UniProt:P51688 SGSH

chain
  • signal peptide:1-20
  • chain:21-502
checksum 90C5CDAB4DCC3808
comment
  • FUNCTION Catalyzes a step in lysosomal heparan sulfate degradation.CATALYTIC ACTIVITY N-sulfo-D-glucosamine + H2O = D-glucosamine + sulfateCOFACTOR Binds 1 Ca(2+) ion per subunit.INTERACTION The conversion to 3-oxoalanine (also known as C-formylglycine, FGly), of a serine or cysteine residue in prokaryotes and of a cysteine residue in eukaryotes, is critical for catalytic activity.DISEASE The disease is caused by variants affecting the gene represented in this entry.SIMILARITY Belongs to the sulfatase family.
databaseName UniProt
dbId 64964
description
  • recommendedName: N-sulphoglucosamine sulphohydrolase ecNumber evidence="7 15 17"3.10.1.1 alternativeName: Sulfoglucosamine sulfamidase alternativeName: Sulphamidase
displayName UniProt:P51688 SGSH
geneName
  • SGSH
  • HSS
identifier P51688
isSequenceChanged false
keyword
  • 3D-structure
  • Calcium
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Hydrolase
  • Lysosome
  • Metal-binding
  • Mucopolysaccharidosis
  • Proteomics identification
  • Reference proteome
  • Signal
moleculeType Protein
name
  • SGSH
otherIdentifier
  • 11721100_a_at
  • 11721101_x_at
  • 11721102_a_at
  • 11761080_at
  • 16849681
  • 204293_PM_at
  • 204293_at
  • 35626_PM_at
  • 35626_at
  • 3773354
  • 3773355
  • 3773356
  • 3773357
  • 3773358
  • 3773359
  • 3773360
  • 3773361
  • 3773362
  • 3773363
  • 3773364
  • 3773365
  • 3773366
  • 3773367
  • 3773368
  • 3773369
  • 3773370
  • 3773371
  • 3773372
  • 3773373
  • 3773374
  • 3773375
  • 3773377
  • 3773378
  • 3773379
  • 3773380
  • 6448
  • 8019061
  • GE59070
  • GO:0005515
  • GO:0005764
  • GO:0006027
  • GO:0006790
  • GO:0008340
  • GO:0008484
  • GO:0016250
  • GO:0016787
  • GO:0030163
  • GO:0030200
  • GO:0043202
  • GO:0046872
  • GO:0061744
  • GO:0070062
  • GO:1901135
  • HMNXSV003004665
  • HMNXSV003032939
  • Hs.128408.0.A1_3p_at
  • ILMN_2133675
  • PH_hs_0002653
  • TC17001934.hg
  • U30894_at
  • g4506918_3p_s_at
  • p7076
schemaClass ReferenceGeneProduct
secondaryIdentifier
  • SPHM_HUMAN
  • A8K5E2
sequenceLength 502
stId uniprot:P51688
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