Species

KNApSAcK Entry

Organism name Combretum micranthum
Genus Combretum
Family Combretaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Combretum micranthum
Linked NCBI taxonomy ID 578542
Linked level species

Family

Family in NCBI taxonomy Combretaceae
ID 3954

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Natural Activity

List (6)

Species Activity
Combretum micranthum G. Don Antibacterial
Combretum micranthum G. Don Antidote, opium
Combretum micranthum G. Don Antiemetic
Combretum micranthum G. Don Astringent
Combretum micranthum G. Don Choleretic
Combretum micranthum G. Don Diuretic

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
C00001345 External link 512 (-)-Betonicine
/ 4-Hydroxyproline betaine
CHEMBL1181451
CHEMBL1373466
CHEMBL1996398
7 / 16 / 14 No. 2627 No. 1
C00002074 External link 512 Stachydrine
CHEMBL394450
CHEMBL1456892
CHEMBL1986864
10 / 8 / 12 No. 2627 No. 1
C00007298 External link 512 Choline
CHEMBL920
D002794
11 / 5 / 5 51 / 20 No. 5945

Human Protein / Gene in interactions

18 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001345 C00002074 C00007298 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001345 C00002074 C00007298 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001345 C00002074 C00007298 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001345 C00002074 C00007298 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001345 C00002074 C00007298 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00001345 3 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00002074 3 / 2
Q92830 Histone acetyltransferase KAT2A Enzyme C00002074 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002074 0 / 0
P02545 Prelamin-A/C Unclassified protein C00001345 11 / 10
P22303 Acetylcholinesterase Hydrolase C00007298 1 / 0
O15245 Solute carrier family 22 member 1 Drug uniporter C00007298 0 / 0
O15244 Solute carrier family 22 member 2 Drug uniporter C00007298 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00007298 0 / 0
O00255 Menin Unclassified protein C00002074 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002074 1 / 2
Q9H015 Solute carrier family 22 member 4 Unclassified protein C00007298 1 / 1
O76082 Solute carrier family 22 member 5 Unclassified protein C00007298 1 / 2

51 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
43 ACHE, ACEE, ARACHE, N-ACHE, YT acetylcholinesterase (EC:3.1.1.7) C00007298
8854 ALDH1A2, RALDH(II), RALDH2, RALDH2-T aldehyde dehydrogenase 1 family, member A2 (EC:1.2.1.36) C00007298
64333 ARHGAP9, 10C, RGL1 Rho GTPase activating protein 9 C00007298
590 BCHE, CHE1, CHE2, E1 butyrylcholinesterase (EC:3.1.1.8) C00007298
701 BUB1B, BUB1beta, BUBR1, Bub1A, MAD3L, MVA1, SSK1, hBUBR1 BUB1 mitotic checkpoint serine/threonine kinase B (EC:2.7.11.1) C00007298
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00007298
9332 CD163, M130, MM130 CD163 molecule C00007298
948 CD36, BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV, PASIV, SCARB3 CD36 molecule (thrombospondin receptor) C00007298
55143 CDCA8, BOR, BOREALIN, DasraB, MESRGP cell division cycle associated 8 C00007298
55349 CHDH choline dehydrogenase (EC:1.1.99.1) C00007298
1111 CHEK1, CHK1 checkpoint kinase 1 (EC:2.7.11.1) C00007298
1137 CHRNA4, BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 cholinergic receptor, nicotinic, alpha 4 (neuronal) C00007298
1139 CHRNA7, CHRNA7-2, NACHRA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) C00007298
1141 CHRNB2, EFNL3, nAChRB2 cholinergic receptor, nicotinic, beta 2 (neuronal) C00007298
81035 COLEC12, CLP1, NSR2, SCARA4, SRCL collectin sub-family member 12 C00007298
1440 CSF3, C17orf33, CSF3OS, GCSF, G-CSF colony stimulating factor 3 (granulocyte) C00007298
1471 CST3, ARMD11 cystatin C C00007298
1514 CTSL, CATL, CTSL1, MEP cathepsin L (EC:3.4.22.15) C00007298
1524 CX3CR1, CCRL1, CMKBRL1, CMKDR1, GPR13, GPRV28, V28 chemokine (C-X3-C motif) receptor 1 C00007298
1794 DOCK2 dedicator of cytokinesis 2 C00007298
3169 FOXA1, HNF3A, TCF3A forkhead box A1 C00007298
2632 GBE1, APBD, GBE, GSD4 glucan (1,4-alpha-), branching enzyme 1 (EC:2.4.1.18) C00007298
3003 GZMK, TRYP2 granzyme K (granzyme 3; tryptase II) (EC:3.4.21.-) C00007298
3309 HSPA5, BIP, GRP78, MIF2 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) C00007298
396742 C00007298
3560 IL2RB, CD122, IL15RB, P70-75 interleukin 2 receptor, beta C00007298
10112 KIF20A, MKLP2, RAB6KIFL kinesin family member 20A C00007298
9493 KIF23, CHO1, KNSL5, MKLP-1, MKLP1 kinesin family member 23 C00007298
51348 KLRF1, CLEC5C, NKp80 killer cell lectin-like receptor subfamily F, member 1 C00007298
114569 MAL2 mal, T-cell differentiation protein 2 (gene/pseudogene) C00007298
55016 MARCH1, MARCH-I, RNF171 membrane-associated ring finger (C3HC4) 1, E3 ubiquitin protein ligase C00007298
4256 MGP, MGLAP, NTI matrix Gla protein C00007298
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00007298
4522 MTHFD1, MTHFC, MTHFD methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase (EC:1.5.1.5 6.3.4.3 3.5.4.9) C00007298
9172 MYOM2, TTNAP myomesin 2 C00007298
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00007298
11333 PDAP1, HASPP28, PAP, PAP1 PDGFA associated protein 1 C00007298
10400 PEMT, PEAMT, PEMPT, PEMT2, PNMT phosphatidylethanolamine N-methyltransferase (EC:2.1.1.17 2.1.1.71) C00007298
5329 PLAUR, CD87, U-PAR, UPAR, URKR plasminogen activator, urokinase receptor C00007298
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00007298
23532 PRAME, CT130, MAPE, OIP-4, OIP4 preferentially expressed antigen in melanoma C00007298
5790 PTPRCAP, CD45-AP, LPAP protein tyrosine phosphatase, receptor type, C-associated protein C00007298
10287 RGS19, GAIP, RGSGAIP regulator of G-protein signaling 19 C00007298
57140 RNPEPL1 arginyl aminopeptidase (aminopeptidase B)-like 1 C00007298
6422 SFRP1, FRP, FRP-1, FRP1, FrzA, SARP2 secreted frizzled-related protein 1 C00007298
6584 SLC22A5, CDSP, OCTN2, OCTN2VT solute carrier family 22 (organic cation/carnitine transporter), member 5 C00007298
9056 SLC7A7, LAT3, LPI, MOP-2, Y+LAT1, y+LAT-1 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 C00007298
6594 SMARCA1, ISWI, NURF140, SNF2L, SNF2L1, SNF2LB, SNF2LT, SWI, SWI2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 C00007298
7015 TERT, CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1, TP2, TRT, hEST2, hTRT telomerase reverse transcriptase (EC:2.7.7.49) C00007298
7128 TNFAIP3, A20, OTUD7C, TNFA1P2 tumor necrosis factor, alpha-induced protein 3 (EC:3.4.19.12) C00007298
83549 UCK1, URK1 uridine-cytidine kinase 1 (EC:2.7.1.48) C00007298

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#212140 Carnitine deficiency, systemic primary; cdsp O76082
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545
#180300 Rheumatoid arthritis; ra Q9H015
#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 (25)

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)
H00286 Crohn's disease O76082 (related)
Q9H015 (related)
H00525 Disorders of fatty-acid oxidation O76082 (related)
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)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (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)

Diseases related to CTD interactions

20 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00007298
D001321 Autistic Disorder C00007298
D006528 Carcinoma, Hepatocellular C00007298
D003072 Cognition Disorders C00007298
D003866 Depressive Disorder C00007298
D002658 Developmental Disabilities C00007298
D056486 Drug-Induced Liver Injury C00007298
D005234 Fatty Liver C00007298
D005235 Fatty Liver, Alcoholic C00007298
D006505 Hepatitis C00007298
D007249 Inflammation C00007298
D007859 Learning Disorders C00007298
D008103 Liver Cirrhosis C00007298
D008113 Liver Neoplasms C00007298
D008569 Memory Disorders C00007298
C541083 Non-alcoholic Fatty Liver Disease C00007298
D010195 Pancreatitis C00007298
D016137 Spina Bifida Cystica C00007298
D013226 Status Epilepticus C00007298
D052878 Urolithiasis C00007298