Species

KNApSAcK Entry

Organism name Diascia vigilis
Genus Diascia
Family Scrophulariaceae
Kingdom Plantae

Metabolite list (3)

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
C00001238 External link 512 Stearic acid
CHEMBL46403
C031183
15 / 17 / 19 6 / 1 No. 184 No. 68
C00001233 External link 512 Palmitic acid
CHEMBL82293
D019308
16 / 8 / 8 35 / 1 No. 184 No. 68
C00001228 External link 512 Myristic acid
/ Tetradecanoic acid
/ n-Tetradecanoic acid
CHEMBL111077
D019814
17 / 9 / 10 3 / 0 No. 1141 No. 68

Human Protein / Gene in interactions

38 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00001228 C00001233 C00001238 2 / 2
Q96RI1 Bile acid receptor NR1H4 C00001228 C00001233 0 / 0
P15090 Fatty acid-binding protein, adipocyte Other cytosolic protein C00001233 C00001238 0 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00001228 C00001233 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001228 C00001238 1 / 1
O60603 Toll-like receptor 2 Membrane receptor C00001228 C00001233 1 / 1
P04150 Glucocorticoid receptor NR3C1 C00001233 C00001238 0 / 1
O75496 Geminin Unclassified protein C00001228 C00001233 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00001228 C00001238 2 / 3
Q9UGP5 DNA polymerase lambda Enzyme C00001238 0 / 0
P08183 Multidrug resistance protein 1 drug C00001233 1 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00001228 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00001228 2 / 2
P39748 Flap endonuclease 1 Enzyme C00001228 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001228 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00001238 3 / 1
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00001238 0 / 0
P12104 Fatty acid-binding protein, intestinal Other cytosolic protein C00001233 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001228 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00001233 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001228 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001233 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00001238 3 / 2
P08047 Transcription factor Sp1 Unclassified protein C00001233 0 / 0
P05413 Fatty acid-binding protein, heart Other cytosolic protein C00001233 0 / 0
Q01469 Fatty acid-binding protein, epidermal Other cytosolic protein C00001233 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001238 3 / 3
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00001228 0 / 0
P03372 Estrogen receptor NR3A1 C00001233 1 / 1
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00001238 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00001238 0 / 0
P10275 Androgen receptor NR3C4 C00001233 3 / 4
Q05193 Dynamin-1 Structural C00001228 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001238 0 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00001228 0 / 0
O00255 Menin Unclassified protein C00001238 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001238 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001228 1 / 1

36 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00001228 C00001233 C00001238
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00001228 C00001233 C00001238
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001233 C00001238
1906 EDN1, ET1, HDLCQ7, PPET1 endothelin 1 C00001233 C00001238
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00001233 C00001238
9619 ABCG1, ABC8, WHITE1 ATP-binding cassette, sub-family G (WHITE), member 1 C00001233 C00001238
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00001233
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00001233
581 BAX, BCL2L4 BCL2-associated X protein C00001233
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00001233
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00001233
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00001233
1374 CPT1A, CPT1, CPT1-L, L-CPT1 carnitine palmitoyltransferase 1A (liver) (EC:2.3.1.21) C00001233
2876 GPX1, GPXD, GSHPX1 glutathione peroxidase 1 (EC:1.11.1.9) C00001233
3034 HAL, HIS, HSTD histidine ammonia-lyase (EC:4.3.1.3) C00001233
57817 HAMP, HEPC, HFE2B, LEAP1, PLTR hepcidin antimicrobial peptide C00001233
3481 IGF2, C11orf43, IGF-II, PP9974 insulin-like growth factor 2 (somatomedin A) C00001233
3630 INS, IDDM2, ILPR, IRDN, MODY10 insulin C00001233
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00001233
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00001233
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00001233
4493 MT1E, MT1, MTD metallothionein 1E C00001233
4494 MT1F, MT1 metallothionein 1F C00001233
4496 MT1H, MT-0, MT-1H, MT-IH, MT1 metallothionein 1H C00001233
4501 MT1X, MT-1l, MT1 metallothionein 1X C00001233
4502 MT2A, MT2 metallothionein 2A C00001233
4843 NOS2, HEP-NOS, INOS, NOS, NOS2A nitric oxide synthase 2, inducible (EC:1.14.13.39) C00001233
3651 PDX1, GSF, IDX-1, IPF1, IUF1, MODY4, PDX-1, STF-1 pancreatic and duodenal homeobox 1 C00001233
29893 PSMC3IP, GT198, HOP2, HUMGT198A, ODG3, TBPIP PSMC3 interacting protein C00001233
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00001233
5054 SERPINE1, PAI, PAI-1, PAI1, PLANH1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 C00001233
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00001233
23216 TBC1D1, TBC, TBC1 TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1 C00001233
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00001233
7351 UCP2, BMIQ4, SLC25A8, UCPH uncoupling protein 2 (mitochondrial, proton carrier) C00001233
199974 CYP4Z1, CYP4A20 cytochrome P450, family 4, subfamily Z, polypeptide 1 (EC:1.14.14.1) C00001228

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (26)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#615363 Estrogen resistance; estrr P03372
#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
#612244 Inflammatory bowel disease 13; ibd13 P08183
#246300 Leprosy, susceptibility to, 3; lprs3 O60603
#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
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (28)

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)
H00344 Leprosy O60603 (related)
H00026 Endometrial Cancer P03372 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00794 Aromatase excess syndrome P11511 (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)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003072 Cognition Disorders C00001238
C00001233