Species

KNApSAcK Entry

Organism name Laurencia aldingensis
Genus
Family
Kingdom

NCBI taxonomy

Entry

Linked NCBI taxonomy name Laurencia aldingensis
Linked NCBI taxonomy ID 1167835
Linked level species

Family

Family in NCBI taxonomy Rhodomelaceae
ID 2803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Eukaryota
ID 2759

Plant class

Plant class
ID

Metabolite list (2)

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
C00003648 External link 512 Cholesterol
/ Cholesterin
/ Cholest-5-en-3beta-ol
CHEMBL112570
CHEMBL1597825
CHEMBL1867358
D002784
20 / 28 / 24 45 / 23 No. 53 No. 11
C00001233 External link 512 Palmitic acid
CHEMBL82293
D019308
16 / 8 / 8 35 / 1 No. 184 No. 68

Human Protein / Gene in interactions

33 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04150 Glucocorticoid receptor NR3C1 C00001233 C00003648 0 / 1
P10275 Androgen receptor NR3C4 C00001233 C00003648 3 / 4
P08183 Multidrug resistance protein 1 drug C00001233 C00003648 1 / 0
O60603 Toll-like receptor 2 Membrane receptor C00001233 1 / 1
P05413 Fatty acid-binding protein, heart Other cytosolic protein C00001233 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003648 0 / 0
P02545 Prelamin-A/C Unclassified protein C00003648 11 / 10
P08047 Transcription factor Sp1 Unclassified protein C00001233 0 / 0
P37840 Alpha-synuclein Unclassified protein C00003648 4 / 2
Q16850 Lanosterol 14-alpha demethylase Cytochrome P450 51A1 C00003648 0 / 0
P15090 Fatty acid-binding protein, adipocyte Other cytosolic protein C00001233 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00001233 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00003648 2 / 3
O75496 Geminin Unclassified protein C00001233 0 / 0
P12104 Fatty acid-binding protein, intestinal Other cytosolic protein C00001233 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001233 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00003648 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00001233 2 / 2
Q96RI1 Bile acid receptor NR1H4 C00001233 0 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00003648 0 / 0
Q01469 Fatty acid-binding protein, epidermal Other cytosolic protein C00001233 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00003648 2 / 0
P03372 Estrogen receptor NR3A1 C00001233 1 / 1
P09884 DNA polymerase alpha catalytic subunit Transferase C00003648 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003648 0 / 0
O00204 Sulfotransferase family cytosolic 2B member 1 Enzyme C00003648 0 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00001233 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00003648 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003648 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00003648 0 / 0
Q9NY46 Sodium channel protein type 3 subunit alpha SCN alpha, NaV1.x C00003648 0 / 0
Q99250 Sodium channel protein type 2 subunit alpha SCN alpha, NaV1.x C00003648 2 / 2
P35498 Sodium channel protein type 1 subunit alpha SCN alpha, NaV1.x C00003648 3 / 2

77 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
9619 ABCG1, ABC8, WHITE1 ATP-binding cassette, sub-family G (WHITE), member 1 C00001233 C00003648
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00001233 C00003648
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00001233 C00003648
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001233
177 AGER, RAGE advanced glycosylation end product-specific receptor C00003648
64240 ABCG5, STSL ATP-binding cassette, sub-family G (WHITE), member 5 C00003648
335 APOA1 apolipoprotein A-I C00003648
857 CAV1, BSCL3, CGL3, MSTP085, PPH3, VIP21, CAV caveolin 1, caveolae protein, 22kDa C00003648
859 CAV3, LGMD1C, LQT9, VIP-21, VIP21 caveolin 3 C00003648
1050 CEBPA, C/EBP-alpha, CEBP CCAAT/enhancer binding protein (C/EBP), alpha C00003648
1066 CES1, ACAT, CE-1, CEH, CES2, HMSE, HMSE1, PCE-1, REH, SES1, TGH, hCE-1 carboxylesterase 1 (EC:3.1.1.1 3.1.1.56) C00003648
1583 CYP11A1, CYP11A, CYPXIA1, P450SCC cytochrome P450, family 11, subfamily A, polypeptide 1 (EC:1.14.15.6) C00003648
1593 CYP27A1, CP27, CTX, CYP27 cytochrome P450, family 27, subfamily A, polypeptide 1 (EC:1.14.13.15) C00003648
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) C00003648
10858 CYP46A1, CP46, CYP46 cytochrome P450, family 46, subfamily A, polypeptide 1 (EC:1.14.13.98) C00003648
1581 CYP7A1, CP7A, CYP7, CYPVII cytochrome P450, family 7, subfamily A, polypeptide 1 (EC:1.14.13.17) C00003648
1718 DHCR24, DCE, Nbla03646, SELADIN1, seladin-1 24-dehydrocholesterol reductase (EC:1.3.1.72) C00003648
1717 DHCR7, SLOS 7-dehydrocholesterol reductase (EC:1.3.1.21) C00003648
355 FAS, ALPS1A, APO-1, APT1, CD95, FAS1, FASTM, TNFRSF6 Fas cell surface death receptor C00003648
2222 FDFT1, DGPT, ERG9, SQS, SS farnesyl-diphosphate farnesyltransferase 1 (EC:2.5.1.21) C00003648
2252 FGF7, HBGF-7, KGF fibroblast growth factor 7 C00003648
2264 FGFR4, CD334, JTK2, TKF fibroblast growth factor receptor 4 (EC:2.7.10.1) C00003648
2773 GNAI3, 87U6, ARCND1 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3 C00003648
2778 GNAS, AHO, C20orf45, GNAS1, GPSA, GSA, GSP, NESP, PHP1A, PHP1B, PHP1C, POH GNAS complex locus C00003648
338442 HCAR2, GPR109A, HCA2, HM74a, HM74b, NIACR1, PUMAG, Puma-g hydroxycarboxylic acid receptor 2 C00003648
3156 HMGCR, LDLCQ3 3-hydroxy-3-methylglutaryl-CoA reductase (EC:1.1.1.34) C00003648
3667 IRS1, HIRS-1 insulin receptor substrate 1 C00003648
3931 LCAT lecithin-cholesterol acyltransferase (EC:2.3.1.43) C00003648
3949 LDLR, FH, FHC, LDLCQ2 low density lipoprotein receptor C00003648
4481 MSR1, CD204, SCARA1, SR-A, SRA, phSR1, phSR2 macrophage scavenger receptor 1 C00003648
4864 NPC1, NPC Niemann-Pick disease, type C1 C00003648
7376 NR1H2, LXR-b, LXRB, NER, NER-I, RIP15, UNR nuclear receptor subfamily 1, group H, member 2 C00003648
10062 NR1H3, LXR-a, LXRA, RLD-1 nuclear receptor subfamily 1, group H, member 3 C00003648
9970 NR1I3, CAR, CAR1, MB67 nuclear receptor subfamily 1, group I, member 3 C00003648
5338 PLD2 phospholipase D2 (EC:3.1.4.4) C00003648
5444 PON1, ESA, MVCD5, PON paraoxonase 1 (EC:3.1.1.2 3.1.8.1 3.1.1.81) C00003648
19 ABCA1, ABC-1, ABC1, CERP, HDLDT1, TGD ATP-binding cassette, sub-family A (ABC1), member 1 C00003648
5468 PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARgamma peroxisome proliferator-activated receptor gamma C00003648
5879 RAC1, Rac-1, TC-25, p21-Rac1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1) C00003648
6256 RXRA, NR2B1 retinoid X receptor, alpha C00003648
6319 SCD, FADS5, MSTP008, SCD1, SCDOS stearoyl-CoA desaturase (delta-9-desaturase) (EC:1.14.19.1) C00003648
6721 SREBF2, SREBP-2, SREBP2, bHLHd2 sterol regulatory element binding transcription factor 2 C00003648
6770 STAR, STARD1 steroidogenic acute regulatory protein C00003648
27346 TMEM97, MAC30 transmembrane protein 97 C00003648
7421 VDR, NR1I1 vitamin D (1,25- dihydroxyvitamin D3) receptor C00003648
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00001233
581 BAX, BCL2L4 BCL2-associated X protein C00001233
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00001233
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00001233
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00001233
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00001233
1374 CPT1A, CPT1, CPT1-L, L-CPT1 carnitine palmitoyltransferase 1A (liver) (EC:2.3.1.21) C00001233
1906 EDN1, ET1, HDLCQ7, PPET1 endothelin 1 C00001233
2876 GPX1, GPXD, GSHPX1 glutathione peroxidase 1 (EC:1.11.1.9) C00001233
3034 HAL, HIS, HSTD histidine ammonia-lyase (EC:4.3.1.3) C00001233
57817 HAMP, HEPC, HFE2B, LEAP1, PLTR hepcidin antimicrobial peptide C00001233
3481 IGF2, C11orf43, IGF-II, PP9974 insulin-like growth factor 2 (somatomedin A) C00001233
64241 ABCG8, GBD4, STSL ATP-binding cassette, sub-family G (WHITE), member 8 C00003648
3630 INS, IDDM2, ILPR, IRDN, MODY10 insulin C00001233
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00001233
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00001233
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00001233
4493 MT1E, MT1, MTD metallothionein 1E C00001233
4494 MT1F, MT1 metallothionein 1F C00001233
4496 MT1H, MT-0, MT-1H, MT-IH, MT1 metallothionein 1H C00001233
4501 MT1X, MT-1l, MT1 metallothionein 1X C00001233
4502 MT2A, MT2 metallothionein 2A C00001233
4843 NOS2, HEP-NOS, INOS, NOS, NOS2A nitric oxide synthase 2, inducible (EC:1.14.13.39) C00001233
3651 PDX1, GSF, IDX-1, IPF1, IUF1, MODY4, PDX-1, STF-1 pancreatic and duodenal homeobox 1 C00001233
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00001233
29893 PSMC3IP, GT198, HOP2, HUMGT198A, ODG3, TBPIP PSMC3 interacting protein C00001233
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00001233
5054 SERPINE1, PAI, PAI-1, PAI1, PLANH1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 C00001233
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00001233
23216 TBC1D1, TBC, TBC1 TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1 C00001233
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00001233
7351 UCP2, BMIQ4, SLC25A8, UCPH uncoupling protein 2 (mitochondrial, proton carrier) C00001233

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (32)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614490 Blood group, junior system; jr Q9UNQ0
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#127750 Dementia, lewy body; dlb P37840
#607208 Dravet syndrome P35498
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#613721 Epileptic encephalopathy, early infantile, 11; eiee11 Q99250
#615363 Estrogen resistance; estrr P03372
#604403 Generalized epilepsy with febrile seizures plus, type 2; gefsp2 P35498
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#612244 Inflammatory bowel disease 13; ibd13 P08183
#246300 Leprosy, susceptibility to, 3; lprs3 O60603
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#609634 Migraine, familial hemiplegic, 3; fhm3 P35498
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#275210 Restrictive dermopathy, lethal P02545
#607745 Seizures, benign familial infantile, 3; bfis3 Q99250
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (27)

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)
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)
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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00775 Familial or sporadic hemiplegic migraine P35498 (related)
H00783 Febrile seizures P35498 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00606 Early infantile epileptic encephalopathy Q99250 (related)
H00806 Benign familial neonatal and infantile epilepsies Q99250 (related)

Diseases related to CTD interactions

24 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D001161 Arteriosclerosis C00003648
D050197 Atherosclerosis C00003648
D006528 Carcinoma, Hepatocellular C00003648
D002779 Cholestasis C00003648
D003327 Coronary Disease C00003648
D056486 Drug-Induced Liver Injury C00003648
D050171 Dyslipidemias C00003648
D005234 Fatty Liver C00003648
D006471 Gastrointestinal Hemorrhage C00003648
D006529 Hepatomegaly C00003648
D006937 Hypercholesterolemia C00003648
D006949 Hyperlipidemias C00003648
D006951 Hyperlipoproteinemias C00003648
D006965 Hyperplasia C00003648
D015228 Hypertriglyceridemia C00003648
D007037 Hypothyroidism C00003648
D007680 Kidney Neoplasms C00003648
D007859 Learning Disorders C00003648
D009336 Necrosis C00003648
D009369 Neoplasms C00003648
D052556 Niemann-Pick Disease, Type C C00003648
D058226 Plaque, Atherosclerotic C00003648
D014456 Ulcer C00003648
D003072 Cognition Disorders C00001233