MPDU1 M1T [endoplasmic reticulum membrane]

Stable Identifier
R-HSA-4717381
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Mannose-P-dolichol utilization defect 1 protein, MPU1_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
MPDU1
Chain
initiator methionine:1, chain:2-247
Other Identifiers
0002190136
11716227_a_at
11716228_x_at
11747202_x_at
11747542_a_at
11747543_x_at
11762319_at
16830589
209208_at
35791_at
3708876
3708880
3708881
3708882
3708885
3708886
3708889
3708890
3708892
3708893
3708894
3708895
8004521
9526
A_14_P118957
A_14_P121020
A_23_P26799
A_24_P198844
A_33_P3268464
A_33_P3268466
GE54333
GO:0003674
GO:0005515
GO:0005575
GO:0005789
GO:0005975
GO:0006457
GO:0006464
GO:0006488
GO:0006629
GO:0008150
GO:0009058
GO:0009312
GO:0016020
GO:0016021
GO:0043226
ILMN_1655654
PH_hs_0000676
PH_hs_0035492
TC17002037.hg
g12001955_3p_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-methionine 1 replaced with L-threonine
Coordinate
1
PsiMod
A protein modification that effectively converts a source amino acid residue to L-threonine.
A protein modification that effectively removes or replaces an L-methionine.
Disease
Name Identifier Synonyms
congenital disorder of glycosylation type I 0050570
Interactors (1)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:Q9NQG1 MANBL      0.556 3
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