Structure of IDP91384

Crystal structure of unliganded anabolic ornithine carbamoyltransferase from Vibrio vulnificus at 1.86 A resolution

Edit deposit information
CSGID target
IDP91384 
PDB Id
4KWT (NCBI MMDB
Authors
I.G.Shabalin,P.Bacal,J.Bajor,J.Winsor,S.Grimshaw,W.F.Anderson,W.Minor,Center For Structural Genomics Of Infectious Diseases (Csgid) 
Responsible person
Ivan Shabalin 
Responsible lab
University of Virginia 
Deposition Date
May 24, 2013 
Release Date
Jun 05, 2013 

Annotation

Description
Ornithine carbamoyltransferase (OTC) catalyzes the reversible transfer of the carbamoyl group from carbamoyl phosphate (CP) to the Nε atom of L-ornithine (ORN) to produce L-citrulline. There are two types of the enzyme – anabolic (aOTC) and catabolic (cOTC). Anabolic OTCs participate in the urea cycle and L-arginine biosynthesis. Catabolic OTCs are part of the catabolic arginine deiminase pathway found in a number of microorganisms. The reported structure is for the anabolic enzyme from pathogen Vibrio vulnificus. The structure has three monomers in the asymmetric unit which form the physiologically active trimer. All three enzyme subunits are unliganded. This structure provides insights into native state of the enzyme featuring open interdomain cleft, disordered SMG loop and catalytic loop B2–H3 located out of the active site. 
Functional assignment
transferase 

Ligands

Ligand code Name Ligand type
PEG crystallization
175 3,5-dihydro-5-methylidene-4h-imidazol-4-on

Structure information

Unit cell parameters

Space Group
P 21 21 21  
Unit Cell

a=77.81Å, b=82.65Å, c=150.91Å
α=90.00, β=90.00, γ=90.00 
Solvent content
 
Matthews coefficient
 

Refinement

Data for the highest resolution shell is in parentheses.
Resolution range
35.50-1.86Å (1.91-1.86Å)  
Rall(%)
16.1 
Rwork(%)
16.0 (25.9) 
Rfree(%)
19.5 (30.4) 
Num. observed reflections
81046 (5944) 
Num. Rfree reflections
4052 (300) 
Completeness(%)
98.3 (98.6) 

Model parameters

Num Atoms
7535  
Num Waters
487  
Num Hetatoms
501  
Model mean isotropic B factor
39.730Å2  
RMSD bond length
0.019Å  
RMSD bond angle
1.738°  
Filename uploaded
hkl_refine_62_tls_ters.pdb (uploaded on May 24, 2013 2:40 PM)  
Inserted
May 24, 2013