KCF-S cluster No. 7732 (1 metabolites)

Corresponding Phytochemical cluster No. 4


Plant Species


Cumulative plant class count

class name count
rosids 3

Cumulative family count

class name count
Malpighiaceae 1
Passifloraceae 1
Nitrariaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Indole alkaloids 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Indole alkaloids C06536 C00001735

Metabolite list (1)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00001735 External link 512 Harmaline
CHEMBL340807
D006246
101 / 52 / 45 6 / 4

Human Protein / Gene in interactions

101 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001735 1 / 0
Q02750 Dual specificity mitogen-activated protein kinase kinase 1 Ste7 C00001735 1 / 1
Q9P1W9 Serine/threonine-protein kinase pim-2 Pim C00001735 0 / 0
Q8TDX7 Serine/threonine-protein kinase Nek7 Nek C00001735 0 / 0
Q99700 Ataxin-2 Unclassified protein C00001735 1 / 1
Q15759 Mitogen-activated protein kinase 11 p38 C00001735 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00001735 0 / 0
P06746 DNA polymerase beta Enzyme C00001735 0 / 0
O15530 3-phosphoinositide-dependent protein kinase 1 Pdk1 C00001735 0 / 0
P41240 Tyrosine-protein kinase CSK Csk C00001735 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00001735 1 / 1
P45984 Mitogen-activated protein kinase 9 Jnk C00001735 0 / 0
P29466 Caspase-1 C14 C00001735 0 / 0
P17252 Protein kinase C alpha type Alpha C00001735 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00001735 0 / 0
O14757 Serine/threonine-protein kinase Chk1 Chk1 C00001735 0 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00001735 1 / 4
Q8IWQ3 Serine/threonine-protein kinase BRSK2 CAMK serine/threonine protein kinase BRSK subfamily C00001735 0 / 0
P27448 MAP/microtubule affinity-regulating kinase 3 CAMK serine/threonine protein kinase MARK subfamily C00001735 0 / 0
P02545 Prelamin-A/C Unclassified protein C00001735 11 / 10
P16473 Thyrotropin receptor Glycohormone receptor C00001735 3 / 2
Q05513 Protein kinase C zeta type Iota C00001735 0 / 0
P47898 5-hydroxytryptamine receptor 5A Serotonin receptor C00001735 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00001735 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00001735 0 / 0
P23443 Ribosomal protein S6 kinase beta-1 p70 C00001735 0 / 0
Q00535 Cyclin-dependent kinase 5 Cdk5 C00001735 0 / 0
Q9UQB9 Aurora kinase C Aur C00001735 1 / 1
Q9HBH9 MAP kinase-interacting serine/threonine-protein kinase 2 CAMK serine/threonine protein kinase MNK subfamily C00001735 0 / 0
Q9NQU5 Serine/threonine-protein kinase PAK 6 STE serine/threonine protein kinase PAKB subfamily C00001735 0 / 0
Q16644 MAP kinase-activated protein kinase 3 CAMK serine/threonine protein kinase MAPKAPK C00001735 0 / 0
Q9H422 Homeodomain-interacting protein kinase 3 CMGC dual-specificity kinase HIPK C00001735 0 / 0
Q14680 Maternal embryonic leucine zipper kinase Melk C00001735 0 / 0
P54132 Bloom syndrome protein Enzyme C00001735 1 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001735 1 / 0
Q15746 Myosin light chain kinase, smooth muscle Mlck C00001735 1 / 1
Q13188 Serine/threonine-protein kinase 3 STE serine/threonine protein kinase MST subfamily C00001735 0 / 0
P31751 RAC-beta serine/threonine-protein kinase Akt C00001735 2 / 2
O75582 Ribosomal protein S6 kinase alpha-5 CAMK serine/threonine protein kinase MSKB subfamily C00001735 0 / 0
O14920 Inhibitor of nuclear factor kappa-B kinase subunit beta Other serine/threonine protein kinase C00001735 0 / 0
Q16513 Serine/threonine-protein kinase N2 Pkn C00001735 0 / 0
Q15139 Serine/threonine-protein kinase D1 Pkd C00001735 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001735 0 / 0
Q8N5S9 Calcium/calmodulin-dependent protein kinase kinase 1 META serine/threonine protein kinase subfamily C00001735 0 / 0
Q9P286 Serine/threonine-protein kinase PAK 7 STE serine/threonine protein kinase PAKB subfamily C00001735 0 / 0
Q96SB4 SRSF protein kinase 1 Srpk C00001735 0 / 0
Q92630 Dual specificity tyrosine-phosphorylation-regulated kinase 2 CMGC dual-specificity kinase DYRK2 C00001735 0 / 0
O43781 Dual specificity tyrosine-phosphorylation-regulated kinase 3 CMGC dual-specificity kinase DYRK2 C00001735 0 / 0
O96013 Serine/threonine-protein kinase PAK 4 STE serine/threonine protein kinase PAKB subfamily C00001735 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001735 0 / 0
P42858 Huntingtin Unclassified protein C00001735 1 / 1
O75496 Geminin Unclassified protein C00001735 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00001735 0 / 0
Q15418 Ribosomal protein S6 kinase alpha-1 Rskb C00001735 0 / 0
O15264 Mitogen-activated protein kinase 13 p38 C00001735 0 / 0
P53779 Mitogen-activated protein kinase 10 Jnk C00001735 0 / 1
P51955 Serine/threonine-protein kinase Nek2 Nek C00001735 0 / 0
Q96RR4 Calcium/calmodulin-dependent protein kinase kinase 2 META serine/threonine protein kinase subfamily C00001735 0 / 0
Q9BUB5 MAP kinase-interacting serine/threonine-protein kinase 1 CAMK serine/threonine protein kinase MNK subfamily C00001735 0 / 0
P48730 Casein kinase I isoform delta Ck1 C00001735 1 / 0
P06280 Alpha-galactosidase A Enzyme C00001735 1 / 1
Q96GD4 Aurora kinase B Aur C00001735 0 / 0
P49137 MAP kinase-activated protein kinase 2 CAMK serine/threonine protein kinase MAPKAPK C00001735 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00001735 0 / 0
P45983 Mitogen-activated protein kinase 8 Jnk C00001735 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001735 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001735 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001735 0 / 0
P22303 Acetylcholinesterase Hydrolase C00001735 1 / 0
P53350 Serine/threonine-protein kinase PLK1 PLK serine/threonine protein kinase subfamily C00001735 0 / 0
Q8IW41 MAP kinase-activated protein kinase 5 CAMK serine/threonine protein kinase MAPKAPK C00001735 0 / 0
O75116 Rho-associated protein kinase 2 Rock C00001735 0 / 0
P55210 Caspase-7 C14 C00001735 0 / 0
P31749 RAC-alpha serine/threonine-protein kinase Akt C00001735 4 / 1
O00141 Serine/threonine-protein kinase Sgk1 AGC serine/threonine protein kinase SGK subfamily C00001735 0 / 0
P51812 Ribosomal protein S6 kinase alpha-3 Rskb C00001735 2 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001735 0 / 1
Q9HC98 Serine/threonine-protein kinase Nek6 Nek C00001735 0 / 0
Q9H2X6 Homeodomain-interacting protein kinase 2 CMGC dual-specificity kinase HIPK C00001735 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001735 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001735 4 / 3
O96017 Serine/threonine-protein kinase Chk2 Rad53 C00001735 4 / 1
Q14012 Calcium/calmodulin-dependent protein kinase type 1 Camk1 C00001735 0 / 0
P17612 cAMP-dependent protein kinase catalytic subunit alpha Pka C00001735 0 / 0
Q13627 Dual specificity tyrosine-phosphorylation-regulated kinase 1A CMGC dual-specificity kinase DYRK1 C00001735 1 / 0
P53778 Mitogen-activated protein kinase 12 p38 C00001735 0 / 0
O00418 Eukaryotic elongation factor 2 kinase Atypical serine/threonine protein kinase alpha subfamily C00001735 0 / 0
Q8TD08 Mitogen-activated protein kinase 15 Mapk C00001735 0 / 0
Q86V86 Serine/threonine-protein kinase pim-3 Pim C00001735 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001735 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001735 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00001735 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001735 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001735 1 / 1
O00255 Menin Unclassified protein C00001735 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001735 1 / 2
P20248 Cyclin-A2 Other cytosolic protein C00001735 0 / 0
P78396 Cyclin-A1 Other cytosolic protein C00001735 0 / 0
P68400 Casein kinase II subunit alpha Ck2 C00001735 0 / 0
P19784 Casein kinase II subunit alpha' Ck2 C00001735 0 / 0
P67870 Casein kinase II subunit beta REG serine/threonine protein kinase family C00001735 0 / 0

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00001735
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00001735
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00001735
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001735
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 C00001735
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00001735

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (52)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#615224 Advanced sleep phase syndrome, familial, 2; fasps2 P48730
#613780 Aortic aneurysm, familial thoracic 7; aat7 Q15746
#208900 Ataxia-telangiectasia; at Q13315
#210900 Bloom syndrome; blm P54132
#114480 Breast cancer O96017
P31749
#615279 Cardiofaciocutaneous syndrome 3; cfc3 Q02750
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#303600 Coffin-lowry syndrome; cls P51812
#114500 Colorectal cancer; crc P31749
#615109 Cowden syndrome 6; cws6 P31749
#125853 Diabetes mellitus, noninsulin-dependent; niddm P31751
#119900 Digital clubbing, isolated congenital P15428
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#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
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#240900 Hypoinsulinemic hypoglycemia with hemihypertrophy; hihghh P31751
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#609265 Li-fraumeni syndrome 2; lfs2 O96017
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#614104 Mental retardation, autosomal dominant 7; mrd7 Q13627
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300844 Mental retardation, x-linked 19; mrx19 P51812
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#259500 Osteogenic sarcoma O96017
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#176807 Prostate cancer O96017
#176920 Proteus syndrome P31749
#275210 Restrictive dermopathy, lethal P02545
#243060 Spermatogenic failure 5; spgf5 Q9UQB9
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#112100 Yt blood group antigen P22303

KEGG DISEASE (45)

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)
H00881 Li-Fraumeni syndrome O96017 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P31751 (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)
H00125 Fabry disease P06280 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)
H00539 PTEN hamartoma tumor syndrome (PHTS) P31749 (related)
H00027 Ovarian cancer P31751 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00480 Non-syndromic X-linked mental retardation P51812 (related)
Q99714 (related)
H00574 Coffin-Lowry syndrome (CLS) P51812 (related)
H00606 Early infantile epileptic encephalopathy P53779 (related)
H00094 DNA repair defects P54132 (related)
Q13315 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00523 Noonan syndrome and related disorders Q02750 (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)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00801 Familial thoracic aortic aneurysm and dissection (TAAD) Q15746 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H01282 Spermatogenic failure Q9UQB9 (related)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00001735
D020329 Essential Tremor C00001735
D006212 Hallucinations C00001735
D014202 Tremor C00001735