Species

KNApSAcK Entry

Organism name Melodinus morsei
Genus Melodinus
Family Apocynaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Melodinus
Linked NCBI taxonomy ID 141584
Linked level genus

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 (12)

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
C00024480 External link 512 11-Hydroxytabersonine
CHEMBL2011510
No. 61 No. 4
C00024463 External link 512 Vincadifformine
/ (-)-Vincadifformine
/ 6,7-Dihydrotabersonine
CHEMBL251690
CHEMBL1617045
C456406
No. 61 No. 4
C00007204 External link 512 Isolariciresinol
/ (+)-Isolariciresinol
CHEMBL399512
CHEMBL1760593
C060284
2 / 1 / 1 No. 406
C00024464 External link 512 (+)-Aspidospermidine
No. 430 No. 4
C00024612 External link 512 Vincoline
/ 20-Epimelobaline
No. 527
C00024498 External link 512 19S-Vindolinine
/ 19-Epivindolinine
/ 20-Epivindolinine
/ 20-epi-Vindolinine
CHEMBL1165590
CHEMBL1330793
15 / 8 / 12 No. 527
C00024454 External link 512 Kopsinine
/ (-)-Kopsinine
CHEMBL93355
CHEMBL253984
C061491
No. 571
C00002591 External link 512 (-)-Cubebin
/ beta-Cubebin
/ (-)-beta-Cubebin
/ (8R,8'R,9S)-Cubebin
CHEMBL182001
CHEMBL399831
C433065
2 / 1 / 1 0 / 2 No. 629 No. 21
C00024497 External link 512
/ 19-Epivindolinine N-oxide
/ 20-Epivindolinine N-oxide
/ 20-Epivindolinine Nb-oxide
No. 2586
C00024615 External link 512 Vindolinine
/ 19R-vindolinine
/ (-)-Vindolinine
C009668
No. 2586
C00024614 External link 512 Vindolinine N-oxide
/ Vindolinine Nb-oxide
No. 2586
C00024594 External link 512 Rhazidine
C003301
No. 6782

Human Protein / Gene in interactions

17 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002591 C00007204 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002591 C00007204 0 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00024498 0 / 0
O75496 Geminin Unclassified protein C00024498 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00024498 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00024498 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00024498 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00024498 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00024498 2 / 0
Q99700 Ataxin-2 Unclassified protein C00024498 1 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00024498 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00024498 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00024498 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00024498 1 / 0
O00255 Menin Unclassified protein C00024498 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00024498 1 / 2
P01215 Glycoprotein hormones alpha chain Unclassified protein C00024498 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#608902 Drug metabolism, poor, cyp2d6-related P10635
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#257220 Niemann-pick disease, type c1; npc1 O15118
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (13)

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)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00036 Osteosarcoma P08684 (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)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D004487 Edema C00002591
D010146 Pain C00002591