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CAZyme Information: MGYG000003035_01263

You are here: Home > Sequence: MGYG000003035_01263

Basic Information | Genomic context | Full Sequence | Enzyme annotations |  CAZy signature domains |  CDD domains | CAZyme hits | PDB hits | Swiss-Prot hits | SignalP and Lipop annotations | TMHMM annotations

Basic Information help

Species CAG-485 sp900542185
Lineage Bacteria; Bacteroidota; Bacteroidia; Bacteroidales; Muribaculaceae; CAG-485; CAG-485 sp900542185
CAZyme ID MGYG000003035_01263
CAZy Family GH10
CAZyme Description Choline-sulfatase
CAZyme Property
Protein Length CGC Molecular Weight Isoelectric Point
522 59635.06 7.6666
Genome Property
Genome Assembly ID Genome Size Genome Type Country Continent
MGYG000003035 3548444 MAG Netherlands Europe
Gene Location Start: 36524;  End: 38092  Strand: +

Full Sequence      Download help

Enzyme Prediction      help

No EC number prediction in MGYG000003035_01263.

CDD Domains      download full data without filtering help

Cdd ID Domain E-Value qStart qEnd sStart sEnd Domain Description
cd16030 iduronate-2-sulfatase 0.0 29 501 2 435
iduronate-2-sulfatase. Iduronate 2-sulfatase is a sulfatase enzyme that catalyze the hydrolysis of sulfate ester bonds from a wide variety of substrates, including steroids, carbohydrates and proteins. Iduronate 2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in the iduronate 2-sulfatase gene that result in enzymatic deficiency lead to the sex-linked mucopolysaccharidosis type II, also known as Hunter syndrome.
cd16031 G6S_like 2.70e-85 28 510 1 424
unchracterized sulfatase homologous to glucosamine (N-acetyl)-6-sulfatase(G6S, GNS). N-acetylglucosamine-6-sulfatase also known as glucosamine (N-acetyl)-6-sulfatase hydrolyzes of the 6-sulfate groups of the N-acetyl-D-glucosamine 6-sulfate units of heparan sulfate and keratan sulfate. Deficiency of N-acetylglucosamine-6-sulfatase results in the disease of Sanfilippo Syndrome type IIId or Mucopolysaccharidosis III (MPS-III), a rare autosomal recessive lysosomal storage disease.
cd16027 SGSH 5.82e-83 30 510 1 366
N-sulfoglucosamine sulfohydrolase (SGSH; sulfamidase). N-sulfoglucosamine sulfohydrolase (SGSH) belongs to the sulfatase family and catalyses the cleavage of N-linked sulfate groups from the GAGs heparin sulfate and heparin. The active site is characterized by the amino-acid sequence motif C(X)PSR that is highly conserved among most sulfatases. The cysteine residue is post-translationally converted to a formylglycine (FGly) residue, which is crucial for the catalytic process. Loss of function of SGSH results a disease called mucopolysaccharidosis type IIIA (Sanfilippo A syndrome), a fatal childhood-onset neurodegenerative disease with mild facial, visceral and skeletal abnormalities.
cd16037 sulfatase_like 1.13e-76 30 490 1 321
uncharacterized sulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.
cd16033 sulfatase_like 1.69e-74 30 509 1 399
uncharacterized sulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.

CAZyme Hits      help

Hit ID E-Value Query Start Query End Hit Start Hit End
QWG09488.1 5.00e-153 29 517 23 511
AZQ64847.1 1.10e-151 29 517 23 511
AOR25410.1 3.68e-150 22 509 18 506
ANQ52496.2 1.13e-147 23 519 17 514
QWG04788.1 1.13e-147 23 519 17 514

PDB Hits      download full data without filtering help

Hit ID E-Value Query Start Query End Hit Start Hit End Description
6HHM_A 3.39e-80 29 509 16 453
Crystalstructure of the family S1_7 ulvan-specific sulfatase FA22070 from Formosa agariphila [Formosa agariphila]
5FQL_A 1.16e-75 25 498 7 513
Insightsinto Hunter syndrome from the structure of iduronate-2- sulfatase [Homo sapiens]
6IOZ_A 2.62e-75 31 498 5 505
Structuralinsights of idursulfase beta [Homo sapiens]
4UG4_A 8.88e-33 26 499 5 432
ChainA, Choline Sulfatase [Sinorhizobium meliloti],4UG4_B Chain B, Choline Sulfatase [Sinorhizobium meliloti],4UG4_C Chain C, Choline Sulfatase [Sinorhizobium meliloti],4UG4_D Chain D, Choline Sulfatase [Sinorhizobium meliloti],4UG4_E Chain E, Choline Sulfatase [Sinorhizobium meliloti],4UG4_F Chain F, Choline Sulfatase [Sinorhizobium meliloti],4UG4_G Chain G, Choline Sulfatase [Sinorhizobium meliloti],4UG4_H Chain H, Choline Sulfatase [Sinorhizobium meliloti]
6G5Z_A 3.27e-31 29 499 1 425
ChainA, Choline-sulfatase [Sinorhizobium meliloti],6G5Z_B Chain B, Choline-sulfatase [Sinorhizobium meliloti],6G5Z_C Chain C, Choline-sulfatase [Sinorhizobium meliloti],6G5Z_D Chain D, Choline-sulfatase [Sinorhizobium meliloti],6G60_A Choline sulfatase from Ensifer (Sinorhizobium) meliloti cocrystalized with choline [Sinorhizobium meliloti 1021],6G60_B Choline sulfatase from Ensifer (Sinorhizobium) meliloti cocrystalized with choline [Sinorhizobium meliloti 1021],6G60_C Choline sulfatase from Ensifer (Sinorhizobium) meliloti cocrystalized with choline [Sinorhizobium meliloti 1021],6G60_D Choline sulfatase from Ensifer (Sinorhizobium) meliloti cocrystalized with choline [Sinorhizobium meliloti 1021]

Swiss-Prot Hits      download full data without filtering help

Hit ID E-Value Query Start Query End Hit Start Hit End Description
T2KM04 2.36e-93 29 508 32 461
Ulvan-active sulfatase OS=Formosa agariphila (strain DSM 15362 / KCTC 12365 / LMG 23005 / KMM 3901 / M-2Alg 35-1) OX=1347342 GN=BN863_22000 PE=1 SV=1
Q08890 1.76e-79 31 509 40 551
Iduronate 2-sulfatase OS=Mus musculus OX=10090 GN=Ids PE=2 SV=3
T2KPK5 1.87e-79 24 509 25 466
Ulvan-active sulfatase OS=Formosa agariphila (strain DSM 15362 / KCTC 12365 / LMG 23005 / KMM 3901 / M-2Alg 35-1) OX=1347342 GN=BN863_22070 PE=1 SV=2
P22304 1.16e-74 25 498 32 538
Iduronate 2-sulfatase OS=Homo sapiens OX=9606 GN=IDS PE=1 SV=1
T2KMG4 8.94e-56 29 509 30 463
Sulfatase OS=Formosa agariphila (strain DSM 15362 / KCTC 12365 / LMG 23005 / KMM 3901 / M-2Alg 35-1) OX=1347342 GN=BN863_22030 PE=1 SV=2

SignalP and Lipop Annotations help

This protein is predicted as OTHER

Other SP_Sec_SPI LIPO_Sec_SPII TAT_Tat_SPI TATLIP_Sec_SPII PILIN_Sec_SPIII
0.759044 0.239138 0.001267 0.000210 0.000144 0.000196

TMHMM  Annotations      help

There is no transmembrane helices in MGYG000003035_01263.