| EC Tree |
| 2. Transferases |
| 2.5 Transferring alkyl or aryl groups, other than methyl groups |
| 2.5.1 Transferring alkyl or aryl groups, other than methyl groups (only sub-subclass identified to date) |
| ID: | 2.5.1.43 |
|---|---|
| Description: | Nicotianamine synthase. |
| Prosite: | PDOC51142; |
| PDB: |
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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 2.5.1.43 |
| BRENDA Enzyme Link: | BRENDA 2.5.1.43 |
| KEGG Enzyme Link: | KEGG2.5.1.43 |
| BioCyc Enzyme Link: | BioCyc 2.5.1.43 |
| ExPASy Enzyme Link: | ExPASy2.5.1.43 |
| EC2PDB Enzyme Link: | EC2PDB 2.5.1.43 |
| ExplorEnz Enzyme Link: | ExplorEnz 2.5.1.43 |
| PRIAM enzyme-specific profiles Link: | PRIAM 2.5.1.43 |
| IntEnz Enzyme Link: | IntEnz 2.5.1.43 |
| MEDLINE Enzyme Link: | MEDLINE 2.5.1.43 |
| RHEA:16481 | 3 S-adenosyl-L-methionine = 3 H(+) + nicotianamine + 3 S-methyl-5'-thioadenosine |
| RULE(radius=1) | [*:1]-[S+;H0:2](-[*:3])-[CH2;+0:4]-[*:5].[*:6]-[S+;H0:7](-[*:8])-[CH2;+0:9]-[*:10]-[*:11]-[NH2;+0:12].[*:13]-[S+;H0:14](-[*:15])-[CH2;+0:16]-[*:17]-[*:18]-[NH2;+0:19]>>[*:5]-[CH2;+0:4]-[NH;+0:12]-[*:11]-[*:10]-[CH2;+0:9]-[N;H0;+0:19]1-[*:18]-[*:17]-[CH2;+0:16]-1.[*:1]-[S;H0;+0:2]-[*:3].[*:6]-[S;H0;+0:7]-[*:8].[*:13]-[S;H0;+0:14]-[*:15] |
| Reaction | ![]() |
| Core-to-Core | No scaffolds atoms were exchanged as a result of the reaction |
| Title | Authors | Date | PubMed ID |
|---|---|---|---|
| The crystallographic structure of thermoNicotianamine synthase with a synthetic reaction intermediate highlights the sequential processing mechanism. | Dreyfus C, Larrouy M, Cavelier F, Martinez J, Pignol D, Arnoux P | 2011 May 28 | 21487608 |