Electronic Supplementary Information (ESI) for Chem. Commun. Unveiling the three- dimensional structure of the green pigment of nitrite- cured meat

Similar documents
GC376 (compound 28). Compound 23 (GC373) (0.50 g, 1.24 mmol), sodium bisulfite (0.119 g,

RNA protects a nucleoprotein complex against radiation damage

Supporting Information

Supporting Information. Synthesis of Aspartame by Thermolysin : An X-ray Structural Study

Acta Crystallographica Section F

Supporting Information. Full and Partial Agonism of a Designed Enzyme Switch

Acta Cryst. (2017). D73, doi: /s

Supplementary Information

Full wwpdb X-ray Structure Validation Report i

Exploiting Protein Conformational Change to Optimize Adenosine-Derived Inhibitors of HSP70

Full wwpdb X-ray Structure Validation Report i

Likelihood and SAD phasing in Phaser. R J Read, Department of Haematology Cambridge Institute for Medical Research

Pathogenic C9ORF72 Antisense Repeat RNA Forms a Double Helix with Tandem C:C Mismatches

Full wwpdb X-ray Structure Validation Report i

Full wwpdb X-ray Structure Validation Report i

Supporting Information

Full wwpdb X-ray Structure Validation Report i

Full wwpdb X-ray Structure Validation Report i

Full wwpdb X-ray Structure Validation Report i

Full wwpdb X-ray Structure Validation Report i

Full wwpdb X-ray Structure Validation Report i

Phaser: Experimental phasing

PHENIX Wizards and Tools

New Delhi Metallo-β-Lactamase: Structural Insights into β- Lactam Recognition and Inhibition

IgE binds asymmetrically to its B cell receptor CD23

Macromolecular Crystallography Part II

wwpdb X-ray Structure Validation Summary Report

This is an author produced version of Privateer: : software for the conformational validation of carbohydrate structures.

Macromolecular Crystallography Part II

SOLVE and RESOLVE: automated structure solution, density modification and model building

In Crystallo Capture of a Covalent Intermediate in the UDP-Galactopyranose Mutase Reaction

Molecular Biology Course 2006 Protein Crystallography Part II

Pipelining Ligands in PHENIX: elbow and REEL

research papers Iterative-build OMIT maps: map improvement by iterative model building and refinement without model bias 1.

Nitrogenase MoFe protein from Clostridium pasteurianum at 1.08 Å resolution: comparison with the Azotobacter vinelandii MoFe protein

Supplementary Materials for

Protein Crystallography Part II

CCP4 Diamond 2014 SHELXC/D/E. Andrea Thorn

SI Text S1 Solution Scattering Data Collection and Analysis. SI references

Trapped intermediates in crystals of the FMN-dependent oxidase PhzG provide insight into the final steps of phenazine biosynthesis

Examples of Protein Modeling. Protein Modeling. Primary Structure. Protein Structure Description. Protein Sequence Sources. Importing Sequences to MOE

X-ray Crystallography I. James Fraser Macromolecluar Interactions BP204

Catalytic Mechanism of the Glycyl Radical Enzyme 4-Hydroxyphenylacetate Decarboxylase from Continuum Electrostatic and QC/MM Calculations

SUPPLEMENTARY INFORMATION

Garib N Murshudov MRC-LMB, Cambridge

SUPPLEMENTARY INFORMATION

The structure of Aquifex aeolicus FtsH in the ADP-bound state reveals a C2-symmetric hexamer

Anisotropy in macromolecular crystal structures. Andrea Thorn July 19 th, 2012

Supporting Information

Conformation-dependent backbone geometry restraints set a new standard for protein crystallographic refinement

research papers A general method for phasing novel complex RNA crystal structures without heavy-atom derivatives

Structural Mechanism for the Fidelity Modulation of DNA Polymerase λ. 128 Academia Road Sec. 2, Nankang, Taipei, 115, Taiwan

The Crystallographic Process

Supporting Information. Structural Insights into Substrate Specificity and Solvent Tolerance in Alcohol

Summary of Experimental Protein Structure Determination. Key Elements

Rational Design of Thermodynamic and Kinetic Binding Profiles by. Optimizing Surface Water Networks Coating Protein Bound Ligands

Supplementary Figures for Tong et al.: Structure and function of the intracellular region of the plexin-b1 transmembrane receptor

Manipulating Ligands Using Coot. Paul Emsley May 2013

SUPPLEMENTARY INFORMATION

shelxl: Refinement of Macromolecular Structures from Neutron Data

Supporting Information

Modelling Macromolecules with Coot

TLS and all that. Ethan A Merritt. CCP4 Summer School 2011 (Argonne, IL) Abstract

Conformation-dependent backbone geometry restraints set a new standard for protein crystallographic refinement

Folding Thermodynamics of Protein-Like Oligomers with Heterogeneous Backbones

Full wwpdb X-ray Structure Validation Report i

Electron Density at various resolutions, and fitting a model as accurately as possible.

High-resolution crystal structure of ERAP1 with bound phosphinic transition-state analogue inhibitor

Experimental Phasing with SHELX C/D/E

Manganese-Calcium Clusters Supported by Calixarenes

Small Molecule Crystallography Lab Department of Chemistry and Biochemistry University of Oklahoma 101 Stephenson Parkway Norman, OK

Rietveld Structure Refinement of Protein Powder Diffraction Data using GSAS

Protein crystallography. Garry Taylor

The Crystallographic Process

HTCondor and macromolecular structure validation

Computational aspects of high-throughput crystallographic macromolecular structure determination

Table 1. Crystallographic data collection, phasing and refinement statistics. Native Hg soaked Mn soaked 1 Mn soaked 2

Small Molecule Crystallography Lab Department of Chemistry and Biochemistry University of Oklahoma 101 Stephenson Parkway Norman, OK

research papers Use of knowledge-based restraints in phenix.refine to improve macromolecular refinement at low resolution 1.

Supplementary Figure 1. Biochemical and sequence alignment analyses the

Supporting Information

Supporting Information

Supporting Information

Direct Method. Very few protein diffraction data meet the 2nd condition

1.b What are current best practices for selecting an initial target ligand atomic model(s) for structure refinement from X-ray diffraction data?!

Charles Ballard (original GáborBunkóczi) CCP4 Workshop 7 December 2011

Table S1. Overview of used PDZK1 constructs and their binding affinities to peptides. Related to figure 1.

SHELXC/D/E. Andrea Thorn

Removing bias from solvent atoms in electron density maps

electronic reprint PHENIX: a comprehensive Python-based system for macromolecular structure solution

Acta Crystallographica Section D

SUPPLEMENTARY INFORMATION

Spin crossover in polymeric and heterometallic Fe II species containing polytopic dipyridylamino-substituted-triazine ligands.

Supplementary Information

SUPPLEMENTARY INFORMATION

Full wwpdb/emdatabank EM Map/Model Validation Report i

Ensemble refinement of protein crystal structures in PHENIX. Tom Burnley Piet Gros

SUPPLEMENTARY INFORMATION

Reaction Landscape of a Pentadentate N5-Ligated Mn II Complex with O 2

Supplementary Materials for

Transcription:

Electronic Supplementary Information (ESI) for Chem. Commun. Unveiling the three- dimensional structure of the green pigment of nitrite- cured meat Jun Yi* and George B. Richter- Addo* Department of Chemistry and Biochemistry, University of Oklahoma, 101 Stephenson Parkway, Norman, OK 73019. USA. yijun@ou.edu; grichteraddo@ou.edu i. X- ray Data Collection and Processing page S1 ii. Structure Solution and Refinement page S1 iii. Table S1. Summary of the X- ray data collection and refinement statistics page S3 iv. Figure S1. The heme vinyl regions of the ferric hh Mb(ONO) complex (PDB entry: 3LR7, 1.60 Å resolution). The close contacts of the terminal Cβ atom at the 4- vinyl position (A) and at the 2- vinyl position ( ) with the side chains of nearby residues are shown in green dashed lines. page S5 v. Figure S2. Superimposition of the hh Mb(ONO) complex (light gray, PDB entry: 3LR7) with the hh NMb(ONO) complex (green, this structure). page S5

X- ray diffraction data collection and processing X- ray data were collected at 100 K on a RigakuMSC RU- H3R X- ray generator operated at 48 kv/98 ma to produce Cu/Kα radiation (λ = 1.5418 Å). 1 oscillation images of the hh nitrimb nitrite derivative crystal were collected over a range of 200 with an exposure time of 5 min per image and a crystal- to- detector distance of 90 mm. Diffraction data were indexed and processed with the d*trek program (Macintosh v.99d). [1] Structure solution and refinement In general, for the R free calculation, 5% of randomly selected reflections were flagged and carried throughout the complete refinement procedure. The CCP4 program REFMAC [2] and the PHENIX [3] refinement program were used for the structure refinement. Bulk- solvent modeling and isotropic scaling of the observed and calculated structural amplitudes were employed during the restrained refinements. COOT [4] was used for visualization and model building/corrections between refinement cycles. The phase information was obtained using the molecular replacement method PHASER [5] as implemented in CCP4. The search model was the 1.45 Å resolution structure of hh MbCO (PDB entry: 1DWR) [6] with all solvent molecules, carbon monoxide and sulfate ions removed. Restrained refinement was carried out for 10 cycles prior to the addition of any solvent, ligand, or sulfate ion, and this resulted in a drop of the R- factor to 0.221 from an initial value of 0.289. In the initial F o - F c difference electron density map, new electron density was evident at the terminus of the 2- vinyl group of the heme moiety, which indicated that the heme had been chemically modified. A triatomic O- N- O fragment was fitted into this new density and the coordinates of the fragment saved into the protein pdb coordinate file. The heme (HEM) group and the added O- N- O fragment were labeled NTE (i.e., nitriheme) as a single ligand in the pdb coordinate file. To generate the NTE ligand library cif file for the needed restrained refinements, we constructed a NTE prosthetic group using Monomer Library Sketcher in CCP4. [2] To begin, the library file and the coordinate file of the unmodified protoporphyrin IX prosthetic group were loaded from the CCP4 monomer library as the starting template. The CBB atom was placed into porphyrin plane from its originally near- perpendicular position. An O- N- O fragment was then attached to the CBB atom of the CAB- CBB vinyl group. The N atom was single bonded to the CBB atom and also bonded to two O atoms with delocalized bonds. The create library descriptions and regularize structure commands were then used to generate the library description and geometry restraints for this NTE molecule. This newly generated NTE cif file was used for further refinements. One nitrite anion bound to the heme and one sulfate anion were added to the model based on density seen in the initial F o - F c electron density map. An additional 10 cycles of restrained refinement in CCP4 were run to give an R- factor of 0.212%. The structure was checked for sidechains showing low occupancy or multiple conformations. The side chain of residue Ser108 was modeled in two conformations each with 50% occupancy. The C- terminal residues Gln152 and Gly153 were S1

omitted from the structural model due to the lack of defined electron density. Water molecules were added during additional refinement cycles using PHENIX. The crystallographic R and R free for the final model are 0.173 and 0.237, respectively, in the 26.47-1.70 Å range. The hh NMb(ONO) derivative crystallized with one molecule in the asymmetric unit, and the final model of its structure contains 151 amino acid residues, one nitriheme prosthetic group, one nitrite anion, one sulfate anion, and 94 water molecules. S2

Table 1. X- ray data collection and refinement statistics a Data Collection PDB accession code 3VAU Space group P2 1 Unit cell dimensions (Å) 35.14, 28.42, 62.87, 90, 105.5, 90 Wavelength (Å) 1.5418 Temperature (K) 100 Resolution range (Å) 26.47-1.70 Number of observations 52180 Unique reflections 13475 Average multiplicity 3.87 (3.76) Completeness (%) 100 (100) <I/σ(I)> 11.8 (3.4) R b merge 0.053 (0.303) Refinement Number of protein atoms 1188 Number of heteroatoms 158 R- factor c 0.173 R d free 0.237 Average B- factor (Å 2 ) e 22.3 rms deviations f bond lengths (Å) 0.03 bond angles ( o ) 2.3 Ramachandran plot (%) g favored 98.7 outliers 0 rotamer outliers 0 a The data in brackets refer to the highest resolution shell. b R merge = Σ hkl Σ i I i (hkl) <I(hkl)> /Σ hkl Σ i I i (hkl), where I i (hkl) is the ith used observation for unique hkl, and <I(hkl)> is the mean intensity for unique hkl. c R = Σ hkl F obs F calc /Σ hkl F obs, where F obs and F calc are the observed and calculated structure factors, respectively. d R free was calculated using 5% of the randomly selected diffraction data which were excluded from the refinement. e The average for the polypeptide atoms. f deviations from ideal values [7] g calculated using MolProbity as implemented in PHENIX [8] S3

References [1] J. W. Pflugrath, Acta Cryst., 1999, D55, 1718-1725. [2] G. N. Murshudov, A. A. Vagin and E. J. Dodson, Acta Cryst., 1997, D53, 240-255. [3] P. D. Adams, R. W. Grosse- Kunstleve, L. W. Hung, T. R. Ioerger, A. J. McCoy, N. W. Moriarty, R. J. Read, J. C. Sacchettini, N. K. Sauter and T. C. Terwilliger, Acta Cryst., 2002, D58, 1948-1954. [4] P. Emsley and K. Cowtan, Acta Cryst., 2004, D60, 2126-2132. [5] A. J. Mccoy, R. W. Grosse- Kunstleve, P. D. Adams, M. D. Winn, L. C. Storoni and R. J. Read, J Appl Crystallogr, 2007, 40, 658-674. [6] K. Chu, J. Vojtchovsky, B. H. McMahon, R. M. Sweet, J. Berendzen and I. Schlichting, Nature, 2000, 403, 921-923. [7] R. A. Engh and R. Huber, Acta Cryst., 1991, A47, 392-400. [8] V. B. Chen, W. B. Arendall, J. J. Headd, D. A. Keedy, R. M. Immormino, G. J. Kapral, L. W. Murray, J. S. Richardson and D. C. Richardson, Acta Cryst., 2010, D66, 12-21. S4

Figure S1. The heme vinyl regions of the ferric hh Mb(ONO) complex (PDB entry: 3LR7, 1.60 Å resolution). The close contacts of the terminal Cβ atom at the 4- vinyl position (A) and at the 2- vinyl position ( ) with the side chains of nearby residues are shown in green dashed lines. Figure S2. Superimposition of the hh Mb(ONO) complex (light gray, PDB entry: 3LR7) with the hh NMb(ONO) complex (green, this structure). Helices E, F, G and H are labeled. S5