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Difference between revisions of "Glycoside Hydrolase Family 138"

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* [[Author]]: ^^^Didier Ndeh^^^
 
* [[Author]]: ^^^Didier Ndeh^^^
 
* [[Responsible Curator]]:  ^^^Harry Gilbert^^^
 
* [[Responsible Curator]]:  ^^^Harry Gilbert^^^
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|-
 
|'''Clan'''     
 
|'''Clan'''     
|GH-x
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|none
 
|-
 
|-
 
|'''Mechanism'''
 
|'''Mechanism'''
|retaining/inverting
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|unknown
 
|-
 
|-
 
|'''Active site residues'''
 
|'''Active site residues'''
|known/not known
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|unknown
 
|-
 
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|{{Hl2}} colspan="2" align="center" |'''CAZy DB link'''
 
|{{Hl2}} colspan="2" align="center" |'''CAZy DB link'''
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== Substrate specificities ==
 
== Substrate specificities ==
Content is to be added here.
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[[Glycoside hydrolases]] of family 138 exhibit α-D-galacturonidase activity. This is based on data from the characterisation of the founding member of the family BT0997 encoded by the human gut bacterium ''B. thetaiotaomicron'' <cite>Ndeh2017</cite>. BT0997 hydrolyses a fragment (GalA-α1,2(GalA-β1,3)(2MeXyl-α1,3-Fuc-α1,4)Rha-&alpha;1,3-Api) of chain A from the pectic polysaccharide rhamnogalacturonan II, producing D-galacturonic acid and the resulting oligosaccharide GalA-β1,3(2MeXyl-α1,3Fuc-α1,4)Rha-α1,3Api <cite>Ndeh2017</cite>.  Several members of this family have been identified in gut and environmental bacteria with a majority of the encoding microbes belonging to the Bacteroidetes phylum <cite>Lombard2014 Cantarel2009</cite>. This phylum is highly represented in human gut microbial populations <cite>Qin2010</cite>.
 
 
Authors may get an idea of what to put in each field from ''Curator Approved'' [[Glycoside Hydrolase Families]]. ''(TIP: Right click with your mouse and open this link in a new browser window...)''
 
 
 
In the meantime, please see these references for an essential introduction to the CAZy classification system: <cite>DaviesSinnott2008 Cantarel2009</cite>.
 
  
 
== Kinetics and Mechanism ==
 
== Kinetics and Mechanism ==
Content is to be added here.
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The kinetic mechanism for this family has not been reported.
  
 
== Catalytic Residues ==
 
== Catalytic Residues ==
Content is to be added here.
+
The catalytic residues for this family have not yet been identified.
  
 
== Three-dimensional structures ==
 
== Three-dimensional structures ==
Content is to be added here.
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No 3D structure for a member of this family has been currently reported.
  
 
== Family Firsts ==
 
== Family Firsts ==
;First stereochemistry determination: Content is to be added here.
+
;First stereochemistry determination:Currently unknown.
;First catalytic nucleophile identification: Content is to be added here.
+
;First catalytic nucleophile identification:Currently unknown.
;First general acid/base residue identification: Content is to be added here.
+
;First general acid/base residue identification:Currently unknown.
;First 3-D structure: Content is to be added here.
+
;First 3-D structure:Currently unknown.
  
 
== References ==
 
== References ==
 
<biblio>
 
<biblio>
 
#Cantarel2009 pmid=18838391
 
#Cantarel2009 pmid=18838391
#DaviesSinnott2008 Davies, G.J. and Sinnott, M.L. (2008) Sorting the diverse: the sequence-based classifications of carbohydrate-active enzymes. ''The Biochemist'', vol. 30, no. 4., pp. 26-32. [http://www.biochemist.org/bio/03004/0026/030040026.pdf Download PDF version].
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#Ndeh2017 pmid=28329766
 +
#Qin2010 pmid=20203603
 +
#Lombard2014 pmid=24270786
 +
 
 +
 
 
</biblio>
 
</biblio>
  
 
[[Category:Glycoside Hydrolase Families|GH138]]
 
[[Category:Glycoside Hydrolase Families|GH138]]

Revision as of 14:52, 16 February 2018

Approve icon-50px.png

This page has been approved by the Responsible Curator as essentially complete. CAZypedia is a living document, so further improvement of this page is still possible. If you would like to suggest an addition or correction, please contact the page's Responsible Curator directly by e-mail.


Glycoside Hydrolase Family GH138
Clan none
Mechanism unknown
Active site residues unknown
CAZy DB link
http://www.cazy.org/GH138.html


Substrate specificities

Glycoside hydrolases of family 138 exhibit α-D-galacturonidase activity. This is based on data from the characterisation of the founding member of the family BT0997 encoded by the human gut bacterium B. thetaiotaomicron [1]. BT0997 hydrolyses a fragment (GalA-α1,2(GalA-β1,3)(2MeXyl-α1,3-Fuc-α1,4)Rha-α1,3-Api) of chain A from the pectic polysaccharide rhamnogalacturonan II, producing D-galacturonic acid and the resulting oligosaccharide GalA-β1,3(2MeXyl-α1,3Fuc-α1,4)Rha-α1,3Api [1]. Several members of this family have been identified in gut and environmental bacteria with a majority of the encoding microbes belonging to the Bacteroidetes phylum [2, 3]. This phylum is highly represented in human gut microbial populations [4].

Kinetics and Mechanism

The kinetic mechanism for this family has not been reported.

Catalytic Residues

The catalytic residues for this family have not yet been identified.

Three-dimensional structures

No 3D structure for a member of this family has been currently reported.

Family Firsts

First stereochemistry determination
Currently unknown.
First catalytic nucleophile identification
Currently unknown.
First general acid/base residue identification
Currently unknown.
First 3-D structure
Currently unknown.

References

  1. Ndeh D, Rogowski A, Cartmell A, Luis AS, Baslé A, Gray J, Venditto I, Briggs J, Zhang X, Labourel A, Terrapon N, Buffetto F, Nepogodiev S, Xiao Y, Field RA, Zhu Y, O'Neil MA, Urbanowicz BR, York WS, Davies GJ, Abbott DW, Ralet MC, Martens EC, Henrissat B, and Gilbert HJ. (2017). Complex pectin metabolism by gut bacteria reveals novel catalytic functions. Nature. 2017;544(7648):65-70. DOI:10.1038/nature21725 | PubMed ID:28329766 [Ndeh2017]
  2. Lombard V, Golaconda Ramulu H, Drula E, Coutinho PM, and Henrissat B. (2014). The carbohydrate-active enzymes database (CAZy) in 2013. Nucleic Acids Res. 2014;42(Database issue):D490-5. DOI:10.1093/nar/gkt1178 | PubMed ID:24270786 [Lombard2014]
  3. Cantarel BL, Coutinho PM, Rancurel C, Bernard T, Lombard V, and Henrissat B. (2009). The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics. Nucleic Acids Res. 2009;37(Database issue):D233-8. DOI:10.1093/nar/gkn663 | PubMed ID:18838391 [Cantarel2009]
  4. Qin J, Li R, Raes J, Arumugam M, Burgdorf KS, Manichanh C, Nielsen T, Pons N, Levenez F, Yamada T, Mende DR, Li J, Xu J, Li S, Li D, Cao J, Wang B, Liang H, Zheng H, Xie Y, Tap J, Lepage P, Bertalan M, Batto JM, Hansen T, Le Paslier D, Linneberg A, Nielsen HB, Pelletier E, Renault P, Sicheritz-Ponten T, Turner K, Zhu H, Yu C, Li S, Jian M, Zhou Y, Li Y, Zhang X, Li S, Qin N, Yang H, Wang J, Brunak S, Doré J, Guarner F, Kristiansen K, Pedersen O, Parkhill J, Weissenbach J, MetaHIT Consortium, Bork P, Ehrlich SD, and Wang J. (2010). A human gut microbial gene catalogue established by metagenomic sequencing. Nature. 2010;464(7285):59-65. DOI:10.1038/nature08821 | PubMed ID:20203603 [Qin2010]

All Medline abstracts: PubMed