Species

KNApSAcK Entry

Organism name Pleurocybella porrigens
Genus Pleurocybella
Family Marasmiaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pleurocybella porrigens
Linked NCBI taxonomy ID 71910
Linked level species

Family

Family in NCBI taxonomy Tricholomataceae
ID 5351

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (11)

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
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
C00001216 External link 512 alpha-Eleostearic acid
No. 367 No. 68
C00029815 External link 512 beta-Eleostearic acid
/ .psi-Eleostearic acid
No. 367 No. 68
C00000170 External link 512 trans-Cinnamate
/ trans-Cinnamic acid
CHEMBL27246
5 / 2 / 2 No. 904 No. 6
C00001396 External link 512 L-Tryptophan
CHEMBL54976
CHEMBL292303
CHEMBL484901
49 / 41 / 39 No. 1432 No. 4
C00030752 External link 512 Methyl alpha-Eleostearate
No. 1785
C00030901 External link 512 Ostopanic acid
/ (8E,10E)-7,12-dioxo-8,10-octadecadienoic acid
CHEMBL478594
C053593
No. 2892
C00031076 External link 512 Porrigenic acid
/ (-)-Porrigenic acid
No. 2892
C00029308 External link 512 (10E,12E)-9,14-Dioxo-10,12-octadecadienoic acid
No. 2892
C00001490 External link 512 Adenine
CHEMBL226345
D000225
52 / 44 / 38 1 / 6 No. 6151
C00032423 External link 512 Triolein
/ Glycerol trioleate
D014304
No. 8113

Human Protein / Gene in interactions

108 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001396 C00003652 1 / 0
P08254 Stromelysin-1 M10A C00001396 C00001490 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001396 C00003652 4 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001396 C00003652 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001396 C00003652 1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00001396 C00003652 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001396 C00003652 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001396 C00003652 0 / 1
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00000170 C00001490 1 / 1
P02545 Prelamin-A/C Unclassified protein C00001396 C00001490 11 / 10
Q99683 Mitogen-activated protein kinase kinase kinase 5 Ste11 C00001490 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00001396 0 / 0
P22894 Neutrophil collagenase M10A C00001490 0 / 0
P42336 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform Enzyme C00001490 9 / 1
P45984 Mitogen-activated protein kinase 9 Jnk C00001490 0 / 0
Q16773 Kynurenine--oxoglutarate transaminase 1 Enzyme C00001396 0 / 0
P17252 Protein kinase C alpha type Alpha C00001490 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00001490 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00001490 2 / 2
Q15303 Receptor tyrosine-protein kinase erbB-4 TK tyrosine-protein kinase EGFR subfamily C00001490 0 / 0
O14965 Aurora kinase A Aur C00001490 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00001396 0 / 0
Q9Y263 Phospholipase A-2-activating protein Unclassified protein C00001396 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00001396 3 / 2
Q16539 Mitogen-activated protein kinase 14 p38 C00001490 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00001396 1 / 2
P02768 Serum albumin Secreted protein C00001396 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00001490 0 / 0
P06493 Cyclin-dependent kinase 1 Cdc2 C00001490 0 / 0
P08069 Insulin-like growth factor 1 receptor TK tyrosine-protein kinase INSR subfamily C00001490 1 / 3
P54132 Bloom syndrome protein Enzyme C00001396 1 / 2
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00001396 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00001490 1 / 8
P11473 Vitamin D3 receptor NR1I1 C00003652 2 / 3
P23280 Carbonic anhydrase 6 Lyase C00001396 0 / 0
P31751 RAC-beta serine/threonine-protein kinase Akt C00001490 2 / 2
O14920 Inhibitor of nuclear factor kappa-B kinase subunit beta Other serine/threonine protein kinase C00001490 0 / 0
Q13464 Rho-associated protein kinase 1 Rock C00001490 0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00001396 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00003652 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00001396 1 / 2
O43353 Receptor-interacting serine/threonine-protein kinase 2 Ripk C00001490 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001396 0 / 0
Q8TDS4 Hydroxycarboxylic acid receptor 2 Hydroxycarboxylic acid receptor C00000170 0 / 0
P07332 Tyrosine-protein kinase Fes/Fps Fer C00001490 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001396 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001396 0 / 0
P42858 Huntingtin Unclassified protein C00001396 1 / 1
O75496 Geminin Unclassified protein C00001396 0 / 0
P15121 Aldose reductase Enzyme C00000170 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00001396 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00001490 0 / 0
Q05397 Focal adhesion kinase 1 Fak C00001490 0 / 0
P03956 Interstitial collagenase M10A C00001490 0 / 1
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00001396 0 / 0
P15056 Serine/threonine-protein kinase B-raf Raf C00001490 6 / 3
P09923 Intestinal-type alkaline phosphatase Enzyme C00001396 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00001396 3 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001396 1 / 2
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00003652 0 / 0
Q99816 Tumor susceptibility gene 101 protein Unclassified protein C00001490 0 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00001490 5 / 9
Q96GD4 Aurora kinase B Aur C00001490 0 / 0
P49137 MAP kinase-activated protein kinase 2 CAMK serine/threonine protein kinase MAPKAPK C00001490 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00001490 0 / 0
P45983 Mitogen-activated protein kinase 8 Jnk C00001490 0 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00001490 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00001396 0 / 1
P08253 72 kDa type IV collagenase M10A C00001490 1 / 3
Q13177 Serine/threonine-protein kinase PAK 2 STE serine/threonine protein kinase PAKA subfamily C00001490 0 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00001396 1 / 1
Q01453 Peripheral myelin protein 22 Unclassified protein C00001396 5 / 2
P03372 Estrogen receptor NR3A1 C00000170 1 / 1
Q08881 Tyrosine-protein kinase ITK/TSK Tec C00001490 1 / 1
O00329 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform Enzyme C00001490 0 / 0
P48775 Tryptophan 2,3-dioxygenase Enzyme C00001396 0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein C00001490 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00001396 2 / 0
P31749 RAC-alpha serine/threonine-protein kinase Akt C00001490 4 / 1
Q15118 [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 1, mitochondrial Pdhk C00001490 0 / 0
O00141 Serine/threonine-protein kinase Sgk1 AGC serine/threonine protein kinase SGK subfamily C00001490 0 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00001396 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001396 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001396 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001396 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00003652 5 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000170 0 / 0
Q99549 M-phase phosphoprotein 8 Unclassified protein C00001396 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00001490 0 / 0
P07451 Carbonic anhydrase 3 Lyase C00001396 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00001490 0 / 1
P31939 Bifunctional purine biosynthesis protein PURH Enzyme C00003652 1 / 1
P52333 Tyrosine-protein kinase JAK3 Jakb C00001490 1 / 1
P04049 RAF proto-oncogene serine/threonine-protein kinase Raf C00001490 2 / 0
P43405 Tyrosine-protein kinase SYK Syk C00001490 0 / 0
Q02750 Dual specificity mitogen-activated protein kinase kinase 1 Ste7 C00001490 1 / 1
P48736 Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform Enzyme C00001490 0 / 0
P22748 Carbonic anhydrase 4 Lyase C00001396 1 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001396 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001396 0 / 0
O00255 Menin Unclassified protein C00001396 2 / 5
Q13951 Core-binding factor subunit beta Unclassified protein C00001396 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001396 1 / 4
Q05BR4 SLC16A10 protein Unclassified protein C00001396 0 / 0
P22694 cAMP-dependent protein kinase catalytic subunit beta Pka C00001490 0 / 0
P17612 cAMP-dependent protein kinase catalytic subunit alpha Pka C00001490 0 / 0
P22612 cAMP-dependent protein kinase catalytic subunit gamma Pka C00001490 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001490 1 / 1

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001490

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (82)

OMIM preferred title UniProt
#608688 Aicar transformylase/imp cyclohydrolase deficiency P31939
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#210900 Bloom syndrome; blm P54132
#114480 Breast cancer P31749
P42336
#115150 Cardiofaciocutaneous syndrome 1; cfc1 P15056
#615279 Cardiofaciocutaneous syndrome 3; cfc3 Q02750
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#114500 Colorectal cancer; crc P15056
P31749
P42336
#612918 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi P42336
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#615108 Cowden syndrome 5; cws5 P42336
#615109 Cowden syndrome 6; cws6 P31749
#218800 Crigler-najjar syndrome, type i P22309
#606785 Crigler-najjar syndrome, type ii P22309
#125853 Diabetes mellitus, noninsulin-dependent; niddm P31751
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#237500 Dubin-johnson syndrome; djs Q92887
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#143500 Gilbert syndrome P22309
#137800 Glioma susceptibility 1; glm1 P04626
#139393 Guillain-barre syndrome, familial; gbs Q01453
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#114550 Hepatocellular carcinoma P42336
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#240900 Hypoinsulinemic hypoglycemia with hemihypertrophy; hihghh P31751
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#270450 Insulin-like growth factor i, resistance to P08069
#603932 Intervertebral disc disease; idd P14780
#182000 Keratosis, seborrheic P42336
#611554 Leopard syndrome 2 P04049
#613707 Leopard syndrome 3 P15056
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#211980 Lung cancer P00533
P04626
P15056
#605027 Lymphoma, non-hodgkin, familial P15056
#613011 Lymphoproliferative syndrome 1; lpfs1 Q08881
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#602501 Megalencephaly-capillary malformation-polymicrogyria syndrome; mcap P42336
#603387 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome; mpph P42336
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#611553 Noonan syndrome 5; ns5 P04049
#613706 Noonan syndrome 7; ns7 P15056
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
P42336
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#176920 Proteus syndrome P31749
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#600802 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative P52333
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278300 Xanthinuria, type i P47989

KEGG DISEASE (70)

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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
P08253 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P31751 (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)
P04626 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
P31751 (related)
P42336 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
H00213 Hypophosphatasia P05186 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00015 Malignant pleural mesothelioma P08069 (related)
H00050 Synovial sarcoma P08069 (related)
H01274 Growth delay due to insulin-like growth factor I resistance P08069 (related)
H00025 Penile cancer P08253 (related)
P14780 (related)
H00472 Torg-Winchester syndrome P08253 (related)
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)
H00479 Metaphyseal dysplasias P14780 (related)
H00032 Thyroid cancer P15056 (related)
H00038 Malignant melanoma P15056 (related)
H00523 Noonan syndrome and related disorders P15056 (related)
Q02750 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00208 Hyperbilirubinemia P22309 (related)
Q92887 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H00539 PTEN hamartoma tumor syndrome (PHTS) P31749 (related)
H00966 AICA-ribosiduria P31939 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00192 Xanthinuria P47989 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P52333 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00107 Other well-defined immunodeficiency syndromes Q08881 (related)

Diseases related to CTD interactions

6 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000855 Anorexia C00001490
D002779 Cholestasis C00001490
D056486 Drug-Induced Liver Injury C00001490
D007565 Jaundice C00001490
D009325 Nausea C00001490
D051437 Renal Insufficiency C00001490