Species

KNApSAcK Entry

Organism name Pachygone dasycarpa
Genus Pachygone
Family Menispermaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pachygone
Linked NCBI taxonomy ID 152360
Linked level genus

Family

Family in NCBI taxonomy Menispermaceae
ID 3455

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (7)

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
C00001814 External link 512 (+)-Atherospermoline
No. 10 No. 4
C00001844 External link 512 Daphnoline
/ Trilobamin
/ Trilobamine
No. 10 No. 4
C00027513 External link 512 Angchibangkine
/ (+)-Angchibangkine
CHEMBL524668
No. 10 No. 4
C00025306 External link 512 Fangchinoline
/ dl-Fangchinoline
/ 7-O-Demethyltetrandrine
CHEMBL504256
CHEMBL509803
CHEMBL500614
12 / 6 / 3 No. 10 No. 4
C00001919 External link 512 Tetrandrine
/ (+)-Tetrandrine
CHEMBL176045
CHEMBL367260
CHEMBL445477
CHEMBL449690
CHEMBL504958
CHEMBL504757
C009438
26 / 23 / 48 6 / 16 No. 10 No. 4
C00001869 External link 512 Isoboldine
/ (S)-Isoboldine
CHEMBL462880
19 / 22 / 55 No. 20 No. 4
C00027250 External link 512 14-Hydroxyisostephodeline
No. 346 No. 4

Human Protein / Gene in interactions

42 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001869 C00001919 1 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00001869 C00001919 7 / 37
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001869 C00001919 1 / 2
O00255 Menin Unclassified protein C00001869 C00001919 2 / 5
Q99700 Ataxin-2 Unclassified protein C00001919 C00025306 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001919 C00025306 1 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00001919 C00025306 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001869 C00001919 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001869 C00001919 1 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001919 C00025306 0 / 0
P08183 Multidrug resistance protein 1 drug C00001919 C00025306 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001869 C00001919 0 / 1
O75496 Geminin Unclassified protein C00001919 C00025306 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00001919 C00025306 2 / 0
P39748 Flap endonuclease 1 Enzyme C00001919 C00025306 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001919 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00001919 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00025306 0 / 0
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00025306 0 / 1
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00001919 0 / 0
P06280 Alpha-galactosidase A Enzyme C00001919 1 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00001869 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001869 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001869 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001919 0 / 0
P55210 Caspase-7 C14 C00001869 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00001919 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001919 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001919 0 / 0
P29466 Caspase-1 C14 C00001869 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001869 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001869 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00001869 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001869 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00001869 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001919 1 / 1
P10253 Lysosomal alpha-glucosidase Hydrolase C00025306 1 / 1
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00025306 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001919 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00001919 4 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00001869 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001869 1 / 4

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
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) C00001919
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00001919
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00001919
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00001919
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) C00001919
1577 CYP3A5, CP35, CYPIIIA5, P450PCN3, PCN3 cytochrome P450, family 3, subfamily A, polypeptide 5 (EC:1.14.14.1) C00001919

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (34)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#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
#133239 Esophageal cancer P04637
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (60)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00125 Fabry disease P06280 (related)
H00079 Asthma P07550 (related)
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)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (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)

Diseases related to CTD interactions

16 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000860 Anoxia C00001919
D001855 Bone Marrow Diseases C00001919
D006331 Heart Diseases C00001919
D006470 Hemorrhage C00001919
D007239 Infection C00001919
D007511 Ischemia C00001919
D015470 Leukemia, Myeloid, Acute C00001919
D008106 Liver Cirrhosis, Experimental C00001919
D055370 Lung Injury C00001919
D028361 Mitochondrial Diseases C00001919
D052016 Mucositis C00001919
D009203 Myocardial Infarction C00001919
D009336 Necrosis C00001919
D016066 Pleural Effusion, Malignant C00001919
D013280 Stomatitis C00001919
D013927 Thrombosis C00001919