Found 518 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: Chitinase A; domain 3

Total Genus Sequence Length pdb Title
17 151 1ix5A Solution structure of the methanococcus thermolithotrophicus fkbp
14 96 1eq3A Nmr structure of human parvulin hpar14
17 120 1j6yA Solution structure of pin1at from arabidopsis thaliana
8 85 1hxvA Ppiase domain of the mycoplasma genitalium trigger factor
28 107 1f40A Solution structure of fkbp12 complexed with gpi-1046, a neurotrophic ligand
13 107 1fkrA Solution structure of fkbp, a rotamase enzyme and receptor for fk506 and rapamycin
8 106 1l1pA Solution structure of the ppiase domain from e. coli trigger factor
16 92 1jnsA Nmr structure of the e. coli peptidyl-prolyl cis/trans-isomerase parvulin 10
12 104 1fjdA Human parvulin-like peptidyl prolyl cis/trans isomerase, hpar14
49 190 3uqaA Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation a54e from burkholderia pseudomallei complexed with fk506
49 192 3uqbA Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with fk506
101 317 5jh8A Crystal structure of chitinase from chromobacterium violaceum atcc 12472
27 111 5j6eA Structure of disulfide crosslinked a. fumigatus fkbp12(v91c)
26 120 5i98A Structure of apo fkbp12(p104g) from c. albicans
30 113 5hwcA Aspergillus fumigatus fkbp12 p90g protein bound with fk506 in p212121 space group
27 122 5htgA Structure of apo p1 form of candida albicans fkbp12
27 111 5hwbA Aspergillus fumigatus fkbp12 apo protein in p212121 space group
25 120 5hw8A Candida albicans fkbp12 p104g protein bound with fk506 in c2 space group
28 122 5hw7A Candida albicans fkbp12 apo protein in p21212 space group
25 120 5hw6A Candida albicans fkbp12 apo protein in c2 space group
27 113 5huaA Structure of c. glabrata fkbp12-fk506 complex
137 452 5hbfA Crystal structure of human full-length chitotriosidase (chit1)
25 107 5hkgA Total chemical synthesis, refolding and crystallographic structure of a fully active immunophilin: calstabin 2 (fkbp12.6).
32 127 5bxjA Complex of the fk1 domain mutant a19t of fkbp51 with 4-nitrophenol
28 119 5b8iC Crystal structure of calcineurin a and calcineurin b in complex with fkbp12 and fk506 from coccidioides immitis rs
162 498 4z2iA Serratia marcescens chitinase b complexed with macrolide inhibitor 30
156 498 4z2gA Serratia marcescens chitinase b complexed with macrolide inhibitor 26
163 498 4z2hA Serratia marcescens chitinase b complexed with macrolide inhibitor 29
161 498 4z2jA Serratia marcescens chitinase b complexed with macrolide inhibitor 31
161 498 4z2lA Serratia marcescens chitinase b complexed with macrolide inhibitor 33
26 107 4fapA Atomic structures of the rapamycin analogs in complex with both human fkbp12 and frb domain of frap
191 539 4dwsD Crystal structure of a chitinase from the yersinia entomophaga toxin complex
36 128 4drpA Evaluation of synthetic fk506 analogs as ligands for the fk506-binding proteins 51 and 52: complex of fkbp51 with 2-(3-((r)-3-(3,4-dimethoxyphenyl)-1-((s)-1-(2-((1r,2s)-2-ethyl-1-hydroxy-cyclohexyl)-2-oxoacetyl)piperidine-2-carbonyloxy)propyl)phenoxy)acetic acid from cocrystallization
184 539 4dwsC Crystal structure of a chitinase from the yersinia entomophaga toxin complex
30 132 4drhA Co-crystal structure of the ppiase domain of fkbp51, rapamycin and the frb fragment of mtor at low ph
190 540 4dwsB Crystal structure of a chitinase from the yersinia entomophaga toxin complex
25 113 4dz2A Crystal structure of a peptidyl-prolyl cis-trans isomerase with surface mutation r92g from burkholderia pseudomallei complexed with fk506
29 113 4dz3A Crystal structure of a peptidyl-prolyl cis-trans isomerase with surface mutation m61h from burkholderia pseudomallei complexed with fk506
27 121 4drjA O-crystal structure of the ppiase domain of fkbp52, rapamycin and the frb fragment of mtor
186 543 4dwsA Crystal structure of a chitinase from the yersinia entomophaga toxin complex
34 128 4drmA 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
35 128 4drqA 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
32 121 4driA Co-crystal structure of the ppiase domain of fkbp51, rapamycin and the frb fragment of mtor
28 160 4dt4A Crystal structure of the ppiase-chaperone slpa with the chaperone binding site occupied by the linker of the purification tag
36 128 4droA 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
34 128 4drkA 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
39 128 4drnA 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
27 121 4dipA Crystal structure of human peptidyl-prolyl cis-trans isomerase fkbp14
26 107 4dh0A X-ray crystal structure of 28-o-methylrapamycin complexed with fkbp12: is the cyclohexyl moiety part of the effector domain of rapamycin?
24 108 4c02B Crystal structure of human acvr1 (alk2) in complex with fkbp12.6 and dorsomorphin