EC Tree |
1. Oxidoreductases |
1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen |
1.14.18 With another compound as one donor, and incorporation of one atom of oxygen into the other donor |
ID: | 1.14.18.7 |
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Description: | Dihydroceramide fatty acyl 2-hydroxylase. |
Alternative Name: |
Plant sphingolipid fatty acid 2-hydroxylase. |
Click one PDB to see exact 3D structure provided by NGL.
Note: Use your mouse to drag, rotate, and zoom in and out of the structure. Mouse-over to identify atoms and bonds. Mouse controls documentation.UniProtKB Enzyme Link: | UniProtKB 1.14.18.7 |
BRENDA Enzyme Link: | BRENDA 1.14.18.7 |
KEGG Enzyme Link: | KEGG1.14.18.7 |
BioCyc Enzyme Link: | BioCyc 1.14.18.7 |
ExPASy Enzyme Link: | ExPASy1.14.18.7 |
EC2PDB Enzyme Link: | EC2PDB 1.14.18.7 |
ExplorEnz Enzyme Link: | ExplorEnz 1.14.18.7 |
PRIAM enzyme-specific profiles Link: | PRIAM 1.14.18.7 |
IntEnz Enzyme Link: | IntEnz 1.14.18.7 |
MEDLINE Enzyme Link: | MEDLINE 1.14.18.7 |
MSA: | |
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Phylogenetic Tree: | |
Uniprot: | |
M-CSA: |
RHEA:46512 | 2 [Fe(II)-cytochrome b5] + a N-(1,2-saturated acyl)sphinganine + 2 H(+) + O2 = 2 [Fe(III)-cytochrome b5] + a N-[(2'R)-hydroxyacyl]sphinganine + H2O |
RULE(radius=1) | [*:1]-[CH2;+0:2]-[*:3].[Fe+2;H0:4].[Fe+2;H0:5].[H+;H0:6].[H+;H0:7].[O;H0;+0:8]=[O;H0;+0:9]>>[*:1]-[CH;+0:2](-[*:3])-[OH;+0:8].[Fe+3;H0:4].[Fe+3;H0:5].[OH2;+0:9] |
Reaction | ![]() |
Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
Title | Authors | Date | PubMed ID |
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Plant sphingolipid fatty acid 2-hydroxylases have unique characters unlike their animal and fungus counterparts. | Nagano M, Uchimiya H, Kawai-Yamada M | 2012 Nov | 22918503 |
Arabidopsis sphingolipid fatty acid 2-hydroxylases (AtFAH1 and AtFAH2) are functionally differentiated in fatty acid 2-hydroxylation and stress responses. | Nagano M, Takahara K, Fujimoto M, Tsutsumi N, Uchimiya H, Kawai-Yamada M | 2012 Jul | 22635113 |
Functional association of cell death suppressor, Arabidopsis Bax inhibitor-1, with fatty acid 2-hydroxylation through cytochrome b₅. | Nagano M, Ihara-Ohori Y, Imai H, Inada N, Fujimoto M, Tsutsumi N, Uchimiya H, Kawai-Yamada M | 2009 Apr | 19054355 |