Species

KNApSAcK Entry

Organism name Stenocereus eruca
Genus Stenocereus
Family Cactaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Stenocereus eruca
Linked NCBI taxonomy ID 867530
Linked level species

Family

Family in NCBI taxonomy Cactaceae
ID 3593

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (11)

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
C00032378 External link 512 Treleasegenic acid
CHEMBL1904698
3 / 2 / 3 No. 13 No. 51
C00019064 External link 512 Oleanolic acid
/ Astrantiagenin C
/ Virgaureagenin B
/ 3beta-Hydroxyolean-12-en-28-oic acid
CHEMBL56615
CHEMBL168
CHEMBL180553
CHEMBL365375
CHEMBL486382
CHEMBL1413646
CHEMBL1436454
D009828
30 / 8 / 12 21 / 15 No. 13 No. 51
C00031116 External link 512 Queretaroic acid
CHEMBL1733823
CHEMBL1886861
4 / 0 / 0 No. 13 No. 51
C00030794 External link 512 Morolic acid
CHEMBL463665
3 / 0 / 0 No. 13 No. 51
C00030702 External link 512 Machaerogenin
CHEMBL1710708
1 / 0 / 0 No. 13 No. 51
C00030701 External link 512 Machaeroceric acid
No. 23 No. 51
C00029446 External link 512 22beta-Hydroxystellatogenin
No. 23 No. 51
C00029445 External link 512 21-ketobetulinic acid
No. 23 No. 51
C00032200 External link 512 Stellatogenin
CHEMBL2144823
2 / 4 / 2 No. 23 No. 51
C00032354 External link 512 Thurberogenin
No. 23 No. 51
C00003741 External link 512 Betulinic acid
CHEMBL269277
CHEMBL71690
CHEMBL519059
CHEMBL1318530
CHEMBL2005635
C002070
34 / 17 / 14 10 / 2 No. 23 No. 51

Human Protein / Gene in interactions

60 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00003741 C00019064 C00032200 C00032378 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00003741 C00031116 C00032378 0 / 0
P24666 Low molecular weight phosphotyrosine protein phosphatase Tyr C00019064 C00030794 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00003741 C00019064 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00019064 C00031116 0 / 0
P06746 DNA polymerase beta Enzyme C00003741 C00019064 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00019064 C00030794 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00003741 C00019064 0 / 0
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00003741 C00019064 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003741 C00019064 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003741 C00019064 0 / 0
P15121 Aldose reductase Enzyme C00003741 C00019064 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00019064 C00031116 0 / 0
P10586 Receptor-type tyrosine-protein phosphatase F Receptor tyrosine-protein phosphatase C00019064 C00030794 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003741 0 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003741 0 / 1
P15559 NAD(P)H dehydrogenase [quinone] 1 Enzyme C00003741 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00003741 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003741 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00032378 2 / 3
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00019064 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00003741 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00019064 0 / 0
P08151 Zinc finger protein GLI1 Unclassified protein C00003741 0 / 0
Q02156 Protein kinase C epsilon type Eta C00003741 0 / 0
P37840 Alpha-synuclein Unclassified protein C00032200 4 / 2
P02545 Prelamin-A/C Unclassified protein C00003741 11 / 10
Q06124 Tyrosine-protein phosphatase non-receptor type 11 Tyr C00019064 4 / 2
P51684 C-C chemokine receptor type 6 CC chemokine receptor C00030702 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00003741 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00003741 1 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00019064 0 / 3
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00003741 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00019064 2 / 2
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003741 2 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00003741 0 / 0
P18433 Receptor-type tyrosine-protein phosphatase alpha Receptor tyrosine-protein phosphatase C00019064 0 / 0
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00019064 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003741 0 / 0
P55055 Oxysterols receptor LXR-beta NR1H3 C00003741 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00019064 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00003741 0 / 0
P05771 Protein kinase C beta type Alpha C00003741 0 / 0
P35228 Nitric oxide synthase, inducible Enzyme C00019064 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003741 1 / 1
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00019064 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003741 1 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00031116 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00019064 0 / 0
P17706 Tyrosine-protein phosphatase non-receptor type 2 Tyr C00019064 0 / 1
P29350 Tyrosine-protein phosphatase non-receptor type 6 Tyr C00019064 0 / 0
P04054 Phospholipase A2 Enzyme C00019064 0 / 0
P23469 Receptor-type tyrosine-protein phosphatase epsilon Receptor tyrosine-protein phosphatase C00019064 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00003741 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00003741 1 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00003741 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00019064 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00019064 1 / 4
Q9UBT2 SUMO-activating enzyme subunit 2 Enzyme C00003741 0 / 0
Q9UBE0 SUMO-activating enzyme subunit 1 Unclassified protein C00003741 0 / 0

26 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00003741 C00019064
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00003741 C00019064
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00003741 C00019064
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00003741 C00019064
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00003741 C00019064
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00019064
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00003741
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00003741
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00003741
581 BAX, BCL2L4 BCL2-associated X protein C00003741
177 AGER, RAGE advanced glycosylation end product-specific receptor C00019064
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00019064
847 CAT catalase (EC:1.11.1.6) C00019064
1956 EGFR, ERBB, ERBB1, HER1, PIG61, mENA epidermal growth factor receptor (EC:2.7.10.1) C00003741
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00019064
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00019064
3065 HDAC1, GON-10, HD1, RPD3, RPD3L1 histone deacetylase 1 (EC:3.5.1.98) C00019064
3146 HMGB1, HMG1, HMG3, SBP-1 high mobility group box 1 C00019064
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00019064
4233 MET, AUTS9, HGFR, RCCP2, c-Met met proto-oncogene (EC:2.7.10.1) C00019064
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00019064
5052 PRDX1, MSP23, NKEF-A, NKEFA, PAG, PAGA, PAGB, PRX1, PRXI, TDPX2 peroxiredoxin 1 (EC:1.11.1.15) C00019064
5728 PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) C00019064
6401 SELE, CD62E, ELAM, ELAM1, ESEL, LECAM2 selectin E C00019064
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00019064
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00019064

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (31)

OMIM preferred title UniProt
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#127750 Dementia, lewy body; dlb P37840
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#607785 Juvenile myelomonocytic leukemia; jmml Q06124
#151100 Leopard syndrome 1 Q06124
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#611162 Malaria, susceptibility to P35228
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#156250 Metachondromatosis; metcds Q06124
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#163950 Noonan syndrome 1; ns1 Q06124
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (31)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00036 Osteosarcoma P08684 (marker)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00408 Type I diabetes mellitus P17706 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35228 (related)
P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (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)
H00523 Noonan syndrome and related disorders Q06124 (related)
H01018 Metachondromatosis Q06124 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

16 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008103 Liver Cirrhosis C00003741
C00019064
D007674 Kidney Diseases C00019064
D002252 Carbon Tetrachloride Poisoning C00019064
D056486 Drug-Induced Liver Injury C00019064
D050171 Dyslipidemias C00019064
D018149 Glucose Intolerance C00019064
D006949 Hyperlipidemias C00019064
D007249 Inflammation C00019064
D008545 Melanoma C00003741
D008106 Liver Cirrhosis, Experimental C00019064
D008107 Liver Diseases C00019064
D017202 Myocardial Ischemia C00019064
D009369 Neoplasms C00019064
D009765 Obesity C00019064
D011041 Poisoning C00019064
D011230 Precancerous Conditions C00019064