Structure-based mutation analysis BCKDHA

Structure selection

The following table presents the PDB structures for BCKDHA to date:

PDB id	resolution [Å]	R-factor	ph-value
1DTW	2.70	0.224	7.5*
1OLS	1.85	0.172	5.5
1OLU	1.90	0.161	5.5
1OLX	2.25	0.161	5.5
1U5B	1.83	0.156	5.8
1V11	1.95	0.139*	5.5
1V16	1.90	0.132*	5.5
1V1M	2.00	0.130*	5.5
1V1R	1.80	0.158	5.5
1WCI	1.84	0.149	5.5
1X7W	1.73	0.148	5.8
1X7X	2.10	0.149	5.8
1X7Y	1.57	0.150	5.8
1X7Z	1.72	0.154	5.8
1X80	2.00	0.161	5.8
2BEU	1.89	0.171	5.5
2BEV	1.80	0.139	5.5
2BEW	1.79	0.147	5.5
2BFB	1.77	0.145	5.5
2BFC	1.64	0.144	5.5
2BFD	1.39*	0.150	5.5
2BFE	1.69	0.150	5.5
2BFF	1.46	0.150	5.5
2J9F	1.88	0.171	5.5

The following PDB Structure was chosen because of its good experimental resolution: <bold></bold>

resultion:
R-factor
ph-value

Comparison energies

Mapping of the mutations on the crystal structure

SCWRL

Before we could use SCWRL we first had to get the sequence of our model: repairPDB bckdha.pdb -seq >> bckdha.seq

When we have the sequence we have to make one file for each mutation. In these files we copied the bckdha.seq and changed the sequence to lower case letters. Then we add the mutation in an upper case letter.

To run SCWRL we used the command: scwrl -i bckdha.pdb -s mutation1.seq -o mutation1Model.pdb

Total minimal energy of the graph

Position	Energy
M82L	642.213
Q125E	616.85
Y166N	616.293
G249S	633.378
C264W	805.257
R265W	710.647
I326T	619.424
F409C	617.305
Y438N	615.951

foldX

To use foldX we first build a runscript. Additionally we had to create one file with all PDB Ids each in a new line (list.txt).

<TITLE>FOLDX_runscript;
<JOBSTART>#;
<PDBS>#;
<BATCH>foldx_protein.txt;
<COMMANDS>FOLDX_commandfile;
<Stability>list.txt;
<END>#;
<OPTIONS>FOLDX_optionfile;
//<Temperature>298;
<R>#;
<pH>5.5;
<IonStrength>0.050;
<water>-CRYSTAL;
<metal>-CRYSTAL;
<VdWDesign>2;
<OutPDB>false;
<pdb_hydrogens>false;
<END>#;
<JOBEND>#;
<ENDFILE>#;

	total energy	difference
wildtype	401.00	0
mutant1	437.88	-36.88
mutant2	431.77	-30.77
mutant3	432.24	-31.24
mutant4	432.22	-31.22
mutant5	488.43	-87.43
mutant6	460.43	-59.43
mutant7	432.94	-31.94
mutant8	433.33	-32.33
mutant9	431.56	-30.56

Minimise

gromacs

Gromacs

1. fetchpdb

The fetch-pdb script first checks, if it was called with an valid PDB-id. If the entered PDB code has 4letters, the script tries to download the pdb-file from the server. The successfully downloaded folder gets unzipped and everything except the actual pdb file is removed.

2. repairPDB

repairPDB bckdha_mod.pdb -noh -nosol > bckdha_clean.pdb

3. SCWRL

scwrl -i bckdha_mod.pdb -s extractedPDB.seq -o bckdha_scwrl.pdb

pdb including HEATOMS

4.pdb2gmx

use clean pdb without HEATOMS

pdb2gmx -f bckdha_clean.pdb -o bckdha.gro -p bckdha.top -water tip3p -ff amber03

5. MDP

6.grompp

grompp -v -f MDP_bckdha.mdp -c bckdha.gro -p bckdha.top -o bckdha.tpr

7.System Minimization

mdrun -v -deffnm bckdha 2> mdrun_out.txt

8.Analyzation

g_energy -f bckdha.edr -o energy_1.xvg

Links

go back to Maple syrup urine disease main page

go back to Task 6 Sequence based mutation analysis

go to Reference Sequence BCKDHA

Structure-based mutation analysis BCKDHA

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