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Search Count: 32

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9O6S image
Structure Of The Human Prohibitin Complex In The Closed State

9O6T image
Structure Of The Human Prohibitin Complex In The Open State

5T19 image
Structure Of Ptp1B Complexed With N-(3'-(1,1-Dioxido-4-Oxo-1,2,5-Thiadiazolidin-2-Yl)-4'-Methyl-[1,1'-Biphenyl]-4-Yl)Acetamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.10 Å Release Date: 2017-04-12
Classification: HYDROLASE
Ligands: MG, 73U, CL

4LLD image
Structure Of Wild-Type Igg1 Antibody Heavy Chain Constant Domain 1 And Light Chain Lambda Constant Domain (Igg1 Ch1:Clambda) At 1.19A

4LLM image
Structure Of Redesigned Igg1 First Constant And Lambda Domains (Ch1:Clambda Constant Redesign 1, Crd1) At 1.75A

4LLQ image
Structure Of Redesigned Igg1 First Constant And Lambda Domains (Ch1:Clambda Constant Redesign 2 Beta, Crd2B) At 1.42A

4LLU image
Structure Of Pertuzumab Fab With Light Chain Clambda At 2.16A

4LLW image
Crystal Structure Of Pertuzumab Clambda Fab With Variable Domain Redesign (Vrd2) At 1.95A

4LLY image
Crystal Structure Of Pertuzumab Clambda Fab With Variable And Constant Domain Redesigns (Vrd2 And Crd2) At 1.6A

4LCD image
Structure Of An Rsp5Xubxsna3 Complex: Mechanism Of Ubiquitin Ligation And Lysine Prioritization By A Hect E3

2YOW image
Bacillus Amyloliquefaciens Cbm33

2YOX image
Bacillus Amyloliquefaciens Cbm33 In Complex With Cu(I) After Photoreduction

2YOY image
Bacillus Amyloliquefaciens Cbm33 In Complex With Cu(I) Reduced Using Ascorbate

3SME image
Structure Of Ptp1B Inactivated By H2O2/Bicarbonate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.70 Å Release Date: 2011-10-19
Classification: HYDROLASE
Ligands: MG

3C1K image
Crystal Structure Of Thrombin In Complex With Inhibitor 15

1ZGI image
Thrombin In Complex With An Oxazolopyridine Inhibitor 21

1ZGV image
Thrombin In Complex With An Oxazolopyridine Inhibitor 2

1ZRB image
Thrombin In Complex With An Azafluorenyl Inhibitor 23B

1Z71 image
Thrombin And P2 Pyridine N-Oxide Inhibitor Complex Structure

1SL3 image
Crystal Structue Of Thrombin In Complex With A Potent P1 Heterocycle-Aryl Based Inhibitor
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