MMADHC T182N [cytosol]

Stable Identifier
R-HSA-3318599
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Methylmalonic aciduria and homocystinuria type D protein, mitochondrial, MMAD_HUMAN, MMADHC
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
MMADHC, C2orf25, CL25022, HSPC161, My011
Chain
transit peptide:1-38, chain:39-296
Reference Transcript
Other Identifiers
0001230239
11722207_a_at
16903461
217883_at
2580643
2580644
2580645
2580646
2580652
2580653
2580654
2580655
2580657
2580658
2580663
2580664
2580665
2580666
2580667
27249
3369042
65896_at
8055672
A_23_P94932
GE61183
GO:0003674
GO:0005515
GO:0005575
GO:0005622
GO:0005737
GO:0005739
GO:0005829
GO:0008150
GO:0009235
GO:0043226
GO:0044281
GO:0051186
ILMN_1810759
ILMN_2090558
ILMN_3248966
PH_hs_0000545
TC02002415.hg
g7661547_3p_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-threonine 182 replaced with L-asparagine
Coordinate
182
PsiMod
A protein modification that effectively removes or replaces an L-threonine.
A protein modification that effectively converts a source amino acid residue to an L-asparagine.
Disease
Name Identifier Synonyms
methylmalonic aciduria and homocystinuria type cblD 0050716 Cobalamin D deficiency
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