Species

KNApSAcK Entry

Organism name Coffea eugenioides
Genus Coffea
Family Rubiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Coffea eugenioides
Linked NCBI taxonomy ID 49369
Linked level species

Family

Family in NCBI taxonomy Rubiaceae
ID 24966

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (6)

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
C00033727 External link 512 Clerosterol
/ (-)-Clerosterol
/ (-)-(3beta,24S)-Stigmasta-5,25-dien-3-ol
CHEMBL252365
No. 53 No. 11
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00032163 External link 512 Sitostanol
/ Stigmastanol
/ beta-Sitostanol
CHEMBL305498
CHEMBL252364
C021255
No. 68 No. 11
C00007322 External link 512 delta7-Avenasterol
No. 111 No. 11
C00033758 External link 512 delta7 Stigmastenol
/ (3beta)-Stigmast-7-en-3-ol
CHEMBL238597
C031313
No. 111 No. 11
C00001492 External link 512 Caffeine
CHEMBL113
D002110
115 / 59 / 49 109 / 161 No. 3446 No. 12

Human Protein / Gene in interactions

124 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001492 C00003672 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001492 C00003672 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001492 C00003672 1 / 1
P03372 Estrogen receptor NR3A1 C00001492 C00003672 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001492 C00003672 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001492 C00003672 0 / 1
P08183 Multidrug resistance protein 1 drug C00001492 C00003672 1 / 0
P06746 DNA polymerase beta Enzyme C00001492 C00003672 0 / 0
P41143 Delta-type opioid receptor Opioid receptor C00001492 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00001492 0 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00001492 2 / 2
P08246 Neutrophil elastase S1A C00001492 2 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00001492 0 / 0
P78527 DNA-dependent protein kinase catalytic subunit Atypical serine/threonine protein kinase PIKK subfamily C00001492 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00001492 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00001492 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00001492 0 / 0
Q9Y2T3 Guanine deaminase Enzyme C00001492 0 / 0
P29466 Caspase-1 C14 C00001492 0 / 0
P17252 Protein kinase C alpha type Alpha C00001492 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00001492 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00001492 2 / 2
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00001492 1 / 4
O15245 Solute carrier family 22 member 1 Drug uniporter C00001492 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00001492 3 / 1
P29275 Adenosine receptor A2b Adenosine receptor C00001492 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00001492 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00001492 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00001492 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00001492 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00001492 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00001492 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00001492 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00001492 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00001492 0 / 0
P02768 Serum albumin Secreted protein C00001492 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00001492 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00001492 0 / 0
Q08828 Adenylate cyclase type 1 Enzyme C00001492 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00001492 0 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00001492 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00001492 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00001492 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00001492 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00001492 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00001492 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00001492 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00001492 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00001492 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00001492 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00001492 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00001492 1 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00001492 0 / 0
O75496 Geminin Unclassified protein C00001492 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00001492 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00001492 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00001492 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00001492 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00001492 1 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00001492 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00001492 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00001492 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00001492 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00001492 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00001492 1 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 0 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00001492 0 / 0
P08311 Cathepsin G S1A C00001492 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00001492 1 / 0
P03956 Interstitial collagenase M10A C00001492 0 / 1
Q13535 Serine/threonine-protein kinase ATR Atypical serine/threonine protein kinase PIKK subfamily C00001492 2 / 2
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00001492 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001492 0 / 0
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00001492 1 / 0
P00734 Prothrombin S1A C00003672 4 / 2
P04150 Glucocorticoid receptor NR3C1 C00001492 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00001492 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00001492 0 / 0
P14679 Tyrosinase Oxidoreductase C00003672 4 / 2
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00001492 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00001492 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00001492 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00001492 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00001492 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00001492 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00001492 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00001492 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00001492 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00001492 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00001492 2 / 1
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00001492 1 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00001492 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 0 / 0
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00001492 1 / 0
P22303 Acetylcholinesterase Hydrolase C00001492 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001492 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001492 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00001492 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00001492 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00001492 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00001492 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00001492 0 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00001492 0 / 0
P11217 Glycogen phosphorylase, muscle form Enzyme C00001492 1 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00001492 0 / 0
P10275 Androgen receptor NR3C4 C00001492 3 / 4
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00001492 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00001492 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00001492 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00001492 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00001492 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00001492 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00001492 0 / 0
P04156 Major prion protein Surface antigen C00001492 6 / 2
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00001492 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001492 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 1 / 1
Q9NY46 Sodium channel protein type 3 subunit alpha SCN alpha, NaV1.x C00001492 0 / 0
Q99250 Sodium channel protein type 2 subunit alpha SCN alpha, NaV1.x C00001492 2 / 2
P35498 Sodium channel protein type 1 subunit alpha SCN alpha, NaV1.x C00001492 3 / 2

109 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
39 ACAT2 acetyl-CoA acetyltransferase 2 (EC:2.3.1.9) C00001492
22985 ACIN1, ACINUS, ACN, fSAP152 apoptotic chromatin condensation inducer 1 C00001492
2181 ACSL3, ACS3, FACL3, PRO2194 acyl-CoA synthetase long-chain family member 3 (EC:6.2.1.3) C00001492
135 ADORA2A, A2aR, ADORA2, RDC8 adenosine A2a receptor C00001492
136 ADORA2B, ADORA2 adenosine A2b receptor C00001492
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00001492
5832 ALDH18A1, ARCL3A, GSAS, P5CS, PYCS aldehyde dehydrogenase 18 family, member A1 (EC:1.2.1.41 2.7.2.11) C00001492
283 ANG, ALS9, HEL168, RNASE4, RNASE5 angiogenin, ribonuclease, RNase A family, 5 (EC:3.1.27.-) C00001492
335 APOA1 apolipoprotein A-I C00001492
336 APOA2, Apo-AII, ApoA-II, apoAII apolipoprotein A-II C00001492
338 APOB, FLDB, LDLCQ4 apolipoprotein B C00001492
341 APOC1 apolipoprotein C-I C00001492
344 APOC2, APO-CII, APOC-II apolipoprotein C-II C00001492
345 APOC3, APOCIII, HALP2 apolipoprotein C-III C00001492
23204 ARL6IP1, AIP1, ARL6IP, ARMER ADP-ribosylation factor-like 6 interacting protein 1 C00001492
440 ASNS, TS11 asparagine synthetase (glutamine-hydrolyzing) (EC:6.3.5.4) C00001492
472 ATM, AT1, ATA, ATC, ATD, ATDC, ATE, TEL1, TELO1 ataxia telangiectasia mutated (EC:2.7.11.1) C00001492
9551 ATP5J2, ATP5JL ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 (EC:3.6.1.14) C00001492
545 ATR, FCTCS, FRP1, MEC1, SCKL, SCKL1 ataxia telangiectasia and Rad3 related (EC:2.7.11.1) C00001492
581 BAX, BCL2L4 BCL2-associated X protein C00001492
27113 BBC3, JFY-1, JFY1, PUMA BCL2 binding component 3 C00001492
637 BID, FP497 BH3 interacting domain death agonist C00001492
699 BUB1, BUB1A, BUB1L, hBUB1 BUB1 mitotic checkpoint serine/threonine kinase (EC:2.7.11.1) C00001492
813 CALU calumenin C00001492
823 CAPN1, CANP, CANP1, CANPL1, muCANP, muCL calpain 1, (mu/I) large subunit (EC:3.4.22.52) C00001492
835 CASP2, CASP-2, ICH1, NEDD-2, NEDD2, PPP1R57 caspase 2, apoptosis-related cysteine peptidase (EC:3.4.22.55) C00001492
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00001492
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00001492
891 CCNB1, CCNB cyclin B1 C00001492
995 CDC25C, CDC25, PPP1R60 cell division cycle 25C (EC:3.1.3.48) C00001492
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00001492
1017 CDK2, p33(CDK2) cyclin-dependent kinase 2 (EC:2.7.11.22) C00001492
1019 CDK4, CMM3, PSK-J3 cyclin-dependent kinase 4 (EC:2.7.11.22) C00001492
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00001492
1111 CHEK1, CHK1 checkpoint kinase 1 (EC:2.7.11.1) C00001492
11200 CHEK2, CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, hCds1 checkpoint kinase 2 (EC:2.7.11.1) C00001492
1508 CTSB, APPS, CPSB cathepsin B (EC:3.4.22.1) C00001492
1537 CYC1, MC3DN6, UQCR4 cytochrome c-1 C00001492
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00001492
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00001492
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00001492
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) C00001492
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00001492
1580 CYP4B1, CYPIVB1, P-450HP cytochrome P450, family 4, subfamily B, polypeptide 1 (EC:1.14.14.1) C00001492
1603 DAD1, OST2 defender against cell death 1 (EC:2.4.99.18) C00001492
1638 DCT, TRP-2, TYRP2 dopachrome tautomerase (EC:5.3.3.12) C00001492
1813 DRD2, D2DR, D2R dopamine receptor D2 C00001492
10209 EIF1, A121, EIF-1, EIF1A, ISO1, SUI1 eukaryotic translation initiation factor 1 C00001492
1978 EIF4EBP1, 4E-BP1, 4EBP1, BP-1, PHAS-I eukaryotic translation initiation factor 4E binding protein 1 C00001492
2688 GH1, GH, GH-N, GHN, IGHD1B, hGH-N growth hormone 1 C00001492
2745 GLRX, GRX, GRX1 glutaredoxin (thioltransferase) (EC:1.8.4.1) C00001492
55830 GLT8D1, MSTP139 glycosyltransferase 8 domain containing 1 C00001492
2746 GLUD1, GDH, GDH1, GLUD glutamate dehydrogenase 1 (EC:1.4.1.3) C00001492
2932 GSK3B glycogen synthase kinase 3 beta (EC:2.7.11.1 2.7.11.26) C00001492
9446 GSTO1, GSTO_1-1, GSTTLp28, P28, SPG-R glutathione S-transferase omega 1 (EC:2.5.1.18 1.8.5.1 1.20.4.2) C00001492
3014 H2AFX, H2A.X, H2A/X, H2AX H2A histone family, member X C00001492
3291 HSD11B2, AME, AME1, HSD11K, HSD2, SDR9C3 hydroxysteroid (11-beta) dehydrogenase 2 (EC:1.1.1.146) C00001492
3484 IGFBP1, AFBP, IBP1, IGF-BP25, PP12, hIGFBP-1 insulin-like growth factor binding protein 1 C00001492
3630 INS, IDDM2, ILPR, IRDN, MODY10 insulin C00001492
3708 ITPR1, INSP3R1, IP3R, IP3R1, SCA15, SCA16, SCA29 inositol 1,4,5-trisphosphate receptor, type 1 C00001492
3939 LDHA, GSD11, LDH1, LDHM lactate dehydrogenase A (EC:1.1.1.27) C00001492
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00001492
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00001492
4257 MGST1, GST12, MGST, MGST-I microsomal glutathione S-transferase 1 (EC:2.5.1.18) C00001492
4277 MICB, PERB11.2 MHC class I polypeptide-related sequence B C00001492
4495 MT1G, MT1, MT1K metallothionein 1G C00001492
2475 MTOR, FRAP, FRAP1, FRAP2, RAFT1, RAPT1 mechanistic target of rapamycin (serine/threonine kinase) (EC:2.7.11.1) C00001492
10 NAT2, AAC2, NAT-2, PNAT N-acetyltransferase 2 (arylamine N-acetyltransferase) (EC:2.3.1.5) C00001492
4942 OAT, GACR, HOGA, OATASE, OKT ornithine aminotransferase (EC:2.6.1.13) C00001492
5062 PAK2, PAK65, PAKgamma p21 protein (Cdc42/Rac)-activated kinase 2 (EC:2.7.11.1) C00001492
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00001492
5354 PLP1, GPM6C, HLD1, MMPL, PLP, PLP/DM20, PMD, SPG2 proteolipid protein 1 C00001492
5521 PPP2R2B, B55BETA, PP2AB55BETA, PP2ABBETA, PP2APR55B, PP2APR55BETA, PR2AB55BETA, PR2ABBETA, PR2APR55BETA, PR52B, PR55-BETA, PR55BETA, SCA12 protein phosphatase 2, regulatory subunit B, beta (EC:3.1.3.16) C00001492
27166 PRELID1, PRELI, PX19, SBBI12 PRELI domain containing 1 C00001492
5591 PRKDC, DNA-PKcs, DNAPK, DNPK1, HYRC, HYRC1, XRCC7, p350 protein kinase, DNA-activated, catalytic polypeptide (EC:2.7.11.1) C00001492
5621 PRNP, ASCR, AltPrP, CD230, CJD, GSS, KURU, PRIP, PrP, PrP27-30, PrP33-35C, PrPc, p27-30 prion protein C00001492
10197 PSME3, Ki, PA28-gamma, PA28G, PA28gamma, REG-GAMMA proteasome (prosome, macropain) activator subunit 3 (PA28 gamma; Ki) C00001492
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) C00001492
5925 RB1, OSRC, RB, p105-Rb, pRb, pp110 retinoblastoma 1 C00001492
5972 REN, HNFJ2 renin (EC:3.4.23.15) C00001492
6194 RPS6, S6 ribosomal protein S6 C00001492
6197 RPS6KA3, CLS, HU-3, ISPK-1, MAPKAPK1B, MRX19, RSK, RSK2, S6K-alpha3, p90-RSK2, pp90RSK2 ribosomal protein S6 kinase, 90kDa, polypeptide 3 (EC:2.7.11.1) C00001492
6198 RPS6KB1, PS6K, S6K, S6K-beta-1, S6K1, STK14A, p70_S6KA, p70(S6K)-alpha, p70-S6K, p70-alpha ribosomal protein S6 kinase, 70kDa, polypeptide 1 (EC:2.7.11.1) C00001492
23212 RRS1 RRS1 ribosome biogenesis regulator homolog (S. cerevisiae) C00001492
6261 RYR1, CCO, MHS, MHS1, RYDR, RYR, RYR-1, SKRR ryanodine receptor 1 (skeletal) C00001492
23256 SCFD1, C14orf163, RA410, SLY1, SLY1P, STXBP1L2 sec1 family domain containing 1 C00001492
6396 SEC13, D3S1231E, SEC13L1, SEC13R, npp-20 SEC13 homolog (S. cerevisiae) C00001492
10484 SEC23A, CLSD Sec23 homolog A (S. cerevisiae) C00001492
5265 SERPINA1, A1A, A1AT, AAT, PI, PI1, PRO2275, alpha1AT serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1 C00001492
866 SERPINA6, CBG serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6 C00001492
6566 SLC16A1, HHF7, MCT, MCT1 solute carrier family 16 (monocarboxylate transporter), member 1 C00001492
54498 SMOX, C20orf16, PAO, PAO-1, PAOH1, SMO spermine oxidase (EC:1.5.3.16) C00001492
6713 SQLE squalene epoxidase (EC:1.14.13.132) C00001492
8878 SQSTM1, A170, OSIL, PDB3, ZIP3, p60, p62, p62B sequestosome 1 C00001492
6426 SRSF1, ASF, SF2, SF2p33, SFRS1, SRp30a serine/arginine-rich splicing factor 1 C00001492
6770 STAR, STARD1 steroidogenic acute regulatory protein C00001492
55342 STRBP, ILF3L, SPNR, p74 spermatid perinuclear RNA binding protein C00001492
7027 TFDP1, DP1, DRTF1, Dp-1 transcription factor Dp-1 C00001492
10548 TM9SF1, HMP70, MP70 transmembrane 9 superfamily member 1 C00001492
9911 TMCC2, HUCEP11 transmembrane and coiled-coil domain family 2 C00001492
27346 TMEM97, MAC30 transmembrane protein 97 C00001492
7292 TNFSF4, CD134L, CD252, GP34, OX-40L, OX4OL, TXGP1 tumor necrosis factor (ligand) superfamily, member 4 C00001492
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00001492
7296 TXNRD1, GRIM-12, TR, TR1, TRXR1, TXNR thioredoxin reductase 1 (EC:1.8.1.9) C00001492
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00001492
7385 UQCRC2, MC3DN5, QCR2, UQCR2 ubiquinol-cytochrome c reductase core protein II (EC:1.10.2.2) C00001492
7498 XDH, XO, XOR xanthine dehydrogenase (EC:1.17.1.4 1.17.3.2) C00001492
10971 YWHAQ, 14-3-3, 1C5, HS1 tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, theta polypeptide C00001492
7587 ZNF37A, KOX21, ZNF37 zinc finger protein 37A C00001492

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (74)

OMIM preferred title UniProt
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#218030 Apparent mineralocorticoid excess; ame P80365
#208900 Ataxia-telangiectasia; at Q13315
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#300615 Brunner syndrome P21397
#123400 Creutzfeldt-jakob disease; cjd P04156
#614564 Cutaneous telangiectasia and cancer syndrome, familial; fctcs Q13535
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#607208 Dravet syndrome P35498
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#613721 Epileptic encephalopathy, early infantile, 11; eiee11 Q99250
#615363 Estrogen resistance; estrr P03372
#600072 Fatal familial insomnia; ffi P04156
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#604403 Generalized epilepsy with febrile seizures plus, type 2; gefsp2 P35498
#137440 Gerstmann-straussler disease; gsd P04156
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 P04626
#232600 Glycogen storage disease v P11217
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#603218 Huntington disease-like 1; hdl1 P04156
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#603932 Intervertebral disc disease; idd P14780
#245300 Kuru, susceptibility to P04156
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
#608516 Major depressive disorder; mdd P08172
%300852 Mental retardation, x-linked 88; mrx88 P50052
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#609634 Migraine, familial hemiplegic, 3; fhm3 P35498
#126200 Multiple sclerosis, susceptibility to; ms P08575
#159900 Myoclonic dystonia P14416
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#607276 Resting heart rate, variation in P08588
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#210600 Seckel syndrome 1; sckl1 Q13535
#607745 Seizures, benign familial infantile, 3; bfis3 Q99250
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#606688 Spongiform encephalopathy with neuropsychiatric features P04156
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#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
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (57)

KEGG name UniProt
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00061 Prion diseases P04156 (related)
H01243 Huntington's disease-like syndrome P04156 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
P35354 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (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)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00069 Glycogen storage diseases (GSD) P11217 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00548 Brunner syndrome P21397 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00775 Familial or sporadic hemiplegic migraine P35498 (related)
H00783 Febrile seizures P35498 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00037 Alveolar rhabdomyosarcoma Q13535 (related)
H00992 Seckel syndrome Q13535 (related)
H00606 Early infantile epileptic encephalopathy Q99250 (related)
H00806 Benign familial neonatal and infantile epilepsies Q99250 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

161 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000014 Abnormalities, Drug-Induced C00001492
D000015 Abnormalities, Multiple C00001492
D000230 Adenocarcinoma C00001492
D000236 Adenoma C00001492
D017542 Aneurysm, Ruptured C00001492
D001008 Anxiety Disorders C00001492
D001018 Aortic Diseases C00001492
D001049 Apnea C00001492
D001167 Arteritis C00001492
D001281 Atrial Fibrillation C00001492
D001282 Atrial Flutter C00001492
D054537 Atrioventricular Block C00001492
D001289 Attention Deficit Disorder with Hyperactivity C00001492
D001480 Basal Ganglia Diseases C00001492
D001714 Bipolar Disorder C00001492
D001766 Blindness C00001492
D018488 Bone Demineralization, Pathologic C00001492
D001929 Brain Edema C00001492
D001930 Brain Injuries C00001492
D001943 Breast Neoplasms C00001492
D002294 Carcinoma, Squamous Cell C00001492
D002295 Carcinoma, Transitional Cell C00001492
D009202 Cardiomyopathies C00001492
D002318 Cardiovascular Diseases C00001492
D002375 Catalepsy C00001492
D002389 Catatonia C00001492
D002543 Cerebral Hemorrhage C00001492
D023341 Chills C00001492
D019970 Cocaine-Related Disorders C00001492
D003072 Cognition Disorders C00001492
D003110 Colonic Neoplasms C00001492
D003327 Coronary Disease C00001492
D003329 Coronary Vasospasm C00001492
D003645 Death, Sudden C00001492
D003866 Depressive Disorder C00001492
D003967 Diarrhea C00001492
D004065 Digestive System Abnormalities C00001492
D004195 Disease Models, Animal C00001492
D004244 Dizziness C00001492
D003875 Drug Eruptions C00001492
D064420 Drug-Related Side Effects and Adverse Reactions C00001492
D004409 Dyskinesia, Drug-Induced C00001492
D004487 Edema C00001492
D004715 Endometriosis C00001492
D004830 Epilepsy, Tonic-Clonic C00001492
D005234 Fatty Liver C00001492
D005317 Fetal Growth Retardation C00001492
D005327 Fetal Resorption C00001492
D005334 Fever C00001492
D005348 Fibrocystic Breast Disease C00001492
D005355 Fibrosis C00001492
D005767 Gastrointestinal Diseases C00001492
D005831 Genital Diseases, Female C00001492
D005832 Genital Diseases, Male C00001492
D005923 Glomerulosclerosis, Focal Segmental C00001492
D006029 Glycosuria C00001492
D006130 Growth Disorders C00001492
D006212 Hallucinations C00001492
D006261 Headache C00001492
D006323 Heart Arrest C00001492
D006330 Heart Defects, Congenital C00001492
D006331 Heart Diseases C00001492
D006345 Heart Septal Defects, Ventricular C00001492
D006417 Hematuria C00001492
D006470 Hemorrhage C00001492
D006505 Hepatitis C00001492
D006620 Hip Fractures C00001492
D006849 Hydrocephalus C00001492
D006930 Hyperalgesia C00001492
D006940 Hyperemia C00001492
D006941 Hyperesthesia C00001492
D006948 Hyperkinesis C00001492
D006965 Hyperplasia C00001492
D006973 Hypertension C00001492
D006974 Hypertension, Malignant C00001492
D006977 Hypertension, Renal C00001492
D020343 Hypertensive Encephalopathy C00001492
D007008 Hypokalemia C00001492
D007022 Hypotension C00001492
D007035 Hypothermia C00001492
D007235 Infant, Premature, Diseases C00001492
D007249 Inflammation C00001492
D007333 Insulin Resistance C00001492
D007674 Kidney Diseases C00001492
D007680 Kidney Neoplasms C00001492
D007681 Kidney Papillary Necrosis C00001492
D007683 Kidney Tubular Necrosis, Acute C00001492
D007859 Learning Disorders C00001492
D007905 Lens Diseases C00001492
D017114 Liver Failure, Acute C00001492
D008113 Liver Neoplasms C00001492
D008133 Long QT Syndrome C00001492
D008175 Lung Neoplasms C00001492
D008206 Lymphatic Diseases C00001492
D015674 Mammary Neoplasms, Animal C00001492
D008325 Mammary Neoplasms, Experimental C00001492
D008569 Memory Disorders C00001492
D008881 Migraine Disorders C00001492
D019964 Mood Disorders C00001492
D019957 Motor Skills Disorders C00001492
D009069 Movement Disorders C00001492
D020267 MPTP Poisoning C00001492
D009120 Muscle Cramp C00001492
D018908 Muscle Weakness C00001492
D009135 Muscular Diseases C00001492
D009139 Musculoskeletal Abnormalities C00001492
D009203 Myocardial Infarction C00001492
D017202 Myocardial Ischemia C00001492
D009325 Nausea C00001492
D009336 Necrosis C00001492
D009357 Neonatal Abstinence Syndrome C00001492
D009374 Neoplasms, Experimental C00001492
D009395 Nephritis, Interstitial C00001492
D009436 Neural Tube Defects C00001492
D009765 Obesity C00001492
D009798 Ocular Hypertension C00001492
D010024 Osteoporosis C00001492
D010146 Pain C00001492
D016584 Panic Disorder C00001492
D010300 Parkinson Disease C00001492
C537181 Paroxysmal nonkinesigenic dyskinesia C00001492
D010911 Pituitary Neoplasms C00001492
D010922 Placenta Diseases C00001492
D010488 Polyarteritis Nodosa C00001492
D011141 Polyuria C00001492
D051299 Post-Dural Puncture Headache C00001492
D011230 Precancerous Conditions C00001492
D011297 Prenatal Exposure Delayed Effects C00001492
D011507 Proteinuria C00001492
D011596 Psychomotor Disorders C00001492
D011605 Psychoses, Substance-Induced C00001492
D012148 Restless Legs Syndrome C00001492
D012509 Sarcoma C00001492
D012512 Sarcoma, Ewing C00001492
D012559 Schizophrenia C00001492
D012640 Seizures C00001492
D012652 Self Mutilation C00001492
D012878 Skin Neoplasms C00001492
D012892 Sleep Deprivation C00001492
D012893 Sleep Disorders C00001492
D007319 Sleep Initiation and Maintenance Disorders C00001492
D013272 Stomach Diseases C00001492
D013274 Stomach Neoplasms C00001492
D020521 Stroke C00001492
D013345 Subarachnoid Hemorrhage C00001492
D019966 Substance-Related Disorders C00001492
D013375 Substance Withdrawal Syndrome C00001492
D013575 Syncope C00001492
D013610 Tachycardia C00001492
D013614 Tachycardia, Paroxysmal C00001492
D013617 Tachycardia, Supraventricular C00001492
D017180 Tachycardia, Ventricular C00001492
C572845 Thyroid cancer, follicular C00001492
D013981 Tic Disorders C00001492
D014202 Tremor C00001492
D014516 Ureteral Neoplasms C00001492
D014555 Urination Disorders C00001492
D014581 Urticaria C00001492
D014693 Ventricular Fibrillation C00001492
D018879 Ventricular Premature Complexes C00001492
D015431 Weight Loss C00001492