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25679-93-0

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25679-93-0 Usage

General Description

L-Histidinol Phosphate is a biochemical compound belonging to a class of organic compounds known as peptides. It is an essential intermediate in the biosynthesis of the essential amino acid histidine, which plays a crucial role in the growth and repair of tissues. L-HISTIDINOL PHOSPHATE is produced through a series of enzymatic reactions, where it is progressively converted to histidine. Its formation involves phosphorylation, which adds a phosphate group to the hydroxyl group of L-histidinol, catalyzed by the enzyme histidinol-phosphate phosphatase. Intracellularly, L-Histidinol Phosphate plays a vital role in protein synthesis and is also involved in the regulation of a host of physiological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 25679-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,7 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25679-93:
(7*2)+(6*5)+(5*6)+(4*7)+(3*9)+(2*9)+(1*3)=150
150 % 10 = 0
So 25679-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N3O4P/c7-5(3-13-14(10,11)12)1-6-2-8-4-9-6/h2,4-5H,1,3,7H2,(H,8,9)(H2,10,11,12)/t5-/m0/s1

25679-93-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name L-histidinol phosphate

1.2 Other means of identification

Product number -
Other names [(2S)-2-amino-3-(1H-imidazol-5-yl)propyl] dihydrogen phosphate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25679-93-0 SDS

25679-93-0Downstream Products

25679-93-0Relevant articles and documents

Library Selection with a Randomized Repertoire of (βα)8-Barrel Enzymes Results in Unexpected Induction of Gene Expression

Rohweder, Bettina,Lehmann, Gerhard,Eichner, Norbert,Polen, Tino,Rajendran, Chitra,Ruperti, Fabian,Linde, Mona,Treiber, Thomas,Jung, Oona,Dettmer, Katja,Meister, Gunter,Bott, Michael,Gronwald, Wolfram,Sterner, Reinhard

, p. 4207 - 4217 (2019)

The potential of the frequently encountered (βα)8-barrel fold to acquire new functions was tested by an approach combining random mutagenesis and selection in vivo. For this purpose, the genes encoding 52 different phosphate-binding (βα)8-barrel proteins were subjected to error-prone PCR and cloned into an expression plasmid. The resulting mixed repertoire was used to transform different auxotrophic Escherichia coli strains, each lacking an enzyme with a phosphate-containing substrate. After plating of the different transformants on minimal medium, growth was observed only for two strains, lacking either the gene for the serine phosphatase SerB or the phosphoserine aminotransferase SerC. The same mutants of the E. coli genes nanE (encoding a putative N-acetylmannosamine-6-phosphate 2-epimerase) and pdxJ (encoding the pyridoxine 5′-phosphate synthase) were responsible for rescuing both ΔserB and ΔserC. Unexpectedly, the complementing NanE and PdxJ variants did not catalyze the SerB or SerC reactions in vitro. Instead, RT-qPCR, RNAseq, and transcriptome analysis showed that they rescue the deletions by enlisting the help of endogenous E. coli enzymes HisB and HisC through exclusive up-regulation of histidine operon transcription. While the promiscuous SerB activity of HisB is well-established, our data indicate that HisC is promiscuous for the SerC reaction, as well. The successful rescue of ΔserB and ΔserC through point mutations and recruitment of additional amino acids in NanE and PdxJ provides another example for the adaptability of the (βα)8-barrel fold.

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