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SRP0383

EHMT1 human

recombinant, expressed in E. coli, ≥63% (SDS-PAGE)

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Synonym(s):

EHMT1, KMT1D

NACRES:

NA.32

biological source

human

recombinant

expressed in E. coli

Assay

≥63% (SDS-PAGE)

form

aqueous solution

mol wt

72.4 kDa

packaging

pkg of 50 μg

NCBI accession no.

NM_024757

UniProt accession no.

Q9H9B1

shipped in

dry ice

storage temp.

−70°C

Gene Information

human ... EHMT1(79813)

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This Item	SRP0135	SRP0140	SRP0136
Sigma-Aldrich SRP0383 EHMT1 human	Sigma-Aldrich SRP0135 G9a human	Sigma-Aldrich SRP0140 PRMT1 human	Sigma-Aldrich SRP0136 G9a human
recombinant expressed in E. coli	recombinant expressed in E. coli	recombinant expressed in E. coli	recombinant expressed in baculovirus infected insect cells
assay ≥63% (SDS-PAGE)	assay ≥70% (SDS-PAGE)	assay ≥50% (SDS-PAGE)	assay ≥70% (SDS-PAGE)
form aqueous solution	form aqueous solution	form aqueous solution	form aqueous solution
mol wt 72.4 kDa	mol wt 74.6 kDa	mol wt 68 kDa	mol wt 74.6 kDa
NCBI accession no. NM_024757	NCBI accession no. NM_006709	NCBI accession no. NM_001536	NCBI accession no. NM_006709

General description

Human euchromatic histone-lysine N-methyltransferase (EHMT1), also known as G9a-like protein (GLP) or KMT1D, (GenBank Accession No. NM_024757), amino acids 894-1298 (end) with N-terminal GST-tag, MW= 72.4 kDa, expressed in an E. coli expression system.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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N+-C-H···O Hydrogen bonds in protein-ligand complexes.

Yukihiro Itoh et al.

Scientific reports, 9(1), 767-767 (2019-01-27)

In the context of drug design, C-H···O hydrogen bonds have received little attention so far, mostly because they are considered weak relative to other noncovalent interactions such as O-H···O hydrogen bonds, π/π interactions, and van der Waals interactions. Herein, we

Molecular and clinical roles of incretin-based drugs in patients with heart failure.

Bassant Orabi et al.

Heart failure reviews, 23(3), 363-376 (2018-04-24)

Glucagon-like peptide-1 (GLP-1) agonists and dipeptidyl peptidase-4 (DPP-4) inhibitors produce some beneficial and deleterious effects in diabetic patients not mediated by their glycemic lowering effects, and there is a need for better understanding of the molecular basis of these effects.

Comparative analysis of glucagonergic cells, glia, and the circumferential marginal zone in the reptilian retina.

Levi Todd et al.

The Journal of comparative neurology, 524(1), 74-89 (2015-06-09)

Retinal progenitors in the circumferential marginal zone (CMZ) and Müller glia-derived progenitors have been well described for the eyes of fish, amphibians, and birds. However, there is no information regarding a CMZ and the nature of retinal glia in species

G9a and Glp methylate lysine 373 in the tumor suppressor p53.

Jing Huang et al.

The Journal of biological chemistry, 285(13), 9636-9641 (2010-02-02)

The tumor suppressor p53 is regulated by numerous post-translational modifications. Lysine methylation has recently emerged as a key post-translational modification that alters the activity of p53. Here, we describe a novel lysine methylation site in p53 that is carried out

Zinc finger protein Wiz links G9a/GLP histone methyltransferases to the co-repressor molecule CtBP.

Jun Ueda et al.

The Journal of biological chemistry, 281(29), 20120-20128 (2006-05-17)

G9a is a SET-domain mammalian histone methyltransferase responsible for mono- and dimethylation of lysine 9 in histone H3 (H3K9) at euchromatic regions. Recently we reported that G9a forms a stoichiometric heteromeric complex with another SET-domain-containing molecule, GLP/Eu-HMTase1. Although G9a and

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