Analysing the visible conformational substates of the FK506-binding protein FKBP12.

Crystal Structure Of The Cytoplasmic Domain Of The Type I Tgf-Beta Receptor In Complex With Fkbp12

Fk506 Binding Protein Fkbp Mutant R42kH87V COMPLEX WITH Immunosuppressant Fk506

Fkbp Mutant F36v Complexed With Remodeled Synthetic Ligand

Fkbp Complexed With Methyl Methylsulfinylmethyl Sulfide (Dss)

Fkbp Complexed With 4-Hydroxy-2-Butanone

Fk506 Binding Protein Mutant, Homodimeric Complex

Solution Structure Of Fkbp12 Complexed With Gpi-1046, A Neurotrophic Ligand

The Structure Of The Immunophilin-Immunosuppressant Fkbp12- Rapamycin Complex Interacting With Human Frap

Atomic Structure Of The Rapamycin Human Immunophilin Fkbp- 12 Complex

Fk-506 Binding Protein: Three-Dimensional Structure Of The Complex With The Antagonist L-685,818

Atomic Structure Of Fkbp-Fk506, An Immunophilin-Immunosuppressant Complex

Design, Synthesis, And Kinetic Evaluation Of High-Affinity Fkbp Ligands, And The X-Ray Crystal Structures Of Their Complexes Wi

Atomic Structure Of Fkbp12-Fk506, An Immunophilin Immunosuppressant Complex

Atomic Structure Of Fkbp12, An Immunophilin Binding Protein

Atomic Structure Of Fkbp12-Rapaymycin, An Immunophilin- Immunosuppressant Complex

Solution Structure Of Fkbp, A Rotamase Enzyme And Receptor For Fk506 And Rapamycin

Crystal Structure Analysis Of The Fkbp12 Complexed With 000107 Small Molecule

Crystal Structure Analysis Of The Fkbp12 Complexed With 000308 Small Molecule

Fk506 Binding Protein Complexed With Fkb-001

The Structure Of The Immunophilin-immunosuppressant Fkbp12-rapamycin Complex Interacting With Human Frap

Fk506 Binding Protein (12 Kda, Human) Complex With L-709,858

Fk506 Binding Protein (12 Kda, Human) Complex With L-707,587

Ternary Complex Of A Calcineurin A Fragment, Calcineurin B, Fkbp12 And The Immunosuppressant Drug Fk506 (tacrolimus)

Wildtype Fk506-Binding Protein Complexed With Rapamycin

Fk506-Binding Protein Mutant Wf59 Complexed With Rapamycin

Fk506-Binding Protein Mutant Wl59 Complexed With Rapamycin

The Structure Of The Immunophilin-immunosuppressant Fkbp12-(c16)- Ethoxy Rapamycin Complex Interacting With Huma

Fk-506-Binding Protein: Three-Dimensional Structure Of The Complex With The Antagonist L-685,818

Crystal Structure Of E60a Mutant Of Fkbp12

Crystal Structure Of E60q Mutant Of Fkbp12

Nmr Structure Of Fkbp12-Mtor Frb Domain-Rapamycin Complex Structure Determined Based On Pcs

Atomic Structures Of The Rapamycin Analogs In Complex With Both Human Fkbp12 And Frb Domain Of Frap

Crystal Structure Of The Kinase Domain Of Type I Activin Receptor (Acvr1) In Complex With Fkbp12 And Dorsomorphin

Crystal Structure Of The Cytoplasmic Domain Of The Bone Morp Protein Receptor Type-1b (Bmpr1b) In Complex With Fkbp12 An 193189

X-Ray Crystal Structure Of 28-O-Methylrapamycin Complexed With Fkbp12: Is The Cyclohexyl Moiety Part Of The Effector Domain Of

Analyzing The Visible Conformational Substates Of The Fk506 Binding Protein Fkbp12

Structural Basis Of Conformational Transitions In The Active Site And 80 S Loop In The Fk506 Binding Protein Fkbp12

FK506-binding protein (FKBP) [Homo sapiens]

peptidyl-prolyl cis-trans isomerase FKBP1A isoform a [Homo sapiens]

peptidyl-prolyl cis-trans isomerase FKBP1A [Bos taurus]

peptidyl-prolyl cis-trans isomerase FKBP1A [Sus scrofa]

peptidyl-prolyl cis-trans isomerase FKBP1A [Oryctolagus cuniculus]

peptidyl-prolyl cis-trans isomerase FKBP1A [Canis lupus familiaris]

RecName: Full=Peptidyl-prolyl cis-trans isomerase FKBP1A; Short=PPIase FKBP1A; AltName: Full=12 kDa FK506-binding protein; Shor

TPA: peptidyl-prolyl cis-trans isomerase FKBP1A [Bos taurus]

School of Public Health, University at Albany SUNY

Partial list of chemical shifts for Human FKBP12

Analyzing the visible conformational substates of the FK506-binding protein FKBP12, major form