|
64
|
255
|
6obyA |
The nucleotide-binding protein af_226 in complex with adp from archaeoglobus fulgidus with co found by pixe. based on 3kb1. |
|
57
|
259
|
6tb2C |
Structure of human haptoglobin-hemoglobin bound to s. aureus isdh |
|
54
|
141
|
6tb2A |
Structure of human haptoglobin-hemoglobin bound to s. aureus isdh |
|
54
|
146
|
6tb2B |
Structure of human haptoglobin-hemoglobin bound to s. aureus isdh |
|
75
|
333
|
6tb2D |
Structure of human haptoglobin-hemoglobin bound to s. aureus isdh |
|
68
|
252
|
6om5A |
Structure of a haemophore from haemophilus haemolyticus |
|
60
|
349
|
6n7eA |
Crystal structure of the cytosolic domain of human cnnm2 in complex with amp-pnp and mg2+ |
|
68
|
216
|
6i8vA |
Ktrc with atp bound |
|
105
|
251
|
6sngA |
Efem structure from the pseudomonas syringae efeuob/m iron-transport system: a new family of periplasmic solute-binding proteins with unique fold |
|
35
|
277
|
6nj8A |
Encapsulin iron storage compartment from quasibacillus thermotolerans |
|
25
|
91
|
6haoA |
Mamm ctd h264e - cadmium form 2 |
|
24
|
79
|
6h8dA |
Mamm ctd d249n - nickel form |
|
24
|
81
|
6h85A |
Mamm ctd h264e-e289h - cadmium form |
|
26
|
92
|
6h5kA |
Mamm ctd d249e - zinc form |
|
24
|
79
|
6ha2A |
Mamm ctd d249h-h285d |
|
24
|
80
|
6h8aA |
Mamm ctd d249n - cadmium form |
|
25
|
80
|
6h9qA |
Mamm ctd d249e - cadmium form |
|
25
|
82
|
6h5vA |
Mamm ctd h264e |
|
22
|
83
|
6hhsA |
Mamm ctd e289d - cadmium form |
|
24
|
79
|
6h8gA |
Mamm ctd h264e - cadmium form 1 |
|
25
|
84
|
6h88A |
Mamm ctd d249n |
|
26
|
81
|
6h9tA |
Mamm ctd h285d - cadmium form |
|
27
|
91
|
6h87A |
Mamm ctd d249n - zinc form |
|
25
|
82
|
6h84A |
Mamm ctd d249h - cadmium form |
|
23
|
79
|
6h89A |
Mamm ctd d249n - copper form |
|
27
|
94
|
6hanA |
Mamm ctd h264e-e289h |
|
23
|
80
|
6h83A |
Mamm ctd d249h - copper form |
|
25
|
79
|
6h81A |
Mamm ctd e289h - nickel form |
|
26
|
92
|
6h9pA |
Mamm ctd e289d - manganese form |
|
23
|
89
|
6h5mA |
Mamm ctd h264e - zinc form 1 |
|
1
|
8
|
6hhsM |
Mamm ctd e289d - cadmium form |
|
24
|
80
|
6h8iA |
Mamm ctd h285d |
|
24
|
90
|
6h5uA |
Mamm ctd h264e - zinc form 2 |
|
60
|
348
|
6mn6A |
Crystal structure of the cytosolic domain of human cnnm3 |
|
66
|
213
|
6j6pA |
Crystal structure of diamondback moth ryanodine receptor phosphorylation domain(2836-3050) mutant s2946d |
|
87
|
332
|
6m85A |
Crystal structure of inward rectifier kir2.2 in a different salt condition |
|
89
|
272
|
6q1cA |
Apo yfea extracted from the e. coli periplasm |
|
90
|
326
|
6m84A |
Crystal structure of ckir2.2 force open mutant in complex with pi(4,5)p2 |
|
96
|
274
|
6q1dA |
Holo yfea reconstituted by zinc soaking |
|
85
|
330
|
6m86A |
Crystal structure of inward rectifier kir2.2 force open mutant |
|
69
|
213
|
6j6oA |
Crystal structure of diamondback moth ryanodine receptor phosphorylation domain(2836-3050) |
|
4
|
25
|
1ckwA |
Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the phe508 region, the most common site of disease-causing delta-f508 mutation |
|
2
|
74
|
1k9cA |
Solution structure of calreticulin p-domain subdomain (residues 189-261) |
|
0
|
26
|
1ckyA |
Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the phe508 region, the most common site of disease-causing delta-f508 mutation |
|
6
|
26
|
1ckxA |
Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the phe508 region, the most common site of disease-causing delta-f508 mutation |
|
0
|
25
|
1ckzA |
Cystic fibrosis transmembrane conductance regulator: solution structures of peptides based on the phe508 region, the most common site of disease-causing delta-f508 mutation |
|
16
|
73
|
1bo9A |
Nmr solution structure of domain 1 of human annexin i |
|
2
|
37
|
1k91A |
Solution structure of calreticulin p-domain subdomain (residues 221-256) |
|
11
|
73
|
1k0vA |
Copper trafficking: the solution structure of bacillus subtilis copz |
|
215
|
677
|
6ctcA |
Crystal structure of human transferrin bound to triferic fpc iron pyrophosphate |