Species

KNApSAcK Entry

Organism name Erythrina fusca
Genus Erythrina
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Erythrina fusca
Linked NCBI taxonomy ID 556509
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

Natural Activity

List (17)

Species Activity
Erythrina fusca Lour. Analgesic
Erythrina fusca Lour. Analgesic
Erythrina fusca Lour. Antipyretic
Erythrina fusca Lour. Antiseptic
Erythrina fusca Lour. Antiseptic
Erythrina fusca Lour. Antitussive
Erythrina fusca Lour. Antitussive
Erythrina fusca Lour. Diaphoretic
Erythrina fusca Lour. Febrifuge
Erythrina fusca Lour. Hallucinogen
Erythrina fusca Lour. Hallucinogenic
Erythrina fusca Lour. Narcotic
Erythrina fusca Lour. Narcotic
Erythrina fusca Lour. Purgative
Erythrina fusca Lour. Sudorific
Erythrina fusca Lour. Vermifuge
Erythrina fusca Lour. Vermifuge

Metabolite list (9)

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
C00019155 External link 512 8-Prenyldaidzein
No. 15 No. 15
C00000954 External link 512 Senegalensein
/ Lonchocarpol A
/ 6,8-Diprenylnaringenin
CHEMBL477969
CHEMBL1545584
C068505
16 / 26 / 18 No. 19 No. 14
C00000977 External link 512 Liquiritigenin
CHEMBL252642
CHEMBL271939
C083152
5 / 4 / 4 1 / 1 No. 25 No. 14
C00008249 External link 512 Cajaflavanone
/ Erythrisenegalone
CHEMBL557692
No. 39
C00008262 External link 512 Lupinifolin
CHEMBL559980
No. 39
C00008450 External link 512 Citflavanone
No. 127 No. 14
C00019388 External link 512 3-Hydroxy-9-methoxy-10-(3-hydroxy-3-methylbutyl)pterocarpan
No. 188 No. 15
C00009687 External link 512 Sandwicarpin
/ 6a-Hydroxyphaseollidin
No. 325 No. 15
C00002515 External link 512 Cristacarpin
/ Erythrabyssin I
CHEMBL454849
C085157
2 / 1 / 1 No. 325 No. 15

Human Protein / Gene in interactions

23 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 C00000977 0 / 0
P17861 X-box-binding protein 1 Unclassified protein C00000954 1 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000954 0 / 0
Q99700 Ataxin-2 Unclassified protein C00000954 1 / 1
P06746 DNA polymerase beta Enzyme C00000954 0 / 0
P04062 Glucosylceramidase Enzyme C00000954 6 / 4
P14780 Matrix metalloproteinase-9 M10A C00000977 2 / 2
P39748 Flap endonuclease 1 Enzyme C00000954 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000954 2 / 0
O75496 Geminin Unclassified protein C00000954 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00002515 0 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000954 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000954 7 / 3
Q04206 Transcription factor p65 Transcription Factor C00000977 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00000977 2 / 2
P03372 Estrogen receptor NR3A1 C00002515 1 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00000954 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000954 4 / 3
P05412 Transcription factor AP-1 Transcription Factor C00000977 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00000954 1 / 0
O00255 Menin Unclassified protein C00000954 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000954 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000954 1 / 1

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1831 TSC22D3, DIP, DSIPI, GILZ, TSC-22R, hDIP TSC22 domain family, member 3 C00000977

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (31)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#114500 Colorectal cancer; crc P84022
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603932 Intervertebral disc disease; idd P14780
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#612371 Major affective disorder 7; mafd7 P17861
#174800 Mccune-albright syndrome; mas P63092
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#166350 Osseous heteroplasia, progressive; poh P63092
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (23)

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)
H00026 Endometrial Cancer P03372 (marker)
Q92731 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
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)
H00025 Penile cancer P14780 (related)
H00479 Metaphyseal dysplasias P14780 (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) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D009120 Muscle Cramp C00000977