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found for this hinge, as lactoferrin crystals grown at 277 and 303 K show rotation between the two lobes (Karthikeyan et al). None of the predictive measures identify a hinge point at 90/91 in the open form structure. However TLSMD analysis of the closed form of the same protein (PDB entry 1LFH; Morph ID f964705-18231) finds segment boundaries at 91/92 and 249/250 for the 3-segment partition, corresponding exactly to the lactoferrin mobile domain boundaries (not shown). 224
Figure 4.6: Troponin C (TNC) Morph ID: f960267-11022, PDB ID: 4TNC HAG hinges (residues 38-39, 65-66, and 104-105) were identified manually by comparison of the 2-calcium bound form of Troponin C (PDB ID: 4TNC, used in (a) and (b) with the 4-calcium bound (2TN4) form (the MolMovDB animation illustrates this, reference morph ID 333010-30921). Green crosses in (b) designate the HAG hinges for 4TNC. This motion is particularly challenging to predict by general-purpose methods such as those presented here, since they cannot directly treat the ion binding and release required[83] for motion. Further, the HAG hinges only reflect the domain motion that 225
Page 1 and 2:
Abstract Flexibility and domain dyn
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Flexibility and domain dynamics of
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Table of Contents Table of figures
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Can hinges be predicted by a simple
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FlexOracle (FO1, FO1M, FO) 176 Defi
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Conclusions 279 References 281 Tabl
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Table of tables Table 2.1: Amino ac
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Acknowledgements Committee: Mark Ge
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Introduction The problem of predict
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Ab initio methods attempt to model
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potential for simplification, motio
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Chapter 1: The molecular motions da
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MolMovDB is a resource for studying
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voids in proteins, helix-helix pack
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A full-feature version of FIRST5 wi
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gradual transition from the initial
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energy. Thus the first residue list
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activity, DNA-directed DNA polymera
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homology table to an entry in the C
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Highlight active sites from the CSA
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Figure 1.3: Conformational change a
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particular, we found that hinges te
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and the holo. In this case it is po
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Our molecular motions database serv
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We first made a simple GOR(Garnier-
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The morph trajectory was sterically
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protein in the Jmol window to his/h
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of the hinge was otherwise unclear,
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Catalytic Sites Atlas (nonredundant
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! ! ! ! ! h c = number of times res
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! ! ! ! µ h " d c D # H . It is eq
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As mentioned earlier, the fact that
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STRIDE[50] recognizes secondary str
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! ! alignment at this position[24,
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To test this idea, we decided to ca
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GOR method is useful for predicting
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! HI active"site (i) as 0.4 for res
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lowered, and the area under the cur
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would be preferable to the other, o
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Discussion Correlations were found
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Sequence in the immediate neighborh
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Figures p-value 0.5 0.25 0 .01 PHE
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Figure 2.3: Secondary structure Res
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Figure 2.5: Conservation: full set
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Figure 2.7: Solvent accessible surf
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completely random predictor, with a
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samples 1800 1600 1400 1200 1000 80
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m = distance from nearest residues
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Hinge All Hinge Residues residues R
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in hinge residues HI p-value 1 277
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Total resid. in Hinge Atlas 54839 H
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Chi- Computer annotated set Hinge A
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BMC: Bioinformatics, we present the
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hinges. Kundu et al. use the lowest
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Domains can move relative to each o
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The quantity ! E(i) represents the
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Identification of local minima As w
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compute FoldX_energy (stability of
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energy element of each cluster was
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At least two sets of atomic coordin
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! FN (false negatives): Number of r
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We observed qualitatively (figures
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pairs of structures used to generat
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coordinate set does not significant
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The LIR family is composed of eight
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CaM is a major calcium-binding prot
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The results of running FlexOracle a
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Figure 3.2: Results for individual
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a. 139
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Figure 3.3: Folylpolyglutamate Synt
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. c. 143
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a. 145
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Figure 3.5: Lir-1 (closed) Morph ID
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. c. 149
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a. 151
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Figure 3.7: Ribose binding protein
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. c. 155
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Tables GNM 157 Single-cut predictor
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Chapter 4: HingeMaster: normal mode
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The problem of hinge prediction is
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Translation Libration Screw Motion
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! [ K] = [ U] " [ ] 2 [ U] T Where
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generated one ROC curve for each mo
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! ! 1 (l " k) A(k,l) = 2 % ' $ C(i,
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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: Figure 4.5: Human lactoferrin (open
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
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Table 5.1: MolMovDB ID, PDB ID, fre
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with sRMSD; however its main utilit
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morph server, and left confident th
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9. M Gerstein RJ, T Johnson, J Tsai
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28. Wriggers W, Schulten K: Protein
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45. Dumontier M, Yao R, Feldman HJ,
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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
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