Protein Name: 1,4-alpha-glucan-branching enzyme
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UniprotKB/SwissProt ID: GLGB_HUMAN (Q04446)
Gene Name: GBE1
Organism: Homo sapiens (Human).
Function: Required for sufficient glycogen accumulation. The alpha 1-6 branches of glycogen play an important role in increasing the solubility of the molecule and, consequently, in reducing the osmotic pressure within cells.
Other Modifications: View all modification sites in dbPTM
Protein Subcellular Localization:
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Protein disease:
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| Disease database |
Database Entry |
Disease information | | HPRD | 01985 | Glycogen storage disease IV, childhood neuromuscular | | HPRD | 01985 | Glycogen storage disease IV, classic hepatic | | HPRD | 01985 | Glycogen storage disease IV, combined hepatic and myopathic | | HPRD | 01985 | Glycogen storage disease IV, congenital neuromuscular | | HPRD | 01985 | Glycogen storage disease IV, fatal perinatal neuromuscular | | HPRD | 01985 | Glycogen storage disease IV, nonprogressive hepatic |
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Network with metabolic pathway:
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Graphical Visualization of S-nitrosylation Sites:
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| Overview of Protein S-nitrosylation Sites with Functional and Structural Information |  |
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