4w9q:A (GLY32) to (GLY139) THE FK1 DOMAIN OF FKBP51 IN COMPLEX WITH (1S,5S,6R)-10-[(3,5- DICHLOROPHENYL)SULFONYL]-3-[2-(3,4-DIMETHOXYPHENOXY)ETHYL]-5-ETHYL-3, 10-DIAZABICYCLO[4.3.1]DECAN-2-ONE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, LIGAND SELECTIVITY, ISOMERASE
1a7x:A (SER8) to (LYS105) FKBP12-FK1012 COMPLEX | ISOMERASE, IMMUNOPHILIN
1nsg:A (ILE7) to (LYS105) THE STRUCTURE OF THE IMMUNOPHILIN-IMMUNOSUPPRESSANT FKBP12-RAPAMYCIN COMPLEX INTERACTING WITH HUMAN FRAP | COMPLEX (ISOMERASE-KINASE), TRANSFERASE, FKBP12, FRAP, RAPAMYCIN, COMPLEX (ISOMERASE-KINASE) COMPLEX
1b6c:A (SER8) to (LYS105) CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF THE TYPE I TGF-BETA RECEPTOR IN COMPLEX WITH FKBP12 | COMPLEX (ISOMERASE/PROTEIN KINASE), RECEPTOR SERINE/THREONINE KINASE
1b6c:C (SER8) to (LYS105) CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF THE TYPE I TGF-BETA RECEPTOR IN COMPLEX WITH FKBP12 | COMPLEX (ISOMERASE/PROTEIN KINASE), RECEPTOR SERINE/THREONINE KINASE
1b6c:E (SER8) to (LYS105) CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF THE TYPE I TGF-BETA RECEPTOR IN COMPLEX WITH FKBP12 | COMPLEX (ISOMERASE/PROTEIN KINASE), RECEPTOR SERINE/THREONINE KINASE
1b6c:G (SER8) to (LYS105) CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF THE TYPE I TGF-BETA RECEPTOR IN COMPLEX WITH FKBP12 | COMPLEX (ISOMERASE/PROTEIN KINASE), RECEPTOR SERINE/THREONINE KINASE
1bkf:A (GLY1) to (LYS105) FK506 BINDING PROTEIN FKBP MUTANT R42K/H87V COMPLEX WITH IMMUNOSUPPRESSANT FK506 | ISOMERASE, ROTAMASE
3fap:A (SER8) to (LYS105) ATOMIC STRUCTURES OF THE RAPAMYCIN ANALOGS IN COMPLEX WITH BOTH HUMAN FKBP12 AND FRB DOMAIN OF FRAP | FKBP12, FRAP, RAPAMYCIN, COMPLEX, GENE THERAPY, CELL CYCLE
2ppn:A (SER8) to (LYS105) CRYSTAL STRUCTURE OF FKBP12 | HIGH RESOLUTION PROTEIN STRUCTURE, ISOMERASE
2ppo:A (SER8) to (LYS105) CRYSTAL STRUCTURE OF E60A MUTANT OF FKBP12 | HIGH RESOLUTION PROTEIN STRUCTURE, LYASE
1d6o:A (SER8) to (LYS105) NATIVE FKBP | ISOMERASE, IMMUNOPHILIN
1d6o:B (SER8) to (LYS105) NATIVE FKBP | ISOMERASE, IMMUNOPHILIN
1d7h:A (SER8) to (LYS105) FKBP COMPLEXED WITH DMSO | ISOMERASE, IMMUNOPHILIN, DMSO, FKBP
1d7j:A (SER8) to (LYS105) FKBP COMPLEXED WITH 4-HYDROXY-2-BUTANONE | ISOMERASE, IMMUNOPHILIN, FKBP, BUQ, 4-HYDROXY-2-BUTANONE
1d7j:B (SER8) to (LYS105) FKBP COMPLEXED WITH 4-HYDROXY-2-BUTANONE | ISOMERASE, IMMUNOPHILIN, FKBP, BUQ, 4-HYDROXY-2-BUTANONE
4iq2:A (ILE7) to (ASN105) P21 CRYSTAL FORM OF FKBP12.6 | FKBP12.6, ISOMERASE
4iqc:A (GLY1) to (ASN105) P3121 CRYSTAL FORM OF FKBP12.6 | FKBP12.6, ISOMERASE
4iqc:B (SER8) to (ASN105) P3121 CRYSTAL FORM OF FKBP12.6 | FKBP12.6, ISOMERASE
4j4n:C (GLY17) to (GLU127) CRYSTAL STRUCTURE OF FK506 BINDING DOMAIN OF PLASMODIUM FALCIPARUM FKBP35 IN COMPLEX WITH D44 | D44, FKBP35, FK506 BINDING, ISOMERASE-ISOMERASE INHIBITOR COMPLEX
4j4o:A (GLY16) to (GLU126) CRYSTAL STRUCTURE OF FK506 BINDING DOMAIN OF PLASMODIUM VIVAX FKBP35 IN COMPLEX WITH D44 | D44, FKBP35, FK506, ISOMERASE-ISOMERASE INHIBITOR COMPLEX
1q1c:A (GLY32) to (THR143) CRYSTAL STRUCTURE OF N(1-260) OF HUMAN FKBP52 | ROTAMASE, TPR REPEAT, NUCLEAR PROTEIN, PHOSPHORYLATION, ISOMERASE
2dg3:A (GLY1) to (LYS105) WILDTYPE FK506-BINDING PROTEIN COMPLEXED WITH RAPAMYCIN | IMMUNOPHILIN, ISOMERASE, ROTAMASE
2dg4:A (GLY1) to (LYS105) FK506-BINDING PROTEIN MUTANT WF59 COMPLEXED WITH RAPAMYCIN | IMMUNOPHILIN, ISOMERASE, ROTAMASE
1q6h:A (VAL128) to (ASP222) CRYSTAL STRUCTURE OF A TRUNCATED FORM OF FKPA FROM ESCHERICHIA COLI | CHAPERONE, PEPTIDYL-PROLYL ISOMERASE, HEAT SHOCK PROTEIN, FKBP FAMILY, ISOMERASE
1q6h:B (VAL128) to (ASP222) CRYSTAL STRUCTURE OF A TRUNCATED FORM OF FKPA FROM ESCHERICHIA COLI | CHAPERONE, PEPTIDYL-PROLYL ISOMERASE, HEAT SHOCK PROTEIN, FKBP FAMILY, ISOMERASE
1q6i:A (VAL128) to (ASP222) CRYSTAL STRUCTURE OF A TRUNCATED FORM OF FKPA FROM ESCHERICHIA COLI, IN COMPLEX WITH IMMUNOSUPPRESSANT FK506 | CHAPERONE, PEPTIDYL-PROLYL ISOMERASE, HEAT SHOCK PROTEIN, FKBP FAMILY, IMMUNOSUPPRESSANT FK506, ASCOMYCIN, ISOMERASE
4jfi:A (GLY32) to (GLY139) INCREASING THE EFFICIENCY EFFICIENCY OF LIGANDS FOR THE FK506-BINDING PROTEIN 51 BY CONFORMATIONAL CONTROL: COMPLEX OF FKBP51 WITH COMPOUND 1-[(9S,13R,13AR)-1,3-DIMETHOXY-8-OXO-5,8,9,10,11,12,13,13A-OCTAHYDRO- 6H-9,13-EPIMINOAZOCINO[2,1-A]ISOQUINOLIN-14-YL]-2-(3,4,5- TRIMETHOXYPHENYL)ETHANE-1,2-DIONE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4jfj:A (GLY32) to (GLY139) INCREASING THE EFFICIENCY EFFICIENCY OF LIGANDS FOR THE FK506-BINDING PROTEIN 51 BY CONFORMATIONAL CONTROL: COMPLEX OF FKBP51 WITH COMPOUND (1S,6R)-10-(1,3-BENZOTHIAZOL-6-YLSULFONYL)-3-[2-(3,4- DIMETHOXYPHENOXY)ETHYL]-3,10-DIAZABICYCLO[4.3.1]DECAN-2-ONE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
2rse:A (GLY902) to (LYS1006) NMR STRUCTURE OF FKBP12-MTOR FRB DOMAIN-RAPAMYCIN COMPLEX STRUCTURE DETERMINED BASED ON PCS | FKBP12, RAPAMYCIN, FK506, LANTHANIDE, PCS, ISOMERASE-TRANSFERASE COMPLEX
1eym:A (SER8) to (LYS105) FK506 BINDING PROTEIN MUTANT, HOMODIMERIC COMPLEX | ROTAMASE; ISOMERASE; LIGAND-REVERSIBLE DIMER
1qpf:D (SER208) to (LYS305) FK506 BINDING PROTEIN (12 KDA, HUMAN) COMPLEX WITH L-709,858 | IMMUNOPHILIN-DRUG COMPLEX, CIS-TRANS ISOMERASE, PEPTIDYL-PROLYL ISOMERASE, ISOMERASE
1qpl:A (GLY1) to (LYS105) FK506 BINDING PROTEIN (12 KDA, HUMAN) COMPLEX WITH L-707,587 | IMMUNOPHILIN-DRUG COMPLEX, CIS-TRANS ISOMERASE, PEPTIDYL- PROLYL ISOMERASE
1qpl:C (SER208) to (LYS305) FK506 BINDING PROTEIN (12 KDA, HUMAN) COMPLEX WITH L-707,587 | IMMUNOPHILIN-DRUG COMPLEX, CIS-TRANS ISOMERASE, PEPTIDYL- PROLYL ISOMERASE
1f40:A (GLY1) to (LYS105) SOLUTION STRUCTURE OF FKBP12 COMPLEXED WITH GPI-1046, A NEUROTROPHIC LIGAND | ISOMERASE
3h9r:B (SER9) to (LYS106) CRYSTAL STRUCTURE OF THE KINASE DOMAIN OF TYPE I ACTIVIN RECEPTOR (ACVR1) IN COMPLEX WITH FKBP12 AND DORSOMORPHIN | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP- BINDING, DISEASE MUTATION, GLYCOPROTEIN, KINASE, MAGNESIUM, MANGANESE, MEMBRANE, METAL-BINDING, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, TRANSMEMBRANE, ISOMERASE, ROTAMASE, ISOMERASE-PROTEIN KINASE COMPLEX
1fap:A (SER8) to (LYS105) THE STRUCTURE OF THE IMMUNOPHILIN-IMMUNOSUPPRESSANT FKBP12- RAPAMYCIN COMPLEX INTERACTING WITH HUMAN FRAP | FKBP12, FRAP, RAPAMYCIN, COMPLEX (ISOMERASE/KINASE)
1fkb:A (GLY1) to (LYS105) ATOMIC STRUCTURE OF THE RAPAMYCIN HUMAN IMMUNOPHILIN FKBP- 12 COMPLEX | ISOMERASE
1fkd:A (GLY1) to (LYS105) FK-506 BINDING PROTEIN: THREE-DIMENSIONAL STRUCTURE OF THE COMPLEX WITH THE ANTAGONIST L-685,818 | CIS-TRANS ISOMERASE
1fkf:A (GLY1) to (LYS105) ATOMIC STRUCTURE OF FKBP-FK506, AN IMMUNOPHILIN-IMMUNOSUPPRESSANT COMPLEX | ISOMERASE
1fkg:A (GLY1) to (LYS105) DESIGN, SYNTHESIS, AND KINETIC EVALUATION OF HIGH-AFFINITY FKBP LIGANDS, AND THE X-RAY CRYSTAL STRUCTURES OF THEIR COMPLEXES WITH FKBP12 | CIS-TRANS ISOMERASE
1fkh:A (SER8) to (LYS105) DESIGN, SYNTHESIS, AND KINETIC EVALUATION OF HIGH-AFFINITY FKBP LIGANDS, AND THE X-RAY CRYSTAL STRUCTURES OF THEIR COMPLEXES WITH FKBP12 | CIS-TRANS ISOMERASE
1fki:B (SER8) to (LYS105) DESIGN, SYNTHESIS, AND KINETIC EVALUATION OF HIGH-AFFINITY FKBP LIGANDS, AND THE X-RAY CRYSTAL STRUCTURES OF THEIR COMPLEXES WITH FKBP12 | CIS-TRANS ISOMERASE
1fkl:A (GLY1) to (LYS105) ATOMIC STRUCTURE OF FKBP12-RAPAYMYCIN, AN IMMUNOPHILIN- IMMUNOSUPPRESSANT COMPLEX | FK506 BINDING PROTEIN, FKBP12, FKBP, CIS-TRANS PROLYL- ISOMERASE, ROTAMASE
1r9h:A (GLY15) to (ALA122) STRUCTURAL GENOMICS OF C.ELEGANS: FKBP-TYPE PEPTIDYLPROLYL ISOMERASE | STRUCTURAL GENOMICS, PEPTIDYLPROLYL ISOMERASE, PSI, PROTEIN STRUCTURE INITIATIVE, SOUTHEAST COLLABORATORY FOR STRUCTURAL GENOMICS, SECSG
2fap:A (ILE7) to (LYS105) THE STRUCTURE OF THE IMMUNOPHILIN-IMMUNOSUPPRESSANT FKBP12-(C16)- ETHOXY RAPAMYCIN COMPLEX INTERACTING WITH HUMA | FKBP12, FRAP, RAPAMYCIN, COMPLEX (ISOMERASE-KINASE), COMPLEX (ISOMERASE-KINASE) COMPLEX
3uqa:A (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE WITH SURFACE MUTATION A54E FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH FK506 | SSGCID, ISOMERASE, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, PROTEIN BINDING
3uqi:A (GLY2) to (ARG106) CRYSTALLOGRAPHIC STRUCTURE OF FKBP12 FROM AEDES AEGYPTI | FKBP12, ISOMERASE, FK506 BINDING
2fke:A (GLY1) to (LYS105) FK-506-BINDING PROTEIN: THREE-DIMENSIONAL STRUCTURE OF THE COMPLEX WITH THE ANTAGONIST L-685,818 | CIS-TRANS ISOMERASE
3vaw:A (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE WITH SURFACE MUTATION V3I FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH FK506 | SSGCID, ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, PROTEIN BINDING, PROTEIN BINDING- INHIBITOR COMPLEX
3ihz:A (GLY16) to (GLU126) CRYSTAL STRUCTURE OF THE FK506 BINDING DOMAIN OF PLASMODIUM VIVAX FKBP35 IN COMPLEX WITH FK506 | PLASMODIUM VIVAX, FKBP35, FK506, ISOMERASE
3ihz:B (ARG23) to (GLU126) CRYSTAL STRUCTURE OF THE FK506 BINDING DOMAIN OF PLASMODIUM VIVAX FKBP35 IN COMPLEX WITH FK506 | PLASMODIUM VIVAX, FKBP35, FK506, ISOMERASE
4lav:A (GLY32) to (ASP141) CRYSTAL STRUCTURE ANALYSIS OF FKBP52, CRYSTAL FORM II | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, PROTEIN FOLDING, ISOMERASE
1tco:C (SER8) to (LYS105) TERNARY COMPLEX OF A CALCINEURIN A FRAGMENT, CALCINEURIN B, FKBP12 AND THE IMMUNOSUPPRESSANT DRUG FK506 (TACROLIMUS) | COMPLEX (HYDROLASE/ISOMERASE), IMMUNOSUPPRESSANT
1j4h:A (GLY1) to (LYS105) CRYSTAL STRUCTURE ANALYSIS OF THE FKBP12 COMPLEXED WITH 000107 SMALL MOLECULE | ISOMERASE, ROTAMASE
1j4i:A (GLY1) to (LYS105) CRYSTAL STRUCTURE ANALYSIS OF THE FKBP12 COMPLEXED WITH 000308 SMALL MOLECULE | ISOMERASE, ROTAMASE
1jvw:A (GLY67) to (SER169) TRYPANOSOMA CRUZI MACROPHAGE INFECTIVITY POTENTIATOR (TCMIP) | MACROPHAGE INFECTIVITY POTENTIATOR, TRYPANOSOMA CRUZI, CHAGAS DISEASE, X-RAY CRYSTAL STRUCTURE, ROTAMASE, ISOMERASE
4n19:A (SER8) to (LYS105) STRUCTURAL BASIS OF CONFORMATIONAL TRANSITIONS IN THE ACTIVE SITE AND 80 S LOOP IN THE FK506 BINDING PROTEIN FKBP12 | ISOMERASE
5b8i:C (GLY11) to (GLY123) CRYSTAL STRUCTURE OF CALCINEURIN A AND CALCINEURIN B IN COMPLEX WITH FKBP12 AND FK506 FROM COCCIDIOIDES IMMITIS RS | SSGCID, NIH, NIAID, SBRI, UW, BERYLLIUM, PHOSPHATASE, CALCINEURIN, FKBP12, FK506, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, HYDROLASE
5bxj:A (GLY32) to (GLY139) COMPLEX OF THE FK1 DOMAIN MUTANT A19T OF FKBP51 WITH 4-NITROPHENOL | COCHAPERONE, FK506, 4-NITROPHENOL, ISOMERASE
2y78:A (LEU15) to (ASP112) CRYSTAL STRUCTURE OF BPSS1823, A MIP-LIKE CHAPERONE FROM BURKHOLDERIA PSEUDOMALLEI | ISOMERASE, MIP, PPIASE, VIRULENCE
3mdy:B (ILE8) to (LYS106) CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF THE BONE MORPHOGENETIC PROTEIN RECEPTOR TYPE-1B (BMPR1B) IN COMPLEX WITH FKBP12 AND LDN- 193189 | COMPLEX (ISOMERASE-PROTEIN KINASE), RECEPTOR SERINE/THREONINE KINASE, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, DISEASE MUTATION, KINASE, TRANSFERASE, ROTAMASE, TRANSFERASE-ISOMERASE COMPLEX
3mdy:D (ILE8) to (LYS106) CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF THE BONE MORPHOGENETIC PROTEIN RECEPTOR TYPE-1B (BMPR1B) IN COMPLEX WITH FKBP12 AND LDN- 193189 | COMPLEX (ISOMERASE-PROTEIN KINASE), RECEPTOR SERINE/THREONINE KINASE, STRUCTURAL GENOMICS CONSORTIUM, SGC, ATP-BINDING, DISEASE MUTATION, KINASE, TRANSFERASE, ROTAMASE, TRANSFERASE-ISOMERASE COMPLEX
4qt2:A (LYS24) to (LEU128) CRYSTAL STRUCTURE OF THE FK506-BINDING DOMAIN OF PLASMODIUM FALCIPARUM FKBP35 IN COMPLEX WITH RAPAMYCIN | PPIASE, ENZYME, RAPAMYCIN, FKBP35, ISOMERASE
4qt3:A (GLY17) to (GLU129) CRYSTAL STRUCTURE RESOLUTION OF PLASMODIUM FALCIPARUM FK506 BINDING DOMAIN (FKBP35) IN COMPLEX WITH RAPAMYCIN AT 1.4A RESOLUTION | PPIASE, ENZYME, RAPAMYCIN, FKBP35, ISOMERASE
3ni6:A (GLY16) to (GLU126) CRYSTAL STRUCTURE OF THE FK506 BINDING DOMAIN OF PLASMODIUM VIVAX FKBP35 | FK506 BINDING DOMAIN, ISOMERASE
3ni6:B (GLY16) to (GLU126) CRYSTAL STRUCTURE OF THE FK506 BINDING DOMAIN OF PLASMODIUM VIVAX FKBP35 | FK506 BINDING DOMAIN, ISOMERASE
3o5i:A (GLY32) to (GLY139) FK1 DOMAIN OF FKBP51, CRYSTAL FORM II | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5i:B (GLY32) to (GLY139) FK1 DOMAIN OF FKBP51, CRYSTAL FORM II | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5j:A (GLY32) to (GLY139) FK1 DOMAIN OF FKBP51, CRYSTAL FORM III | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5l:A (GLY32) to (GLY139) FK1 DOMAIN MUTANT A19T OF FKBP51, CRYSTAL FORM I | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5m:A (GLY32) to (GLY139) FK1 DOMAIN MUTANT A19T OF FKBP51, CRYSTAL FORM II | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5m:B (GLY32) to (GLY139) FK1 DOMAIN MUTANT A19T OF FKBP51, CRYSTAL FORM II | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5o:A (GLY32) to (GLY139) FK1 DOMAIN MUTANT A19T OF FKBP51, CRYSTAL FORM III | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5p:A (GLY32) to (GLU140) FK1 DOMAIN MUTANT A19T OF FKBP51, CRYSTAL FORM IV | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5q:A (GLY32) to (GLY139) FK1 DOMAIN MUTANT A19T OF FKBP51, CRYSTAL FORM IV, IN PRESENCE OF DMSO | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
3o5r:A (GLY32) to (GLY139) COMPLEX OF FK506 WITH THE FK1 DOMAIN MUTANT A19T OF FKBP51 | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4tw7:A (GLY32) to (GLY139) THE FK1 DOMAIN OF FKBP51 IN COMPLEX WITH IFIT4 | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, LIGAND SELECTIVITY, ISOMERASE
4tw8:A (GLY32) to (GLU144) THE FK1-FK2 DOMAINS OF FKBP52 IN COMPLEX WITH IFIT-FL | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, LIGAND SELECTIVITY, ISOMERASE
4tw8:B (GLY32) to (THR143) THE FK1-FK2 DOMAINS OF FKBP52 IN COMPLEX WITH IFIT-FL | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, LIGAND SELECTIVITY, ISOMERASE
4tx0:A (GLY32) to (GLY139) THE FK1 DOMAIN OF FKBP51 IN COMPLEX WITH (1S,5S,6R)-10-[(3,5- DICHLOROPHENYL)SULFONYL]-5-(2-METHOXYETHOXY)-3-(2-METHOXYETHYL)-3,10- DIAZABICYCLO[4.3.1]DECAN-2-ONE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4dh0:A (ILE7) to (LYS105) X-RAY CRYSTAL STRUCTURE OF 28-O-METHYLRAPAMYCIN COMPLEXED WITH FKBP12: IS THE CYCLOHEXYL MOIETY PART OF THE EFFECTOR DOMAIN OF RAPAMYCIN? | PEPTIDYL-PROLYL CIS-TRANS ISOMERASE, ISOMERASE-IMMUNOSUPPRESSANT COMPLEX
4dip:B (LEU32) to (ASN136) CRYSTAL STRUCTURE OF HUMAN PEPTIDYL-PROLYL CIS-TRANS ISOMERASE FKBP14 | STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, PEPTIDYL- PROLYL CIS-TRANS ISOMERASE, ISOMERASE
5hkg:A (GLY1) to (ASN105) TOTAL CHEMICAL SYNTHESIS, REFOLDING AND CRYSTALLOGRAPHIC STRUCTURE OF A FULLY ACTIVE IMMUNOPHILIN: CALSTABIN 2 (FKBP12.6). | SYNTHETIC PROTEIN, REFOLDING, IMMUNOPHILIN, ISOMERASE
4dri:A (GLY32) to (GLY139) CO-CRYSTAL STRUCTURE OF THE PPIASE DOMAIN OF FKBP51, RAPAMYCIN AND THE FRB FRAGMENT OF MTOR | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, MAMMALIAN TARGET OF RAPAMYCIN, KINASE, SIGNALLING, IMMUNOSUPPRESSION, CANCER, ISOMERASE-TRANSFERASE COMPLEX
4drj:A (GLY32) to (GLY139) O-CRYSTAL STRUCTURE OF THE PPIASE DOMAIN OF FKBP52, RAPAMYCIN AND THE FRB FRAGMENT OF MTOR | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, KINASE, SIGNALLING, MAMMALIAN TARGET OF RAPAMYCIN, IMMUNOSUPPRESSION, CANCER, ISOMERASE-TRANSFERASE COMPLEX
4drm:A (GLY32) to (GLY139) EVALUATION OF SYNTHETIC FK506 ANALOGS AS LIGANDS FOR FKBP51 AND FKBP52: COMPLEX OF FKBP51 WITH {3-[(1R)-3-(3,4-DIMETHOXYPHENYL)-1- ({[(2S)-1-{[(1S,2R)-2-ETHYL-1-HYDROXYCYCLOHEXYL](OXO) ACETYL}PIPERIDIN-2-YL]CARBONYL}OXY)PROPYL]PHENOXY}ACETIC ACID | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4drn:A (GLY32) to (GLY139) EVALUATION OF SYNTHETIC FK506 ANALOGS AS LIGANDS FOR FKBP51 AND FKBP52: COMPLEX OF FKBP51 WITH {3-[(1R)-3-(3,4-DIMETHOXYPHENYL)-1- ({[(2S)-1-{[(1S,2R)-2-ETHYL-1-HYDROXYCYCLOHEXYL](OXO) ACETYL}PIPERIDIN-2-YL]CARBONYL}OXY)PROPYL]PHENOXY}ACETIC ACID | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4dro:A (GLY32) to (GLY139) EVALUATION OF SYNTHETIC FK506 ANALOGS AS LIGANDS FOR FKBP51 AND FKBP52: COMPLEX OF FKBP51 WITH (1R)-3-(3,4-DIMETHOXYPHENYL)-1- PHENYLPROPYL (2S)-1-{[(1R,2S)-2-ETHYL-1-HYDROXYCYCLOHEXYL](OXO) ACETYL}PIPERIDINE-2-CARBOXYLATE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4drq:A (GLY32) to (GLU140) EXPLORATION OF PIPECOLATE SULFONAMIDES AS BINDERS OF THE FK506-BINDING PROTEINS 51 AND 52: COMPLEX OF FKBP51 WITH 2-(3-((R)-1-((S)-1-(3,5- DICHLOROPHENYLSULFONYL)PIPERIDINE-2-CARBONYLOXY)-3-(3,4-DIMETHOXY - PHENYL)PROPYL)PHENOXY)ACETIC ACID | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
5hw6:A (GLU3) to (GLY120) CANDIDA ALBICANS FKBP12 APO PROTEIN IN C2 SPACE GROUP | FKBP12, PROLYL ISOMERASE, ISOMERASE
5hw7:A (GLN12) to (GLY120) CANDIDA ALBICANS FKBP12 APO PROTEIN IN P21212 SPACE GROUP | FKBP12, PROLYL ISOMERASE, ISOMERASE
5hwb:A (LYS8) to (GLY106) ASPERGILLUS FUMIGATUS FKBP12 APO PROTEIN IN P212121 SPACE GROUP | FKBP12, PROLYL ISOMERASE, FK506, ISOMERASE
5hwb:B (GLY2) to (GLY106) ASPERGILLUS FUMIGATUS FKBP12 APO PROTEIN IN P212121 SPACE GROUP | FKBP12, PROLYL ISOMERASE, FK506, ISOMERASE
5hwc:A (GLY2) to (GLY106) ASPERGILLUS FUMIGATUS FKBP12 P90G PROTEIN BOUND WITH FK506 IN P212121 SPACE GROUP | FKBP12, PROLYL ISOMERASE, FK506, ISOMERASE
5i98:A (GLU3) to (GLY120) STRUCTURE OF APO FKBP12(P104G) FROM C. ALBICANS | FKBP12, SELF-CATALYSIS, ISOMERASE
5i98:B (GLN7) to (GLY120) STRUCTURE OF APO FKBP12(P104G) FROM C. ALBICANS | FKBP12, SELF-CATALYSIS, ISOMERASE
5j6e:A (SER9) to (GLY106) STRUCTURE OF DISULFIDE CROSSLINKED A. FUMIGATUS FKBP12(V91C) | FKBP12, DISULFIDE TRAPPING, CROSSLINKED DIMER, ISOMERASE
4fn2:A (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE WITH SURFACE MUTATION D44G FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ37 | SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, ISOMERASE, PROTEIN BINDING
4ggq:C (THR16) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ40 | SSGCID, ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, PROTEIN BINDING
4ggq:A (THR16) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ40 | SSGCID, ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, PROTEIN BINDING
4ggq:B (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ40 | SSGCID, ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, PROTEIN BINDING
4ggq:D (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ40 | SSGCID, ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, PROTEIN BINDING
4giv:B (GLY9) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE WITH SURFACE MUTATION D44G FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ183 | SSGCID, ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, PROTEIN BINDING
2ppp:A (SER8) to (LYS105) CRYSTAL STRUCTURE OF E60Q MUTANT OF FKBP12 | HIGH RESOLUTION PROTEIN STRUCTURE, LYASE
1d7i:A (SER8) to (LYS105) FKBP COMPLEXED WITH METHYL METHYLSULFINYLMETHYL SULFIDE (DSS) | ISOMERASE, IMMUNOPHILIN, FKBP,METHYL METHYLSULFINYLMETHYL SULFIDE, DSS
1d7i:B (SER8) to (LYS105) FKBP COMPLEXED WITH METHYL METHYLSULFINYLMETHYL SULFIDE (DSS) | ISOMERASE, IMMUNOPHILIN, FKBP,METHYL METHYLSULFINYLMETHYL SULFIDE, DSS
1pbk:A (TYR111) to (ASP222) HOMOLOGOUS DOMAIN OF HUMAN FKBP25 | FKBP12 HOMOLOGOUS DOMAIN OF HFKBP25, ISOMERASE
4jfk:A (GLY32) to (GLY139) INCREASING THE EFFICIENCY EFFICIENCY OF LIGANDS FOR THE FK506-BINDING PROTEIN 51 BY CONFORMATIONAL CONTROL: COMPLEX OF FKBP51 WITH (1S,6R)- 3-[2-(3,4-DIMETHOXYPHENOXY)ETHYL]-10-[(2-OXO-2,3-DIHYDRO-1,3- BENZOTHIAZOL-6-YL)SULFONYL]-3,10-DIAZABICYCLO[4.3.1]DECAN-2-ONE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
1fkk:A (GLY1) to (LYS105) ATOMIC STRUCTURE OF FKBP12, AN IMMUNOPHILIN BINDING PROTEIN | FK506 BINDING PROTEIN, FKBP12, CIS-TRANS PROLYL-ISOMERASE, ROTAMASE
1fkt:A (ILE7) to (LYS105) SOLUTION STRUCTURE OF FKBP, A ROTAMASE ENZYME AND RECEPTOR FOR FK506 AND RAPAMYCIN | CIS-TRANS ISOMERASE
2vcd:A (LEU32) to (ILE131) SOLUTION STRUCTURE OF THE FKBP-DOMAIN OF LEGIONELLA PNEUMOPHILA MIP IN COMPLEX WITH RAPAMYCIN | MIP, FKBP, PPIASE, MEMBRANE, ROTAMASE, SIROLIMUS, VIRULENCE, ISOMERASE, RAPAMYCIN, FKBP-DOMAIN, OUTER MEMBRANE, LEGIONNAIRES DISEASE, MACROLIDE ANTIBIOTIC, LEGIONELLA PNEUMOPHILA
2vn1:A (LYS24) to (GLU129) CRYSTAL STRUCTURE OF THE FK506-BINDING DOMAIN OF PLASMODIUM FALCIPARUM FKBP35 IN COMPLEX WITH FK506 | FKBP, FK506, ISOMERASE, TPR REPEAT, PLASMODIUM FALCIPARUM
2vn1:B (LYS24) to (GLU127) CRYSTAL STRUCTURE OF THE FK506-BINDING DOMAIN OF PLASMODIUM FALCIPARUM FKBP35 IN COMPLEX WITH FK506 | FKBP, FK506, ISOMERASE, TPR REPEAT, PLASMODIUM FALCIPARUM
1yat:A (ILE7) to (LYS105) IMPROVED CALCINEURIN INHIBITION BY YEAST FKBP12-DRUG COMPLEXES. CRYSTALLOGRAPHIC AND FUNCTIONAL ANALYSIS | BINDING PROTEIN
5d75:A (TYR111) to (LEU225) CRYSTAL STRUCTURE OF HUMAN FKBD25 IN COMPLEX WITH FK506 | FK506, FKBP25, FKBP3, IMMUNOPHILIN, INHIBITOR, ISOMERASE-INHIBITOR COMPLEX
5dit:A (GLY32) to (GLY139) THE FK1 DOMAIN OF FKBP51 IN COMPLEX WITH THE NEW SYNTHETIC LIGAND (1R)-3-(3,4-DIMETHOXYPHENYL)-1-F3-[2-(MORPHOLIN-4-YL) ETHOXY]PHENYLGPROPYL(2S)-1-[(2S,3R)-2-CYCLOHEXYL-3- HYDROXYBUTANOYL]PIPERIDINE-2-CARBOXYLATE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, LIGAND SELECTIVITY, ISOMERASE
5div:A (GLY32) to (GLY139) THE FK1 DOMAIN OF FKBP51 IN COMPLEX WITH THE NEW SYNTHETIC LIGAND (S)- N-(1-CARBAMOYLCYCLOPENTYL)-1-((S)-2-CYCLOHEXYL-2-(3,4,5- TRIMETHOXYPHENYL)ACETYL)PIPERIDINE-2-CARBOXAMIDE | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, LIGAND SELECTIVITY, ISOMERASE
4c02:B (GLY1) to (ASN105) CRYSTAL STRUCTURE OF HUMAN ACVR1 (ALK2) IN COMPLEX WITH FKBP12.6 AND DORSOMORPHIN | TRANSFERASE-ISOMERASE COMPLEX, TRANSFERASE, DORSOMORPHIN,
3o5k:B (GLY32) to (GLY139) FK1 DOMAIN OF FKBP51, CRYSTAL FORM VIII | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILINE, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
5gpg:A (TYR111) to (ASP222) CO-CRYSTAL STRUCTURE OF THE FK506 BINDING DOMAIN OF HUMAN FKBP25, RAPAMYCIN AND THE FRB DOMAIN OF HUMAN MTOR | COMPLEX, KINASE, ISOMERASE-TRANSFERASE COMPLEX
5ht1:A (SER15) to (LYS112) STRUCTURE OF APO C. GLABRATA FKBP12 | FKBP12, C. GLABRATA, PAHTOGENESIS, ISOMERASE
4drk:A (LYS38) to (GLY139) EVALUATION OF SYNTHETIC FK506 ANALOGS AS LIGANDS FOR FKBP51 AND FKBP52: COMPLEX OF FKBP51 WITH {3-[(1R)-3-(3,4-DIMETHOXYPHENYL)-1- ({[(2S)-1-(3,3-DIMETHYL-2-OXOPENTANOYL)PIPERIDIN-2-YL]CARBONYL}OXY) PROPYL]PHENOXY}ACETIC ACID | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4drk:B (GLY32) to (GLY139) EVALUATION OF SYNTHETIC FK506 ANALOGS AS LIGANDS FOR FKBP51 AND FKBP52: COMPLEX OF FKBP51 WITH {3-[(1R)-3-(3,4-DIMETHOXYPHENYL)-1- ({[(2S)-1-(3,3-DIMETHYL-2-OXOPENTANOYL)PIPERIDIN-2-YL]CARBONYL}OXY) PROPYL]PHENOXY}ACETIC ACID | FK-506 BINDING DOMAIN, HSP90 COCHAPERONE, IMMUNOPHILIN, PEPTIDYL- PROLYL ISOMERASE, ISOMERASE
4dz2:B (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A PEPTIDYL-PROLYL CIS-TRANS ISOMERASE WITH SURFACE MUTATION R92G FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH FK506 | SSGCID, ISOMERASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE
4g50:A (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE WITH SURFACE MUTATION D44G FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ168 | SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, ISOMERASE, PROTEIN BINDING
4g50:B (LEU15) to (ASP112) CRYSTAL STRUCTURE OF A SMT FUSION PEPTIDYL-PROLYL CIS-TRANS ISOMERASE WITH SURFACE MUTATION D44G FROM BURKHOLDERIA PSEUDOMALLEI COMPLEXED WITH CJ168 | SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, ISOMERASE, PROTEIN BINDING