Species

KNApSAcK Entry

Organism name Gossypium hirsutum
Genus Gossypium
Family Malvaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Gossypium hirsutum
Linked NCBI taxonomy ID 3635
Linked level species

Family

Family in NCBI taxonomy Malvaceae
ID 3629

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (25)

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
C00005361 External link 512 Sexangularetin 3-glucoside-7-rhamnoside
No. 1 No. 15
C00005386 External link 512 Quercetin 3'-glucoside
/ 3,5,7,3',4'-Pentahydroxyflavone
CHEMBL1222354
No. 2 No. 15
C00005382 External link 512 Quercimeritrin
/ Quercetin 7-glucoside
/ Quercetin 7-O-beta-D-glucoside
CHEMBL248726
C089996
No. 2 No. 15
C00004636 External link 512 Tamarixetin
/ 4'-O-Methylquercetin
/ 3,3',5,7-Tetrahydroxy-4'-methoxyflavone
/ 3,5,7-Trihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL226034
5 / 6 / 5 No. 3 No. 15
C00004644 External link 512 Dillenetin
/ 3',4'-Dimethoxyquercetin
/ 3,5,7-Trihydroxy-3',4'-dimethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one
CHEMBL2043330
No. 3 No. 15
C00004651 External link 512 Quercetin 3,5,7,4'-tetramethyl ether
CHEMBL77553
No. 8 No. 15
C00004652 External link 512 Quercetin 3,5,3',4'-tetramethyl ether
No. 8 No. 15
C00000003 External link 512 GA3
/ Gibberellin A3
CHEMBL513241
CHEMBL566653
CHEMBL1232952
CHEMBL1476967
CHEMBL1487394
C007842
10 / 18 / 17 No. 40 No. 41
C00000004 External link 512 GA4
/ Gibberellin A4
No. 40 No. 41
C00000013 External link 512 GA13
/ Gibberellin A13
No. 187 No. 41
C00020170 External link 512 Lacinilene A
No. 647 No. 38
C00000096 External link 512 9-Ribosyl-trans-zeatin
/ Zeatin-9-beta-D-ribofuranoside
No. 989
C00000134 External link 512 (s)-(+)-Abscisic acid
/ 2,4-Pentadienoic acid
CHEMBL288040
CHEMBL379808
CHEMBL1318134
CHEMBL1469719
CHEMBL1741460
CHEMBL1965138
D000040
10 / 9 / 10 No. 1435 No. 38
C00003486 External link 512 Strigol
/ (+)-Strigol
No. 1816 No. 38
C00000094 External link 512 2iP
/ N6-(delta2-Isopentenyl)adenine
CHEMBL476189
C001478
5 / 2 / 3 18 / 0 No. 2879
C00000091 External link 512 trans-Zeatin
CHEMBL525239
D015026
2 / 3 / 2 0 / 1 No. 2879
C00003143 External link 512 Hemigossypol
No. 2950 No. 38
C00020116 External link 512 Lacinilene C
CHEMBL254803
C023021
No. 3777 No. 38
C00003158 External link 512 Lacinilene C 7-methyl ether
CHEMBL2206801
C029267
No. 3777 No. 38
C00013227 External link 512 Lacinilene D
/ Lacinilene B
/ 21,7-Dihydroxy-1-methyl-4-(1-methylethyl)-(1H)-naphthalenone
No. 3777 No. 38
C00007452 External link 512 Sucrose 6-phosphate
C535046
No. 3949
C00001151 External link 512 Sucrose
/ (+)-Sucrose
CHEMBL253582
CHEMBL1976550
D013395
1 / 0 / 0 4 / 10 No. 3949
C00001239 External link 512 Sterculic acid
C003345
No. 4256 No. 70
C00011606 External link 512 beta-Bisabolol
No. 4385
C00011650 External link 512 Bisabolene oxide
No. 4675

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000003 C00000094 C00000134 C00004636 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000003 C00000094 C00000134 0 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000003 C00000094 C00000134 1 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000003 C00000094 C00000134 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000003 C00000094 C00000134 0 / 1
P10275 Androgen receptor NR3C4 C00000003 C00000134 3 / 4
P16473 Thyrotropin receptor Glycohormone receptor C00000091 C00000134 3 / 2
P10145 Interleukin-8 Secreted protein C00000134 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000003 2 / 0
O75496 Geminin Unclassified protein C00000003 0 / 0
P04792 Heat shock protein beta-1 Unclassified protein C00004636 2 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00000003 0 / 0
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00004636 4 / 4
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00004636 0 / 0
P03372 Estrogen receptor NR3A1 C00000134 1 / 1
P02768 Serum albumin Secreted protein C00001151 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000003 11 / 10
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000134 0 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00004636 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000091 0 / 0

22 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
440 ASNS, TS11 asparagine synthetase (glutamine-hydrolyzing) (EC:6.3.5.4) C00000094
694 BTG1 B-cell translocation gene 1, anti-proliferative C00000094
10681 GNB5, GB5 guanine nucleotide binding protein (G protein), beta 5 C00000094
182 JAG1, AGS, AHD, AWS, CD339, HJ1, JAGL1 jagged 1 C00000094
9818 NUPL1, PRO2463 nucleoporin like 1 C00000094
5142 PDE4B, DPDE4, PDE4B5, PDEIVB phosphodiesterase 4B, cAMP-specific (EC:3.1.4.17) C00000094
8544 PIR pirin (iron-binding nuclear protein) (EC:1.13.11.24) C00000094
5366 PMAIP1, APR, NOXA phorbol-12-myristate-13-acetate-induced protein 1 C00000094
9360 PPIG, CARS-Cyp, CYP, SCAF10, SRCyp peptidylprolyl isomerase G (cyclophilin G) (EC:5.2.1.8) C00000094
5782 PTPN12, PTP-PEST, PTPG1 protein tyrosine phosphatase, non-receptor type 12 (EC:3.1.3.48) C00000094
5774 PTPN3, PTP-H1, PTPH1 protein tyrosine phosphatase, non-receptor type 3 (EC:3.1.3.48) C00000094
6004 RGS16, A28-RGS14, A28-RGS14P, RGS-R regulator of G-protein signaling 16 C00000094
6016 RIT1, NS8, RIBB, RIT, ROC1 Ras-like without CAAX 1 C00000094
6286 S100P, MIG9 S100 calcium binding protein P C00000094
7029 TFDP2, DP2 transcription factor Dp-2 (E2F dimerization partner 2) C00000094
7127 TNFAIP2, B94, EXOC3L3 tumor necrosis factor, alpha-induced protein 2 C00000094
7296 TXNRD1, GRIM-12, TR, TR1, TRXR1, TXNR thioredoxin reductase 1 (EC:1.8.1.9) C00000094
7431 VIM, CTRCT30 vimentin C00000094
3630 INS, IDDM2, ILPR, IRDN, MODY10 insulin C00001151
55630 SLC39A4, AEZ, AWMS2, ZIP4 solute carrier family 39 (zinc transporter), member 4 C00001151
80834 TAS1R2, GPR71, T1R2, TR2 taste receptor, type 1, member 2 C00001151
83756 TAS1R3, T1R3 taste receptor, type 1, member 3 C00001151

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (28)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#606595 Charcot-marie-tooth disease, axonal, type 2f; cmt2f P04792
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#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
#608634 Neuronopathy, distal hereditary motor, type iib; hmn2b P04792
#604229 Peters anomaly Q16678
#275210 Restrictive dermopathy, lethal P02545
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275

KEGG DISEASE (25)

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)
H00026 Endometrial Cancer P03372 (marker)
H00856 Distal hereditary motor neuropathies (dHMN) P04792 (related)
H00036 Osteosarcoma P08684 (marker)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (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)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (related)

Diseases related to CTD interactions

11 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D019969 Amphetamine-Related Disorders C00001151
D018149 Glucose Intolerance C00001151
D006461 Hemolysis C00001151
D006946 Hyperinsulinism C00001151
D006948 Hyperkinesis C00001151
D006973 Hypertension C00001151
D007333 Insulin Resistance C00001151
D009401 Nephrosis C00001151
C541083 Non-alcoholic Fatty Liver Disease C00001151
D019966 Substance-Related Disorders C00001151
D000647 Amnesia C00000091