L-Allothreonine (BioDeep_00000399985)
Main id: BioDeep_00000014513
natural product PANOMIX_OTCML-2023 BioNovoGene_Lab2019
描述信息
The L-enantiomer of allothreonine.
L-Allothreonine (H-allo-Thr-OH) is an endogenous metabolite.
同义名列表
5 个代谢物同义名
L-Allothreonine; D-(+)-Threonine; H-Allo-Thr-OH; L-Allothreonine; D-threonine
数据库引用编号
17 个数据库交叉引用编号
- ChEBI: CHEBI:28718
- KEGG: C05519
- PubChem: 99289
- ChEMBL: CHEMBL59238
- CAS: 28954-12-3
- CAS: 144-98-9
- MoNA: EMBL-MCF_spec133558
- MoNA: CCMSLIB00000578041
- MetaboLights: MTBLC28718
- PubChem: 7864
- PDB-CCD: ALO
- 3DMET: B01870
- NIKKAJI: J1.327G
- medchemexpress: HY-W008315
- LOTUS: LTS0115582
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-339
- KNApSAcK: 28718
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
50 个相关的物种来源信息
- 3630 - Abutilon: LTS0115582
- 318060 - Abutilon indicum: 10.1055/S-0028-1097714
- 318060 - Abutilon indicum: LTS0115582
- 4150 - Antirrhinum: LTS0115582
- 4151 - Antirrhinum majus: 10.1055/S-0028-1097736
- 4151 - Antirrhinum majus: LTS0115582
- 4890 - Ascomycota: LTS0115582
- 2 - Bacteria: LTS0115582
- 5204 - Basidiomycota: LTS0115582
- 123403 - Catha: LTS0115582
- 123405 - Catha edulis: 10.1002/ARDP.19602931105
- 123405 - Catha edulis: LTS0115582
- 4305 - Celastraceae: LTS0115582
- 5110 - Claviceps: LTS0115582
- 5111 - Claviceps purpurea: 10.1055/S-0028-1100051
- 5111 - Claviceps purpurea: LTS0115582
- 34397 - Clavicipitaceae: LTS0115582
- 41218 - Colchicaceae: LTS0115582
- 13444 - Colchicum: LTS0115582
- 1094124 - Colchicum trigynum: 10.1055/S-0028-1097874
- 1094124 - Colchicum trigynum: LTS0115582
- 543 - Enterobacteriaceae: LTS0115582
- 561 - Escherichia: LTS0115582
- 562 - Escherichia coli: LTS0115582
- 2759 - Eukaryota: LTS0115582
- 3803 - Fabaceae: LTS0115582
- 4751 - Fungi: LTS0115582
- 1236 - Gammaproteobacteria: LTS0115582
- 4447 - Liliopsida: LTS0115582
- 3963 - Loranthaceae: LTS0115582
- 3398 - Magnoliopsida: LTS0115582
- 3629 - Malvaceae: LTS0115582
- 3881 - Onobrychis: LTS0115582
- 1441993 - Onobrychis kachetica: 10.1007/BF00565728
- 1441993 - Onobrychis kachetica: LTS0115582
- 156152 - Plantaginaceae: LTS0115582
- 5296 - Puccinia: LTS0115582
- 5297 - Puccinia graminis: 10.1139/V60-033
- 5297 - Puccinia graminis: LTS0115582
- 5262 - Pucciniaceae: LTS0115582
- 162484 - Pucciniomycetes: LTS0115582
- 3958 - Santalaceae: LTS0115582
- 147550 - Sordariomycetes: LTS0115582
- 35493 - Streptophyta: LTS0115582
- 58023 - Tracheophyta: LTS0115582
- 33090 - Viridiplantae: LTS0115582
- 1003255 - Viscaceae: LTS0115582
- 3971 - Viscum: LTS0115582
- 3972 - Viscum album: 10.1515/BCHM2.1960.322.1.273
- 3972 - Viscum album: LTS0115582
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
| 亚细胞结构定位 | 关联基因列表 |
|---|
文献列表
- Gilles Curien, Olivier Bastien, Mylène Robert-Genthon, Athel Cornish-Bowden, María Luz Cárdenas, Renaud Dumas. Understanding the regulation of aspartate metabolism using a model based on measured kinetic parameters.
Molecular systems biology.
2009; 5(?):271. doi:
10.1038/msb.2009.29. [PMID: 19455135] - Valérie de Crécy-Lagard, Basma El Yacoubi, Rocío Díaz de la Garza, Alexandre Noiriel, Andrew D Hanson. Comparative genomics of bacterial and plant folate synthesis and salvage: predictions and validations.
BMC genomics.
2007 Jul; 8(?):245. doi:
10.1186/1471-2164-8-245. [PMID: 17645794] - Andrea Scaloni, Mauro Dalla Serra, Pietro Amodeo, Luisa Mannina, Rosa Maria Vitale, Anna Laura Segre, Oscar Cruciani, Francesca Lodovichetti, Maria Luigia Greco, Alberto Fiore, Monica Gallo, Chiara D'Ambrosio, Manuela Coraiola, Gianfranco Menestrina, Antonio Graniti, Vincenzo Fogliano. Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: cormycin A.
The Biochemical journal.
2004 Nov; 384(Pt 1):25-36. doi:
10.1042/bj20040422. [PMID: 15196052] - Hua Zhao, Kenji Hamase, Akiko Morikawa, Zongyin Qiu, Kiyoshi Zaitsu. Determination of d- and l-enantiomers of threonine and allo-threonine in mammals using two-step high-performance liquid chromatography.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2004 Oct; 810(2):245-50. doi:
10.1016/j.jchromb.2004.08.006. [PMID: 15380721] - Sonja Hess, Kirk R Gustafson, Dennis J Milanowski, Edgardo Alvira, Mark A Lipton, Lewis K Pannell. Chirality determination of unusual amino acids using precolumn derivatization and liquid chromatography-electrospray ionization mass spectrometry.
Journal of chromatography. A.
2004 May; 1035(2):211-9. doi:
10.1016/j.chroma.2004.02.068. [PMID: 15124814] - Kwang-Hwan Jhee, Dimitri Niks, Peter McPhie, Michael F Dunn, Edith Wilson Miles. Yeast cystathionine beta-synthase reacts with L-allothreonine, a non-natural substrate, and L-homocysteine to form a new amino acid, 3-methyl-L-cystathionine.
Biochemistry.
2002 Feb; 41(6):1828-35. doi:
10.1021/bi011756t. [PMID: 11827527]
