l - People

More documents

Recommendations

Info

References 1. Taverna DM, Goldstein RA: Why are proteins marginally stable? Proteins 2002, 46(1):105-109. 2. Efficient Mo nte-Carlo Simulation of Proteins [robotics.stanford.edu/~itayl/mcs/] 3. Gerstein M, Krebs W: A database of macromolecular motions. Nucleic Acids Res 1998, 26(18):4280-4290. 4. Murzin AG, Brenner SE, Hubbard T, Chothia C: SCOP: a structural classification of proteins database for the investigation of sequences and structures. J Mol Biol 1995, 247(4):536-540. 5. Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res 2000, 28(1):235-242. 6. Pearl F, Todd A, Sillitoe I, Dibley M, Redfern O, Lewis T, Bennett C, Marsden R, Grant A, Lee D et al: The CATH Domain Structure Database and related resources Gene3D and DHS provide comprehensive domain family information for genome analysis. Nucleic Acids Res 2005, 33(Database issue):D247-251. 7. Janin J, Wodak SJ: Structural domains in proteins and their role in the dynamics of protein function. Prog Biophys Mol Biol 1983, 42(1):21-78. 8. Gerstein M, Lesk AM, Chothia C: Structural mechanisms for domain movements in proteins. Biochemistry 1994, 33(22):6739-6749. 280
9. M Gerstein RJ, T Johnson, J Tsai, W Krebs: Studying Macromolecular Motions in a Database Framework: from Structure to Sequence. Rigidity Theory and Applications 1999:401-442. 10. Krebs WG, Alexandrov V, Wilson CA, Echols N, Yu H, Gerstein M: Normal mode analysis of macromolecular motions in a database framework: developing mode concentration as a useful classifying statistic. Proteins 2002, 48(4):682-695. 11. Camon E, Magrane M, Barrell D, Lee V, Dimmer E, Maslen J, Binns D, Harte N, Lopez R, Apweiler R: The Gene Ontology Annotation (GOA) Database: sharing knowledge in Uniprot with Gene Ontology. Nucleic Acids Res 2004, 32(Database issue):D262-266. 12. Wells S, Menor, S., Hespenheide, B.M. and Thorpe, M.F: Physical Biology 2005, 2:S127. 13. Samuel Flores EY, Nicholas Carriero, and Mark Gerstein: submitted 2005. 14. Keating K, Flores, S., Kuhn, L., Gerstein, M.: in preparation 2005. 15. Jacobs DJ, Rader AJ, Kuhn LA, Thorpe MF: Protein flexibility predictions using graph theory. Proteins 2001, 44(2):150-165. 16. B. Brooks RB, B. Olafson, D. States, S. Swaminathan, and M. Karplus: CHARMM: A Program for Macromolecular Energy, Minimization, and Dynamics Calculations. Comp Chem 1983, 4:87-217. 17. Lindahl E, Hess B, van der Spoel D: GROMACS: A package for molecular simulation and trajectory analysis. J Mol Mod 2001, 7:306-317. 18. Rader AJ, Hespenheide BM, Kuhn LA, Thorpe MF: Protein unfolding: rigidity lost. Proc Natl Acad Sci U S A 2002, 99(6):3540-3545. 281
Page 1 and 2:
Abstract Flexibility and domain dyn
Page 3 and 4:
Flexibility and domain dynamics of
Page 5 and 6:
Table of Contents Table of figures
Page 7 and 8:
Can hinges be predicted by a simple
Page 9 and 10:
FlexOracle (FO1, FO1M, FO) 176 Defi
Page 11 and 12:
Conclusions 279 References 281 Tabl
Page 13 and 14:
Table of tables Table 2.1: Amino ac
Page 15 and 16:
Acknowledgements Committee: Mark Ge
Page 17 and 18:
Introduction The problem of predict
Page 19 and 20:
Ab initio methods attempt to model
Page 21 and 22:
potential for simplification, motio
Page 23 and 24:
Chapter 1: The molecular motions da
Page 25 and 26:
MolMovDB is a resource for studying
Page 27 and 28:
voids in proteins, helix-helix pack
Page 29 and 30:
A full-feature version of FIRST5 wi
Page 31 and 32:
gradual transition from the initial
Page 33 and 34:
energy. Thus the first residue list
Page 35 and 36:
activity, DNA-directed DNA polymera
Page 37 and 38:
homology table to an entry in the C
Page 39 and 40:
Highlight active sites from the CSA
Page 43 and 44:
Figure 1.3: Conformational change a
Page 45 and 46:
particular, we found that hinges te
Page 47 and 48:
and the holo. In this case it is po
Page 49 and 50:
Our molecular motions database serv
Page 51 and 52:
We first made a simple GOR(Garnier-
Page 53 and 54:
The morph trajectory was sterically
Page 55 and 56:
protein in the Jmol window to his/h
Page 57 and 58:
of the hinge was otherwise unclear,
Page 59 and 60:
Catalytic Sites Atlas (nonredundant
Page 61 and 62:
! ! ! ! ! h c = number of times res
Page 63 and 64:
! ! ! ! µ h " d c D # H . It is eq
Page 65 and 66:
As mentioned earlier, the fact that
Page 67 and 68:
STRIDE[50] recognizes secondary str
Page 69 and 70:
! ! alignment at this position[24,
Page 71 and 72:
To test this idea, we decided to ca
Page 73 and 74:
GOR method is useful for predicting
Page 75 and 76:
! HI active"site (i) as 0.4 for res
Page 77 and 78:
lowered, and the area under the cur
Page 79 and 80:
would be preferable to the other, o
Page 81 and 82:
Discussion Correlations were found
Page 83 and 84:
Sequence in the immediate neighborh
Page 85 and 86:
Figures p-value 0.5 0.25 0 .01 PHE
Page 87 and 88:
Figure 2.3: Secondary structure Res
Page 89 and 90:
Figure 2.5: Conservation: full set
Page 91 and 92:
Figure 2.7: Solvent accessible surf
Page 93 and 94:
completely random predictor, with a
Page 95 and 96:
samples 1800 1600 1400 1200 1000 80
Page 97 and 98:
m = distance from nearest residues
Page 99 and 100:
Hinge All Hinge Residues residues R
Page 101 and 102:
in hinge residues HI p-value 1 277
Page 103 and 104:
Total resid. in Hinge Atlas 54839 H
Page 105 and 106:
Chi- Computer annotated set Hinge A
Page 107 and 108:
BMC: Bioinformatics, we present the
Page 109 and 110:
hinges. Kundu et al. use the lowest
Page 111 and 112:
Domains can move relative to each o
Page 113 and 114:
The quantity ! E(i) represents the
Page 115 and 116:
Identification of local minima As w
Page 117 and 118:
compute FoldX_energy (stability of
Page 119 and 120:
energy element of each cluster was
Page 121 and 122:
At least two sets of atomic coordin
Page 123 and 124:
! FN (false negatives): Number of r
Page 125 and 126:
We observed qualitatively (figures
Page 127 and 128:
pairs of structures used to generat
Page 129 and 130:
coordinate set does not significant
Page 131 and 132:
The LIR family is composed of eight
Page 133 and 134:
CaM is a major calcium-binding prot
Page 135 and 136:
The results of running FlexOracle a
Page 137 and 138:
Figure 3.2: Results for individual
Page 139 and 140:
a. 139
Page 141 and 142:
Figure 3.3: Folylpolyglutamate Synt
Page 143 and 144:
. c. 143
Page 145 and 146:
a. 145
Page 147 and 148:
Figure 3.5: Lir-1 (closed) Morph ID
Page 149 and 150:
. c. 149
Page 151 and 152:
a. 151
Page 153 and 154:
Figure 3.7: Ribose binding protein
Page 155 and 156:
. c. 155
Page 157 and 158:
Tables GNM 157 Single-cut predictor
Page 159 and 160:
Chapter 4: HingeMaster: normal mode
Page 161 and 162:
The problem of hinge prediction is
Page 163 and 164:
Translation Libration Screw Motion
Page 165 and 166:
! [ K] = [ U] " [ ] 2 [ U] T Where
Page 167 and 168:
generated one ROC curve for each mo
Page 169 and 170:
! ! 1 (l " k) A(k,l) = 2 % ' $ C(i,
Page 171 and 172:
however, since we found that the Co
Page 173 and 174:
A key part of this analysis involve
Page 175 and 176:
describe its net vibrational displa
Page 177 and 178:
! Because it cuts the backbone at t
Page 179 and 180:
! ! x HingeMaster = x" # y . [6] 2
Page 181 and 182:
different values of ! " * and gener
Page 183 and 184:
manually select domains and color p
Page 185 and 186:
E. coli resides in the periplasmic
Page 187 and 188:
The results for this protein are sh
Page 189 and 190:
esidues (62). As is customary we al
Page 191 and 192:
FlexOracle (FO) The FlexOracle algo
Page 193 and 194:
extra breakpoints based on visual i
Page 195 and 196:
hinge, it is usually predicted by a
Page 197 and 198:
Supplementary methods Statistical t
Page 199 and 200:
! ! ! eigenvector. The resulting re
Page 201 and 202:
TNC induces a conformational change
Page 203 and 204:
possibility that unexpected results
Page 205 and 206:
UDP-N-acetylglucosamine enolpyruvyl
Page 207 and 208:
predicted both hinges, again with m
Page 209 and 210:
Most predictors (including FO, Ston
Page 211 and 212:
FO, hNMb, and hNMd were completely
Page 213 and 214:
HingeMaster makes a strong predicti
Page 215 and 216:
Figure 4.2: ROC curves for HingeMas
Page 217 and 218:
Figure 4.3: HingeMaster results for
Page 219 and 220:
d. e. 219
Page 221 and 222:
221
Page 223 and 224:
Figure 4.5: Human lactoferrin (open
Page 225 and 226:
Figure 4.6: Troponin C (TNC) Morph
Page 227 and 228:
Figure 4.7: Calmodulin, calcium fre
Page 229 and 230: 229
Page 231 and 232: Tables Predictor Basis Max. hinge p
Page 233 and 234: test true c positive positive sensi
Page 235 and 236: 235 Closed Metal bound # of hinge p
Page 237 and 238: Chapter 5: The Conformation Explore
Page 239 and 240: ending, which involves a rigid regi
Page 241 and 242: lengths and angles)[89]. The equili
Page 243 and 244: for holo as well as apo forms, but
Page 245 and 246: queried using the “?” button. O
Page 247 and 248: coordinate. This phenomenon is know
Page 249 and 250: ! At the end of each equilibration
Page 251 and 252: aborted. This marked the correspond
Page 253 and 254: sRMSD has a major limitation that m
Page 255 and 256: with respect to the starting struct
Page 257 and 258: generated structure with respect to
Page 259 and 260: Ribose Binding Protein (RBP) As des
Page 261 and 262: strikingly similar both to the holo
Page 263 and 264: energy minimization. The minimizati
Page 265 and 266: Figures Figure 5.1: Assignment of r
Page 267 and 268: Figure 5.3: Results for glutamine b
Page 269 and 270: Figure 5.4: Results for biotin carb
Page 271 and 272: Figure 5.6: Results for Adenylate K
Page 273 and 274: close to the holo. The structure wi
Page 275 and 276: Table 5.1: MolMovDB ID, PDB ID, fre
Page 277 and 278: with sRMSD; however its main utilit
Page 279: morph server, and left confident th
Page 283 and 284: 28. Wriggers W, Schulten K: Protein
Page 285 and 286: 45. Dumontier M, Yao R, Feldman HJ,
Page 287 and 288: 62. Thorpe MF, D.J. Jacobs, M.V. Ch
Page 289 and 290: 81. Winn MD, Isupov MN, Murshudov G
Page 291 and 292: 98. Morris GM, Goodsell DS, Hallida
Page 293 and 294: 115. Miyazawa T: Normal Vibrations
show all

l - People

Create successful ePaper yourself

Delete template?

Save as template?