Structural Entry Filters:

Search Count: 34

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8ZH7 image
Crystal Structure Of N-Terminal Domain Of N-Methyl-D-Aspartate Receptor Subunit Nr1 In Complex With Patient-Derived Antibody

7XLP image
Mek1 Bound To Ds03090629

7XNC image
Mek1 Bound To Ds94070624

7AG1 image
Crystal Structure Of E. Coli Sfp Aldolase (Yiht) From Sulfo-Emp Pathway

7AG4 image
Crystal Structure Of Active Site Mutant Of Sq Isomerase (Yihs-H248A) From Salmonella Enterica In Complex With Sulfofructose (Sf)

7AG6 image
Crystal Structure Of Sf Kinase Yihv From E. Coli In Complex With Sulfofructose (Sf), Adp-Mg

7AG7 image
Crystal Structure Of Sfp Aldolase Yiht From Salmonella Enterica In Complex With Sulfate Bound At The Active Site

7AGH image
Crystal Structure Of Sf Kinase Yihv From E. Coli In Complex With Amppnp-Mg

7AGK image
Crystal Structure Of E. Coli Sf Kinase (Yihv) In Complex With Product Sulfofructose Phosphate (Sfp)

7NE2 image
Crystal Structure Of Class I Sfp Aldolase Yiht From Salmonella Enterica With Sfp/ Dhap (Schiff Base Complex With Active Site Lys193)

7CEE image
Crystal Structure Of Mouse Neuroligin-3

7CEG image
Crystal Structure Of The Complex Between Mouse Ptp Delta And Neuroligin-3

6YPE image
Crystal Structure Of The Human Neuronal Pentraxin 1 (Np1) Pentraxin (Ptx) Domain.

6LUR image
Human Puf60 Uhm Domain (Thioredoxin Fusion) In Complex With A Small Molecule Binder

6P5M image
Discovery Of A Novel, Highly Potent, And Selective Thieno[3,2-D]Pyrimidinone-Based Cdc7 Inhibitor With A Quinuclidine Moiety (Tak-931) As An Orally Active Investigational Anti-Tumor Agent

6P5P image
Discovery Of A Novel, Highly Potent, And Selective Thieno[3,2-D]Pyrimidinone-Based Cdc7 Inhibitor With A Quinuclidine Moiety (Tak-931) As An Orally Active Investigational Anti-Tumor Agent

6KG2 image
Human Mthfd2 In Complex With Compound 18

6E3E image
Structure Of Rorgt In Complex With A Novel Inverse Agonist.

6E3G image
Structure Of Rorgt In Complex With A Novel Agonist.

6JIB image
Human Mthfd2 In Complex With Ds44960156
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