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N-acetylglucosamine-1-phosphate transferase

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(Redirected from UDP-N-acetylglucosamine-1-phosphotransferase) Mammalian protein found in Homo sapiens
N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
Identifiers
SymbolGNPTAB
Alt. symbolsGNPTA
NCBI gene79158
HGNC29670
OMIM607840
RefSeqNM_024312
UniProtQ3T906
Other data
LocusChr. 12 q23.3
Search for
StructuresSwiss-model
DomainsInterPro
N-acetylglucosamine-1-phosphate transferase, gamma subunit
Identifiers
SymbolGNPTG
Alt. symbolsGNPTAG
NCBI gene84572
HGNC23026
OMIM607838
RefSeqNM_032520
UniProtQ9UJJ9
Other data
LocusChr. 16 p13.3
Search for
StructuresSwiss-model
DomainsInterPro

N-acetylglucosamine-1-phosphate transferase (GlcNAc-1-phosphotransferase) is a transferase enzyme.

Function

It is made up of two alpha (α), two betas (β), and two gammas (γ) subunits. GNPTAB produces the alpha and beta subunits, GNPTG produces the gamma subunit. GlcNAc-1-phosphotransferase functions to prepare newly made enzymes for lysosome transportation (lysosomal hydrolases to the lysosome). Lysosomes, a part of an animal cell, helps break down large molecules into smaller ones that can be reused. GlcNAc-1-phosphotransferase phosphorylates carbon 6 of one or more mannosyl residues of N linked glycoproteins being processed in Golgi Apparatus . UDP-GLcNAc provides the phosphate in a reaction catalysed by this enzyme. M6P acts as an indicator of whether a hydrolase should be transported to the lysosome or not. Once a hydrolase indicates an M6P, it can be transported to a lysosome. Surprisingly some lysosomal enzymes are only tagged at a rate of 5% or lower.

Clinical significance

It is associated with the following conditions:

In melanocytic cells, GNPTG gene expression may be regulated by MITF.

References

  1. Online Mendelian Inheritance in Man (OMIM): MUCOLIPIDOSIS II ALPHA/BETA - 252500
  2. Online Mendelian Inheritance in Man (OMIM): MUCOLIPIDOSIS III GAMMA - 252605
  3. Hoek KS, Schlegel NC, Eichhoff OM, et al. (2008). "Novel MITF targets identified using a two-step DNA microarray strategy". Pigment Cell Melanoma Res. 21 (6): 665–76. doi:10.1111/j.1755-148X.2008.00505.x. PMID 19067971. S2CID 24698373.

Kang, C., Riazuddin, S., Mundorff, J., Krasnewich, D., Friedman, P., Mullikin, J.C., and Drayna, D. (2010). Mutations in the Lysosomal Enzyme–Targeting Pathway and Persistent Stuttering. New England Journal of Medicine 362, 677–685.

External links

Transferases: phosphorus-containing groups (EC 2.7)
2.7.1-2.7.4:
phosphotransferase/kinase
(PO4)
2.7.1: OH acceptor
2.7.2: COOH acceptor
2.7.3: N acceptor
2.7.4: PO4 acceptor
2.7.6: diphosphotransferase
(P2O7)
2.7.7: nucleotidyltransferase
(PO4-nucleoside)
Polymerase
DNA polymerase
DNA-directed DNA polymerase
I/A
γ
θ
ν
T7
Taq
II/B
α
δ
ε
ζ
Pfu
III/C
IV/X
β
λ
μ
TDT
V/Y
η
ι
κ
RNA-directed DNA polymerase
Reverse transcriptase
Telomerase
RNA polymerase
Template-directed
RNA polymerase I
II
III
IV
V
ssRNAP
POLRMT
Primase
1
2
PrimPol
RNA-dependent RNA polymerase
Polyadenylation
PAP
PNPase
Phosphorolytic
3' to 5' exoribonuclease
Nucleotidyltransferase
Guanylyltransferase
Other
2.7.8: miscellaneous
Phosphatidyltransferases
Glycosyl-1-phosphotransferase
2.7.10-2.7.13: protein kinase
(PO4; protein acceptor)
2.7.10: protein-tyrosine
2.7.11: protein-serine/threonine
2.7.12: protein-dual-specificity
2.7.13: protein-histidine
Metabolism: carbohydrate metabolism · glycoprotein enzymes
Anabolism
Catabolism
Transport
M6P tagging


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