinitis pigmentosa 37; rp37 Q9Y5X4
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (17)

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)
H00101 Other phagocyte defects P11413 (related)
H00668 Anemia due to disorders of glutathione metabolism P11413 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (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)
H00527 Retinitis pigmentosa (RP) Q9Y5X4 (related)
H00805 Vitreoretinal degeneration Q9Y5X4 (related)