PCIDB

Tabernaemontana psorocarpa (Pierre ex Stapf)Pichon

Species

KNApSAcK Entry

Organism name Tabernaemontana psorocarpa (Pierre ex Stapf)Pichon
Genus Tabernaemontana
Family Apocynaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Tabernaemontana psorocarpa
Linked NCBI taxonomy ID 761091
Linked level species

Family

Family in NCBI taxonomy Apocynaceae
ID 4056

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (2)

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
C00025214 External link 512 Tetrahydroalstonine
CHEMBL122404
CHEMBL123325
CHEMBL498734
CHEMBL486933
CHEMBL1604074
CHEMBL2079609
32 / 28 / 31 No. 246 No. 4
C00026074 External link 512 Vallesiachotamine
CHEMBL454571
CHEMBL449796
No. 4951

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00025214 1 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00025214 0 / 0
P29466 Caspase-1 C14 C00025214 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00025214 0 / 0
P02545 Prelamin-A/C Unclassified protein C00025214 11 / 10
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00025214 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00025214 0 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00025214 1 / 0
P68871 Hemoglobin subunit beta Secreted protein C00025214 4 / 4
P17405 Sphingomyelin phosphodiesterase Enzyme C00025214 2 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00025214 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00025214 0 / 0
P42858 Huntingtin Unclassified protein C00025214 1 / 1
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00025214 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00025214 0 / 0
Q99816 Tumor susceptibility gene 101 protein Unclassified protein C00025214 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00025214 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00025214 3 / 3
P55210 Caspase-7 C14 C00025214 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00025214 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00025214 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00025214 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00025214 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00025214 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00025214 0 / 0
Q14145 Kelch-like ECH-associated protein 1 Unclassified protein C00025214 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00025214 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00025214 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00025214 1 / 1
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00025214 0 / 0
O00255 Menin Unclassified protein C00025214 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00025214 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (28)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#613985 Beta-thalassemia P68871
#603902 Beta-thalassemia, dominant inclusion body type P68871
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#140700 Heinz body anemias P68871
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#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
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#275210 Restrictive dermopathy, lethal P02545
#603903 Sickle cell anemia P68871
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (31)

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)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (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)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00228 Thalassemia P68871 (related)
H00229 Sickle cell anemia (SCA) P68871 (related)
H00020 Colorectal cancer P68871 (marker)
H00022 Bladder cancer P68871 (marker)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)