Species

KNApSAcK Entry

Organism name Frullania incumbens
Genus Frullania
Family Jubulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Frullania incumbens
Linked NCBI taxonomy ID 642320
Linked level species

Family

Family in NCBI taxonomy Frullaniaceae
ID 400721

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Embryophyta
ID 3193

Metabolite list (9)

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
C00032087 External link 512 Octadecanoic acid
CHEMBL46403
C031183
15 / 17 / 19 6 / 1 No. 184 No. 68
C00001232 External link 512 Oleic acid
/ (Z)-9-Octadecenoic acid
CHEMBL8659
CHEMBL460657
D019301
30 / 19 / 20 26 / 9 No. 184 No. 68
C00030345 External link 512 gamma-Cadinene
C054278
No. 283 No. 39
C00036669 External link 512 9,12-Octadecadienoic acid
CHEMBL267476
D019787
29 / 31 / 28 42 / 11 No. 367 No. 68
C00003116 External link 512 beta-Chamigrene
No. 451 No. 38
C00012425 External link 512 Bicyclogermacren
/ Bicyclogermacrene
/ (+)-Bicyclogermacrene
CHEMBL509566
No. 699 No. 38
C00001228 External link 512 Myristic acid
/ Tetradecanoic acid
/ n-Tetradecanoic acid
CHEMBL111077
D019814
17 / 9 / 10 3 / 0 No. 1141 No. 68
C00007453 External link 512 Cyclohexane
/ beta-Elemene
CHEMBL448502
CHEMBL479707
No. 1400
C00037851 External link 512 Striatene
No. 4896

Human Protein / Gene in interactions

59 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00001228 C00001232 C00032087 C00036669 2 / 2
Q9UGP5 DNA polymerase lambda Enzyme C00001232 C00032087 C00036669 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001232 C00032087 C00036669 0 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00001228 C00001232 C00036669 0 / 0
P15090 Fatty acid-binding protein, adipocyte Other cytosolic protein C00001232 C00032087 C00036669 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001228 C00032087 C00036669 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001232 C00032087 C00036669 3 / 3
Q96RI1 Bile acid receptor NR1H4 C00001228 C00001232 C00036669 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001228 C00001232 C00036669 0 / 0
O75496 Geminin Unclassified protein C00001228 C00001232 C00036669 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00001232 C00036669 5 / 3
P16473 Thyrotropin receptor Glycohormone receptor C00032087 C00036669 3 / 2
P13726 Tissue factor Membrane receptor C00001232 C00036669 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001232 C00036669 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001228 C00001232 0 / 0
P05413 Fatty acid-binding protein, heart Other cytosolic protein C00001232 C00036669 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00032087 C00036669 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00001228 C00032087 2 / 3
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00001232 C00032087 0 / 0
P35610 Sterol O-acyltransferase 1 Enzyme C00001232 C00036669 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001232 C00032087 1 / 2
P17405 Sphingomyelin phosphodiesterase Enzyme C00001228 2 / 2
P39748 Flap endonuclease 1 Enzyme C00001228 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00036669 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00001228 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00036669 0 / 0
O00519 Fatty-acid amide hydrolase 1 Enzyme C00001232 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001228 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00001232 0 / 0
P54132 Bloom syndrome protein Enzyme C00001232 1 / 2
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00036669 0 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00036669 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00032087 0 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00032087 3 / 1
P02545 Prelamin-A/C Unclassified protein C00036669 11 / 10
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00001232 1 / 4
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00036669 0 / 0
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00036669 0 / 0
Q01469 Fatty acid-binding protein, epidermal Other cytosolic protein C00001232 0 / 0
P17252 Protein kinase C alpha type Alpha C00001232 0 / 0
P07148 Fatty acid-binding protein, liver Unclassified protein C00001232 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00036669 2 / 2
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00001232 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001232 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00001228 0 / 0
P03372 Estrogen receptor NR3A1 C00036669 1 / 1
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00032087 0 / 0
Q05193 Dynamin-1 Structural C00001228 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00036669 0 / 1
O14842 Free fatty acid receptor 1 Free fatty acid receptor C00036669 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00001232 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001232 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001232 4 / 3
P10275 Androgen receptor NR3C4 C00036669 3 / 4
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00001232 2 / 2
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00001228 0 / 0
O60603 Toll-like receptor 2 Membrane receptor C00001228 1 / 1
O00255 Menin Unclassified protein C00032087 2 / 5
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001228 1 / 1

57 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00001228 C00001232 C00032087 C00036669
1906 EDN1, ET1, HDLCQ7, PPET1 endothelin 1 C00001232 C00032087 C00036669
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00001228 C00032087 C00036669
9619 ABCG1, ABC8, WHITE1 ATP-binding cassette, sub-family G (WHITE), member 1 C00001232 C00032087 C00036669
6256 RXRA, NR2B1 retinoid X receptor, alpha C00001232 C00036669
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00001232 C00036669
19 ABCA1, ABC-1, ABC1, CERP, HDLDT1, TGD ATP-binding cassette, sub-family A (ABC1), member 1 C00001232 C00036669
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001232 C00032087
5468 PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARgamma peroxisome proliferator-activated receptor gamma C00001232 C00036669
335 APOA1 apolipoprotein A-I C00001232 C00036669
5467 PPARD, FAAR, NR1C2, NUC1, NUCI, NUCII, PPARB peroxisome proliferator-activated receptor delta C00001232 C00036669
847 CAT catalase (EC:1.11.1.6) C00001232 C00036669
100136658 C00001232 C00036669
5444 PON1, ESA, MVCD5, PON paraoxonase 1 (EC:3.1.1.2 3.1.8.1 3.1.1.81) C00001232 C00036669
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00001232 C00036669
196 AHR, bHLHe76 aryl hydrocarbon receptor C00036669
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00001232
1869 E2F1, E2F-1, RBAP1, RBBP3, RBP3 E2F transcription factor 1 C00001232
778733 C00001232
1401 CRP, PTX1 C-reactive protein, pentraxin-related C00001232
338 APOB, FLDB, LDLCQ4 apolipoprotein B C00001232
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00001232
5925 RB1, OSRC, RB, p105-Rb, pRb, pp110 retinoblastoma 1 C00001232
9429 ABCG2, ABC15, ABCP, BCRP, BCRP1, BMDP, CD338, CDw338, EST157481, GOUT1, MRX, MXR, MXR1, UAQTL1 ATP-binding cassette, sub-family G (WHITE), member 2 C00001232
5054 SERPINE1, PAI, PAI-1, PAI1, PLANH1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 C00001232
6514 SLC2A2, GLUT2 solute carrier family 2 (facilitated glucose transporter), member 2 C00001232
6720 SREBF1, SREBP-1c, SREBP1, bHLHd1 sterol regulatory element binding transcription factor 1 C00001232
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00032087
3630 INS, IDDM2, ILPR, IRDN, MODY10 insulin C00001232
430 ASCL2, ASH2, HASH2, MASH2, bHLHa45 achaete-scute family bHLH transcription factor 2 C00036669
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00036669
1082 CGB, CGB3, CGB5, CGB7, CGB8, hCGB chorionic gonadotropin, beta polypeptide C00036669
1387 CREBBP, CBP, KAT3A, RSTS CREB binding protein (EC:2.3.1.48) C00036669
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00036669
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00036669
1557 CYP2C19, CPCJ, CYP2C, P450C2C, P450IIC19 cytochrome P450, family 2, subfamily C, polypeptide 19 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00036669
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00036669
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00036669
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00036669
2168 FABP1, FABPL, L-FABP fatty acid binding protein 1, liver C00036669
2170 FABP3, FABP11, H-FABP, M-FABP, MDGI, O-FABP fatty acid binding protein 3, muscle and heart (mammary-derived growth inhibitor) C00036669
9415 FADS2, D6D, DES6, FADSD6, LLCDL2, SLL0262, TU13 fatty acid desaturase 2 (EC:1.14.19.-) C00036669
3458 IFNG, IFG, IFI interferon, gamma C00036669
3586 IL10, CSIF, GVHDS, IL-10, IL10A, TGIF interleukin 10 C00036669
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00036669
3558 IL2, IL-2, TCGF, lymphokine interleukin 2 C00036669
3565 IL4, BCGF-1, BCGF1, BSF-1, BSF1, IL-4 interleukin 4 C00036669
3567 IL5, EDF, IL-5, TRF interleukin 5 (colony-stimulating factor, eosinophil) C00036669
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00036669
653361 NCF1, NCF1A, NOXO2, SH3PXD1A, p47phox neutrophil cytosolic factor 1 C00036669
4688 NCF2, NCF-2, NOXA2, P67-PHOX, P67PHOX neutrophil cytosolic factor 2 C00036669
8648 NCOA1, F-SRC-1, KAT13A, RIP160, SRC1, bHLHe42, bHLHe74 nuclear receptor coactivator 1 (EC:2.3.1.48) C00036669
10499 NCOA2, GRIP1, KAT13C, NCoA-2, SRC2, TIF2, bHLHe75 nuclear receptor coactivator 2 C00036669
5338 PLD2 phospholipase D2 (EC:3.1.4.4) C00036669
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00036669
6319 SCD, FADS5, MSTP008, SCD1, SCDOS stearoyl-CoA desaturase (delta-9-desaturase) (EC:1.14.19.1) C00036669
199974 CYP4Z1, CYP4A20 cytochrome P450, family 4, subfamily Z, polypeptide 1 (EC:1.14.14.1) C00001228

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (51)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#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
#208900 Ataxia-telangiectasia; at Q13315
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#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
#119900 Digital clubbing, isolated congenital P15428
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#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
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613688 Long qt syndrome 2; lqt2 Q12809
#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
#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
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#601665 Obesity P37231
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#609620 Short qt syndrome 1; sqt1 Q12809
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#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 (52)

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)
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)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00036 Osteosarcoma P08684 (marker)
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)
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)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00094 DNA repair defects P54132 (related)
Q13315 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (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

18 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003072 Cognition Disorders C00032087
C00001232
D006520 Hepatitis, Animal C00001232
C00036669
D005234 Fatty Liver C00001232
C00036669
D001321 Autistic Disorder C00036669
D055371 Acute Lung Injury C00001232
D007333 Insulin Resistance C00001232
D055370 Lung Injury C00001232
D011654 Pulmonary Edema C00001232
D012128 Respiratory Distress Syndrome, Adult C00001232
D000860 Anoxia C00001232
D019970 Cocaine-Related Disorders C00036669
D017453 Dermatitis, Irritant C00036669
D006526 Hepatitis C C00036669
D006937 Hypercholesterolemia C00036669
D006949 Hyperlipidemias C00036669
D015228 Hypertriglyceridemia C00036669
D007414 Intestinal Neoplasms C00036669
D008175 Lung Neoplasms C00036669