Organism name | Puccinia graminis |
---|---|
Genus | Puccinia |
Family | Pucciniaceae |
Kingdom | Fungi |
Linked NCBI taxonomy name | Puccinia graminis |
---|---|
Linked NCBI taxonomy ID | 5297 |
Linked level | species |
Family in NCBI taxonomy | Pucciniaceae |
---|---|
ID | 5262 |
Kingdom (Superkingdom) in NCBI taxonomy | Fungi |
---|---|
ID | 4751 |
Plant class | |
---|---|
ID |
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 |
---|---|---|---|---|---|---|---|---|
C00003786
![]() |
Torulene
/ 3',4'-Didehydro-beta,psi-carotene |
C078922
|
No. 131 | No. 59 |
![]() |
|||
C00002476
![]() |
Herniarin
/ 7-Methoxycoumarin |
CHEMBL49732
|
C007929
|
23 / 10 / 12 | No. 864 | No. 25 |
![]() |
|
C00002462
![]() |
Daphnetin
|
CHEMBL244948
|
C039952
|
40 / 43 / 40 | No. 1030 | No. 25 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002462 C00002476 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002462 C00002476 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00002462 C00002476 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002462 C00002476 | 0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002462 C00002476 | 2 / 2 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002462 C00002476 | 3 / 3 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002462 | 0 / 0 |
P43166 | Carbonic anhydrase 7 | Lyase | C00002476 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00002462 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00002462 | 11 / 10 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00002462 | 1 / 1 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00002462 | 3 / 1 |
P00918 | Carbonic anhydrase 2 | Lyase | C00002476 | 1 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002462 | 0 / 1 |
P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00002462 | 1 / 8 |
P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00002462 | 0 / 0 |
P23280 | Carbonic anhydrase 6 | Lyase | C00002476 | 0 / 0 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00002462 | 0 / 0 |
Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00002476 | 0 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002462 | 1 / 0 |
P28845 | Corticosteroid 11-beta-dehydrogenase isozyme 1 | Enzyme | C00002476 | 1 / 1 |
O43570 | Carbonic anhydrase 12 | Lyase | C00002476 | 1 / 2 |
P39748 | Flap endonuclease 1 | Enzyme | C00002462 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002462 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00002462 | 0 / 0 |
P15121 | Aldose reductase | Enzyme | C00002476 | 0 / 0 |
P00915 | Carbonic anhydrase 1 | Lyase | C00002476 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00002462 | 1 / 1 |
P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00002476 | 0 / 0 |
P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00002462 | 0 / 0 |
P56817 | Beta-secretase 1 | A1A | C00002476 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002462 | 0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00002476 | 0 / 1 |
Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00002476 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00002462 | 0 / 0 |
Q01453 | Peripheral myelin protein 22 | Unclassified protein | C00002462 | 5 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00002462 | 0 / 0 |
Q00796 | Sorbitol dehydrogenase | Enzyme | C00002476 | 0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002462 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002462 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002462 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002462 | 0 / 0 |
Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00002462 | 1 / 0 |
P21728 | D(1A) dopamine receptor | Dopamine receptor | C00002462 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002462 | 4 / 3 |
Q99549 | M-phase phosphoprotein 8 | Unclassified protein | C00002462 | 0 / 0 |
P07451 | Carbonic anhydrase 3 | Lyase | C00002476 | 0 / 0 |
P22748 | Carbonic anhydrase 4 | Lyase | C00002476 | 1 / 1 |
P80365 | Corticosteroid 11-beta-dehydrogenase isozyme 2 | Enzyme | C00002476 | 1 / 1 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00002462 | 2 / 0 |
O14980 | Exportin-1 | Unclassified protein | C00002476 | 0 / 0 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00002462 | 4 / 1 |
P40225 | Thrombopoietin | Unclassified protein | C00002462 | 1 / 1 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002462 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002462 | 1 / 1 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00002462 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00002462 | 1 / 4 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#218030 | Apparent mineralocorticoid excess; ame |
P80365
|
#608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
#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
|
#604931 | Cortisone reductase deficiency 1; cortrd1 |
P28845
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#139393 | Guillain-barre syndrome, familial; gbs |
Q01453
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#145900 | Hypertrophic neuropathy of dejerine-sottas |
Q01453
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#211980 | Lung cancer |
P00533
|
#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
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp |
Q01453
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#600852 | Retinitis pigmentosa 17; rp17 |
P22748
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#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
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#187950 | Thrombocythemia 1; thcyt1 |
P40225
|
#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
|
#278300 | Xanthinuria, type i |
P47989
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
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)
|
H00022 | Bladder cancer |
P00533
(related)
|
H00028 | Choriocarcinoma |
P00533
(related)
|
H00030 | Cervical cancer |
P00533
(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)
|
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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00527 | Retinitis pigmentosa (RP) |
P22748
(related)
|
H01111 | Cortisone reductase deficiency (CRD) |
P28845
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00227 | Congenital amegakaryocytic thrombocytopenia (CAMT) |
P40225
(marker)
|
H00192 | Xanthinuria |
P47989
(related)
|
H00259 | Apparent mineralocorticoid excess syndrome |
P80365
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (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)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(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)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|