Species

KNApSAcK Entry

Organism name Esenbeckia yaxhoob Lundell
Genus Esenbeckia
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Rutaceae
Linked NCBI taxonomy ID 23513
Linked level family

Family

Family in NCBI taxonomy Rutaceae
ID 23513

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (5)

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
C00003749 External link 512 Lupeol
/ Lupenol
/ (+)-Lupenol
CHEMBL289191
CHEMBL459702
C010480
3 / 0 / 0 2 / 6 No. 23 No. 51
C00000970 External link 512 Hesperidin
CHEMBL265606
CHEMBL449317
CHEMBL1314714
CHEMBL1328143
CHEMBL1535112
CHEMBL1574000
CHEMBL2140112
D006569
24 / 9 / 14 10 / 5 No. 48 No. 14
C00002477 External link 512 Imperatorin
CHEMBL453805
C031534
18 / 7 / 6 1 / 1 No. 606 No. 25
C00035530 External link 512 Asarinin
C006637
No. 621 No. 21
C00036263 External link 512 2-Tridecanone
CHEMBL480097
C009541
No. 1611

Human Protein / Gene in interactions

41 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P83916 Chromobox protein homolog 1 Unclassified protein C00000970 C00002477 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000970 C00002477 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00000970 C00002477 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000970 C00002477 0 / 1
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002477 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000970 0 / 0
P62158 Calmodulin Unclassified protein C00000970 1 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003749 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00002477 0 / 0
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00002477 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000970 0 / 1
Q9GZU7 Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 Enzyme C00000970 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00003749 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003749 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00002477 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00002477 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002477 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00000970 1 / 1
P11308 Transcriptional regulator ERG Unclassified protein C00000970 1 / 2
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000970 1 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002477 1 / 1
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00002477 0 / 0
P56817 Beta-secretase 1 A1A C00002477 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000970 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000970 1 / 1
P06746 DNA polymerase beta Enzyme C00000970 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000970 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00002477 2 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000970 0 / 0
Q9Y251 Heparanase Enzyme C00000970 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000970 0 / 0
O00167 Eyes absent homolog 2 Enzyme C00002477 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002477 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000970 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002477 1 / 0
O00255 Menin Unclassified protein C00000970 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000970 1 / 2
Q02410 Amyloid beta A4 precursor protein-binding family A member 1 Unclassified protein C00000970 0 / 0
Q00975 Voltage-dependent N-type calcium channel subunit alpha-1B N-TYPE C00000970 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000970 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002477 1 / 1

13 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1499 CTNNB1, CTNNB, MRD19, armadillo catenin (cadherin-associated protein), beta 1, 88kDa C00003749
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) C00003749
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00002477
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00000970
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00000970
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00000970
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00000970
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00000970
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00000970
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00000970
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00000970
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00000970
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00000970

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (16)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#612219 Ewing sarcoma; es P11308
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#614916 Ventricular tachycardia, catecholaminergic polymorphic, 4; cpvt4 P62158
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (19)

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)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P11308 (related)
H00035 Ewing's sarcoma P11308 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

11 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00002477
C00000970
D014947 Wounds and Injuries C00003749
D006937 Hypercholesterolemia C00003749
D009374 Neoplasms, Experimental C00003749
D012878 Skin Neoplasms C00003749
D009202 Cardiomyopathies C00003749
D006528 Carcinoma, Hepatocellular C00003749
D058186 Acute Kidney Injury C00000970
D055371 Acute Lung Injury C00000970
D008171 Lung Diseases C00000970
D012128 Respiratory Distress Syndrome, Adult C00000970