Unusual ligand structure in Ni–Fe active center and an additional Mg site in hydrogenase revealed by high resolution X-ray structure analysis  Yoshiki.

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Unusual ligand structure in Ni–Fe active center and an additional Mg site in hydrogenase revealed by high resolution X-ray structure analysis  Yoshiki Higuchi, Tatsuhiko Yagi, Noritake Yasuoka  Structure  Volume 5, Issue 12, Pages 1671-1680 (December 1997) DOI: 10.1016/S0969-2126(97)00313-4

Figure 1 Overall structure of Miyazaki hydrogenase and comparison to D. gigas hydrogenase. (a) Schematic drawing of Miyazaki hydrogenase. The large subunit is composed of four domains, one α-helical domain composed of helices (denoted α) 4, 4a, 5, 6, 7, 8, 9, 9a, 10, 11, 12, 13a and 13, and βstrands (β) Ca and Cb colored in blue; two α/β-type domains (α/βI: with helices 15, 16 and 17, and with βstrands A, B and C colored in magenta, and α/βII: with helices 1, 2, 3 and 14, and with βstrands Ha, H, I and J colored in green); and one β/random-coil domain composed of βstrands D, E, Ea, F, Fa, Fb, G and Ga colored in yellow. The flavodoxin module and the remaining part of the small subunit are colored in cyan and pale pink, respectively. The metal centers are presented in balls (Fe: magenta, Ni: yellow, S=O: green, C≡O or C≡N: purple and Mg: orange). The secondary structures are labeled according to the naming scheme of D. gigas hydrogenase [3], and additionally assigned ones are denoted by lower case letters, such as α4a, which exists between two αhelices (α4 and α5). (b) The comparison of the mainchain folding between the Miyazaki (pink) and the D. gigas (blue) hydrogenases. The figure (both parts) was generated using MOLSCRIPT [36] and Raster3D [37]. Structure 1997 5, 1671-1680DOI: (10.1016/S0969-2126(97)00313-4)

Figure 2 Stereo view of the dispersive (in magenta) (F1.000 Å–F1.743 Å) and Bijvoet (in blue) (F+1.730 Å–F−1.730 Å) anomalous difference Fourier maps for the Fe atoms, and dispersive (in light green) (F1.000 Å–F1.487 Å) anomalous difference map for the Ni atom. The maps are calculated at 3.0 Åand shown at contour level of 5.0σ with ball-and-stick models shown for Ni: light green, Fe: magenta and S: green. The electron-density peaks are roughly centered at the position of the anomalous scatterers. Structure 1997 5, 1671-1680DOI: (10.1016/S0969-2126(97)00313-4)

Figure 3 Stereo view of the omitted (Fe, Ni and ligands including cysteine residues were omitted) map (1.8 Å) in the vicinity of the Ni–Fe center contoured at 1.5σ. Two small ligands (C≡O or C≡N, currently assigned as C≡O) are fitted as the L2 and the L3 ligands, and one big ligand (S=O) as the L1 ligand. The ligand coordination geometry of the Fe atom is a slightly distorted octahedron, whereas the ligands for the Ni atom take a penta-coordinate system (square pyramid) constructed with five sulfur atoms. The atoms that comprise the Ni–Fe center are shown in ball and stick model (Fe: magenta, Ni: orange, C≡O/C≡N: blue, S=O: pink, S: violet and cysteine: green). The omitted map was calculated after the first stage of the simulated annealing refinement with four non-protein ligands. Structure 1997 5, 1671-1680DOI: (10.1016/S0969-2126(97)00313-4)

Figure 4 Stereo view of the 2Fo–Fc electron-density map (1.8 Å) around the Mg atom contoured at 1.5σ with a ball-and-stick model of the ligands (Mg: green, Glu: purple, Gln: cyan, Leu: yellow, Arg, Lys, His: sky-blue and Wat: pink). The ligands to the metal are the Nϵ2 atom of the imidazole ring of His552, the oxygen atom (Oϵ2) of the sidechain of Glu62, the carbonyl oxygen of Leu498 and three water oxygen molecules, Wat1, Wat2 and Wat3, which are further hydrogen bonded by Oϵ1 and Oϵ2 of Glu337 and Oϵ1 of Glu62, respectively. There exist various hydrogen-bonding networks including some sidechain atoms and water molecules. Structure 1997 5, 1671-1680DOI: (10.1016/S0969-2126(97)00313-4)