6fm9
Crystal structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1)Crystal structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1)
Structural highlights
Disease[GPT_HUMAN] DPAGT1-CDG;Congenital myasthenic syndromes with glycosylation defect. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Function[GPT_HUMAN] Catalyzes the initial step in the synthesis of dolichol-P-P-oligosaccharides. |
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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
- Arrowsmith, C H
- Beeson, D
- Belaya, K
- Berridge, G
- Bountra, C
- Burgess-Brown, N
- Carpenter, E P
- Chalk, R
- Chu, A
- Dong, L
- Dong, Y Y
- Edwards, A M
- Goubin, S
- Kupinska, K
- Mahajan, P
- Mukhopadhyay, S
- Pike, A C.W
- Structural genomic
- Tessitore, A
- Wang, D
- Congenital myasthenic syndrome 13
- Integral membrane protein
- Protein glycosylation
- Sgc
- Transferase