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PDBsum entry 1m1a

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Top Page protein dna_rna ligands metals Protein-protein interface(s) links
Structural protein/DNA PDB id
1m1a
Contents
Protein chains
99 a.a. *
80 a.a. *
105 a.a. *
93 a.a. *
93 a.a. *
DNA/RNA
Ligands
IMT-IMT-PYB-PYB-
ABU-PYB-PYB-PYB-
PYB-BAL-DIB
Metals
_MN ×10
Waters ×220
* Residue conservation analysis

References listed in PDB file
Key reference
Title Crystal structures of nucleosome core particles in complex with minor groove DNA-Binding ligands.
Authors R.K.Suto, R.S.Edayathumangalam, C.L.White, C.Melander, J.M.Gottesfeld, P.B.Dervan, K.Luger.
Ref. J Mol Biol, 2003, 326, 371-380. [DOI no: 10.1016/S0022-2836(02)01407-9]
PubMed id 12559907
Abstract
We determined the crystal structures of three nucleosome core particles in complex with site-specific DNA-binding ligands, the pyrrole-imidazole polyamides. While the structure of the histone octamer and its interaction with the DNA remain unaffected by ligand binding, nucleosomal DNA undergoes significant structural changes at the ligand-binding sites and in adjacent regions to accommodate the ligands. Our findings suggest that twist diffusion occurs over long distances through tightly bound nucleosomal DNA. This may be relevant to the mechanism of ATP-dependent and spontaneous nucleosome translocation, and to the effect of bound factors on nucleosome dynamics.
Figure 2.
Figure 2. DNA parameters. (a) Minor groove widths were averaged for the 10 -- 11 base-pairs between indi- vidual protein -- DNA contact points, and are plotted against the superhelix location. Values for X-NCP, NCP-PA1, NCP-PA2, and NCP-PA3 are plotted against SHLs in black, blue, green, and magenta, respectively. The location of polyamides in each structure is indicated by blue, green, and magenta boxes, respectively. Data points for SHLs at which stretching occurs are circled; the equivalent regions in the long half are indicated by broken-line circles. (b) DNA twist angles, averaged as in (a). The position of stretch sites is indicated as in (a). A vertical line indicates the location of the dyad axis (SHL 0).
Figure 4.
Figure 4. Stretching of nucleosomal DNA. (a) A schematic describing the alignment procedure. Long (turquoise) and short DNA halves (black and brown, respectively for NCP-PA1,2 and X-NCP) were aligned using LSQMAN (Uppsala Software Factory). Base-pair 73 is indicated by F. Stretching of the short half occurs at SHL-5 in NCP-PA1 and 2, and at SHL-2 in X-NCP. Hatched regions indicate those regions of the short half where the sequence is out of register by one base-pair compared to the long half. (b) Overview of parts of the structure of NCP-PA1, viewed down the superhelical axis as in Figure 1(a). Only base-pairs 13 -- 78 (short half) and associated proteins are shown. The long half (turquoise, base-pairs 68 -- 134) was superimposed onto the short half (white) as described for (a). Polyamide 1 is shown in blue; histone coloring is as described for Figure 1. The dyad axis is indicated by a broken line, base-pair 73 is indicated by F, the L1L2 DNA-binding motif is indicated by O, the a1 -- a1 motif is indicated by *. (c) X-NCP with aligned long and short halves (turquoise and gold, respectively) was superimposed onto NCP-PA1 by a structural alignment of 30 base-pairs centered on either stretching site, as shown in (a). All other labels are as in (b).
The above figures are reprinted by permission from Elsevier: J Mol Biol (2003, 326, 371-380) copyright 2003.
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