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PDBsum entry 2xm1

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protein ligands Protein-protein interface(s) links
Hydrolase PDB id
2xm1

 

 

 

 

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Contents
Protein chains
645 a.a.
Ligands
GOL ×4
LTM ×2
Waters ×1045
PDB id:
2xm1
Name: Hydrolase
Title: Btgh84 in complex with n-acetyl gluconolactam
Structure: O-glcnacase bt_4395. Chain: a, b. Synonym: btgh84, beta-hexosaminidase, hexosaminidase b, gh84, n- acetyl-beta-glucosaminidase, beta-n-acetylhexosaminidase,. Engineered: yes
Source: Bacteroides thetaiotaomicron vpi-5482. Organism_taxid: 226186. Atcc: 29148. Expressed in: escherichia coli. Expression_system_taxid: 511693.
Resolution:
2.00Å     R-factor:   0.182     R-free:   0.220
Authors: Y.He,G.J.Davies
Key ref: Y.He et al. (2011). Inhibition of a bacterial O-GlcNAcase homologue by lactone and lactam derivatives: structural, kinetic and thermodynamic analyses. Amino Acids, 40, 829-839. PubMed id: 20689974
Date:
22-Jul-10     Release date:   03-Aug-11    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q89ZI2  (OGA_BACTN) -  O-GlcNAcase BT_4395 from Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50)
Seq:
Struc:
 
Seq:
Struc:
737 a.a.
645 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.3.2.1.169  - protein O-GlcNAcase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction:
1. 3-O-(N-acetyl-beta-D-glucosaminyl)-L-seryl-[protein] + H2O = N-acetyl-D-glucosamine + L-seryl-[protein]
2. 3-O-(N-acetyl-beta-D-glucosaminyl)-L-threonyl-[protein] + H2O = L-threonyl-[protein] + N-acetyl-D-glucosamine
3-O-(N-acetyl-beta-D-glucosaminyl)-L-seryl-[protein]
+ H2O
= N-acetyl-D-glucosamine
+ L-seryl-[protein]
Bound ligand (Het Group name = LTM)
matches with 87.50% similarity
3-O-(N-acetyl-beta-D-glucosaminyl)-L-threonyl-[protein]
+ H2O
= L-threonyl-[protein]
+
N-acetyl-D-glucosamine
Bound ligand (Het Group name = LTM)
matches with 87.50% similarity
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
Amino Acids 40:829-839 (2011)
PubMed id: 20689974  
 
 
Inhibition of a bacterial O-GlcNAcase homologue by lactone and lactam derivatives: structural, kinetic and thermodynamic analyses.
Y.He, A.K.Bubb, K.A.Stubbs, T.M.Gloster, G.J.Davies.
 
  ABSTRACT  
 
No abstract given.

 

 

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