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CAZyme Information: KIV98786.1

You are here: Home > Sequence: KIV98786.1

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 Verruconis gallopava
Lineage Ascomycota; Dothideomycetes; ; Sympoventuriaceae; Verruconis; Verruconis gallopava
CAZyme ID KIV98786.1
CAZy Family AA1
CAZyme Description Cutinase [Source:UniProtKB/TrEMBL;Acc:A0A0D1YDG7]
CAZyme Property
Protein Length CGC Molecular Weight Isoelectric Point
526 KN847597|CGC2 57957.42 5.8130
Genome Property
Genome Version/Assembly ID Genes Strain NCBI Taxon ID Non Protein Coding Genes Protein Coding Genes
FungiDB-61_VgallopavaCBS43764 9871 N/A 53 9818
Gene Location

Full Sequence      Download help

Enzyme Prediction      help

EC 3.1.1.74:3

CAZyme Signature Domains help

Family Start End Evalue family coverage
CE5 356 518 5.2e-38 0.9576719576719577

CDD Domains      download full data without filtering help

Cdd ID Domain E-Value qStart qEnd sStart sEnd Domain Description
293755 G6S_like 2.79e-145 3 321 1 290
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.
293758 sulfatase_like 5.88e-49 4 318 1 277
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.
293766 G6S 6.31e-47 4 318 1 293
glucosamine (N-acetyl)-6-sulfatase(G6S, GNS) AND sulfatase 1(SULF1). 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. Deficient of N-acetylglucosamine-6-sulfatase results in disease of Sanfilippo Syndrome type IIId or Mucopolysaccharidosis III (MPS-III), a rare autosomal recessive lysosomal storage disease. SULF1 encodes an extracellular heparan sulfate endosulfatase, that removes 6-O-sulfate groups from heparan sulfate chains of heparan sulfate proteoglycans (HSPGs).
395860 Cutinase 9.94e-47 356 510 1 158
Cutinase.
293751 SGSH 4.81e-46 5 306 1 227
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.

CAZyme Hits      help

Hit ID E-Value Query Start Query End Hit Start Hit End
2.71e-124 78 321 1 250
2.80e-124 78 321 1 250
3.30e-60 3 206 2 228
2.17e-54 338 526 114 303
1.33e-51 347 526 188 368

PDB Hits      download full data without filtering help

Hit ID E-Value Query Start Query End Hit Start Hit End Description
1.83e-84 4 321 28 366
Structure of BT4656 in complex with its substrate D-Glucosamine-2-N, 6-O-disulfate. [Bacteroides thetaiotaomicron VPI-5482]
1.65e-74 2 379 7 415
Chain A, Sulfatase [Akkermansia muciniphila ATCC BAA-835],7EBP_B Chain B, Sulfatase [Akkermansia muciniphila ATCC BAA-835],7EBQ_A Chain A, Sulfatase [Akkermansia muciniphila ATCC BAA-835]
4.21e-61 6 321 28 345
Chain A, Exo-L-galactose-6-sulfatase [Bacteroides uniformis],7LHA_B Chain B, Exo-L-galactose-6-sulfatase [Bacteroides uniformis],7LJ2_A Chain A, Exo-L-galactose-6-sulfatase [Bacteroides uniformis],7LJ2_B Chain B, Exo-L-galactose-6-sulfatase [Bacteroides uniformis]
4.26e-32 331 523 48 246
Structure of cutinase from Trichoderma reesei in its native form. [Trichoderma reesei QM6a],4PSD_A Structure of Trichoderma reesei cutinase native form. [Trichoderma reesei QM6a],4PSE_A Trichoderma reesei cutinase in complex with a C11Y4 phosphonate inhibitor [Trichoderma reesei QM6a],4PSE_B Trichoderma reesei cutinase in complex with a C11Y4 phosphonate inhibitor [Trichoderma reesei QM6a]
4.45e-25 344 509 16 191
Chain A, CUTINASE [Fusarium vanettenii]

Swiss-Prot Hits      download full data without filtering help

Hit ID E-Value Query Start Query End Hit Start Hit End Description
1.73e-83 4 321 52 390
N-acetylglucosamine-6-O-sulfatase OS=Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) OX=226186 GN=BT_4656 PE=1 SV=1
6.60e-40 350 518 24 194
Cutinase OS=Botryotinia fuckeliana OX=40559 GN=cutA PE=1 SV=1
1.20e-38 344 526 47 223
Cutinase 4 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) OX=227321 GN=cut4 PE=2 SV=1
5.57e-32 323 525 9 200
Cutinase OS=Monilinia fructicola OX=38448 GN=CUT1 PE=2 SV=1
1.89e-31 331 523 48 246
Cutinase OS=Hypocrea jecorina (strain QM6a) OX=431241 GN=TRIREDRAFT_60489 PE=3 SV=2

SignalP and Lipop Annotations help

This protein is predicted as OTHER

Other SP_Sec_SPI CS Position
1.000059 0.000002

TMHMM  Annotations      help

There is no transmembrane helices in KIV98786.1.