Species

KNApSAcK Entry

Organism name Erythrina abyssinica
Genus Erythrina
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Erythrina abyssinica
Linked NCBI taxonomy ID 1237573
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (27)

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
C00038344 External link 512 Abyssinoflavanone VII
CHEMBL229220
1 / 0 / 0 No. 19 No. 14
C00000936 External link 512 Abyssinone V
CHEMBL255890
CHEMBL454332
C056679
2 / 0 / 0 No. 19 No. 14
C00014176 External link 512 Abyssinin III
/ Abyssinoflavanone III
/ 5,7,3',4'-Tetrahydroxy-5',6'-diprenylflavanone
No. 19 No. 14
C00014175 External link 512 Abyssinone V 4'-methyl ether
/ 5,7-Dihydroxy-4'-methoxy-3',5'-diprenylflavanone
CHEMBL470249
CHEMBL1425525
20 / 20 / 13 No. 19 No. 14
C00008202 External link 512 Abyssinone IV
CHEMBL470454
1 / 0 / 0 No. 19 No. 14
C00008319 External link 512 Sigmoidin A
CHEMBL229506
C064221
1 / 0 / 0 No. 19 No. 14
C00001869 External link 512 Isoboldine
/ (S)-Isoboldine
CHEMBL462880
19 / 22 / 55 No. 20 No. 4
C00000996 External link 512 Abyssinin II
/ Abyssinoflavanone II
/ 5'-Prenylhomoeriodictyol
CHEMBL388722
1 / 0 / 0 No. 28 No. 14
C00014213 External link 512 Abyssinoflavanone IV
/ 5,7,3'-Trihydroxy-2'-prenyl-[2'',3'':4',5']furanoflavanone
No. 28 No. 14
C00008201 External link 512 Abyssinone II
CHEMBL389924
CHEMBL558103
CHEMBL1688178
2 / 2 / 2 No. 28 No. 14
C00008318 External link 512 Sigmoidin B
CHEMBL229454
C064222
1 / 0 / 0 No. 28 No. 14
C00008203 External link 512 Abyssinone III
CHEMBL454077
CHEMBL1688179
CHEMBL1688180
1 / 0 / 0 No. 39
C00008465 External link 512 Sigmoidin F
CHEMBL229222
C062901
1 / 0 / 0 No. 39
C00008320 External link 512 Sigmoidin C
CHEMBL229617
1 / 0 / 0 No. 127 No. 14
C00014240 External link 512 Abyssinin I
/ Abyssinoflavanone I
/ (2S)-5,7-Dihydroxy-3'-methoxy-6'',6''-dimethylpyrano[2'',3'':4',5']flavanone
CHEMBL389736
1 / 0 / 0 No. 127 No. 14
C00014456 External link 512 Licoagrochalcone A
/ 3-Prenyl-4,2',4'-trihydroxychalcone
CHEMBL229885
2 / 2 / 2 No. 133 No. 13
C00035796 External link 512 5-Prenylbutein
CHEMBL253677
No. 133 No. 13
C00002559 External link 512 Phaseolin
/ (-)-Phaseollin
CHEMBL448350
No. 135 No. 15
C00002371 External link 512 Abyssinone VI
CHEMBL508727
1 / 0 / 0 No. 190 No. 13
C00014257 External link 512 Abyssinoflavanone V
/ 5,7,3'-Trihydroxy-2'-prenyl-(5''-hydroxy-6'',6''-dimethyldihydropyrano[2'',3'':4',5'])flavanone
No. 235
C00001852 External link 512 Erythratidine
No. 273 No. 4
C00002515 External link 512 Cristacarpin
/ Erythrabyssin I
CHEMBL454849
C085157
2 / 1 / 1 No. 325 No. 15
C00001851 External link 512 Erysotrine
CHEMBL442947
No. 446 No. 4
C00009669 External link 512 Erythrabyssin II
/ 3,9-Dihydroxy-2,10-diprenylpterocarpan
CHEMBL455372
1 / 0 / 0 No. 460
C00008457 External link 512 Sigmoidin D
CHEMBL516331
C051738
1 / 0 / 0 No. 740
C00014261 External link 512 Abyssinoflavanone VI
/ 5,7-Dihydroxy-(5''-hydroxy-6'',6''-dimethylpyrano[2'',3'':7,6])-6''',6'''-dimethyldihydropyrano[2''',3''':4',3']flavanone
No. 2013
C00000935 External link 512 Abyssinone I
No. 8287 No. 14

Human Protein / Gene in interactions

40 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000936 C00000996 C00002371 C00008201 C00008202 C00008203 C00008318 C00008319 C00008320 C00008457 C00008465 C00009669 C00014175 C00014240 C00014456 C00038344 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001869 C00014175 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001869 C00014175 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00008201 C00014456 2 / 2
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001869 C00014175 1 / 2
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001869 2 / 2
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00014175 0 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00014175 1 / 4
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001869 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00001869 0 / 0
P39748 Flap endonuclease 1 Enzyme C00014175 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00014175 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00014175 2 / 0
O75496 Geminin Unclassified protein C00014175 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00002515 0 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00014175 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00014175 7 / 3
Q99700 Ataxin-2 Unclassified protein C00014175 1 / 1
P17861 X-box-binding protein 1 Unclassified protein C00014175 1 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001869 3 / 3
P29466 Caspase-1 C14 C00001869 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00014175 0 / 0
P03372 Estrogen receptor NR3A1 C00002515 1 / 1
P55210 Caspase-7 C14 C00001869 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001869 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001869 0 / 1
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00014175 1 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00014175 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001869 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00001869 7 / 37
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00014175 0 / 0
P04054 Phospholipase A2 Enzyme C00000936 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001869 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001869 1 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00001869 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00014175 1 / 0
O00255 Menin Unclassified protein C00001869 2 / 5
Q13951 Core-binding factor subunit beta Unclassified protein C00001869 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001869 1 / 4
Q13148 TAR DNA-binding protein 43 Unclassified protein C00014175 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (40)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#208900 Ataxia-telangiectasia; at Q13315
#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
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#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
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#612371 Major affective disorder 7; mafd7 P17861
#174800 Mccune-albright syndrome; mas P63092
#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
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (64)

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)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
Q92731 (marker)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
Q13315 (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)
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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (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)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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)