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M1004

Sigma-Aldrich

Met-Ala-Ser

≥97% (TLC)

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About This Item

Empirische Formel (Hill-System):
C11H21N3O5S
CAS-Nummer:
17351-33-6
Molekulargewicht:
307.37
MDL-Nummer:
MFCD00055791
UNSPSC-Code:
12352202
PubChem Substanz-ID:
24896466
NACRES:
NA.26

product name

Met-Ala-Ser,

Assay

≥97% (TLC)

Form

powder

Farbe

white

Lagertemp.

−20°C

SMILES String

CSCC[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(O)=O

InChI

1S/C11H21N3O5S/c1-6(9(16)14-8(5-15)11(18)19)13-10(17)7(12)3-4-20-2/h6-8,15H,3-5,12H2,1-2H3,(H,13,17)(H,14,16)(H,18,19)/t6-,7-,8-/m0/s1

InChIKey

WXHHTBVYQOSYSL-FXQIFTODSA-N

Amino Acid Sequence

Met-Ala-Ser

Anwendung

Met-Ala-Ser has been used as a tripeptide in the OH radical-induced oxidation reaction and analysis by high performance liquid chromatography-diode array detector-fluorescence detector (HPLC-DAD-FLD).

Biochem./physiol. Wirkung

Met-Ala-Ser (MAS) is used to complex with peptide deformylase(s) (PDF) to help delineate mechanisms of recognition of mimic-peptides by N-terminal cleaved expression peptide.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Qing Tang et al.
The Journal of cell biology, 214(2), 167-179 (2016-07-20)
Myo51, a class V myosin in fission yeast, localizes to and assists in the assembly of the contractile ring, a conserved eukaryotic actomyosin structure that facilitates cytokinesis. Rng8 and Rng9 are binding partners that dictate the cellular localization and function
Cong Han et al.
Biochemical and biophysical research communications, 319(4), 1292-1298 (2004-06-15)
Helicobacter pylori is a gram-negative pathogenic bacterium, which is associated with peptic ulcer disease and gastric cancer. It is urgent to discover novel drug targets for appropriate antimicrobial agents against this human pathogen. In bacteria, peptide deformylase (PDF) catalyzes the
Abayomi D Olaitan et al.
Rapid communications in mass spectrometry : RCM, 32(21), 1887-1896 (2018-08-02)
Common surface-assisted laser desorption/ionization (SALDI) surfaces are functionalized to improve mass spectrometric detection. Such surfaces are selective to certain group(s) of compounds. The application of universal and sensitive SALDI surfaces with appropriate size/surface area is paramount. In this study, two
Ki Hyun Nam et al.
Biochemical and biophysical research communications, 381(4), 630-633 (2009-03-03)
PDF (peptide deformylase) plays a critical role in the production of mature proteins by removing the N-formyl polypeptide of nascent proteins in the prokaryote cell system. This protein is essential for bacterial growth, making it an attractive target for the
A Becker et al.
Nature structural biology, 5(12), 1053-1058 (1998-12-10)
Eubacterial proteins are synthesized with a formyl group at the N-terminus which is hydrolytically removed from the nascent chain by the mononuclear iron enzyme peptide deformylase. Catalytic efficiency strongly depends on the identity of the bound metal. We have determined
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