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PDBsum entry 4zm7

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Hydrolase PDB id
4zm7

 

 

 

 

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Contents
Protein chain
180 a.a.
Waters ×469
PDB id:
4zm7
Name: Hydrolase
Title: Pccel45a n105d mutatnt at cryo condition
Structure: Endoglucanase v-like protein. Chain: a. Fragment: unp residues 27-206. Synonym: pccel45a. Engineered: yes. Mutation: yes
Source: Phanerochaete chrysosporium. White-rot fungus. Organism_taxid: 5306. Strain: k-3. Gene: egv. Expressed in: komagataella pastoris. Expression_system_taxid: 4922.
Resolution:
0.70Å     R-factor:   0.127     R-free:   0.135
Authors: A.Nakamura,T.Ishida,M.Samejima,K.Igarashi
Key ref: A.Nakamura et al. (2015). "Newton's cradle" proton relay with amide-imidic acid tautomerization in inverting cellulase visualized by neutron crystallography. Sci Adv, 1, e1500263. PubMed id: 26601228 DOI: 10.1126/sciadv.1500263
Date:
02-May-15     Release date:   02-Sep-15    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
B3Y002  (B3Y002_PHACH) -  Endoglucanase V-like protein from Phanerodontia chrysosporium
Seq:
Struc:
206 a.a.
180 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 

 
DOI no: 10.1126/sciadv.1500263 Sci Adv 1:e1500263 (2015)
PubMed id: 26601228  
 
 
"Newton's cradle" proton relay with amide-imidic acid tautomerization in inverting cellulase visualized by neutron crystallography.
A.Nakamura, T.Ishida, K.Kusaka, T.Yamada, S.Fushinobu, I.Tanaka, S.Kaneko, K.Ohta, H.Tanaka, K.Inaka, Y.Higuchi, N.Niimura, M.Samejima, K.Igarashi.
 
  ABSTRACT  
 
Hydrolysis of carbohydrates is a major bioreaction in nature, catalyzed by glycoside hydrolases (GHs). We used neutron diffraction and high-resolution x-ray diffraction analyses to investigate the hydrogen bond network in inverting cellulase PcCel45A, which is an endoglucanase belonging to subfamily C of GH family 45, isolated from the basidiomycete Phanerochaete chrysosporium. Examination of the enzyme and enzyme-ligand structures indicates a key role of multiple tautomerizations of asparagine residues and peptide bonds, which are finally connected to the other catalytic residue via typical side-chain hydrogen bonds, in forming the "Newton's cradle"-like proton relay pathway of the catalytic cycle. Amide-imidic acid tautomerization of asparagine has not been taken into account in recent molecular dynamics simulations of not only cellulases but also general enzyme catalysis, and it may be necessary to reconsider our interpretation of many enzymatic reactions.
 

 

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