7
|
64
|
1dfdA |
Oxidised desulfovibrio africanus ferredoxin i, nmr, 19 structures |
9
|
65
|
1g25A |
Solution structure of the n-terminal domain of the human tfiih mat1 subunit |
19
|
117
|
1d6tA |
Rnase p protein from staphylococcus aureus |
12
|
91
|
1b64A |
Solution structure of the guanine nucleotide exchange factor domain from human elongation factor-one beta, nmr, 20 structures |
12
|
88
|
1emwA |
Solution structure of the ribosomal protein s16 from thermus thermophilus |
13
|
79
|
1kviA |
Solution structure of the reduced form of the first heavy metal binding motif of the menkes protein |
8
|
46
|
1cxrA |
Automated 2d noesy assignment and structure calculation of crambin(s22/i25) with self-correcting distance geometry based noah/diamod programs |
15
|
129
|
1hpwA |
Structure of a pilin monomer from pseudomonas aeruginosa: implications for the assembly of pili. |
12
|
72
|
1afiA |
Structure of the reduced form of merp, the periplasmic protein from the bacterial mercury detoxification system, nmr, 20 structures |
4
|
52
|
1faqA |
Raf-1 cysteine rich domain, nmr, 27 structures |
10
|
43
|
1hevA |
Hevein: the nmr assignment and an assessment of solution-state folding for the agglutinin-toxin motif |
27
|
98
|
1apsA |
Three-dimensional structure of acylphosphatase. refinement and structure analysis |
22
|
104
|
1kvnA |
Solution structure of protein srp19 of the arhaeoglobus fulgidus signal recognition particle, 10 structures |
25
|
161
|
1bxdA |
Nmr structure of the histidine kinase domain of the e. coli osmosensor envz |
12
|
97
|
1je3A |
Solution structure of ec005 from escherichia coli |
52
|
184
|
1ge9A |
Solution structure of the ribosome recycling factor |
16
|
80
|
1jwwA |
Nmr characterization of the n-terminal domain of a potential copper-translocating p-type atpase from bacillus subtilis |
23
|
77
|
1bc6A |
7-fe ferredoxin from bacillus schlegelii, nmr, 20 structures |
11
|
83
|
1d1rA |
Nmr solution structure of the product of the e. coli ycih gene. |
15
|
96
|
1fjcA |
Solution structure of nucleolin rbd2 |
7
|
64
|
1b3cA |
Solution structure of a beta-neurotoxin from the new world scorpion centruroides sculpturatus ewing |
21
|
85
|
1hdnA |
The high-resolution structure of the histidine-containing phosphocarrier protein hpr from escherichia coli determined by restrained molecular dynamics from nmr nuclear overhauser effect data |
13
|
88
|
1iqoA |
Solution structure of mth1880 from methanobacterium thermoautotrophicum |
27
|
132
|
1ivzA |
Solution structure of the sea domain from murine hypothetical protein homologous to human mucin 16 |
3
|
46
|
1gnfA |
Solution structure of the n-terminal zinc finger of murine gata-1, nmr, 25 structures |
15
|
50
|
1bk8A |
Determination of the three-dimensional solution structure of aesculus hippocastanum antimicrobial protein 1 (ah-amp1) by 1h nmr, 25 structures |
4
|
75
|
1d9nA |
Solution structure of the methyl-cpg-binding domain of the methylation-dependent transcriptional repressor mbd1/pcm1 |
20
|
103
|
1jm7A |
Solution structure of the brca1/bard1 ring-domain heterodimer |
9
|
46
|
1jmpA |
Solution structure of the viscotoxin b |
11
|
112
|
1csyA |
Syk tyrosine kinase c-terminal sh2 domain complexed with a phosphopeptidefrom the gamma chain of the high affinity immunoglobin g receptor, nmr |
11
|
68
|
1cpzA |
Copper chaperone of enterococcus hirae (apo-form) |
10
|
60
|
1i6gA |
Nmr solution structure of the insect-specific neurotoxin variant 5 (cse-v5) from the scorpion centruroides sculpturatus ewing |
6
|
54
|
1ce3A |
Putative ancestral protein encoded by a single sequence repeat of the multidomain proteinase inhibitor from nicotiana alata |
17
|
95
|
1ghuA |
Nmr solution structure of growth factor receptor-bound protein 2 (grb2) sh2 domain, 24 structures |
24
|
112
|
1l4sA |
Solution structure of ribosome associated factor y |
12
|
55
|
1hdlA |
Lekti domain one |
29
|
130
|
1gd5A |
Solution structure of the px domain from human p47phox nadph oxidase |
1
|
80
|
1k0tA |
Nmr solution structure of unbound, oxidized photosystem i subunit psac, containing [4fe-4s] clusters fa and fb |
8
|
46
|
1jmnA |
Solution structure of the viscotoxin a2 |
18
|
111
|
1bfiA |
Solution structure of the c-terminal sh2 domain of the p85alpha regulatory subunit of phosphoinositide 3-kinase, nmr, 30 structures |
44
|
104
|
1cn7A |
Yeast ribosomal protein l30 |
150
|
462
|
5f8jA |
Enterovirus 71 polymerase elongation complex (c1s4 form) |
145
|
462
|
5f8nA |
Enterovirus 71 polymerase elongation complex (c3s6 form) |
105
|
327
|
9icxA |
Dna polymerase beta (pol b) (e.c.2.7.7.7) complexed with six base pairs of dna (non gapped dna only) |
99
|
327
|
7icqA |
Dna polymerase beta (e.c.2.7.7.7)/dna complex, soaked in the presence of zncl2 |
95
|
327
|
7icuA |
Dna polymerase beta (pol b) (e.c.2.7.7.7) complexed with six base pairs of dna; soaked in the presence of cdcl2 (0.1 millimolar) |
95
|
327
|
8icrA |
Dna polymerase beta (pol b) (e.c.2.7.7.7) complexed with seven base pairs of dna; soaked in the presence of datp (1 millimolar) and mncl2 (5 millimolar) |
102
|
327
|
9icuA |
Dna polymerase beta (pol b) (e.c.2.7.7.7) complexed with six base pairs of dna; soaked in the presence of dttp (1 millimolar) and mncl2 (5 millimolar) |
100
|
327
|
8ickA |
Dna polymerase beta (pol b) (e.c.2.7.7.7) complexed with seven base pairs of dna; soaked in the presence of datp (1 millimolar), mgcl2 (5 millimolar), and mncl2 (5 millimolar) |
99
|
327
|
9icvA |
Dna polymerase beta (e.c.2.7.7.7)/dna complex + 2'-deoxyadenosine-5'-triphosphate, soaked in the presence of datp and zncl2 |