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Methylmalonyl Coenzyme A Mutase Proteins (MUT)

MUT encodes the mitochondrial enzyme methylmalonyl Coenzyme A mutase. Additionally we are shipping Methylmalonyl Coenzyme A Mutase Antibodies (20) and Methylmalonyl Coenzyme A Mutase Kits (4) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
MUT 4594 P22033
Rat MUT MUT 688517  
MUT 17850 P16332
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Top Methylmalonyl Coenzyme A Mutase Proteins at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 39 to 44 Days
$9,248.02
Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 39 to 44 Days
$9,248.02
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details

MUT Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine)

More Proteins for Methylmalonyl Coenzyme A Mutase (MUT) Interaction Partners

Human Methylmalonyl Coenzyme A Mutase (MUT) interaction partners

  1. In methylmalonic acidemia,a total of 10 novel MUT mutations were detected in the Chinese population. c.729_730insTT (p.D244Lfs*39) was the most frequent mutation.

  2. Two novel mutations of the MUT gene, including c.581C>T (p.P194L) and c.1219A>T (p.N407Y), are associated with methylmalonic academia in a Chinese family.

  3. Five different known mutations in either MUT or MMACHC (show MMACHC Proteins) genes were identified in seven of the eight Chinese patients with methyl malonic acidemia.

  4. 3 Patients with Isolated methylmalonic acidemia lacked methylmalonyl-CoA mutase (MCM) activity and had no MCM band, patients with the cobalamin defects had high MCM activity levels and an intense MCM band at about 83 kDa, in comparison to those in their parents.

  5. a novel splice site mutation in intron 12 of the MUT gene is a potential highly pathogenic allele via inhibition of alternative splicing leading to Methylmalonic aciduria.

  6. data stratify MUT missense mutations into categories of biochemical defects, including (1) reduced protein level due to misfolding, (2) increased thermolability, (3) impaired enzyme activity, and (4) reduced cofactor response in substrate turnover

  7. Mutations in MUT cause methylmalonic acidemia.

  8. Using alanine-scanning mutagenesis, we demonstrate that the switch III motif is critical for bidirectional signal transmission of the GTPase-activating protein (show RASA1 Proteins) activity of MCM and the chaperone functions of MeaB in the MeaB-MCM complex.

  9. The contribution of Glu338 in human MCM to adenosylcobalamin Co-C bond labilization and catalysis was evaluated by substituting the residue with a glutamine, aspartate, or alanine. The MCM variants showed 16-, 330-, and 12-fold reductions in k(cat).

  10. This work reveals that Mexican patients with MMA have new (p.V136F) as well as worldwide and hispanic reported mutations. The mutation R108C is the most frequent change (40% of total alleles) mainly in patients from Leon, Guanajuato

Pig (Porcine) Methylmalonyl Coenzyme A Mutase (MUT) interaction partners

Mouse (Murine) Methylmalonyl Coenzyme A Mutase (MUT) interaction partners

  1. The mouse methylmalonic aciduria- related genes, Mmaa (show MMAA Proteins), Mmab (show MMAB Proteins), and Mut may have specialized functions depending on the tissue or cell type.

  2. methylmalonyl-CoA mutase has a role in methylmalonic aciduria and early neonatal lethality

  3. Mitochondrial dysfunction in Mut is reported.

Methylmalonyl Coenzyme A Mutase (MUT) Protein Profile

Protein Summary

This gene encodes the mitochondrial enzyme methylmalonyl Coenzyme A mutase. In humans, the product of this gene is a vitamin B12-dependent enzyme which catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA, while in other species this enzyme may have different functions. Mutations in this gene may lead to various types of methylmalonic aciduria.

Gene names and symbols associated with MUT

  • methylmalonyl CoA mutase (MUT)
  • methylmalonyl Coenzyme A mutase (mut)
  • methylmalonyl CoA mutase (mut)
  • methylmalonyl CoA mutase (Mut)
  • methylmalonyl-Coenzyme A mutase (Mut)
  • D230010K02Rik protein
  • Mcm protein

Protein level used designations for MUT

methylmalonyl Coenzyme A mutase , methylmalonyl-CoA mutase, mitochondrial , methylmalonyl CoA mutase , methylmalonyl-CoA isomerase , methylmalonyl-Coenzyme A mutase , MCM

GENE ID SPECIES
422049 Gallus gallus
463198 Pan troglodytes
474930 Canis lupus familiaris
569581 Danio rerio
706189 Macaca mulatta
100357233 Oryctolagus cuniculus
100379804 Xenopus (Silurana) tropicalis
4594 Homo sapiens
688517 Rattus norvegicus
399535 Sus scrofa
280871 Bos taurus
100174196 Pongo abelii
17850 Mus musculus
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