Non-lysosomal glucosylceramidase (GBA2)

Homo sapiens — UniProt Q9HCG7

Gene: GBA2Homo sapiensSwissProt reviewed

About Non-lysosomal glucosylceramidase

Non-lysosomal glucosylceramidase (GBA2) is a protein from Homo sapiens identified by UniProt accession Q9HCG7, 927 residues long. MolForge cross-references it against 0 known binders and 180 disease associations.

Target properties

Protein nameNon-lysosomal glucosylceramidase
UniProt accessionQ9HCG7
GeneGBA2
OrganismHomo sapiens
Length927 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Approved drugs hitting this target (2)

DrugCentral-linked approved drugs that act on this protein.

Disease associations (180)

Diseases linked to this target (Open Targets).

  • Autosomal recessive spastic paraplegia type 46 · score 0.80
  • hereditary spastic paraplegia 46 · score 0.73
  • Spastic paraplegia · score 0.55
  • hereditary spastic paraplegia · score 0.49
  • autosomal recessive cerebellar ataxia with late-onset spasticity · score 0.37
  • Neurodevelopmental disorder · score 0.33
  • CEP290-related ciliopathy · score 0.27
  • Parkinson disease · score 0.26
  • lysosomal storage disease · score 0.26
  • multiple sclerosis · score 0.26

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9HCG7-F1alphafoldPREDICTED89.22—

Amino-acid sequence (927 residues)

MGTQDPGNMG TGVPASEQIS CAKEDPQVYC PEETGGTKDV QVTDCKSPED SRPPKETDCC NPEDSGQLMV SYEGKAMGYQ VPPFGWRICL AHEFTEKRKP FQANNVSLSN MIKHIGMGLR YLQWWYRKTH VEKKTPFIDM INSVPLRQIY GCPLGGIGGG TITRGWRGQF CRWQLNPGMY QHRTVIADQF TVCLRREGQT VYQQVLSLER PSVLRSWNWG LCGYFAFYHA LYPRAWTVYQ LPGQNVTLTC RQITPILPHD YQDSSLPVGV FVWDVENEGD EALDVSIMFS MRNGLGGGDD APGGLWNEPF CLERSGETVR GLLLHHPTLP NPYTMAVAAR VTAATTVTHI TAFDPDSTGQ QVWQDLLQDG QLDSPTGQST PTQKGVGIAG AVCVSSKLRP RGQCRLEFSL AWDMPRIMFG AKGQVHYRRY TRFFGQDGDA APALSHYALC RYAEWEERIS AWQSPVLDDR SLPAWYKSAL FNELYFLADG GTVWLEVLED SLPEELGRNM CHLRPTLRDY GRFGYLEGQE YRMYNTYDVH FYASFALIML WPKLELSLQY DMALATLRED LTRRRYLMSG VMAPVKRRNV IPHDIGDPDD EPWLRVNAYL IHDTADWKDL NLKFVLQVYR DYYLTGDQNF LKDMWPVCLA VMESEMKFDK DHDGLIENGG YADQTYDGWV TTGPSAYCGG LWLAAVAVMV QMAALCGAQD IQDKFSSILS RGQEAYERLL WNGRYYNYDS SSRPQSRSVM SDQCAGQWFL KACGLGEGDT EVFPTQHVVR ALQTIFELNV QAFAGGAMGA VNGMQPHGVP DKSSVQSDEV WVGVVYGLAA TMIQEGLTWE GFQTAEGCYR TVWERLGLAF QTPEAYCQQR VFRSLAYMRP LSIWAMQLAL QQQQHKKASW PKVKQGTGLR TGPMFGPKEA MANLSPE

Explore Non-lysosomal glucosylceramidase with MolForge

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Quick facts

UniProtQ9HCG7
GeneGBA2
OrganismHomo sapiens
Length927
Binders0
Diseases180
View on UniProt