|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||Cat.#||Product name||Source (Host)||Tag||Protein Length||Price|
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.
|GTP binding||ARF6; LGALS6; EEF1A1L2; EIF2S3Y; EEFSEC; RAB30; NMUR2; ARL1; SEPT1; RHOV|
|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.