| Record Information |
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| Version | 2.0 |
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| Creation Date | 2015-06-04 15:14:56 -0600 |
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| Update Date | 2015-09-17 16:25:05 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | L-Lysyl-tRNA |
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| Description | L-Lysyl-tRNA is an intermediate in tRNA charging pathway in E.coli. It is a product for the enzyme lysyl-tRNA synthetase which catalyzes the reaction ATP + L-lysine + tRNALys -> AMP + diphosphate + L-lysyl-tRNALys (BioCyc class: Charged-LYS-tRNAs). |
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| Structure | |
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| Synonyms: | - moco (dioxyo)
- Molybdenum cofactor
- Molybdenum cofactor (dioxyo)
- Molybdopterin
- Molybdopterin cofactor
- MoO2(OH)DTPP-MP
- Pterin molybdenum cofactor
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| Chemical Formula: | C10H16MoN5O8PS2 |
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| Weight: | Average: 525.31
Monoisotopic: 526.923197 |
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| InChI Key: | VUKICSJFFDCESC-UHFFFAOYSA-L |
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| InChI: | InChI=1S/C10H14N5O6PS2.Mo.2H2O/c11-10-14-7-4(8(16)15-10)12-3-6(24)5(23)2(21-9(3)13-7)1-20-22(17,18)19;;;/h2-3,9,12,23-24H,1H2,(H2,17,18,19)(H4,11,13,14,15,16);;2*1H2/q;+2;;/p-2 |
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| CAS number: | Not Available |
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| IUPAC Name: | {[(1R,10R,16R)-5-amino-7,13,13-trioxo-17-oxa-12,14-dithia-2,4,6,9-tetraaza-13-molybdatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-3(8),5,11(15)-trien-16-yl]methoxy}phosphonic acid |
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| Traditional IUPAC Name: | [(1R,10R,16R)-5-amino-7,13,13-trioxo-17-oxa-12,14-dithia-2,4,6,9-tetraaza-13-molybdatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁵]heptadeca-3(8),5,11(15)-trien-16-yl]methoxyphosphonic acid |
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| SMILES: | O.O.[Mo++].[H]C1(COP(O)([O-])=O)OC2([H])NC3=C(NC2([H])C(S)=C1S)C([O-])=NC(=N)N3 |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as molybdopterins. These are cofactors or analogs thereof, with a structure based on a furan ring fused to a pterin. In addition, the pyran ring features two thiolates, which serve as ligands in molybdo- and tungstoenzymes. In some cases, the alkyl phosphate group is replaced by an alkyl diphosphate nucleotide. |
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| Kingdom | Organic compounds |
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| Super Class | Organoheterocyclic compounds |
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| Class | Pteridines and derivatives |
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| Sub Class | Pterins and derivatives |
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| Direct Parent | Molybdopterins |
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| Alternative Parents | |
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| Substituents | - Molybdopterin
- Pyranopterin
- Aminopyrimidine
- Pyrimidone
- Secondary aliphatic/aromatic amine
- Monoalkyl phosphate
- Organic phosphoric acid derivative
- Phosphoric acid ester
- Pyran
- Pyrimidine
- Alkyl phosphate
- Heteroaromatic compound
- Vinylogous amide
- Oxacycle
- Azacycle
- Organic transition metal salt
- Secondary amine
- Organic nitrogen compound
- Amine
- Primary amine
- Hydrocarbon derivative
- Organosulfur compound
- Organooxygen compound
- Organonitrogen compound
- Organic oxide
- Organic salt
- Organic zwitterion
- Organic oxygen compound
- Aromatic heteropolycyclic compound
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| Molecular Framework | Aromatic heteropolycyclic compounds |
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| External Descriptors | |
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| Physical Properties |
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| State: | Not Available |
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| Charge: | -2 |
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| Melting point: | Not Available |
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| Experimental Properties: | |
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| Predicted Properties | |
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| Biological Properties |
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| Cellular Locations: | Cytoplasm |
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| Reactions: | |
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| SMPDB Pathways: | Not Available |
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| KEGG Pathways: | - Aminoacyl-tRNA biosynthesis ec00970
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| EcoCyc Pathways: | Not Available |
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| Concentrations |
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| Not Available |
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| Spectra |
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| Spectra: | |
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| References |
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| References: | Not Available |
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| Synthesis Reference: | Not Available |
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| Material Safety Data Sheet (MSDS) | Not Available |
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| Links |
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| External Links: | | Resource | Link |
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| CHEBI ID | 71306 | | HMDB ID | Not Available | | Pubchem Compound ID | 56928099 | | Kegg ID | C01931 | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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