Species

KNApSAcK Entry

Organism name Couroupita guianensis
Genus Couroupita
Family Lecythidaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Couroupita guianensis
Linked NCBI taxonomy ID 66684
Linked level species

Family

Family in NCBI taxonomy
ID

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (6)

Species Activity
Couroupita guianensis Aubl. Analgesic
Couroupita guianensis Aubl. Antirheumatic
Couroupita guianensis Aubl. Canicide
Couroupita guianensis Aubl. Depilatory
Couroupita guianensis Aubl. Poison
Couroupita guianensis Aubl. Vulnerary

Metabolite list (2)

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
C00002200 External link 512 Tryptanthrin
/ Tryptanthrine
/ Couroupitine A
CHEMBL306946
C046243
20 / 22 / 23 2 / 0 No. 1798 No. 7
C00026982 External link 512 Indirubin
/ Indigo red
/ Couroupitine B
/ Indigopurpurin
CHEMBL259664
CHEMBL1276127
C027185
16 / 11 / 8 40 / 1 No. 4840

Human Protein / Gene in interactions

35 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10636 Microtubule-associated protein tau Unclassified protein C00002200 C00026982 4 / 3
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002200 2 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002200 0 / 3
P02545 Prelamin-A/C Unclassified protein C00002200 11 / 10
P24941 Cyclin-dependent kinase 2 Cdc2 C00026982 0 / 0
P06493 Cyclin-dependent kinase 1 Cdc2 C00026982 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002200 0 / 1
Q00535 Cyclin-dependent kinase 5 Cdk5 C00026982 0 / 0
Q15078 Cyclin-dependent kinase 5 activator 1 REG serine/threonine protein kinase family C00026982 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002200 1 / 0
P11387 DNA topoisomerase 1 Isomerase C00002200 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00002200 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00026982 2 / 3
P17538 Chymotrypsinogen B S1A C00026982 0 / 0
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00026982 1 / 1
Q92830 Histone acetyltransferase KAT2A Enzyme C00002200 0 / 0
P42858 Huntingtin Unclassified protein C00002200 1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002200 0 / 0
O75496 Geminin Unclassified protein C00002200 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002200 0 / 0
P21980 Protein-glutamine gamma-glutamyltransferase 2 Enzyme C00026982 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002200 1 / 2
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00026982 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002200 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002200 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002200 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002200 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00002200 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00026982 4 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002200 0 / 0
O95067 G2/mitotic-specific cyclin-B2 Other cytosolic protein C00026982 0 / 0
P14635 G2/mitotic-specific cyclin-B1 Other cytosolic protein C00026982 0 / 0
Q8WWL7 G2/mitotic-specific cyclin-B3 Other cytosolic protein C00026982 0 / 0
P49840 Glycogen synthase kinase-3 alpha Gsk C00026982 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00026982 0 / 0

42 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
36 ACADSB, 2-MEBCAD, ACAD7, SBCAD acyl-CoA dehydrogenase, short/branched chain (EC:1.3.8.5) C00026982
196 AHR, bHLHe76 aryl hydrocarbon receptor C00026982
378 ARF4, ARF2 ADP-ribosylation factor 4 C00026982
405 ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00026982
10575 CCT4, CCT-DELTA, Cctd, SRB chaperonin containing TCP1, subunit 4 (delta) C00026982
1000 CDH2, CD325, CDHN, CDw325, NCAD cadherin 2, type 1, N-cadherin (neuronal) C00026982
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00026982
1017 CDK2, p33(CDK2) cyclin-dependent kinase 2 (EC:2.7.11.22) C00026982
1195 CLK1, CLK, CLK/STY, STY CDC-like kinase 1 (EC:2.7.12.1) C00026982
9318 COPS2, ALIEN, CSN2, SGN2, TRIP15 COP9 signalosome subunit 2 C00026982
1441 CSF3R, CD114, GCSFR colony stimulating factor 3 receptor (granulocyte) C00026982
3577 CXCR1, C-C, C-C-CKR-1, CD128, CD181, CDw128a, CKR-1, CMKAR1, IL8R1, IL8RA, IL8RBA chemokine (C-X-C motif) receptor 1 C00026982
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00026982
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00026982
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00026982
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00026982
3491 CYR61, CCN1, GIG1, IGFBP10 cysteine-rich, angiogenic inducer, 61 C00026982
1869 E2F1, E2F-1, RBAP1, RBBP3, RBP3 E2F transcription factor 1 C00026982
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00026982
3281 HSBP1, NPC-A-13 heat shock factor binding protein 1 C00026982
3329 HSPD1, CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13 heat shock 60kDa protein 1 (chaperonin) C00026982
10808 HSPH1, HSP105, HSP105A, HSP105B, NY-CO-25 heat shock 105kDa/110kDa protein 1 C00026982
3458 IFNG, IFG, IFI interferon, gamma C00026982
3484 IGFBP1, AFBP, IBP1, IGF-BP25, PP12, hIGFBP-1 insulin-like growth factor binding protein 1 C00026982
3554 IL1R1, CD121A, D2S1473, IL-1R-alpha, IL1R, IL1RA, P80 interleukin 1 receptor, type I C00026982
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00026982
3608 ILF2, NF45, PRO3063 interleukin enhancer binding factor 2 C00026982
3688 ITGB1, CD29, FNRB, GPIIA, MDF2, MSK12, VLA-BETA, VLAB integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12) C00026982
3689 ITGB2, CD18, LAD, LCAMB, LFA-1, MAC-1, MF17, MFI7 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) C00026982
4258 MGST2, GST2, MGST-II microsomal glutathione S-transferase 2 (EC:2.5.1.18) C00026982
4436 MSH2, COCA1, FCC1, HNPCC, HNPCC1, LCFS2 mutS homolog 2 C00026982
653361 NCF1, NCF1A, NOXO2, SH3PXD1A, p47phox neutrophil cytosolic factor 1 C00026982
4864 NPC1, NPC Niemann-Pick disease, type C1 C00026982
5925 RB1, OSRC, RB, p105-Rb, pRb, pp110 retinoblastoma 1 C00026982
4735 SEPT2, DIFF6, NEDD-5, NEDD5, Pnutl3, hNedd5 septin 2 C00026982
6514 SLC2A2, GLUT2 solute carrier family 2 (facilitated glucose transporter), member 2 C00026982
6688 SPI1, OF, PU.1, SFPI1, SPI-1, SPI-A spleen focus forming virus (SFFV) proviral integration oncogene C00026982
6938 TCF12, CRS3, HEB, HTF4, HsT17266, bHLHb20 transcription factor 12 C00026982
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00026982
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00026982
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002200
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00002200

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (29)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#601626 Leukemia, acute myeloid; aml P36888
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257220 Niemann-pick disease, type c1; npc1 O15118
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (28)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00003 Acute myeloid leukemia (AML) P36888 (related)
H00059 Huntington's disease (HD) P42858 (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)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006968 Hypersensitivity, Delayed C00026982