Species

KNApSAcK Entry

Organism name Spongiporus leucomallellus (Murril)
Genus
Family
Kingdom

Metabolite list (36)

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
C00023799 External link 512 Eburicoic acid
CHEMBL179188
CHEMBL1981478
C004867
0 / 1 No. 86 No. 51
C00003652 External link 512 Ergosterol
/ Ergosta-5,7,22-trien-3beta-ol
CHEMBL222608
CHEMBL1232562
CHEMBL1512075
CHEMBL1741735
CHEMBL1965225
D004875
12 / 14 / 11 No. 111 No. 11
C00032307 External link 512 Tetracosane
/ n-Tetracosane
No. 115
C00034834 External link 512 Dotriacontane
No. 115
C00007423 External link 512 Pentadecanoic acid
/ n-Pentadecanoic acid
CHEMBL460025
1 / 2 / 2 No. 184 No. 68
C00020066 External link 512 T-Cadinol
/ epi-alpha-Cadinol
CHEMBL486795
C072576
No. 205 No. 38
C00029671 External link 512 alpha-Muurolene
No. 283 No. 39
C00003118 External link 512 Copaene
/ alpha-Copaene
/ (-)-alpha-Copaene
No. 333 No. 38
C00021886 External link 512 beta-Pompene
/ Gymnomitrene
/ beta-Barbatene
/ beta-Gymnomitrene
No. 365 No. 38
C00001224 External link 512 Linoleic acid
/ (Z,Z)-9,12-Octadecadienoic acid
CHEMBL267476
29 / 31 / 28 No. 367 No. 68
C00034861 External link 512 Isobazzanene
No. 451 No. 38
C00000805 External link 512 alpha-Pinene
CHEMBL442565
C005451
3 / 3 / 2 0 / 1 No. 476 No. 35
C00034818 External link 512 cis-Linalool oxide
CHEMBL29660
CHEMBL282731
CHEMBL63592
CHEMBL397730
14 / 17 / 50 No. 518 No. 6
C00034757 External link 512 (Z)-Nerolidol
/ cis-Nerolidol
CHEMBL25424
CHEMBL508801
CHEMBL561014
CHEMBL1923157
3 / 3 / 1 No. 726 No. 38
C00007535 External link 512 Phenylacetaldehyde
/ Benzeneacetaldehyde
/ Phenylacetic aldehyde
C013192
3 / 0 No. 885
C00010301 External link 512 Coriandrol
/ (S)-Linalool
/ S-(+)-Linalool
/ (+)-S-Linalool
/ (S)-3,7-Dimethyl-1,6-octadien-3-ol
CHEMBL25306
CHEMBL235672
6 / 8 / 2 No. 958 No. 34
C00034888 External link 512 -(-)-Linalool
/ (-)-R-Linalool
CHEMBL25306
CHEMBL235672
6 / 8 / 2 No. 958 No. 34
C00029674 External link 512 alpha-Terpineol
CHEMBL447597
CHEMBL449810
C016775
3 / 16 / 11 No. 983 No. 35
C00001231 External link 512 Caprylic acid
/ Octanoic acid
/ n-Octanoic acid
CHEMBL324846
C031492
10 / 14 / 13 2 / 1 No. 1141 No. 68
C00001228 External link 512 Myristic acid
/ Tetradecanoic acid
/ n-Tetradecanoic acid
CHEMBL111077
D019814
17 / 9 / 10 3 / 0 No. 1141 No. 68
C00030758 External link 512 2-Undecanone
/ Methyl nonyl ketone
No. 1611
C00029335 External link 512 beta-Ocimene
/ E-beta-Ocimene
/ (E)-beta-Ocimene
C443996
No. 1698 No. 34
C00034765 External link 512 3-Octanone
C017582
No. 1738
C00034760 External link 512 2-Decanone
CHEMBL47127
1 / 0 / 0 No. 1738
C00030828 External link 512 Nonanal
/ n-Nonanal
C008664
1 / 1 No. 1993
C00030804 External link 512 n-Decanal
C021170
2 / 0 No. 1993
C00029330 External link 512 (E)-2-Decenal
CHEMBL507518
No. 2140
C00029331 External link 512 (E)-2-Nonenal
/ trans-2-Nonenal
CHEMBL450072
1 / 0 / 0 No. 2140
C00034756 External link 512 (E,E)-2,4-Nonadienal
No. 2201
C00029341 External link 512 (E,E)-2,4-Decadienal
/ 2-trans,4-trans-Decadienal
CHEMBL443949
8 / 12 / 42 No. 2201
C00003029 External link 512 Camphene
CHEMBL506889
CHEMBL510535
C019286
No. 2460 No. 35
C00034755 External link 512 (E)-2-Heptenal
CHEMBL454759
No. 2883
C00029316 External link 512 (2E)-Octenal
/ (E)-2-Octenal
/ trans-Oct-2-en-1-al
CHEMBL448058
No. 2883
C00034763 External link 512 2-Amylfuran
/ 2-Pentylfuran
No. 3145
C00001218 External link 512 Caproic acid
/ Hexanoic acid
/ 1-Hexanoic acid
/ n-Hexanoic acid
CHEMBL14184
C037652
5 / 0 / 0 No. 3692 No. 68
C00034891 External link 512 Sandvicene
/ (+)-Sandvicene
No. 4457

Human Protein / Gene in interactions

70 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P16050 Arachidonate 15-lipoxygenase Enzyme C00001224 C00003652 C00010301 C00034757 C00034818 C00034888 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001224 C00001231 C00003652 C00029341 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000805 C00001224 C00001231 C00029341 3 / 2
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00003652 C00010301 C00029674 C00034888 5 / 1
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00010301 C00029674 C00034888 3 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00001218 C00001228 C00001231 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001228 C00010301 C00034888 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001224 C00003652 C00034757 0 / 0
O75496 Geminin Unclassified protein C00001224 C00001228 C00001231 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00001224 C00001228 C00007423 2 / 2
P11473 Vitamin D3 receptor NR1I1 C00001228 C00003652 C00029341 2 / 3
P02545 Prelamin-A/C Unclassified protein C00001224 C00001231 C00029674 11 / 10
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001224 C00001228 C00034818 1 / 1
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00000805 C00029341 C00034818 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00001218 C00001228 C00001231 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00010301 C00034757 C00034888 3 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001224 C00034818 3 / 3
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00010301 C00034888 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00001224 C00001228 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00001224 C00029341 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001224 C00003652 0 / 1
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00001224 C00001228 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00029341 C00034818 7 / 37
Q92830 Histone acetyltransferase KAT2A Enzyme C00001224 C00001228 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001218 C00001224 0 / 0
Q9UGP5 DNA polymerase lambda Enzyme C00001218 C00001224 0 / 0
P10145 Interleukin-8 Secreted protein C00029341 C00034818 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003652 1 / 1
O00519 Fatty-acid amide hydrolase 1 Enzyme C00029331 0 / 0
P40763 Signal transducer and activator of transcription 3 Transcription Factor C00034818 1 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001228 0 / 0
Q8TCC7 Solute carrier family 22 member 8 Antiporter C00001231 0 / 0
Q4U2R8 Solute carrier family 22 member 6 Antiporter C00001231 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001228 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00001228 2 / 2
P04150 Glucocorticoid receptor NR3C1 C00001231 0 / 1
O15296 Arachidonate 15-lipoxygenase B Enzyme C00001228 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00001224 5 / 3
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00034818 0 / 0
P13726 Tissue factor Membrane receptor C00001224 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00001224 0 / 0
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00001224 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000805 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003652 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003652 0 / 1
P51692 Signal transducer and activator of transcription 5B Unclassified protein C00034818 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001224 2 / 2
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00001224 0 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00001224 0 / 0
P05413 Fatty acid-binding protein, heart Other cytosolic protein C00001224 0 / 0
P03372 Estrogen receptor NR3A1 C00001224 1 / 1
O00748 Cocaine esterase Enzyme C00034760 0 / 0
P15121 Aldose reductase Enzyme C00001218 0 / 0
Q05193 Dynamin-1 Structural C00001228 0 / 0
O14842 Free fatty acid receptor 1 Free fatty acid receptor C00001224 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00034818 0 / 0
P15090 Fatty acid-binding protein, adipocyte Other cytosolic protein C00001224 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00003652 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00029341 0 / 0
P10275 Androgen receptor NR3C4 C00001224 3 / 4
O60603 Toll-like receptor 2 Membrane receptor C00001228 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00034818 0 / 1
P31939 Bifunctional purine biosynthesis protein PURH Enzyme C00003652 1 / 1
P35610 Sterol O-acyltransferase 1 Enzyme C00001224 0 / 0
P42224 Signal transducer and activator of transcription 1-alpha/beta Unclassified protein C00034818 3 / 3
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003652 1 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00034818 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00034818 1 / 4
Q9NSA0 Solute carrier family 22 member 11 Transporter C00001231 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001228 1 / 1

9 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
231 AKR1B1, ADR, ALDR1, ALR2, AR aldo-keto reductase family 1, member B1 (aldose reductase) (EC:1.1.1.21) C00030804 C00030828
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00001228 C00001231
217 ALDH2, ALDH-E2, ALDHI, ALDM aldehyde dehydrogenase 2 family (mitochondrial) (EC:1.2.1.3) C00030804
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00007535
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00007535
128 ADH5, ADH-3, ADHX, FALDH, FDH, GSH-FDH, GSNOR alcohol dehydrogenase 5 (class III), chi polypeptide (EC:1.1.1.1 1.1.1.284) C00001231
1646 AKR1C2, AKR1C-pseudo, BABP, DD, DD2, DDH2, HAKRD, HBAB, MCDR2, SRXY8 aldo-keto reductase family 1, member C2 (EC:1.3.1.20 1.1.1.357) C00007535
199974 CYP4Z1, CYP4A20 cytochrome P450, family 4, subfamily Z, polypeptide 1 (EC:1.14.14.1) C00001228
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00001228

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (65)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#608688 Aicar transformylase/imp cyclohydrolase deficiency P31939
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#209950 Atypical mycobacteriosis, familial P42224
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
%606641 Body mass index; bmi P37231
#614162 Candidiasis, familial, 7; candf7 P42224
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 P37231
#245590 Growth hormone insensitivity with immunodeficiency P51692
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#147060 Hyper-ige recurrent infection syndrome, autosomal dominant P40763
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#246300 Leprosy, susceptibility to, 3; lprs3 O60603
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#211980 Lung cancer P04637
#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
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#613796 Mycobacterial and viral infections, susceptibility to, autosomal recessive P42224
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#601665 Obesity P37231
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (85)

KEGG name UniProt
H00344 Leprosy O60603 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (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)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
P40763 (related)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00208 Hyperbilirubinemia P22309 (related)
H00966 AICA-ribosiduria P31939 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00107 Other well-defined immunodeficiency syndromes P40763 (related)
H00089 IFN-gamma/IL-12 axis P42224 (related)
H00363 Candidiasis P42224 (related)
H01109 Chronic mucocutaneous candidiasis (CMC) P42224 (related)
H00931 Growth hormone insensitivity with immunodeficiency P51692 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (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)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D005909 Glioblastoma C00023799
D003877 Dermatitis, Contact C00000805
D009336 Necrosis C00030828
D003128 COMA C00001231