Species

KNApSAcK Entry

Organism name Podocarpus milanjianus
Genus Podocarpus
Family Podocarpaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Podocarpus milanjianus
Linked NCBI taxonomy ID 85247
Linked level species

Family

Family in NCBI taxonomy Podocarpaceae
ID 3362

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Spermatophyta
ID 58024

Metabolite list (5)

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
C00000263 External link 512 Podolactone A
C008943
No. 463 No. 41
C00000264 External link 512 Podolactone B
No. 463 No. 41
C00000274 External link 512 Nagilactone G
No. 463 No. 41
C00000266 External link 512 Podolactone D
CHEMBL460334
No. 463 No. 41
C00000268 External link 512 Nagilactone A
CHEMBL1381439
13 / 20 / 13 No. 1854 No. 41

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00000268 4 / 1
Q99700 Ataxin-2 Unclassified protein C00000268 1 / 1
P06746 DNA polymerase beta Enzyme C00000268 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000268 11 / 10
P42858 Huntingtin Unclassified protein C00000268 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000268 2 / 0
O75496 Geminin Unclassified protein C00000268 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000268 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000268 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000268 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000268 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000268 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00000268 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#137800 Glioma susceptibility 1; glm1 O75874
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545
#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

KEGG DISEASE (13)

KEGG name UniProt
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)
H00059 Huntington's disease (HD) P42858 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)