Species

KNApSAcK Entry

Organism name Cephalanceropsis gracilis
Genus
Family
Kingdom

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
C00038719 External link 512 Cephalandole A
No. 1963
C00026981 External link 512 Isatin
CHEMBL326294
D007510
8 / 5 / 3 12 / 0 No. 2737
C00000113 External link 512 Indole-3-carboxylic acid
CHEMBL387527
C012382
1 / 3 / 4 No. 3632
C00000112 External link 512 Indole-3-carboxaldehyde
/ 1H-Indole-3-carboxaldehyde
CHEMBL147741
C012381
2 / 1 / 1 No. 4314
C00026982 External link 512 Indirubin
/ Indigo red
/ Couroupitine B
/ Indigopurpurin
CHEMBL259664
CHEMBL1276127
C027185
16 / 11 / 8 40 / 1 No. 4840
C00041602 External link 512 Isatan
No. 5087
C00041427 External link 512 Cephalinone C
/ (-)-Cephalinone C
No. 5087
C00038721 External link 512 Cephathrindole A
No. 5583
C00038722 External link 512 Cephathrindole B
No. 5583
C00041425 External link 512 Cephalinone A
/ (-)-Cephalinone A
No. 6679
C00041424 External link 512 Cephalandole C
/ (+)-Cephalandole C
No. 7370
C00038720 External link 512 Cephalandole B
No. 8325
C00041665 External link 512 Methyl dioxindole-3-acetate
/ (-)-Methyl dioxindole-3-acetate
No. 8330
C00041426 External link 512 Cephalinone B
/ (-)-Cephalinone B
No. 8334
C00041428 External link 512 Cephalinone D
/ (-)-Cephalinone D
No. 8797

Human Protein / Gene in interactions

26 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P21980 Protein-glutamine gamma-glutamyltransferase 2 Enzyme C00026981 C00026982 0 / 0
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00026982 0 / 0
P12268 Inosine-5'-monophosphate dehydrogenase 2 Oxidoreductase C00000112 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00026981 1 / 1
P24941 Cyclin-dependent kinase 2 Cdc2 C00026982 0 / 0
P06493 Cyclin-dependent kinase 1 Cdc2 C00026982 0 / 0
Q00535 Cyclin-dependent kinase 5 Cdk5 C00026982 0 / 0
Q15078 Cyclin-dependent kinase 5 activator 1 REG serine/threonine protein kinase family C00026982 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00026982 2 / 3
P17538 Chymotrypsinogen B S1A C00026982 0 / 0
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00026982 1 / 1
O75496 Geminin Unclassified protein C00026981 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00026982 4 / 1
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00026981 0 / 0
P06276 Cholinesterase Hydrolase C00026981 0 / 0
P00374 Dihydrofolate reductase Oxidoreductase C00000112 1 / 1
P22303 Acetylcholinesterase Hydrolase C00026981 1 / 0
P02766 Transthyretin Secreted protein C00026981 3 / 2
P10636 Microtubule-associated protein tau Unclassified protein C00026982 4 / 3
P10275 Androgen receptor NR3C4 C00000113 3 / 4
P23141 Liver carboxylesterase 1 Enzyme C00026981 0 / 0
O95067 G2/mitotic-specific cyclin-B2 Other cytosolic protein C00026982 0 / 0
P14635 G2/mitotic-specific cyclin-B1 Other cytosolic protein C00026982 0 / 0
Q8WWL7 G2/mitotic-specific cyclin-B3 Other cytosolic protein C00026982 0 / 0
P49840 Glycogen synthase kinase-3 alpha Gsk C00026982 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00026982 0 / 0

52 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
36 ACADSB, 2-MEBCAD, ACAD7, SBCAD acyl-CoA dehydrogenase, short/branched chain (EC:1.3.8.5) C00026982
196 AHR, bHLHe76 aryl hydrocarbon receptor C00026982
378 ARF4, ARF2 ADP-ribosylation factor 4 C00026982
405 ARNT, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00026982
10575 CCT4, CCT-DELTA, Cctd, SRB chaperonin containing TCP1, subunit 4 (delta) C00026982
1000 CDH2, CD325, CDHN, CDw325, NCAD cadherin 2, type 1, N-cadherin (neuronal) C00026982
983 CDK1, CDC2, CDC28A, P34CDC2 cyclin-dependent kinase 1 (EC:2.7.11.23 2.7.11.22) C00026982
1017 CDK2, p33(CDK2) cyclin-dependent kinase 2 (EC:2.7.11.22) C00026982
1195 CLK1, CLK, CLK/STY, STY CDC-like kinase 1 (EC:2.7.12.1) C00026982
9318 COPS2, ALIEN, CSN2, SGN2, TRIP15 COP9 signalosome subunit 2 C00026982
1441 CSF3R, CD114, GCSFR colony stimulating factor 3 receptor (granulocyte) C00026982
3577 CXCR1, C-C, C-C-CKR-1, CD128, CD181, CDw128a, CKR-1, CMKAR1, IL8R1, IL8RA, IL8RBA chemokine (C-X-C motif) receptor 1 C00026982
1588 CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) C00026982
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00026982
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00026982
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00026982
3491 CYR61, CCN1, GIG1, IGFBP10 cysteine-rich, angiogenic inducer, 61 C00026982
1869 E2F1, E2F-1, RBAP1, RBBP3, RBP3 E2F transcription factor 1 C00026982
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00026982
3281 HSBP1, NPC-A-13 heat shock factor binding protein 1 C00026982
3329 HSPD1, CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13 heat shock 60kDa protein 1 (chaperonin) C00026982
10808 HSPH1, HSP105, HSP105A, HSP105B, NY-CO-25 heat shock 105kDa/110kDa protein 1 C00026982
3458 IFNG, IFG, IFI interferon, gamma C00026982
3484 IGFBP1, AFBP, IBP1, IGF-BP25, PP12, hIGFBP-1 insulin-like growth factor binding protein 1 C00026982
3554 IL1R1, CD121A, D2S1473, IL-1R-alpha, IL1R, IL1RA, P80 interleukin 1 receptor, type I C00026982
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00026982
3608 ILF2, NF45, PRO3063 interleukin enhancer binding factor 2 C00026982
3688 ITGB1, CD29, FNRB, GPIIA, MDF2, MSK12, VLA-BETA, VLAB integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12) C00026982
3689 ITGB2, CD18, LAD, LCAMB, LFA-1, MAC-1, MF17, MFI7 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) C00026982
4258 MGST2, GST2, MGST-II microsomal glutathione S-transferase 2 (EC:2.5.1.18) C00026982
4436 MSH2, COCA1, FCC1, HNPCC, HNPCC1, LCFS2 mutS homolog 2 C00026982
653361 NCF1, NCF1A, NOXO2, SH3PXD1A, p47phox neutrophil cytosolic factor 1 C00026982
4864 NPC1, NPC Niemann-Pick disease, type C1 C00026982
5925 RB1, OSRC, RB, p105-Rb, pRb, pp110 retinoblastoma 1 C00026982
4735 SEPT2, DIFF6, NEDD-5, NEDD5, Pnutl3, hNedd5 septin 2 C00026982
6514 SLC2A2, GLUT2 solute carrier family 2 (facilitated glucose transporter), member 2 C00026982
6688 SPI1, OF, PU.1, SFPI1, SPI-1, SPI-A spleen focus forming virus (SFFV) proviral integration oncogene C00026982
6938 TCF12, CRS3, HEB, HTF4, HsT17266, bHLHb20 transcription factor 12 C00026982
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00026982
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00026982
231 AKR1B1, ADR, ALDR1, ALR2, AR aldo-keto reductase family 1, member B1 (aldose reductase) (EC:1.1.1.21) C00026981
8574 AKR7A2, AFAR, AFAR1, AFB1-AR1, AKR7 aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) (EC:1.1.1.n11) C00026981
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00026981
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00026981
874 CBR3, SDR21C2, hCBR3 carbonyl reductase 3 (EC:1.1.1.184) C00026981
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00026981
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00026981
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00026981
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00026981
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00026981
6647 SOD1, ALS, ALS1, IPOA, SOD, hSod1, homodimer superoxide dismutase 1, soluble (EC:1.15.1.1) C00026981
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00026981

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#105210 Amyloidosis, hereditary, transthyretin-related P02766
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#300615 Brunner syndrome P21397
#115430 Carpal tunnel syndrome; cts1 P02766
#145680 Dystransthyretinemic euthyroidal hyperthyroxinemia P02766
#600274 Frontotemporal dementia; ftd P10636
#601626 Leukemia, acute myeloid; aml P36888
#613839 Megaloblastic anemia due to dihydrofolate reductase deficiency P00374
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#112100 Yt blood group antigen P22303

KEGG DISEASE (16)

KEGG name UniProt
H01197 Dihydrofolate reductase (DHFR) deficiency P00374 (related)
H00798 Familial carpal tunnel syndrome P02766 (related)
H00845 Familial amyloidosis P02766 (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)
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)
H00548 Brunner syndrome P21397 (related)
H00003 Acute myeloid leukemia (AML) P36888 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006968 Hypersensitivity, Delayed C00026982