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Official Full Name methylmalonic aciduria (cobalamin deficiency) cblA type
Background The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria.
Synonyms MMAA; methylmalonic aciduria (cobalamin deficiency) cblA type; methylmalonic aciduria (cobalamin deficiency) type A; methylmalonic aciduria type A protein, mitochondrial; cblA; mitochondrial; Methylmalonic aciduria type A protein; Methylmalonic aciduria type A protein mitochondrial; MGC120010; MGC120011; MGC120012; MGC120013; MMAA_HUMAN; OTTHUMP00000220105; OTTHUMP00000220104
    • Species :
    • Human
    • Mouse
    • Zebrafish
    • Source :
    • HEK293
    • HEK293T
    • Mammalian Cell
    • Wheat Germ
    • Tag :
    • GST
    • His
    • MYC/DDK
    • Myc
    • DDK
    • N/A
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human MMAA-2148H Recombinant Human MMAA Protein, Myc/DDK-tagged, C13 and N15-labeled HEK293T Myc/DDK
    Mouse Mmaa-404M Recombinant Mouse Mmaa Protein, MYC/DDK-tagged HEK293T MYC/DDK
    Human MMAA-4286HCL Recombinant Human MMAA 293 Cell Lysate HEK293 N/A
    Human MMAA-5403H Recombinant Human MMAA Protein, GST-tagged Wheat Germ GST
    Human MMAA-573H Recombinant Human MMAA Protein, MYC/DDK-tagged HEK293 Myc/DDK
    Mouse MMAA-9895M Recombinant Mouse MMAA Protein Mammalian Cell His
    Zebrafish MMAA-5990Z Recombinant Zebrafish MMAA Mammalian Cell His

    Mmaa involved in several pathways and played different roles in them. We selected most pathways Mmaa participated on our site, such as Cobalamin (Cbl, vitamin B12) transport and metabolism, Defective MMAA causes methylmalonic aciduria type cblA, Defective MUT causes methylmalonic aciduria mut type, which may be useful for your reference. Also, other proteins which involved in the same pathway with Mmaa were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein
    Cobalamin (Cbl, vitamin B12) transport and metabolism MMADHC; ELA2L; MMAA; AMN; LOC100686744; TCN1; ELA2; MTRR; CBLC-1; CTRC
    Defective MMAA causes methylmalonic aciduria type cblA MMAA
    Defective MUT causes methylmalonic aciduria mut type MMAA
    Defects in cobalamin (B12) metabolism MMADHC; MMAA; MTRR; AMN
    Defects in vitamin and cofactor metabolism MMADHC; MTRR; MMAA; AMN
    Disease KREMEN1; JAG1; STX1B; MIB1; CTBP2; MTRR; GPC5; NA; gag; FDX1
    Diseases of metabolism CYP11A1; MMAA; SFTPC; GYG1; FDXR; FDX1L; MTRR; FDX1; CCDC59; EPM2A
    Fatty acid, triacylglycerol, and ketone body metabolism HELZ2; TIAM2; CYP7A1; CDK19; ACOT13; MED16; CCNC; ELOVL1A; ACOT11; ACOT8

    Mmaa has several biochemical functions, for example, GTP binding, hydrolase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by Mmaa itself. We selected most functions Mmaa had, and list some proteins which have the same functions with Mmaa. You can find most of the proteins on our site.

    Function Related Protein
    hydrolase activity HDHD3; ATP2A1L; PPTC7A; PRSS41; CMBL; CTSLA; INPPL1A; GLS; SHHA; F9A

    Mmaa 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 Mmaa here. Most of them are supplied by our site. Hope this information will be useful for your research of Mmaa.


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