|
52
|
130
|
1b7nA |
Verification of spmp using mutant human lysozymes |
|
51
|
129
|
1ir9A |
Im mutant of lysozyme |
|
51
|
130
|
1b5xA |
Contribution of hydrogen bonds to the conformational stability of human lysozyme: calorimetry and x-ray analysis of six ser->ala mutants |
|
52
|
130
|
1ip1A |
G37a human lysozyme |
|
47
|
129
|
1bgiA |
Orthorhombic lysozyme crystallized at high temperature (310k) |
|
48
|
129
|
1iotA |
Stabilization of hen egg white lysozyme by a cavity-filling mutation |
|
50
|
130
|
1b5uA |
Contribution of hydrogen bonds to the conformational stability of human lysozyme: calorimetry and x-ray analysis of six ser->ala mutant |
|
49
|
129
|
1b0dA |
Structural effects of monovalent anions on polymorphic lysozyme crystals |
|
47
|
130
|
1ip3A |
G68a human lysozyme |
|
46
|
130
|
1bb4A |
Human lysozyme double mutant a96l, w109h |
|
53
|
130
|
1b7lA |
Verification of spmp using mutant human lysozymes |
|
58
|
162
|
1b6iA |
T4 lysozyme mutant with cys 54 replaced by thr, cys 97 replaced by ala, thr 21 replaced by cys and lys 124 replaced by cys (c54t,c97a,t21c,k124c) |
|
48
|
129
|
1ir7A |
Im mutant of lysozyme |
|
51
|
129
|
1iorA |
Stabilization of hen egg white lysozyme by a cavity-filling mutation |
|
53
|
130
|
1ip2A |
G48a human lysozyme |
|
50
|
130
|
1b7rA |
Verification of spmp using mutant human lysozymes |
|
49
|
130
|
1b7qA |
Verification of spmp using mutant human lysozymes |
|
51
|
130
|
1inuA |
Crystal structure of mutant human lysozyme substituted at the surface positions |
|
35
|
129
|
1io5A |
Hydrogen and hydration of hen egg-white lysozyme determined by neutron diffraction |
|
60
|
162
|
195lA |
Thermodynamic and structural compensation in "size-switch" core-repacking variants of t4 lysozyme |
|
54
|
164
|
152lA |
Conservation of solvent-binding sites in 10 crystal forms of t4 lysozyme |
|
60
|
162
|
162lA |
Control of enzyme activity by an engineered disulfide bond |
|
58
|
162
|
183lA |
Specificity of ligand binding in a buried non-polar cavity of t4 lysozyme: linkage of dynamics and structural plasticity |
|
58
|
162
|
129lA |
Structures of randomly generated mutants of t4 lysozyme show that protein stability can be enhanced by relaxation of strain and by improved hydrogen bonding via bound solvent |
|
60
|
162
|
113lA |
Structural basis of alpha-helix propensity at two sites in t4 lysozyme |
|
62
|
164
|
176lA |
Protein flexibility and adaptability seen in 25 crystal forms of t4 lysozyme |
|
59
|
162
|
123lA |
The energetic cost and the structural consequences of burying a hydroxyl group within the core of a protein determined from ala to ser and val to thr substitutions in t4 lysozyme |
|
59
|
162
|
111lA |
Structural basis of alpha-helix propensity at two sites in t4 lysozyme |
|
58
|
164
|
174lA |
Protein flexibility and adaptability seen in 25 crystal forms of t4 lysozyme |
|
60
|
162
|
108lA |
Structural basis of alpha-helix propensity at two sites in t4 lysozyme |
|
61
|
162
|
110lA |
Structural basis of alpha-helix propensity at two sites in t4 lysozyme |
|
60
|
162
|
178lA |
Protein flexibility and adaptability seen in 25 crystal forms of t4 lysozyme |
|
49
|
129
|
135lA |
X-ray structure of monoclinic turkey egg lysozyme at 1.3 angstroms resolution |
|
56
|
162
|
158lA |
Control of enzyme activity by an engineered disulfide bond |
|
58
|
162
|
190lA |
A helix initiation signal in t4 lysozyme identified by polyalanine mutagenesis |
|
38
|
120
|
1iizA |
Crystal structure of the induced antibacterial protein from tasar silkworm, antheraea mylitta |
|
57
|
162
|
144lA |
Role of backbone flexibility in the accommodation of variants that repack the core of t4 lysozyme |
|
56
|
162
|
165lA |
Control of enzyme activity by an engineered disulfide bond |
|
59
|
162
|
187lA |
Specificity of ligand binding in a buried non-polar cavity of t4 lysozyme: linkage of dynamics and structural plasticity |
|
60
|
162
|
128lA |
The energetic cost and the structural consequences of burying a hydroxyl group within the core of a protein determined from ala to ser and val to thr substitutions in t4 lysozyme |
|
59
|
162
|
112lA |
Structural basis of alpha-helix propensity at two sites in t4 lysozyme |
|
48
|
129
|
194lA |
The 1.40 a structure of spacehab-01 hen egg white lysozyme |
|
61
|
162
|
127lA |
The energetic cost and the structural consequences of burying a hydroxyl group within the core of a protein determined from ala to ser and val to thr substitutions in t4 lysozyme |
|
58
|
162
|
115lA |
Structural basis of alpha-helix propensity at two sites in t4 lysozyme |
|
58
|
164
|
167lA |
Protein flexibility and adaptability seen in 25 crystal forms of t4 lysozyme |
|
60
|
162
|
125lA |
The energetic cost and the structural consequences of burying a hydroxyl group within the core of a protein determined from ala to ser and val to thr substitutions in t4 lysozyme |
|
58
|
162
|
141lA |
Role of backbone flexibility in the accommodation of variants that repack the core of t4 lysozyme |
|
58
|
164
|
172lA |
Protein flexibility and adaptability seen in 25 crystal forms of t4 lysozyme |
|
59
|
163
|
102lA |
How amino-acid insertions are allowed in an alpha-helix of t4 lysozyme |
|
58
|
162
|
159lA |
Control of enzyme activity by an engineered disulfide bond |
