General Information of the Protein
Protein ID
PT02448
Protein Name
Non-lysosomal glucosylceramidase
Secondarily
Protein Name
Beta-glucocerebrosidase 2
Bile acid beta-glucosidase GBA2
Bile acid glucosyl transferase GBA2
Cholesterol glucosyltransferase GBA2
Cholesteryl-beta-glucosidase GBA2
Glucosylceramidase 2
Non-lysosomal cholesterol glycosyltransferase
Non-lysosomal galactosylceramidase
Non-lysosomal glycosylceramidase
Gene Name
GBA2
Secondarily
Gene Name
KIAA1605
SPG46
AD035
Sequence
MGTQDPGNMGTGVPASEQISCAKEDPQVYCPEETGGTKDVQVTDCKSPEDSRPPKETDCCNPEDSGQLMVSYEGKAMGYQVPPFGWRICLAHEFTEKRKPFQANNVSLSNMIKHIGMGLRYLQWWYRKTHVEKKTPFIDMINSVPLRQIYGCPLGGIGGGTITRGWRGQFCRWQLNPGMYQHRTVIADQFTVCLRREGQTVYQQVLSLERPSVLRSWNWGLCGYFAFYHALYPRAWTVYQLPGQNVTLTCRQITPILPHDYQDSSLPVGVFVWDVENEGDEALDVSIMFSMRNGLGGGDDAPGGLWNEPFCLERSGETVRGLLLHHPTLPNPYTMAVAARVTAATTVTHITAFDPDSTGQQVWQDLLQDGQLDSPTGQSTPTQKGVGIAGAVCVSSKLRPRGQCRLEFSLAWDMPRIMFGAKGQVHYRRYTRFFGQDGDAAPALSHYALCRYAEWEERISAWQSPVLDDRSLPAWYKSALFNELYFLADGGTVWLEVLEDSLPEELGRNMCHLRPTLRDYGRFGYLEGQEYRMYNTYDVHFYASFALIMLWPKLELSLQYDMALATLREDLTRRRYLMSGVMAPVKRRNVIPHDIGDPDDEPWLRVNAYLIHDTADWKDLNLKFVLQVYRDYYLTGDQNFLKDMWPVCLAVMESEMKFDKDHDGLIENGGYADQTYDGWVTTGPSAYCGGLWLAAVAVMVQMAALCGAQDIQDKFSSILSRGQEAYERLLWNGRYYNYDSSSRPQSRSVMSDQCAGQWFLKACGLGEGDTEVFPTQHVVRALQTIFELNVQAFAGGAMGAVNGMQPHGVPDKSSVQSDEVWVGVVYGLAATMIQEGLTWEGFQTAEGCYRTVWERLGLAFQTPEAYCQQRVFRSLAYMRPLSIWAMQLALQQQQHKKASWPKVKQGTGLRTGPMFGPKEAMANLSPE
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Organism
Homo sapiens, Human
Protein Classification
Enzyme
Function
Non-lysosomal glucosylceramidase that catalyzes the hydrolysis of glucosylceramides/GlcCers (such as beta-D-glucosyl-(1<->1')-N-acylsphing-4-enine) to free glucose and ceramides (such as N-acylsphing-4-enine) (PubMed:17105727, PubMed:30308956, PubMed:32144204). GlcCers are membrane glycosphingolipids that have a wide intracellular distribution (By similarity). They are the main precursors of more complex glycosphingolipids that play a role in cellular growth, differentiation, adhesion, signaling, cytoskeletal dynamics and membrane properties (By similarity). Involved in the transglucosylation of cholesterol, transfers glucose from GlcCer to cholesterol, thereby modifying its water solubility and biological properties (PubMed:32144204). Under specific conditions, may catalyze the reverse reaction, transferring glucose from cholesteryl-3-beta-D-glucoside to ceramide (such as N-acylsphing-4-enine) (Probable). May play a role in the metabolism of bile acids (PubMed:11489889, PubMed:9111029, PubMed:17080196). Able to hydrolyze bile acid 3-O-glucosides as well as to produce bile acid-glucose conjugates thanks to a bile acid glucosyl transferase activity (PubMed:11489889, PubMed:9111029, PubMed:17080196). Catalyzes the hydrolysis of galactosylceramides/GalCers (such as beta-D-galactosyl-(1<->1')-N-acylsphing-4-enine), as well as the galactosyl transfer between GalCers and cholesterol in vitro with lower activity compared with their activity against GlcCers (PubMed:32144204).
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Uniprot ID
Primary ID:
Q9HCG7

Secondarily ID:
D3DRP2
Q5TCV6
Q96A51
Q96LY1
Q96SJ2
Q9H2L8
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Ensembl ID
ENSG00000070610
HGNC ID
HGNC:18986
Subcellular Location
Endoplasmic reticulum membrane
Golgi apparatus membrane
Map of Molecular Bioactivity Related to the Protein
Map of Molecular Bioactivity Related to the Protein

Protein
Cell Line
Compound

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Protein
Cell Line ID: CL000004 , SH-SY5Y
Compound ID Compound Name Compound Formula
CP0166849
(2R,3R,4R,5S)-1-(5-hexoxypentyl)-2-(hydroxymethyl)piperidine-3,4,5-triol
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C17H35NO5
 1
1
IC50 = 0.4 nM
   TI
   LI
   LO
   TS
CP0444073
1-(5-hexoxypentyl)-2-(hydroxymethyl)piperidine-3,4,5-triol
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C17H35NO5
 1
1
IC50 = 1 nM
   TI
   LI
   LO
   TS
CP0038675
(2R,3R,4R,5S)-2-(hydroxymethyl)-1-nonylpiperidine-3,4,5-triol
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C15H31NO4
 1
1
IC50 = 3 nM
   TI
   LI
   LO
   TS
CP0045196
(2R,3R,4R,5S)-1-[5-(Adamantan-1-ylmethoxy)-pentyl]-2-hydroxymethyl-piperidine-3,4,5-triol
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C22H39NO5
 1
1
IC50 = 3 nM
   TI
   LI
   LO
   TS
CP0421966
1-[5-(1-adamantylmethoxy)pentyl]-2-(hydroxymethyl)piperidine-3,4,5-triol
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C22H39NO5
 1
1
IC50 = 4 nM
   TI
   LI
   LO
   TS
CP0052556
(2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol
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C10H21NO4
 1
1
IC50 = 14 nM
   TI
   LI
   LO
   TS
CP0083161
(2R,3R,4R,5S)-2-(hydroxymethyl)-1-(5-nonoxypentyl)piperidine-3,4,5-triol
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C20H41NO5
 1
1
IC50 = 34 nM
   TI
   LI
   LO
   TS
CP0050249
2-Hydroxymethyl-1-nonyl-piperidine-3,4,5-triol
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C15H31NO4
 1
1
IC50 = 35 nM
   TI
   LI
   LO
   TS
CP0444074
2-(hydroxymethyl)-1-(5-nonoxypentyl)piperidine-3,4,5-triol
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C20H41NO5
 1
1
IC50 = 44 nM
   TI
   LI
   LO
   TS
CP0444075
(2S,3S,4S,5R)-1-[5-(1-adamantylmethoxy)pentyl]-2-(hydroxymethyl)piperidine-3,4,5-triol
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C22H39NO5
 1
1
IC50 = 65 nM
   TI
   LI
   LO
   TS
CP0384591
(2S,3S,4S,5R)-2-(hydroxymethyl)-1-(5-nonoxypentyl)piperidine-3,4,5-triol
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C20H41NO5
 1
1
IC50 = 137 nM
   TI
   LI
   LO
   TS
CP0536752
1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol
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C10H21NO4
 1
1
IC50 = 260 nM
   TI
   LI
   LO
   TS
CP0384593
(2S,3S,4S,5R)-2-(hydroxymethyl)-1-nonylpiperidine-3,4,5-triol
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C15H31NO4
 1
1
IC50 = 4600 nM
   TI
   LI
   LO
   TS
CP0181793
(2S,3S,4S,5R)-1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol
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C10H21NO4
 1
1
IC50 = 7700 nM
   TI
   LI
   LO
   TS
CP0536750
(2S,3S,4S,5R)-1-(5-hexoxypentyl)-2-(hydroxymethyl)piperidine-3,4,5-triol
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C17H35NO5
 1
1
IC50 = 36700 nM
   TI
   LI
   LO
   TS
Biochemical Assays
Compound ID Compound Name Compound Formula
CP0045196
(2R,3R,4R,5S)-1-[5-(Adamantan-1-ylmethoxy)-pentyl]-2-hydroxymethyl-piperidine-3,4,5-triol
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C22H39NO5
 2
1 IC50 = 1 nM
2 IC50 = 2 nM
CP0038675
(2R,3R,4R,5S)-2-(hydroxymethyl)-1-nonylpiperidine-3,4,5-triol
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C15H31NO4
 1
1 IC50 = 7 nM
CP0166849
(2R,3R,4R,5S)-1-(5-hexoxypentyl)-2-(hydroxymethyl)piperidine-3,4,5-triol
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C17H35NO5
 1
1 IC50 = 8 nM
CP0083161
(2R,3R,4R,5S)-2-(hydroxymethyl)-1-(5-nonoxypentyl)piperidine-3,4,5-triol
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C20H41NO5
 1
1 IC50 = 40 nM
CP0052556
(2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol
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C10H21NO4
 2
1 IC50 = 230 nM
2 IC50 = 300 nM