Species

KNApSAcK Entry

Organism name Frullania monocera
Genus Frullania
Family Jubulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Frullania monocera
Linked NCBI taxonomy ID 236963
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 (15)

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
C00003647 External link 512 Campesterol
/ 24alpha-Methylcholesterol
/ (24R)24-Methylcholest-5-en-3beta-ol
CHEMBL520535
CHEMBL485421
CHEMBL1836653
C021273
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
C00023770 External link 512 Sitosterol
/ Stigmasta-5,22-dien-3beta-ol
/ (24R)24-Ethylcholesta-5,22-dien-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00015321 External link 512 3,4'-Dimethoxybibenzyl
/ Lunularine dimethyl ether
CHEMBL477915
No. 96 No. 26
C00030479 External link 512 Hexadecanoic acid
/ n-Hexadecanoic acid
CHEMBL82293
D019308
16 / 8 / 8 35 / 1 No. 184 No. 68
C00021886 External link 512 beta-Pompene
/ Gymnomitrene
/ beta-Barbatene
/ beta-Gymnomitrene
No. 365 No. 38
C00000805 External link 512 alpha-Pinene
CHEMBL442565
C005451
3 / 3 / 2 0 / 1 No. 476 No. 35
C00003110 External link 512 Caryophyllene
/ (E)-Caryophyllene
/ beta-Caryophyllene
/ (-)-(E)-Caryophyllene
/ (E)-beta-Caryophyllene
CHEMBL445740
CHEMBL448700
2 / 3 / 7 No. 478 No. 38
C00012425 External link 512 Bicyclogermacren
/ Bicyclogermacrene
/ (+)-Bicyclogermacrene
CHEMBL509566
No. 699 No. 38
C00020283 External link 512 Albicanol
C438910
No. 1202 No. 38
C00020282 External link 512 Drimenol
/ delta7(8)-15-Hydroxyiresane
No. 1202 No. 38
C00007453 External link 512 Cyclohexane
/ beta-Elemene
CHEMBL448502
CHEMBL479707
No. 1400
C00000853 External link 512 Myrcene
CHEMBL455491
C008574
3 / 3 / 3 No. 2285 No. 34
C00036783 External link 512 Atraric acid
/ Methyl beta-Orsellinate
CHEMBL508287
3 / 3 / 1 No. 3641
C00037166 External link 512 Fusicogigantepoxide
No. 3972

Human Protein / Gene in interactions

41 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P16473 Thyrotropin receptor Glycohormone receptor C00000805 C00000853 C00023770 3 / 2
P08183 Multidrug resistance protein 1 drug C00023770 C00030479 1 / 0
Q96RI1 Bile acid receptor NR1H4 C00000853 C00030479 0 / 0
P03372 Estrogen receptor NR3A1 C00023770 C00030479 1 / 1
P04150 Glucocorticoid receptor NR3C1 C00000853 C00030479 0 / 1
P06746 DNA polymerase beta Enzyme C00023770 C00023774 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00023770 C00030479 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00023770 1 / 0
P15090 Fatty acid-binding protein, adipocyte Other cytosolic protein C00030479 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00023774 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00023770 2 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00023770 0 / 1
P11387 DNA topoisomerase 1 Isomerase C00030479 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00036783 2 / 0
O75496 Geminin Unclassified protein C00030479 0 / 0
P12104 Fatty acid-binding protein, intestinal Other cytosolic protein C00030479 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00023770 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00036783 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00030479 0 / 0
P00734 Prothrombin S1A C00023770 4 / 2
P05413 Fatty acid-binding protein, heart Other cytosolic protein C00030479 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00030479 2 / 2
P14679 Tyrosinase Oxidoreductase C00023770 4 / 2
O60603 Toll-like receptor 2 Membrane receptor C00030479 1 / 1
P28482 Mitogen-activated protein kinase 1 Erk C00000805 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00023770 0 / 0
Q01469 Fatty acid-binding protein, epidermal Other cytosolic protein C00030479 0 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00000805 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00023770 0 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00023774 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00023770 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00023770 0 / 1
P10275 Androgen receptor NR3C4 C00030479 3 / 4
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00030479 0 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00023770 1 / 1
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00023770 1 / 1
O00255 Menin Unclassified protein C00003110 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003110 1 / 2
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 C00036783 1 / 1

36 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
9619 ABCG1, ABC8, WHITE1 ATP-binding cassette, sub-family G (WHITE), member 1 C00030479
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00030479
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00030479
581 BAX, BCL2L4 BCL2-associated X protein C00030479
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00030479
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00030479
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00030479
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00030479
1374 CPT1A, CPT1, CPT1-L, L-CPT1 carnitine palmitoyltransferase 1A (liver) (EC:2.3.1.21) C00030479
1906 EDN1, ET1, HDLCQ7, PPET1 endothelin 1 C00030479
2876 GPX1, GPXD, GSHPX1 glutathione peroxidase 1 (EC:1.11.1.9) C00030479
3034 HAL, HIS, HSTD histidine ammonia-lyase (EC:4.3.1.3) C00030479
57817 HAMP, HEPC, HFE2B, LEAP1, PLTR hepcidin antimicrobial peptide C00030479
3481 IGF2, C11orf43, IGF-II, PP9974 insulin-like growth factor 2 (somatomedin A) C00030479
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00030479
3630 INS, IDDM2, ILPR, IRDN, MODY10 insulin C00030479
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00030479
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00030479
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00030479
4493 MT1E, MT1, MTD metallothionein 1E C00030479
4494 MT1F, MT1 metallothionein 1F C00030479
4496 MT1H, MT-0, MT-1H, MT-IH, MT1 metallothionein 1H C00030479
4501 MT1X, MT-1l, MT1 metallothionein 1X C00030479
4502 MT2A, MT2 metallothionein 2A C00030479
4843 NOS2, HEP-NOS, INOS, NOS, NOS2A nitric oxide synthase 2, inducible (EC:1.14.13.39) C00030479
3651 PDX1, GSF, IDX-1, IPF1, IUF1, MODY4, PDX-1, STF-1 pancreatic and duodenal homeobox 1 C00030479
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00030479
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00030479
29893 PSMC3IP, GT198, HOP2, HUMGT198A, ODG3, TBPIP PSMC3 interacting protein C00030479
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00030479
5054 SERPINE1, PAI, PAI-1, PAI1, PLANH1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 C00030479
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00030479
23216 TBC1D1, TBC, TBC1 TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1 C00030479
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00030479
7351 UCP2, BMIQ4, SLC25A8, UCPH uncoupling protein 2 (mitochondrial, proton carrier) C00030479

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (31)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#218030 Apparent mineralocorticoid excess; ame P80365
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#246300 Leprosy, susceptibility to, 3; lprs3 O60603
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (27)

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)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (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)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (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)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003877 Dermatitis, Contact C00000805
D003072 Cognition Disorders C00030479