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Showing all 8 items for (author: bogyo & m)

EMDB-73509: 
Structure of the Plasmodium falciparum 20S proteasome in complex with a beta5-selective covalent syringolin analogue inhibitor.
Method: single particle / : Yan NL, Gu X, Fajtova P, Tse E, Melo A, Southworth DR, O'Donoghue A, Sello JK, Gestwicki JE

EMDB-73510: 
Structure of the human 20S proteasome in complex with a beta5-selective covalent syringolin analogue inhibitor.
Method: single particle / : Yan NL, Gu X, Fajtova P, Tse E, Melo A, Southworth DR, O'Donoghue A, Sello JK, Gestwicki JE

PDB-9yuy: 
Structure of the Plasmodium falciparum 20S proteasome in complex with a beta5-selective covalent syringolin analogue inhibitor.
Method: single particle / : Yan NL, Gu X, Fajtova P, Tse E, Melo A, Southworth DR, O'Donoghue A, Sello JK, Gestwicki JE

PDB-9yuz: 
Structure of the human 20S proteasome in complex with a beta5-selective covalent syringolin analogue inhibitor.
Method: single particle / : Yan NL, Gu X, Fajtova P, Tse E, Melo A, Southworth DR, O'Donoghue A, Sello JK, Gestwicki JE

EMDB-23544: 
Human phosphofructokinase-1 liver type bound to activator NA-11
Method: single particle / : Lynch EM, Kollman JM

PDB-7lw1: 
Human phosphofructokinase-1 liver type bound to activator NA-11
Method: single particle / : Lynch EM, Kollman JM, Webb B

PDB-5fmg: 
Structure and function based design of Plasmodium-selective proteasome inhibitors
Method: single particle / : Li H, O'Donoghue AJ, van der Linden WA, Xie SC, Yoo E, Foe IT, Tilley L, Craik CS, da Fonseca PCA, Bogyo M

EMDB-3231: 
Structure and function based design of Plasmodium-selective proteasome inhibitors
Method: single particle / : Li H, O' Donoghue AJ, van der Linden WA, Xie SC, Yoo E, Foe IT, Tilley L, Craik CS, da Fonseca PCA, Bogyo M
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