Methylmalonic aciduria (cobalamin deficiency) cblA type
mammalian protein found in Homo sapiens
Press Enter · cited answer in seconds
0 sources
Summary
Methylmalonic aciduria (cobalamin deficiency) cblA type is a protein[1].
Key Facts
- Methylmalonic aciduria (cobalamin deficiency) cblA type's instance of is recorded as protein[2].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's UniProt protein ID is recorded as Q8IVH4[3].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's part of is recorded as P-loop containing nucleoside triphosphate hydrolase[4].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's part of is recorded as SIMIBI class G3E GTPase, ArgK/MeaB[5].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's RefSeq protein ID is recorded as NP_758454[6].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's RefSeq protein ID is recorded as XP_011529986[7].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's RefSeq protein ID is recorded as XP_011529987[8].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's RefSeq protein ID is recorded as XP_011529988[9].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's PDB structure ID is recorded as 2WWW[10].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's molecular function is recorded as nucleotide binding[11].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's molecular function is recorded as hydrolase activity[12].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's molecular function is recorded as GTPase activity[13].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's molecular function is recorded as protein binding[14].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's molecular function is recorded as GTP binding[15].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's molecular function is recorded as identical protein binding[16].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's molecular function is recorded as protein homodimerization activity[17].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's cell component is recorded as mitochondrial matrix[18].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's cell component is recorded as mitochondrion[19].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's biological process is recorded as cobalamin metabolic process[20].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's biological process is recorded as cobalamin biosynthetic process[21].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's biological process is recorded as short-chain fatty acid catabolic process[22].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's encoded by is recorded as MMAA[23].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's found in taxon is recorded as Homo sapiens[24].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's Ensembl protein ID is recorded as ENSP00000281317[25].
- Methylmalonic aciduria (cobalamin deficiency) cblA type's Ensembl protein ID is recorded as ENSP00000427422[26].