HEMK1
-
Official Full Name
HemK methyltransferase family member 1 -
Synonyms
HEMK1;HemK methyltransferase family member 1;MTQ1;HEMK;M.HsaHemKP;HEMK homolog 7kb
Recombinant Proteins
- Human
- Zebrafish
- Mouse
- E.coli
- Insect Cells
- Wheat Germ
- Mammalian Cells
- HEK293
- In Vitro Cell Free System
- His
- GST
- Non
- DDK
- Myc
- Avi
- Fc
Involved Pathway
HEMK1 involved in several pathways and played different roles in them. We selected most pathways HEMK1 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with HEMK1 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
Protein Function
HEMK1 has several biochemical functions, for example, DNA binding,N-methyltransferase activity,protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by HEMK1 itself. We selected most functions HEMK1 had, and list some proteins which have the same functions with HEMK1. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| DNA binding | HIVEP2,HIF1AL2,NOSTRIN,TRIM27,ZFP523,ZNF80,CHD6,TCEA3,TOP1L,RORCB |
| protein binding | TPRGL,GJA1,PDCD6IP,SEPT6,TRPC4AP,GSTO1,AIG1,ZNF212,GGA3,CALM3 |
| protein methyltransferase activity | FAM86,NDUFAF5,N6AMT1,PRDM13,PRDM11,CARM1,NTMT1,TRMT10C,PRDM12,METTL21D |
| N-methyltransferase activity | PRMT1,FBLL1,FAM86,METTL8,RNMTL1B,METTL21D,RNMTL1A,PRDM11,PRDM12,TRMT10B |
Interacting Protein
HEMK1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with HEMK1 here. Most of them are supplied by our site. Hope this information will be useful for your research of HEMK1.
CHN1;CDC23
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References
- Zechi-Ceide, RM; Rodrigues, MG; et al. Saethre-Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7. AMERICAN JOURNAL OF MEDICAL GENETICS PART A 158A:1680-1685(2012).
