class name | count |
---|---|
rosids | 3 |
class name | count |
---|---|
Malpighiaceae | 1 |
Passifloraceae | 1 |
Nitrariaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Indole alkaloids | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Indole alkaloids | C06536 | C00001735 |
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
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Harmaline
|
CHEMBL340807
|
D006246
|
101 / 52 / 45 | 6 / 4 |
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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 |
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
|
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 | 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)
|