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Cover illustration: A ribbon diagram of the Kelch domain of human Keap1 showing the conserved water molecules found in each blade of the -propeller (p. 1335). |
Acta Cryst. (2005). D61, 1313-1319 [ doi:10.1107/S0907444905022523 ] Ligand binding at the transthyretin dimer-dimer interface: structure of the transthyretin-T4Ac complex at 2.2 Å resolutionP. Neumann, V. Cody and A. WojtczakSynopsis: The crystal structure of the human transthyretin-tetraiodothyroacetic acid complex was determined. The ligand is in an unusual position, penetrating the dimer-dimer interface and interacting with three TTR monomers simultaneously. PDB reference: 1ked Online 28 September 2005 |
Acta Cryst. (2005). D61, 1320-1334 [ doi:10.1107/S0907444905022638 ] The structure of Cryptococcus neoformans thymidylate synthase suggests strategies for using target dynamics for species-specific inhibitionJ. S. Finer-Moore, A. C. Anderson, R. H. O'Neil, M. P. Costi, S. Ferrari, J. Krucinski and R. M. StroudSynopsis: The ternary complex structures of C. neoformans TS and human TS are highly conserved. A 1,8-naphthalein derivative that selectively inhibits C. neoformans and E. coli TSs over human TS binds to an open conformation of E. coli TS. Disorder of the inhibitor-binding site in the human apoenzyme may explain the inhibitor specificity. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1335-1342 [ doi:10.1107/S0907444905022626 ] Conserved solvent and side-chain interactions in the 1.35 Å structure of the Kelch domain of Keap1L. J. Beamer, X. Li, C. A. Bottoms and M. HanninkSynopsis: Use of 1.35 Å SAD data for de novo structure determination of the Kelch domain and for refinement at atomic resolution is described. PDB reference: 1zgk Online 28 September 2005 |
Acta Cryst. (2005). D61, 1343-1347 [ doi:10.1107/S090744490502264X ] Structure of the hypothetical Mycoplasma protein MPN555 suggests a chaperone functionU. Schulze-Gahmen, S. Aono, S. Chen, H. Yokota, R. Kim and S.-H. KimSynopsis: The crystal structure of a hypothetical protein (MPN555) from M. pneumoniae revealed a trilobal molecule with at least one central binding pocket or channel. The molecule has structural homology with two bacterial chaperone proteins, which suggests a similar chaperone function for MPN555. PDB reference: 1zxj Online 28 September 2005 |
Acta Cryst. (2005). D61, 1348-1353 [ doi:10.1107/S0907444905022997 ] Structures of two minor-groove-binding quinolinium quaternary salts complexed with d(CGCGAATTCGCG)2 at 1.6 and 1.8 Å resolutionA. Adams, C. Leong, W. A. Denny and J. M. GussSynopsis: The high-resolution X-ray crystal structures of two anticancer minor-groove-binding quinolinium quaternary salts complexed with the dodecamer d(CGCGAATTCGCG)2 are reported. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1354-1363 [ doi:10.1107/S0907444905023152 ] Automated crystallographic ligand building using the medial axis transform of an electron-density isosurfaceJ. Aishima, D. S. Russel, L. J. Guibas, P. D. Adams and A. T. BrungerSynopsis: Use of the medial axis for automated crystallographic model building is described. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1364-1372 [ doi:10.1107/S0907444905023565 ] Three-dimensional structure determination of proteins related to human health in their functional context at The Israel Structural Proteomics Center (ISPC)S. Albeck, Y. Burstein, O. Dym, Y. Jacobovitch, N. Levi, R. Meged, Y. Michael, Y. Peleg, J. Prilusky, G. Schreiber, I. Silman, T. Unger and J. L. SussmanSynopsis: The work of the Israel Structural Proteomics Center (ISPC) to determine the structures of proteins related to human health in their functional context is described. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1373-1377 [ doi:10.1107/S0907444905023358 ] Absolute configuration of the hydroxyfarnesylethyl group of haem A, determined by X-ray structural analysis of bovine heart cytochrome c oxidase using methods applicable at 2.8 Å resolutionE. Yamashita, H. Aoyama, M. Yao, K. Muramoto, K. Shinzawa-Itoh, S. Yoshikawa and T. TsukiharaSynopsis: The absolute configuration of haem A, the prosthetic group of cytochrome c oxidase, was determined to be S by analyzing bond angles. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1378-1385 [ doi:10.1107/S0907444905023590 ] A flexible and economical medium-throughput strategy for protein production and crystallizationN. Moreland, R. Ashton, H. M. Baker, I. Ivanovic, S. Patterson, V. L. Arcus, E. N. Baker and J. S. LottSynopsis: A medium-throughput strategy has been developed for academic structural biology that meets the twin goals of research output and graduate-student development. The platform incorporates Gateway cloning and 96-well methods for solubility screening and crystallization. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1386-1394 [ doi:10.1107/S0907444905023851 ] Crystallographic analysis of the NNA7 Fab and proposal for the mode of human blood-group recognitionK. Xie, S.-C. Song, S. L. Spitalnik and J. E. WedekindSynopsis: The NNA7 Fab antibody fragment recognizes the human N blood-group antigen, whereas the NNA7-G91S mutant exhibits reduced antigen binding. To provide insight into how these Fab fragments recognize this clinically relevant glycopeptide antigen, the crystal structures of both Fab fragments were solved. The results provide a model for peptide and sugar recognition based upon crystallographic contacts, as well as a bound 2-(N-morpholino)ethanesulfonic acid (MES) molecule trapped in the antigen-combining site. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1395-1401 [ doi:10.1107/S0907444905024194 ] Structure of free fumarase C from Escherichia coliT. WeaverSynopsis: The crystal structure of fumarase C has been solved in the absence of inhibitors and substrate analogues. This novel crystal structure reports a pH-sensitive shift at the allosteric B site and preservation of the architecture surrounding the conserved active-site water. PDB reference: 1yfe Online 28 September 2005 |
Acta Cryst. (2005). D61, 1402-1405 [ doi:10.1107/S0907444905024029 ] Structural studies on recombinant T = 3 capsids of Sesbania mosaic virus coat protein mutantsV. Sangita, G. L. Lokesh, P. S. Satheshkumar, V. Saravanan, C. S. Vijay, H. S. Savithri and M. R. N. MurthySynopsis: Purified Sesbania mosaic virus coat-protein particles have been crystallized and X-ray crystal structures of their mutant capsids have been determined. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1406-1412 [ doi:10.1107/S0907444905024030 ] Structure of a mutant T = 1 capsid of Sesbania mosaic virus: role of water molecules in capsid architecture and integrityV. Sangita, P. S. Satheshkumar, H. S. Savithri and M. R. N. MurthySynopsis: The role of water molecules in the Sesbania mosaic virus structure has been analyzed. PDB reference: 1x36 Online 28 September 2005 |
Acta Cryst. (2005). D61, 1413-1417 [ doi:10.1107/S0907444905024285 ] High-resolution neutron protein crystallography with radically small crystal volumes: application of perdeuteration to human aldose reductaseI. Hazemann, M. T. Dauvergne, M. P. Blakeley, F. Meilleur, M. Haertlein, A. Van Dorsselaer, A. Mitschler, D. A. A. Myles and A. PodjarnySynopsis: Perdeuterated human aldose reductase neutron diffraction data at 2.2 Å resolution was collected from a 0.15 mm3 crystal. Deuterium atoms were clearly seen in the neutron-scattering density map. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1418-1425 [ doi:10.1107/S0907444905024340 ] Mutation of surface residues to promote crystallization of activated factor XI as a complex with benzamidine: an essential step for the iterative structure-based design of factor XI inhibitorsL. Jin, P. Pandey, R. E. Babine, D. T. Weaver, S. S. Abdel-Meguid and J. E. StricklerSynopsis: The crystallizability of coagulation factor XI has been improved by surface-residue mutation, generating a quadruple mutant that crystallizes easily in the presence of benzamidine and has facilitated the iterative process of structure-based design of factor XI selective inhibitors. PDB references: 1zhm, 1zhp and 1zhr Online 28 September 2005 |
Acta Cryst. (2005). D61, 1426-1431 [ doi:10.1107/S0907444905024984 ] Towards rationalization of crystallization screening for small- to medium-sized academic laboratories: the PACT/JCSG+ strategyJ. Newman, D. Egan, T. S. Walter, R. Meged, I. Berry, M. Ben Jelloul, J. L. Sussman, D. I. Stuart and A. PerrakisSynopsis: A strategy for crystallization screening using nanolitre drops and a combination of a sparse-matrix screen (JCSG+) and a novel systematic screen (PACT) is presented and discussed. Online 28 September 2005 |
Acta Cryst. (2005). D61, 1432-1435 [ doi:10.1107/S090744490502473X ] Notes of a protein crystallographer: my nights with ACTORC. Abad-ZapateroSynopsis: A historical perspective of the steps leading to the current robot technology available for crystal mounting and data collection is presented. The implications for the future of the field are briefly discussed. Online 28 September 2005 |
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