Found 518 chains in Genus chains table. Displaying 151 - 200. Applied filters: Proteins

Search results query: Chitinase A; domain 3

Total Genus Sequence Length pdb Title
121 344 4mnlA Crystal structure of gh18 chitinase (g77w/e119q mutant) from cycas revoluta in complex with (glcnac)4
121 361 4mavA Crystal structure of signaling protein spb-40 complexed with 5-hydroxymethyl oxalanetriol at 2.80 a resolution
122 344 4mnmA Crystal structure of gh18 chitinase (g77w/e119q mutant) from cycas revoluta in complex with (glcnac)4
120 361 4mpkA Crystal structure of the complex of buffalo signaling protein spb-40 with n-acetylglucosamine at 2.65 a resolution
32 122 4mgvA Crystal structure of fk506 binding domain of plasmodium vivax fkbp35 in complex with inhibitor d5
122 344 4mnkA Crystal structure of gh18 chitinase from cycas revoluta in complex with (glcnac)3
128 398 4lgxA Structure of chitinase d from serratia proteamaculans revealed an unusually constrained substrate binding site
51 208 4kqzA Structure of the receptor binding domain (rbd) of mers-cov spike
59 234 4layA Crystal structure analysis of fkbp52, complex with i63
56 235 4lawA Crystal structure analysis of fkbp52, crystal form iii
56 237 4laxA Crystal structure analysis of fkbp52, complex with fk506
44 208 4kr0B Complex structure of mers-cov spike rbd bound to cd26
46 204 4l72B Crystal structure of mers-cov complexed with human dpp4
58 240 4lavA Crystal structure analysis of fkbp52, crystal form ii
56 209 4l3nA Crystal structure of the receptor-binding domain from newly emerged middle east respiratory syndrome coronavirus
30 132 4jysA Crystal structure of fkbp25 from plasmodium vivax
34 128 4jfkA 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
20 117 4it6A Crystal structure of amino acid residues 1-120 of cg17282
34 128 4jfjA 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
21 107 4iq2A P21 crystal form of fkbp12.6
34 128 4jflA Increasing the efficiency efficiency of ligands for the fk506-binding protein 51 by conformational control: complex of fkbp51 with 6-({(1s,5r)-3-[2-(3,4-dimethoxyphenoxy)ethyl]-2-oxo-3,9-diazabicyclo[3.3.1]non-9-yl}sulfonyl)-1,3-benzothiazol-2(3h)-one
34 122 4j4oA Crystal structure of fk506 binding domain of plasmodium vivax fkbp35 in complex with d44
35 127 4jfiA 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
34 128 4jfmA Increasing the efficiency efficiency of ligands for the fk506-binding protein 51 by conformational control: complex of fkbp51 with 2-(3,4-dimethoxyphenoxy)ethyl (2s)-1-[(2-oxo-2,3-dihydro-1,3-benzothiazol-6-yl)sulfonyl]piperidine-2-carboxylate
28 123 4j4nA Crystal structure of fk506 binding domain of plasmodium falciparum fkbp35 in complex with d44
28 107 4ipxA Analyzing the visible conformational substates of the fk506 binding protein fkbp12
33 121 4itzA Crystal structure of the fk506 binding domain of plasmodium vivax fkbp35 in complex with a tetrapeptide substrate
25 107 4iqcA P3121 crystal form of fkbp12.6
59 210 4it4A Crystal structure of residues 1-211 of cg17282
12 98 4harA Crystal structure of rubella virus capsid protein (residues 127-277)
14 98 4hbeA Crystal structure of rubella virus capsid protein (residues 127-277)
8 96 4hboA Crystal structure of rubella virus capsid protein (residues 127-277)
48 191 4ggqA Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase from burkholderia pseudomallei complexed with cj40
46 191 4g50A Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj168
48 192 4givA Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj183
29 108 4g2pA Crystal structure of peptidyl-prolyl cis-trans isomerase domain ii of molecular chaperone sura from salmonella enterica subsp. enterica serovar typhimurium str. 14028s
44 190 4fn2A Crystal structure of a smt fusion peptidyl-prolyl cis-trans isomerase with surface mutation d44g from burkholderia pseudomallei complexed with cj37
124 394 3qokA Crystal structure of putative chitinase ii from klebsiella pneumoniae
30 124 3pa7A Crystal structure of fkbp from plasmodium vivax in complex with tetrapeptide alpf
53 223 3prbA Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26
38 150 3pr9A Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26
33 150 3praA Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26
36 223 3prdA Structural analysis of protein folding by the methanococcus jannaschii chaperone fkbp26
187 515 3oa5A The structure of chi1, a chitinase from yersinia entomophaga
49 158 3oobA Structural and functional insights of directly targeting pin1 by epigallocatechin-3-gallate
42 157 3odkA Discovery of cell-active phenyl-imidazole pin1 inhibitors by structure-guided fragment evolution
34 125 3o5fA Fk1 domain of fkbp51, crystal form vii
33 128 3o5rA Complex of fk506 with the fk1 domain mutant a19t of fkbp51
31 124 3o5jA Fk1 domain of fkbp51, crystal form iii
35 127 3o5mA Fk1 domain mutant a19t of fkbp51, crystal form ii