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6OMK

Crystal structure of a glycylpeptide N-tetradecanoyltransferase (N-myristoyl transferase, NMT) from Leishmania major Friedlin bound to tetradecanoyl-CoA

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU FR-E+ SUPERBRIGHT
Temperature [K]100
Detector technologyCCD
Collection date2018-08-29
DetectorRIGAKU SATURN 944+
Wavelength(s)1.5406
Spacegroup nameP 21 21 21
Unit cell lengths49.250, 89.170, 90.360
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution44.585 - 2.100
R-factor0.1748
Rwork0.170
R-free0.23270
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3h5z
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwareMOLREP
Refinement softwarePHENIX ((1.15_3459))
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]44.58544.5852.150
High resolution limit [Å]2.1009.3902.100
Rmerge0.1030.0580.552
Rmeas0.1120.0630.605
Total number of observations164416
Number of reflections239143141756
<I/σ(I)>12.5428.973.5
Completeness [%]100.098.4100
Redundancy6.8755.8796.032
CC(1/2)0.9970.9960.874
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP5.6287LemaA.18219.a.B1.PS38467 at 3.52 mg/mL with 0.5 mM myristoyl CoA (tetradecanoyl CoA) against 16% PEG 3350, 0.2 M NaCl, 0.1 M sodium cacodylate pH 5.6, supplemented with 20% ethylene glycol as cryo-protectant, crystal tracking ID 303026d4, unique puck ID vle8-4

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PDB entries from 2024-10-30

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