Tutorials for protein data bank and swiss PDB
Tutorials for protein data bank and swiss PDB viewer 2010/04/19 Prof. Jinn-Moon Yang Yen-Fu Chen and Kai-Cheng Hsu http: //gemdock. life. nctu. edu. tw/dock/download/20100419_spv. ppt http: //gemdock. life. nctu. edu. tw/dock/download/20100419_spv. pdf http: //ppt. cc/cnq. T (ppt) http: //ppt. cc/WWxd (pdf)
Contents Introduction of protein structures Using thymidine kinase as an example Download and install Tutorial Download protein structures from PDB Basic Operation Advance Operation Resources for tutorial http: //www. youtube. com/watch? v=y. FE 3 CAHNk. Zg&feat ure=related
Introduction of protein structures Proteins present in all biological organisms Polymers of amino acids (20 L-α-amino acids) Nanoparticles Perform particular biochemical functions Transcription and translation stemcells. nih. go: Early Development Cell regulation and catalysis reactions Nature: Mattson, M. Nature. 422, 385 -387 (2003)
Introduction of protein structures To enable to perform protein’s biological function, protein fold into one or more specific spatial conformations driven by noncovalent interactions Hydrogen bonding, ionic interactions, van der Waals forces and hydrophobic packing 3 D protein structures are necessary for understanding the functions of protein at molecular level Protein structure: from amino acid to quaternary structure Adapted from Protein Structure in Wikipedia Hemoglobin: oxy-deoxy states Adapted from structural biology Wikipedia
Noncovalent interactions for protein structure and function Ionic bond A bond formed by the attraction between two oppositely charged ions Hydrogen bond An attractive interaction of a hydrogen atom with an electronegative atom, like N, O, and F Potential energy of Na and Cl
Noncovalent interactions for protein structure and function van der Waals force Attractive or repulsive force between molecules Hydrophobic interaction The physical property of a molecule (known as a hydrophobe) that is repelled from a mass of water An example of van der Waals force: Gecko climbs on the glass An example of hydrophobic interaction: Water drops on hydrophobic surface
Protein structure database: Protein data bank (PDB) Techniques for determining atomic structures X-ray crystallography, NMR spectroscopy and electron microscopy PDB contains information about experimentallydetermined structures of biological marcomoleculeas (proteins, and DNA/RNA) Proteins (1 kim) X-ray NMR DNAs/RNAs (2 k 7 e) EM http: //www. pdb. org/ Biological complexes (1 zrc)
Search protein structures in PDB provides search by protein name, ligand, or structrue related keywords Search example: thymidine kinase (TK) • Function: DNA synthesis • Therapeutic: Anticancer and antivirus drug target
Example: X-ray structures of virus’ thymidine kinase with substrates/inhibitors Protein name Source spices Experimental method has ligands
Search result of “X-ray structures of virus’ thymidine kinase with substrates/inhibitors” 23 structures for these keywords PDB ID of this structure TK of virus TK with ligand (substrate) X-ray structure
Structure and related data (1 kim) The title of this structure The citation of this structure Related data of this structure Visualization of biological assembly
Structure and ligand data (1 kim) Ligand in this structure
Structure and sequence data (1 kim) Related data of this structure Sequence ID of 1 kim in Uni. Prot. KB Structure classification ID of 1 kim
Advance inspection for protein structure: download structure from PDB 1. Save the data on your PC 2. Open the file on a structure viewer program (swiss PDBviewer, pymol, and etc. )
Classification of Drug Development Unknown query High-Throughput Screening (HTS) Similar compounds Structure-based Drug Design (SBDD) SBDD or de novo design Known Protein (receptor) Structure Compound similarity search Known Compound structure DDT 2002 Unknown
Discovering new leads SBDD HTS Yellow: virtual screening (SBDD) Blue: high-throughput screening (HTS) • • There are more than 5 H-bond donors. The molecular weight is over 500. The Log. P is over 5. There are more than 10 H-bond acceptors. Curr. opin. Chem. Biol. 2002, 439
Drugs derived from structure-based approaches Drug Discovery Today, 10, 895, 2005
Drug Discovery Today, 10, 895, 2005
Tutorial for Swiss PDB viewer
Download and install Download Swiss Pdb. Viewer http: //spdbv. vital-it. ch/download. html Download user guide http: //spdbv. vital-it. ch/Swiss. Pdb. Viewer. Manualv 3. 7. pdf Tutorial video (English) http: //www. youtube. com/watch? v=n. YT 5 qwtf. New&fe ature=related http: //www. youtube. com/watch? v=y. FE 3 CAHNk. Zg
Download page
General Terms Main chain Residue Arginine Chain Secondary Structure (Ribbon) Side chain Gray: C atom Blue: N atom Red: O atom Atom radius A protein may have multiple chains
Install and execute swiss pdb viewer
Workspace Layer info Main window Viewer Control panel
Move & Rotate Center Zoom Translate Rotate
Open control panel
Load PDB 1
Load PDB 2
Display or hide residues -for some residues Press left button of mouse
Display or hide residues -for all residues Press right button of mouse
Display or hide side chains of residues
Display or hide residue labels GLU 111
Display or hide atom radius
Render in solid 3 D
Show secondary structures -Display or hide ribbons
Bond length 1 angstrom (A) or 1 × 10− 10 meters 1. 52 A ? A
Bond length ? A
Bond length
Hydrogen bond length ? A
Hydrogen bonds of helix
Hydrogen bond of helix
Hydrogen bonds of helix Helix
Hydrogen bonds of sheet Sheet Residue 50~55 201~207 323~328
Number of helix ? From residue 46~146
Change color
Visualization of biological assembly -color by chain
Change color by chain -act on Ribbons
Show residue properties -Change color by Type Negative Positive Polar Reisdue ASP GLU HIS LYS ARG SER TYR ASN THR GLN Hydrophobic CYS MET PHE ALA TRP LEU ILE PRO VAL GLY
Show structure flexibility Change color by B-factor A low B-factor meaning that the position of the atom has been determined with accuracy High B-factor Low B-factor
Other color types default atom colors Root mean square between 2 molecules Secondary Structure Selected residues Relative accessibility
Thymidine kinase • Function: DNA synthesis • Therapeutic: Anticancer and antivirus drug target
Analyze protein-ligand interactions -Select ligands (or residues) Press left button of mouse to select the ligand (THM, thymidine) of 1 kim
Identify binding site -Show protein (ribbon) and ligand (stick)
Select residues in the binding site -Neighbors of selected residues
Center selected residues
H-bonds of the binding site -Compute H-bonds
H-bonds between protein and ligand -Show H-bonds of selection
H-bonds between TK and THM -Show residues from selection
Show residue label Press right button of mouse 1. Q 125 recognize thymine moiety 2. Activity was decreased by over 90% if Q 125 mutated (Biochemistry, 2000. 39: p. 4105 -4111)
van der Waal forces -Stacking interactions M 128 and Y 172 sandwich the thymine moiety Stabilize the binding of substrate (JBC, 1999. 274: p. 31967 -31973)
Observe the protein surface -Compute Surface
Surface preference
Show ligand in the surface
Discard surface
Comparison of multiple structures -Import PDB code: 3 vtk Another structure of thymidine kinase
Open layer info Show or hide 1 kim 3 vtk
Superimpose two molecules
Results of superimposition RMS: 0. 63 Ǻ Measure the structure similarity
Comparison of binding sites -Neighbors of selected residues
Comparison of ligands 3 vtk: inhibitor (Green) 1 kim: substrate(CPK)
Save files
Homework Keyword 1. Capture a picture of N 1 neuraminidase (ribbon) and its ligand (stick) 2. Capture a picture of H-bonds between protein and ligand E-mail pikihsu@gmail. com Mail title: 學號姓名_HW 2
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