KNApSAcK Metabolite C00007323
Metabolite
KNApSAcK Entry
| id | C00007323 |
|---|---|
| Name | D-Cysteine |
| CAS RN | 921-01-7 |
| Standard InChI | InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m1/s1 |
| Standard InChI (Main Layer) | InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6) |
Cluster
| Phytochemical cluster | |
|---|---|
| KCF-S cluster | No. 2426 |
Link
ChEMBL
| By standard InChI | CHEMBL171281 |
|---|---|
| By standard InChI Main Layer | CHEMBL863 CHEMBL54943 CHEMBL171281 |
KEGG
| By LinkDB | C00793 |
|---|
CTD
| By CAS RN |
|---|
Species
Summary
Plant class
| class name | count |
|---|---|
| rosids | 1 |
Family
| family name | count |
|---|---|
| Brassicaceae | 1 |
List (1)
* NCBI
| KNApSAcK organism | *ID | *family | *plant class | *kingdom |
|---|---|---|---|---|
| Arabidopsis thaliana | 3702 | Brassicaceae | rosids | Viridiplantae |
Human Protein / Gene in interaction
11 ChEMBL Protein in interactions
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| P02545 | Prelamin-A/C | Unclassified protein | CHEMBL54943 |
CHEMBL1614544
(1)
|
11 / 10 |
| P78536 | Disintegrin and metalloproteinase domain-containing protein 17 | M12B | CHEMBL54943 |
CHEMBL873712
(2)
|
1 / 0 |
| P11473 | Vitamin D3 receptor | NR1I1 | CHEMBL54943 CHEMBL171281 |
CHEMBL1794311
(2)
|
2 / 3 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | CHEMBL54943 |
CHEMBL1794584
(1)
|
2 / 0 |
| Q9Y2Q3 | Glutathione S-transferase kappa 1 | Enzyme | CHEMBL54943 |
CHEMBL683576
(1)
CHEMBL683578
(1)
CHEMBL683580 (1) CHEMBL880099 (1) CHEMBL683582 (1) CHEMBL685223 (1) |
0 / 0 |
| P52732 | Kinesin-like protein KIF11 | Other cytosolic protein | CHEMBL863 |
CHEMBL896510
(1)
|
1 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL171281 |
CHEMBL1614250
(1)
CHEMBL1614421
(1)
|
4 / 3 |
| Q7Z2H8 | Proton-coupled amino acid transporter 1 | Unclassified protein | CHEMBL863 |
CHEMBL1919336
(2)
|
0 / 0 |
| Q9UPY5 | Cystine/glutamate transporter | Unclassified protein | CHEMBL863 |
CHEMBL1072818
(1)
CHEMBL1072820
(1)
CHEMBL1072821 (1) CHEMBL1072824 (1) CHEMBL1112741 (1) CHEMBL1919955 (1) |
0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL54943 |
CHEMBL1738442
(1)
|
0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | CHEMBL54943 |
CHEMBL1614364
(1)
|
1 / 1 |
Related Disease
Diseases related to proteins in ChEMBL interactions
OMIM (22)
| OMIM | preferred title | UniProt |
|---|---|---|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #614328 | Inflammatory skin and bowel disease, neonatal; nisbd |
P78536
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #152950 | Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation; mclmr |
P52732
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG DISEASE (17)
| KEGG | disease name | UniProt |
|---|---|---|
| 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)
|
| 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)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|