Species

KNApSAcK Entry

Organism name Mangifera indica
Genus Mangifera
Family Anacardiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Mangifera indica
Linked NCBI taxonomy ID 29780
Linked level species

Family

Family in NCBI taxonomy Anacardiaceae
ID 4011

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (24)

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
C00006698 External link 512 Myrtillin
/ Delphinidin 3-O-beta-D-glucopyranoside
CHEMBL518846
No. 2 No. 15
C00006680 External link 512 Peonidin galactoside
/ Peonidin 3-galactoside
/ Peonidin 3-O-beta-D-galactopyranoside
CHEMBL1784263
No. 2 No. 15
C00006650 External link 512 Cyanidin 3-arabinoside
No. 2 No. 15
C00006722 External link 512 Petunidin 3-glucoside
/ Petunidin 3-O-beta-D-glucopyranoside
CHEMBL1784264
C455107
No. 2 No. 15
C00002962 External link 512 Aphloiol
/ Mangiferin
/ 2-beta-D-Glucopyranosyl-1,3,6,7-tetrahydroxy xanthone
CHEMBL1329826
C013592
27 / 17 / 17 39 / 41 No. 22 No. 15
C00000945 External link 512 Butin
/ 7,3',4'-Trihydroxyflavanone
CHEMBL451168
C051437
No. 25 No. 14
C00000029 External link 512 GA29
/ Gibberellin A29
No. 40 No. 41
C00000020 External link 512 GA20
/ Gibberellin A20
No. 40 No. 41
C00000003 External link 512 GA3
/ Gibberellin A3
CHEMBL513241
CHEMBL566653
CHEMBL1232952
CHEMBL1476967
CHEMBL1487394
C007842
10 / 18 / 17 No. 40 No. 41
C00000001 External link 512 GA1
/ Gibberellin A1
C422660
No. 40 No. 41
C00003787 External link 512 Violaxanthin
C005613
No. 114 No. 59
C00048268 External link 512 23-Hydroxy-mangiferonic acid
CHEMBL550926
No. 129 No. 11
C00000019 External link 512 GA19
/ Gibberellin A19
C120175
No. 187 No. 41
C00002445 External link 512 Rubrofusarin
CHEMBL475086
C015497
No. 493 No. 65
C00000165 External link 512 gamma-Eudesmol
CHEMBL477900
No. 613 No. 38
C00002662 External link 512 5-Pentadecylresorcinol
CHEMBL98610
2 / 4 / 2 No. 652
C00002655 External link 512 5-(Heptadec-12-enyl)resorcinol
CHEMBL1795548
No. 652
C00002416 External link 512 Aurasperone D
No. 863 No. 65
C00000095 External link 512 9-Ribosyl-cis-zeatin
/ 6-(4-Hydroxy-3-methyl-cis-2-butenylamino)-9-beta-D-ribofuranosylpurine
No. 989
C00000096 External link 512 9-Ribosyl-trans-zeatin
/ Zeatin-9-beta-D-ribofuranoside
No. 989
C00003767 External link 512 5,6-epoxy-beta-Carotene
/ beta-Carotene 5,6-epoxide
C073147
No. 1206 No. 59
C00000093 External link 512 Dihydrozeatin
No. 2879
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

Human Protein / Gene in interactions

39 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000003 C00000094 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000003 C00000094 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000003 C00000094 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000003 C00000094 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000003 C00002962 0 / 0
O75496 Geminin Unclassified protein C00000003 C00002962 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000003 C00000094 0 / 1
P10696 Alkaline phosphatase, placental-like Enzyme C00002962 0 / 1
P02545 Prelamin-A/C Unclassified protein C00000003 11 / 10
P00352 Retinal dehydrogenase 1 Enzyme C00002962 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000003 2 / 0
Q9Y5X4 Photoreceptor-specific nuclear receptor NR2E3 C00002962 2 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002962 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00002962 1 / 1
P09923 Intestinal-type alkaline phosphatase Enzyme C00002962 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00002962 3 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00002962 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002962 0 / 0
P00734 Prothrombin S1A C00002662 4 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00000091 3 / 2
P29466 Caspase-1 C14 C00002962 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002962 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002962 2 / 2
P55210 Caspase-7 C14 C00002962 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002962 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00002662 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002962 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00002962 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002962 0 / 0
P10275 Androgen receptor NR3C4 C00000003 3 / 4
Q9UBT6 DNA polymerase kappa Enzyme C00002962 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002962 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000091 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002962 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00002962 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00002962 1 / 4
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002962 5 / 3
Q9Y618 Nuclear receptor corepressor 2 Unclassified protein C00002962 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002962 0 / 0

57 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
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) C00002962
25 ABL1, ABL, JTK7, bcr/abl, c-ABL, p150, v-abl c-abl oncogene 1, non-receptor tyrosine kinase (EC:2.7.10.2) C00002962
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00002962
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002962
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00002962
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002962
847 CAT catalase (EC:1.11.1.6) C00002962
891 CCNB1, CCNB cyclin B1 C00002962
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00002962
1147 CHUK, IKBKA, IKK-alpha, IKK1, IKKA, NFKBIKA, TCF16 conserved helix-loop-helix ubiquitous kinase (EC:2.7.11.10) C00002962
7852 CXCR4, CD184, D2S201E, FB22, HM89, HSY3RR, LAP3, LCR1, LESTR, NPY3R, NPYR, NPYRL, NPYY3R, WHIM chemokine (C-X-C motif) receptor 4 C00002962
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002962
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00002962
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00002962
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00002962
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00002962
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00002962
355 FAS, ALPS1A, APO-1, APT1, CD95, FAS1, FASTM, TNFRSF6 Fas cell surface death receptor C00002962
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00002962
3551 IKBKB, IKK-beta, IKK2, IKKB, NFKBIKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta (EC:2.7.11.10) C00002962
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00002962
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00002962
4023 LPL, HDLCQ11, LIPD lipoprotein lipase (EC:3.1.1.34) C00002962
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00002962
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002962
4793 NFKBIB, IKBB, TRIP9 nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, beta C00002962
4803 NGF, Beta-NGF, HSAN5, NGFB nerve growth factor (beta polypeptide) C00002962
5320 PLA2G2A, MOM1, PLA2, PLA2B, PLA2L, PLA2S, PLAS1, sPLA2 phospholipase A2, group IIA (platelets, synovial fluid) (EC:3.1.1.4) C00002962
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00002962
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) C00002962
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002962
6716 SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2) (EC:1.3.1.22) C00002962
7015 TERT, CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1, TP2, TRT, hEST2, hTRT telomerase reverse transcriptase (EC:2.7.7.49) C00002962
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00002962
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002962
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00002962
7364 UGT2B7, UDPGT_2B9, UDPGT2B7, UDPGTH2, UGT2B9 UDP glucuronosyltransferase 2 family, polypeptide B7 (EC:2.4.1.17) C00002962
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00002962
331 XIAP, API3, BIRC4, IAP-3, ILP1, MIHA, XLP2, hIAP-3, hIAP3 X-linked inhibitor of apoptosis C00002962

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (42)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
%606641 Body mass index; bmi P37231
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#268100 Enhanced s-cone syndrome; escs Q9Y5X4
#137800 Glioma susceptibility 1; glm1 P37231
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#601665 Obesity P37231
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#275210 Restrictive dermopathy, lethal P02545
#611131 Retinitis pigmentosa 37; rp37 Q9Y5X4
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (37)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (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)
H00213 Hypophosphatasia P05186 (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)
H00023 Testicular cancer P10696 (marker)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)
H00527 Retinitis pigmentosa (RP) Q9Y5X4 (related)
H00805 Vitreoretinal degeneration Q9Y5X4 (related)

Diseases related to CTD interactions

42 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D016301 Alveolar Bone Loss C00002962
D000707 Anaphylaxis C00002962
D050197 Atherosclerosis C00002962
D001847 Bone Diseases C00002962
D001862 Bone Resorption C00002962
D003248 Constipation C00002962
D003457 Cryptosporidiosis C00002962
D003921 Diabetes Mellitus, Experimental C00002962
D003924 Diabetes Mellitus, Type 2 C00002962
D003928 Diabetic Nephropathies C00002962
D056486 Drug-Induced Liver Injury C00002962
D005234 Fatty Liver C00002962
D006331 Heart Diseases C00002962
D006561 Herpes Simplex C00002962
D015658 HIV Infections C00002962
D006946 Hyperinsulinism C00002962
D006949 Hyperlipidemias C00002962
D006967 Hypersensitivity C00002962
D033461 Hyperuricemia C00002962
D007154 Immune System Diseases C00002962
D007249 Inflammation C00002962
D007333 Insulin Resistance C00002962
D007511 Ischemia C00002962
D007674 Kidney Diseases C00002962
D007859 Learning Disorders C00002962
D015464 Leukemia, Myelogenous, Chronic, BCR-ABL Positive C00002962
D015470 Leukemia, Myeloid, Acute C00002962
D008175 Lung Neoplasms C00002962
D008569 Memory Disorders C00002962
D008630 Mercury Poisoning C00002962
D009203 Myocardial Infarction C00002962
D009336 Necrosis C00002962
D009410 Nerve Degeneration C00002962
D009437 Neuralgia C00002962
D010300 Parkinson Disease C00002962
D010518 Periodontitis C00002962
D011470 Prostatic Hyperplasia C00002962
D011833 Radiation Injuries, Experimental C00002962
D012772 Shock, Septic C00002962
D013276 Stomach Ulcer C00002962
D014235 Trichinellosis C00002962
D000647 Amnesia C00000091