Organism name | Combretum micranthum |
---|---|
Genus | Combretum |
Family | Combretaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Combretum micranthum |
---|---|
Linked NCBI taxonomy ID | 578542 |
Linked level | species |
Family in NCBI taxonomy | Combretaceae |
---|---|
ID | 3954 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
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
![]() |
(-)-Betonicine
/ 4-Hydroxyproline betaine |
CHEMBL1181451
CHEMBL1373466 CHEMBL1996398 |
7 / 16 / 14 | No. 2627 | No. 1 |
![]() |
||
C00002074
![]() |
Stachydrine
|
CHEMBL394450
CHEMBL1456892 CHEMBL1986864 |
10 / 8 / 12 | No. 2627 | No. 1 |
![]() |
||
C00007298
![]() |
Choline
|
CHEMBL920
|
D002794
|
11 / 5 / 5 | 51 / 20 | No. 5945 |
![]() |
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 |
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
|
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 | 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)
|
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
|