2XKI

Aquo-met structure of C.lacteus mini-Hb

2XKI の概要

• エントリーDOI: 10.2210/pdb2xki/pdb
• 関連するPDBエントリー: 1KR7 1V07 2VYY 2VYZ 2XKG 2XKH
• 分子名称: NEURAL HEMOGLOBIN, PROTOPORPHYRIN IX CONTAINING FE, SULFATE ION, ... (5 entities in total)
• 機能のキーワード: oxygen storage, metal-binding
• 由来する生物種: CEREBRATULUS LACTEUS (MILKY RIBBON-WORM)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 12351.59

構造登録者

Pesce, A.,Nardini, M.,Dewilde, S.,Capece, L.,Marti, M.A.,Congia, S.,Salter, M.D.,Blouin, G.C.,Estrin, D.A.,Ascenzi, P.,Moens, L.,Bolognesi, M.,Olson, J.S. (登録日: 2010-07-08, 公開日: 2010-12-08, 最終更新日: 2023-12-20)

主引用文献

Pesce, A.,Nardini, M.,Dewilde, S.,Capece, L.,Marti, M.A.,Congia, S.,Salter, M.D.,Blouin, G.C.,Estrin, D.A.,Ascenzi, P.,Moens, L.,Bolognesi, M.,Olson, J.S.
Ligand Migration in the Apolar Tunnel of Cerebratulus Lacteus Mini-Hemoglobin.
J.Biol.Chem., 286:5347-, 2011

PubMed Abstract: The large apolar tunnel traversing the mini-hemoglobin from Cerebratulus lacteus (CerHb) has been examined by x-ray crystallography, ligand binding kinetics, and molecular dynamic simulations. The addition of 10 atm of xenon causes loss of diffraction in wild-type (wt) CerHbO(2) crystals, but Leu-86(G12)Ala CerHbO(2), which has an increased tunnel volume, stably accommodates two discrete xenon atoms: one adjacent to Leu-86(G12) and another near Ala-55(E18). Molecular dynamics simulations of ligand migration in wt CerHb show a low energy pathway through the apolar tunnel when Leu or Ala, but not Phe or Trp, is present at the 86(G12) position. The addition of 10-15 atm of xenon to solutions of wt CerHbCO and L86A CerHbCO causes 2-3-fold increases in the fraction of geminate ligand recombination, indicating that the bound xenon blocks CO escape. This idea was confirmed by L86F and L86W mutations, which cause even larger increases in the fraction of geminate CO rebinding, 2-5-fold decreases in the bimolecular rate constants for ligand entry, and large increases in the computed energy barriers for ligand movement through the apolar tunnel. Both the addition of xenon to the L86A mutant and oxidation of wt CerHb heme iron cause the appearance of an out Gln-44(E7) conformer, in which the amide side chain points out toward the solvent and appears to lower the barrier for ligand escape through the E7 gate. However, the observed kinetics suggest little entry and escape (≤ 25%) through the E7 pathway, presumably because the in Gln-44(E7) conformer is thermodynamically favored.

PubMed: 21147768
DOI: 10.1074/JBC.M110.169045

実験手法

X-RAY DIFFRACTION (1.3 Å)