Species

KNApSAcK Entry

Organism name Nicotiana cavicola
Genus Nicotiana
Family Solanaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Nicotiana cavicola
Linked NCBI taxonomy ID 118690
Linked level species

Family

Family in NCBI taxonomy Solanaceae
ID 4070

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (6)

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
C00003110 External link 512 Caryophyllene
/ (E)-Caryophyllene
/ beta-Caryophyllene
/ (-)-(E)-Caryophyllene
/ (E)-beta-Caryophyllene
CHEMBL445740
CHEMBL448700
2 / 3 / 7 No. 478 No. 38
C00035115 External link 512 Benzenepropanol
/ 3-Phenylpropanol
/ Hydrocinnamic alcohol
CHEMBL1606391
C016655
3 / 1 / 4 No. 885
C00035128 External link 512 m-Cresol
/ m-Oxytoluene
CHEMBL298312
C042041
6 / 4 / 1 1 / 3 No. 1546
C00035059 External link 512 Benzyl salicylate
CHEMBL460124
C039672
9 / 6 / 4 3 / 0 No. 2308
C00019221 External link 512 Benzyl benzoate
CHEMBL1239
C006723
12 / 5 / 8 3 / 2 No. 2308
C00034054 External link 512 Methyl benzoate
CHEMBL16435
C044605
4 / 6 / 6 No. 4170

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00019221 C00034054 C00035059 C00035128 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00035115 C00035128 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00019221 C00035059 1 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00035059 C00035128 3 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00019221 C00035115 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00019221 C00035115 1 / 4
O75164 Lysine-specific demethylase 4A Enzyme C00019221 C00035059 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00019221 C00035059 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003110 C00019221 1 / 2
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00019221 0 / 0
O75496 Geminin Unclassified protein C00035059 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00035128 0 / 0
P10145 Interleukin-8 Secreted protein C00034054 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00019221 0 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00035059 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00035059 0 / 0
P22303 Acetylcholinesterase Hydrolase C00035128 1 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00019221 1 / 1
P40925 Malate dehydrogenase, cytoplasmic Enzyme C00019221 0 / 0
P10275 Androgen receptor NR3C4 C00034054 3 / 4
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00035128 0 / 0
P30556 Type-1 angiotensin II receptor Angiotensin receptor C00019221 1 / 1
O00255 Menin Unclassified protein C00003110 2 / 5
P16473 Thyrotropin receptor Glycohormone receptor C00034054 3 / 2
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00035059 2 / 2

4 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00019221 C00035059
2100 ESR2, ER-BETA, ESR-BETA, ESRB, ESTRB, Erb, NR3A2 estrogen receptor 2 (ER beta) C00019221 C00035059
7031 TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 trefoil factor 1 C00019221 C00035059
6329 SCN4A, HOKPP2, HYKPP, HYPP, NAC1A, Na(V)1.4, Nav1.4, SkM1 sodium channel, voltage-gated, type IV, alpha subunit C00035128

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (19)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#613688 Long qt syndrome 2; lqt2 Q12809
%300852 Mental retardation, x-linked 88; mrx88 P50052
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#267430 Renal tubular dysgenesis; rtd P30556
#609620 Short qt syndrome 1; sqt1 Q12809
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#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
#112100 Yt blood group antigen P22303

KEGG DISEASE (22)

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)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00575 Renal tubular dysgenesis P30556 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (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)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003877 Dermatitis, Contact C00019221
D012532 Scabies C00019221
D002057 Burns, Chemical C00035128
D056486 Drug-Induced Liver Injury C00035128
D006967 Hypersensitivity C00035128