dethiobiotin (BioDeep_00000400006)

 

Secondary id: BioDeep_00000001323

natural product PANOMIX_OTCML-2023 BioNovoGene_Lab2019


代谢物信息卡片


dl-Dithiobiotin

化学式: C10H18N2O3 (214.1317)
中文名称: 5-甲基-2-氧-4-咪唑啉己酸, D-脱硫生物素, d-Desthiobiotin
谱图信息: 最多检出来源 Homo sapiens(otcml) 21.66%

分子结构信息

SMILES: CC1C(NC(=O)N1)CCCCCC(=O)O
InChI: InChI=1S/C10H18N2O3/c1-7-8(12-10(15)11-7)5-3-2-4-6-9(13)14/h7-8H,2-6H2,1H3,(H,13,14)(H2,11,12,15)

描述信息

A hexanoic acid having a 5-methyl-2-oxoimidazolidin-4-yl group at the 6-position.
D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents
D050258 - Mitosis Modulators > D008934 - Mitogens
D-Desthiobiotin is a biotin derivative used in affinity chromatography and protein chromatography. D-Desthiobiotin also can be used for protein and cell labeling, detection and isolation[1].

同义名列表

4 个代谢物同义名

dethiobiotin; dl-Dithiobiotin; D-Desthiobiotin; Dethiobiotin



数据库引用编号

39 个数据库交叉引用编号

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)

1 个相关的物种来源信息

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
Cytoplasm 9 AK4, BIRC5, FABP5, HMGCS1, ISCU, MAP2K2, MAP2K3, PFAS, TLR4
Peripheral membrane protein 1 MAP2K2
Endosome membrane 2 INSR, TLR4
Endoplasmic reticulum membrane 2 HSP90B1, MLANA
Nucleus 5 BIRC5, FABP5, HSP90B1, ISCU, MAP2K2
cytosol 8 BIRC5, FABP5, HMGCS1, HSP90B1, ISCU, MAP2K2, MAP2K3, PFAS
trans-Golgi network 1 MLANA
nucleoplasm 4 ATP2B1, BIRC5, FABP5, MAP2K3
Cell membrane 5 AGTR1, ATP2B1, INSR, SLC5A6, TLR4
Multi-pass membrane protein 4 AGTR1, ATP2B1, SLC5A6, TPRA1
Synapse 2 ATP2B1, FABP5
cell surface 1 TLR4
glutamatergic synapse 2 ATP2B1, FABP5
Golgi apparatus 3 FUT2, MAP2K2, MLANA
Golgi membrane 2 FUT2, INS
presynaptic membrane 1 ATP2B1
smooth endoplasmic reticulum 1 HSP90B1
Lysosome 1 INSR
plasma membrane 8 AGTR1, ATP2B1, FABP5, INSR, MLANA, SLC5A6, TLR4, TPRA1
synaptic vesicle membrane 1 ATP2B1
Membrane 9 AGTR1, ATP2B1, HSP90B1, INSR, MAP2K2, MAP2K3, SLC5A6, TLR4, TPRA1
apical plasma membrane 1 SLC5A6
axon 1 INSR
basolateral plasma membrane 2 ATP2B1, SLC5A6
caveola 1 INSR
extracellular exosome 7 ATP2B1, BTD, FABP5, FUT2, HSP90B1, INSR, PFAS
endoplasmic reticulum 2 HSP90B1, MAP2K2
extracellular space 4 BTD, FABP5, INS, THPO
perinuclear region of cytoplasm 3 HSP90B1, MAP2K2, TLR4
mitochondrion 3 AK4, ISCU, MAP2K2
protein-containing complex 2 BIRC5, HSP90B1
intracellular membrane-bounded organelle 1 ATP2B1
postsynaptic density 1 FABP5
Single-pass type I membrane protein 2 INSR, TLR4
Secreted 3 FABP5, INS, THPO
extracellular region 6 BTD, FABP5, HSP90B1, INS, MAP2K2, THPO
cytoplasmic side of plasma membrane 1 MAP2K2
neuronal cell body membrane 1 INSR
Mitochondrion matrix 1 AK4
mitochondrial matrix 3 AK4, BTD, ISCU
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
external side of plasma membrane 2 INSR, TLR4
microtubule cytoskeleton 1 BIRC5
Melanosome membrane 1 MLANA
midbody 2 BIRC5, HSP90B1
Early endosome 2 MAP2K2, TLR4
cell-cell junction 1 MAP2K2
Single-pass type II membrane protein 1 FUT2
Apical cell membrane 1 SLC5A6
Cytoplasm, cytoskeleton, spindle 1 BIRC5
focal adhesion 2 HSP90B1, MAP2K2
microtubule 2 BIRC5, MAP2K2
spindle 1 BIRC5
peroxisomal membrane 1 MAP2K2
collagen-containing extracellular matrix 1 HSP90B1
lateral plasma membrane 1 ATP2B1
interphase microtubule organizing center 1 BIRC5
Cell projection, ruffle 1 TLR4
Late endosome 2 INSR, MAP2K2
ruffle 1 TLR4
receptor complex 2 INSR, TLR4
cell projection 1 ATP2B1
phagocytic cup 1 TLR4
Chromosome 1 BIRC5
centriole 1 BIRC5
Secreted, extracellular space 1 BTD
[Isoform 1]: Mitochondrion 1 ISCU
brush border membrane 1 SLC5A6
nuclear chromosome 1 BIRC5
postsynaptic density, intracellular component 1 FABP5
Basolateral cell membrane 1 ATP2B1
endosome lumen 1 INS
Chromosome, centromere 1 BIRC5
Chromosome, centromere, kinetochore 1 BIRC5
Melanosome 2 HSP90B1, MLANA
Golgi cisterna membrane 1 FUT2
Presynaptic cell membrane 1 ATP2B1
sperm plasma membrane 1 HSP90B1
basal plasma membrane 1 SLC5A6
lipopolysaccharide receptor complex 1 TLR4
secretory granule lumen 1 INS
secretory granule membrane 1 FABP5
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 HSP90B1, INS
kinetochore 1 BIRC5
transport vesicle 1 INS
azurophil granule lumen 1 FABP5
Golgi apparatus, Golgi stack membrane 1 FUT2
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
iron-sulfur cluster assembly complex 1 ISCU
mitochondrial 1 ISCU
chromosome, centromeric region 1 BIRC5
Sarcoplasmic reticulum lumen 1 HSP90B1
chromosome passenger complex 1 BIRC5
cytoplasmic microtubule 1 BIRC5
spindle microtubule 1 BIRC5
survivin complex 1 BIRC5
dendrite membrane 1 INSR
postsynaptic cytosol 1 FABP5
endocytic vesicle lumen 1 HSP90B1
insulin receptor complex 1 INSR
endoplasmic reticulum chaperone complex 1 HSP90B1
photoreceptor ribbon synapse 1 ATP2B1


文献列表

  • Di Qu, Peng Ge, Laure Botella, Sae Woong Park, Ha-Na Lee, Natalie Thornton, James M Bean, Inna V Krieger, James C Sacchettini, Sabine Ehrt, Courtney C Aldrich, Dirk Schnappinger. Mycobacterial biotin synthases require an auxiliary protein to convert dethiobiotin into biotin. Nature communications. 2024 May; 15(1):4161. doi: 10.1038/s41467-024-48448-1. [PMID: 38755122]
  • Chaoxiang Chen, Mengdi Sun, Jialin Wang, Liyun Su, Junjie Lin, Xiaomei Yan. Active cargo loading into extracellular vesicles: Highlights the heterogeneous encapsulation behaviour. Journal of extracellular vesicles. 2021 11; 10(13):e12163. doi: 10.1002/jev2.12163. [PMID: 34719860]
  • Benjamin Lake, Nickolas Serniuck, Eden Kapcan, Alex Wang, Anthony F Rullo. Covalent Immune Recruiters: Tools to Gain Chemical Control Over Immune Recognition. ACS chemical biology. 2020 04; 15(4):1089-1095. doi: 10.1021/acschembio.0c00112. [PMID: 32100991]
  • Yudi Ding, Nicholas H Williams, Christopher A Hunter. A Synthetic Vesicle-to-Vesicle Communication System. Journal of the American Chemical Society. 2019 11; 141(44):17847-17853. doi: 10.1021/jacs.9b09102. [PMID: 31642667]
  • Kathrin E Witzke, Kristin Rosowski, Christian Müller, Maike Ahrens, Martin Eisenacher, Dominik A Megger, Jürgen Knobloch, Andrea Koch, Thilo Bracht, Barbara Sitek. Quantitative Secretome Analysis of Activated Jurkat Cells Using Click Chemistry-Based Enrichment of Secreted Glycoproteins. Journal of proteome research. 2017 01; 16(1):137-146. doi: 10.1021/acs.jproteome.6b00575. [PMID: 27696881]
  • Anne-Marie Haughey, Benoit Guilhabert, Alexander L Kanibolotsky, Peter J Skabara, Martin D Dawson, Glenn A Burley, Nicolas Laurand. An oligofluorene truxene based distributed feedback laser for biosensing applications. Biosensors & bioelectronics. 2014 Apr; 54(?):679-86. doi: 10.1016/j.bios.2013.11.054. [PMID: 24355421]
  • Joji Grace Villamor, Farnusch Kaschani, Tom Colby, Julian Oeljeklaus, David Zhao, Markus Kaiser, Matthew P Patricelli, Renier A L van der Hoorn. Profiling protein kinases and other ATP binding proteins in Arabidopsis using Acyl-ATP probes. Molecular & cellular proteomics : MCP. 2013 Sep; 12(9):2481-96. doi: 10.1074/mcp.m112.026278. [PMID: 23722185]
  • David Cobessi, Renaud Dumas, Virginie Pautre, Céline Meinguet, Jean-Luc Ferrer, Claude Alban. Biochemical and structural characterization of the Arabidopsis bifunctional enzyme dethiobiotin synthetase-diaminopelargonic acid aminotransferase: evidence for substrate channeling in biotin synthesis. The Plant cell. 2012 Apr; 24(4):1608-25. doi: 10.1105/tpc.112.097675. [PMID: 22547782]
  • Guy Patchornik. Purification of His-tagged proteins with [desthiobiotin-BSA-EDTA] conjugates exhibiting resistance to EDTA. Bioconjugate chemistry. 2008 Mar; 19(3):673-9. doi: 10.1021/bc700368y. [PMID: 18311907]
  • S Chiruvolu, S Walker, J Israelachvili, F J Schmitt, D Leckband, J A Zasadzinski. Higher order self-assembly of vesicles by site-specific binding. Science (New York, N.Y.). 1994 Jun; 264(5166):1753-6. doi: 10.1126/science.8209255. [PMID: 8209255]
  • S M Krassner, B Granger, P Phermsangngnam, T Le, V Linden. Further studies on substrates inducing metacyclogenesis in Trypanosoma cruzi. The Journal of protozoology. 1990 Mar; 37(2):128-32. doi: 10.1111/j.1550-7408.1990.tb05882.x. [PMID: 2181116]
  • T Schneider, R Dinkins, K Robinson, J Shellhammer, D W Meinke. An embryo-lethal mutant of Arabidopsis thaliana is a biotin auxotroph. Developmental biology. 1989 Jan; 131(1):161-7. doi: 10.1016/s0012-1606(89)80047-8. [PMID: 2909401]