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PDBsum entry 5gqh

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protein Protein-protein interface(s) links
Hydrolase/hydrolase inhibitor PDB id
5gqh

 

 

 

 

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Contents
Protein chains
901 a.a.
135 a.a.
PDB id:
5gqh
Name: Hydrolase/hydrolase inhibitor
Title: Cryo-em structure of paecas3-acrf3 complex
Structure: Crispr-associated nuclease/helicase cas3 subtype i-f/ypest. Chain: a. Synonym: type i-f crispr-associated nuclease/helicase cas3. Engineered: yes. Anti-crispr protein 3. Chain: b, c. Synonym: acrf3,uncharacterized protein. Engineered: yes
Source: Pseudomonas aeruginosa ucbpp-pa14. Organism_taxid: 208963. Strain: ucbpp-pa14. Gene: cas3. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008. Pseudomonas phage jbd5. Organism_taxid: 1223261. Gene: jbd5_035.
Authors: X.Zhang,J.Ma,Y.Wang,J.Wang
Key ref: J.Wang et al. (2016). A CRISPR evolutionary arms race: structural insights into viral anti-CRISPR/Cas responses. Cell Res, 26, 1165-1168. PubMed id: 27585537 DOI: 10.1038/cr.2016.103
Date:
07-Aug-16     Release date:   21-Sep-16    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q02ML8  (CAS3_PSEAB) -  CRISPR-associated nuclease/helicase Cas3 subtype I-F/YPEST from Pseudomonas aeruginosa (strain UCBPP-PA14)
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1076 a.a.
901 a.a.
Protein chains
Pfam   ArchSchema ?
L7P7R7  (L7P7R7_9CAUD) -  Phage protein from Pseudomonas phage JBD5
Seq:
Struc:
139 a.a.
135 a.a.
Key:    PfamA domain  Secondary structure

 Enzyme reactions 
   Enzyme class 2: Chain A: E.C.3.1.-.-
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
   Enzyme class 3: Chain A: E.C.3.6.4.-  - ?????
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
Note, where more than one E.C. class is given (as above), each may correspond to a different protein domain or, in the case of polyprotein precursors, to a different mature protein.

 

 
DOI no: 10.1038/cr.2016.103 Cell Res 26:1165-1168 (2016)
PubMed id: 27585537  
 
 
A CRISPR evolutionary arms race: structural insights into viral anti-CRISPR/Cas responses.
J.Wang, J.Ma, Z.Cheng, X.Meng, L.You, M.Wang, X.Zhang, Y.Wang.
 
  ABSTRACT  
 
No abstract given.

 

 

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