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PDB: 8 results

5I94
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BU of 5i94 by Molmil
Crystal structure of human glutaminase C in complex with the inhibitor UPGL-00019
Descriptor: 2-phenyl-N-{5-[4-({5-[(phenylacetyl)amino]-1,3,4-thiadiazol-2-yl}oxy)piperidin-1-yl]-1,3,4-thiadiazol-2-yl}acetamide, Glutaminase kidney isoform, mitochondrial
Authors:Huang, Q, Cerione, R.
Deposit date:2016-02-19
Release date:2016-05-11
Last modified:2023-09-27
Method:X-RAY DIFFRACTION (2.983 Å)
Cite:Design and evaluation of novel glutaminase inhibitors.
Bioorg.Med.Chem., 24, 2016
1AN0
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BU of 1an0 by Molmil
CDC42HS-GDP COMPLEX
Descriptor: CDC42HS-GDP, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION
Authors:Kongsaeree, P, Cerione, R, Clardy, J.
Deposit date:1997-06-26
Release date:1999-01-13
Last modified:2021-11-03
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:The Structure Determination of Cdc42Hs and Gdp Complex
To be Published
1N52
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BU of 1n52 by Molmil
Cap Binding Complex
Descriptor: 20 kDa nuclear cap binding protein, 7-METHYL-GUANOSINE-5'-TRIPHOSPHATE-5'-GUANOSINE, 80 kDa nuclear cap binding protein, ...
Authors:Calero, G, Wilson, K, Ly, T, Rios-Steiner, J, Clardy, J, Cerione, R.
Deposit date:2002-11-04
Release date:2003-02-18
Last modified:2024-02-14
Method:X-RAY DIFFRACTION (2.11 Å)
Cite:Structural basis of m7GpppG binding to the nuclear cap-binding protein complex.
Nat.Struct.Biol., 9, 2002
1N54
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BU of 1n54 by Molmil
Cap Binding Complex m7GpppG free
Descriptor: 20 kDa nuclear cap binding protein, 80 kDa nuclear cap binding protein, GLYCEROL
Authors:Calero, G, Wilson, K, Ly, T, Rios-Steiner, J, Clardy, J, Cerione, R.
Deposit date:2002-11-04
Release date:2003-02-18
Last modified:2024-02-14
Method:X-RAY DIFFRACTION (2.72 Å)
Cite:Structural basis of m7GpppG binding to the nuclear cap-binding protein complex.
Nat.Struct.Biol., 9, 2002
5FI7
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BU of 5fi7 by Molmil
Crystal structure of human GAC in complex with inhibitor UPGL_00015: 2-phenyl-~{N}-[5-[(3~{S})-3-[[5-(2-phenylethanoylamino)-1,3,4-thiadiazol-2-yl]oxy]pyrrolidin-1-yl]-1,3,4-thiadiazol-2-yl]ethanamide
Descriptor: 2-phenyl-~{N}-[5-[(3~{S})-3-[[5-(2-phenylethanoylamino)-1,3,4-thiadiazol-2-yl]oxy]pyrrolidin-1-yl]-1,3,4-thiadiazol-2-yl]ethanamide, Glutaminase kidney isoform, mitochondrial
Authors:Huang, Q, Cerione, R.
Deposit date:2015-12-22
Release date:2016-05-11
Last modified:2023-09-27
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:Design and evaluation of novel glutaminase inhibitors.
Bioorg.Med.Chem., 24, 2016
5FI2
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BU of 5fi2 by Molmil
Crystal structure of human GAC in complex with inhibitor UPGL_00009: 2-phenyl-~{N}-[5-[[(3~{R})-1-[5-(2-phenylethanoylamino)-1,3,4-thiadiazol- 2-yl]pyrrolidin-3-yl]amino]-1,3,4-thiadiazol-2-yl]ethanamide
Descriptor: 2-phenyl-~{N}-[5-[[(3~{R})-1-[5-(2-phenylethanoylamino)-1,3,4-thiadiazol-2-yl]pyrrolidin-3-yl]amino]-1,3,4-thiadiazol-2-yl]ethanamide, Glutaminase kidney isoform, mitochondrial
Authors:Huang, Q, Cerione, R.
Deposit date:2015-12-22
Release date:2016-05-11
Last modified:2023-09-27
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:Design and evaluation of novel glutaminase inhibitors.
Bioorg.Med.Chem., 24, 2016
5FI6
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BU of 5fi6 by Molmil
Crystal structure of human GAC in complex with inhibitor UPGL_00011: 2-phenyl-~{N}-[5-[[(3~{S})-1-[5-(2-phenylethanoylamino)-1,3,4-thiadiazol-2-yl]pyrrolidin-3-yl]amino]-1,3,4-thiadiazol-2-yl]ethanamide
Descriptor: 2-phenyl-~{N}-[5-[[(3~{S})-1-[5-(2-phenylethanoylamino)-1,3,4-thiadiazol-2-yl]pyrrolidin-3-yl]amino]-1,3,4-thiadiazol-2-yl]ethanamide, Glutaminase kidney isoform, mitochondrial
Authors:Huang, Q, Cerione, R.
Deposit date:2015-12-22
Release date:2016-05-11
Last modified:2024-03-06
Method:X-RAY DIFFRACTION (2.52 Å)
Cite:Design and evaluation of novel glutaminase inhibitors.
Bioorg.Med.Chem., 24, 2016
2NGR
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BU of 2ngr by Molmil
TRANSITION STATE COMPLEX FOR GTP HYDROLYSIS BY CDC42: COMPARISONS OF THE HIGH RESOLUTION STRUCTURES FOR CDC42 BOUND TO THE ACTIVE AND CATALYTICALLY COMPROMISED FORMS OF THE CDC42-GAP.
Descriptor: ALUMINUM FLUORIDE, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ...
Authors:Nassar, N, Hoffman, G, Clardy, J, Cerione, R.
Deposit date:1998-07-31
Release date:1999-01-06
Last modified:2023-08-30
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Structures of Cdc42 bound to the active and catalytically compromised forms of Cdc42GAP.
Nat.Struct.Biol., 5, 1998

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