EC Number   |
Reference  |
|---|
   1.14.99.53 | - |
736451 |
| 1.14.99.53 | crystal structure in the Cu(II)-bound form and photoreduction of the crystalline protein in the x-ray beam, leading to conversion from the initial Cu(II)-oxidized form with two coordinated water molecules, which adopts a trigonal bipyramidal geometry, to a reduced Cu(I) form in a T-shaped geometry with no coordinated water molecules |
736451 |
| 1.14.99.53 | 1.1 A resolution room-temperature X-ray structure and 2.1 A resolution neutron structure, show a putative dioxygen species equatorially bound to the active site copper with elongated density for the dioxygen, most consistent with a Cu(II)-bound peroxide |
740090 |
| 1.14.99.53 | comparative analysis of sequences, solved structures, and homology models from AA9 and AA10 LPMO families.The two LPMO families are highly conserved, structurally they have minimal sequence similarity outside the active site residues |
740205 |
| 1.14.99.53 | analysis of the copper active site |
740345 |
| 1.14.99.53 | 1.55 A resolution structure of N-terminal LPMO10A module reveals deletions of interacting loops that protrude from the core beta-sandwich scaffold in larger LPMO10s |
740455 |
| 1.14.99.53 | to 1.85 A resolution, tri-modular enzyme containing a catalytic family AA10 LPMO module, a family 5 chitin-binding module, and a C-terminal unclassified module which displays tight and specific binding to chitin |
740758 |
| 1.14.99.53 | in presence of Zn2+, to 1.55 A resolution, and in presence of Cu2+, to 1.4 AS resolution |
741038 |
| 1.14.99.53 | calculation of solution structure. Ca2+, Mg2+, Fe3+, Co2+, Zn2+, or Cu2+ ions show binding to an interaction site located between His28 and His114 |
741326 |
| 1.14.99.53 | to 1.3 A resolution |
741336 |
