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Open data
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Basic information
Entry | Database: PDB / ID: 2k0x | ||||||
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Title | The actinorhodin holo acyl carrier protein from S. coelicolor | ||||||
![]() | Actinorhodin polyketide synthase acyl carrier protein | ||||||
![]() | TRANSPORT PROTEIN / Acyl carrier protein / polyketide / holo / phosphopantetheine / Antibiotic biosynthesis | ||||||
Function / homology | ![]() lipid A biosynthetic process / acyl binding / antibiotic biosynthetic process / acyl carrier activity / cytosol Similarity search - Function | ||||||
Biological species | ![]() | ||||||
Method | SOLUTION NMR / simulated annealing | ||||||
Model details | This deposit is a set of twenty structures of the holo (phosphopantetheinylated) actinorhodin ...This deposit is a set of twenty structures of the holo (phosphopantetheinylated) actinorhodin polyketide acyl carrier protein (ACP). These datasets form a sister set to the recent apo- coordinates we deposited and can be used to directly compare the two forms. | ||||||
![]() | Crump, M.P. / Evans, S.E. / Williams, C. | ||||||
![]() | ![]() Title: An ACP Structural Switch: Conformational Differences between the Apo and Holo Forms of the Actinorhodin Polyketide Synthase Acyl Carrier Protein. Authors: Evans, S.E. / Williams, C. / Arthur, C.J. / Burston, S.G. / Simpson, T.J. / Crosby, J. / Crump, M.P. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 560.9 KB | Display | ![]() |
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PDB format | ![]() | 495.2 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
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-Related structure data
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Links
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Assembly
Deposited unit | ![]()
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NMR ensembles |
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Components
#1: Protein | Mass: 9239.177 Da / Num. of mol.: 1 / Mutation: C17S Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Description: Actinorhodin acyl carrier protein (act ACP) from S. coelicolor was heterologously overexpressed in its apo form in E. coli BL21 (DE3) cells. These cells contained the plasmid pET11c C17S ...Description: Actinorhodin acyl carrier protein (act ACP) from S. coelicolor was heterologously overexpressed in its apo form in E. coli BL21 (DE3) cells. These cells contained the plasmid pET11c C17S act ACP (courtesy of Dr. Tom Nicholson). This IPTG inducible vector is both easier to use and more reliable than the heat inducible pT7-7 version originally constructed. The protein was modified to the holo form using S. coelicolor ACPS and Enzyme CoA. Gene: actI / Production host: ![]() ![]() |
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#2: Chemical | ChemComp-PNS / |
-Experimental details
-Experiment
Experiment | Method: SOLUTION NMR Details: This deposit is a set of twenty structures of the holo (phosphopantetheinylated) actinorhodin polyketide acyl carrier protein (ACP). These datasets form a sister set to the recent apo- ...Details: This deposit is a set of twenty structures of the holo (phosphopantetheinylated) actinorhodin polyketide acyl carrier protein (ACP). These datasets form a sister set to the recent apo- coordinates we deposited and can be used to directly compare the two forms. | ||||||||||||||||||||||||||||||||||||||||||||
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NMR experiment |
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Sample preparation
Details | Contents: 1-2 mM [U-98% 13C; U-98% 15N] act holo-acp, 1-2 mM Phosphopantetheine side chain, 95 % H2O, 5 % D2O, 20 mM potassium phosphate, 5 mM TCEP, 1 mM sodium azide, 95% H2O/5% D2O Solvent system: 95% H2O/5% D2O | ||||||||||||||||||||||||||||||||
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Sample conditions | pH: 5.5 / Pressure: ambient / Temperature: 298 K |
-NMR measurement
NMR spectrometer | Type: Varian INOVA / Manufacturer: Varian / Model: INOVA / Field strength: 600 MHz |
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Processing
NMR software |
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Refinement | Method: simulated annealing / Software ordinal: 1 Details: All structure calculations were carried out using the Ambiguous Restraints for Iterative Assignment of NOEs (ARIA) protocol Version 1.2, which includes an algorithm that attempts to correct ...Details: All structure calculations were carried out using the Ambiguous Restraints for Iterative Assignment of NOEs (ARIA) protocol Version 1.2, which includes an algorithm that attempts to correct for the effects of spin diffusion, was use. Torsion Angle Likelihood Obtained from Shift and sequence similarity (TALOS) and was used to predict φ and ψ dihedral angle restraints. Initially, structure calculation runs contained 8 iterations of 20 structures each, with the best 7 structures in each iteration (sorted according to total energy) being used for analysis and assignment. The number of dynamics steps was increased over default values to 20000 and 16000 for the first and second cooling stages respectively. After each run, violated restraints were checked, and those arising from noise peaks or incorrect assignments were removed/reassigned. Final ensembles of 100 structures were calculated from calibrated restraint tables. The 20 best structures (sorted according to total energy) were selected for water refinement. Water refined structures were calculated using the slightly modified refinement script applied to the RECOORD database. PROCHECK and WHATCHECK and quality indicators were compared to the average values for the RECOORD database of protein NMR structures. | ||||||||||||||||
NMR representative | Selection criteria: closest to the average | ||||||||||||||||
NMR ensemble | Conformer selection criteria: structures with the lowest energy Conformers calculated total number: 20 / Conformers submitted total number: 20 |