Species

KNApSAcK Entry

Organism name Antrodia camphorata
Genus Antrodia
Family Meripilaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Taiwanofungus camphoratus
Linked NCBI taxonomy ID 196114
Linked level species

Family

Family in NCBI taxonomy Coriolaceae
ID 83233

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (14)

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
C00029821 External link 512 Sitostenone
/ beta-Sitostenone
/ Stigmast-4-en-3-one
/ Stigmast-4-ene-3-one
CHEMBL66926
No. 53 No. 11
C00023774 External link 512 Fucostanol
/ Stigmasterol
/ Dihydro-beta-sitosterol
/ (24S)24-Ethylcholestain-3beta-ol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00030190 External link 512 Epifriedelanol
/ epi-Friedelinol
/ beta-Friedelinol
/ Friedelan-3beta-ol
/ Longan triterpane A
CHEMBL229563
CHEMBL464649
No. 101 No. 52
C00023805 External link 512 Eburicol
/ Obtusifoldienol
/ 24-Methylene dihydrolanosterol
/ 24-Methylene-24,25-dihydrolanosterol
CHEMBL518556
C014520
No. 218 No. 51
C00023803 External link 512 Dehydroeburicoic acid
CHEMBL1744446
No. 551
C00029287 External link 512 L-Sesamin
/ (-)-Sesamin
CHEMBL43469
CHEMBL252915
CHEMBL1572261
CHEMBL1591714
CHEMBL1708854
CHEMBL1904496
CHEMBL1968861
20 / 24 / 15 No. 621 No. 21
C00023758 External link 512 Ergosta-4,6,8(14),22-tetraen-3-one
CHEMBL1801892
CHEMBL2040598
C015860
No. 768
C00038466 External link 512 Antcin B
CHEMBL446448
CHEMBL1644789
CHEMBL1966186
No. 2103
C00038465 External link 512 Antcin A
CHEMBL388526
CHEMBL1644793
No. 2103
C00038468 External link 512 Antrocamphin B
CHEMBL229342
No. 4945
C00038467 External link 512 Antrocamphin A
CHEMBL229169
No. 4945
C00038199 External link 512 2,3,4,5-Tetramethoxybenzoyl chloride
CHEMBL376803
No. 5281
C00038473 External link 512 Antrodioxolanone
CHEMBL229460
No. 6450
C00038414 External link 512 alpha-Tocospiro B
CHEMBL2204408
No. 8560

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00029287 1 / 0
Q16637 Survival motor neuron protein Unclassified protein C00029287 4 / 1
P06746 DNA polymerase beta Enzyme C00023774 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00023774 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00029287 0 / 1
P11473 Vitamin D3 receptor NR1I1 C00029287 2 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00029287 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00029287 2 / 0
O75496 Geminin Unclassified protein C00029287 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00029287 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00029287 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00029287 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00029287 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00029287 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00029287 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00029287 0 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00023774 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00029287 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00029287 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00029287 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00029287 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00029287 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00023774 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00023774 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00029287 1 / 1

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00023774

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (24)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#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
#600274 Frontotemporal dementia; ftd P10636
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#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
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (15)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (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)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)