ライフサイエンスコーパス: be solved at @3 resolution

1 ructures of LS bound with various substrates were solved at 2 A resolution.

2 crystal structure of EcoRII mutant R88A has been solved at 2.1A resolution.

3 tone and 4-keto-5-aminolaevulinic acid, have been solved at high resolution.

4 resolution, and a complex of PNP.ImmH.PO(4) was solved at 1.5 A resolution.

5 , c = 28.11 A and beta = 120.45 degrees) and was solved at 1.9 A resolution.

6 ifferences, the crystal structure of Fe-SODA was solved at 2.2 A resolution.

7 l structure of the major part of F, F(1-94), was solved at 2.3 A resolution.

8 tructure of the antibody Fab fragment, which was solved at 2.4 A resolution.

9 emapsin 2 phosphoserine peptide and GGA1 VHS was solved at 2.6 A resolution.

10 entral domain of Sec16 in complex with Sec13 was solved at 2.7-A resolution.

11 A-DNA complex containing a four-way junction was solved at 3.1 A resolution.

12 ructure of the MGL.l-cycloserine complex has been solved at 1.6 A resolution.

13 gh affinity binding site for Rev protein has been solved at 1.6 A resolution.

14 l lobe of the cockroach allergen Bla g 2 has been solved at 1.8 A resolution.

15 ab fragment and its complex with hapten have been solved at 2.1 A resolution.

16 urinic/ apyrimidinic endonuclease (HAP1) has been solved at 2.2 A resolution.

17 apo, unphosphorylated form of p38 kinase has been solved at 2.3 A resolution.

18 rminal domain of human gammaS-crystallin has been solved at 2.4 A resolution.

19 co-crystallized with UDP-Gal and MnCl(2) has been solved at 2.8 A resolution.

20 e parasitic protozoan Trypanosoma brucei has been solved at 2.8 A resolution.

21 C AmpC beta-lactamase from Escherichia coli was solved at 1.71 A resolution.

22 1-->2) branching sucrase DeltaN(123)-GBD-CD2 was solved at 1.90 A resolution.

23 cting PAS proteins, Atg17, Atg29, and Atg31, was solved at 3.05 A resolution.

24 s of oxidized NQO2 in complex with PQ and CQ were solved at 1.4 A resolution.

25 he absence and presence of bound lipoic acid were solved at 2.1 A resolution.

26 structures of potent inhibitors with PvSHMT were solved at 2.6 A resolution.

27 The crystal structure of DaaE has been solved at 1.48 A resolution.

28 ium caldarium with novel crystal packing has been solved at 1.65-A resolution.

29 ex with nonneutralizing antibody mAb#12, has been solved at 2.90-A resolution.

30 e Thermus thermophilus 30S ribosomal subunit was solved at 2.6 angstrom resolution.

31 470 and HI1471 of Haemophilus influenzae has been solved at 2.4 angstrom resolution.

32 5 of the 6-deoxyerythronolide B synthase has been solved at 2.7 Angstrom resolution.

33 -binding domain of ribosomal protein L11 has been solved at 2.8 angstrom resolution.

34 ) of complex I from Thermus thermophilus has been solved at 3.3 angstrom resolution.

35 Fab' fragment of a monoclonal antibody 7C11 was solved at 2.8-angstroms resolution.

36 he extreme thermophile Thermus aquaticus has been solved at 2.5 Angstroms resolution.

37 , CP-80,794, PD-129,541 and PD-130,328) have been solved at atomic resolution allowing full anisotrop

38 ture of the coxsackievirus B3 polymerase has been solved at 2.25-A resolution and is shown to be high

39 ted muscle myosin, complexed with MgADP, has been solved at 2.5 A resolution and reveals an unusual c

40 tions in circular chromosome separation, has been solved at 2.5 A resolution and reveals that the pro

41 l structure of intact fumarate reductase has been solved at 3.3 angstrom resolution and demonstrates

42 immucillin-H (ImmH) and inorganic phosphate was solved at 1.75 A resolution and confirms the trimeri

43 The crystal structure of NAE:I was solved at 2.3 A resolution and shows that NAE:I is a

44 tructure of calcium-bound cotton annexin Gh1 was solved at 2.5 A resolution and shows three metal ion

45 structure of the KIR2DS2-HLA-A*11:01 complex was solved at 2.5-A resolution and revealed residue-bind

46 tructure of OD4.2.2 in complex with VRC-PG04 was solved at 3.0-A resolution and compared to known cry

47 d with the inhibitors vanadate and molybdate were solved at 2.2 A resolution and compared to a newly

48 Two new crystal forms of IIAGlc have been solved at high resolution, and the models were comp

49 The X-ray crystal structure of free ImmH was solved at 0.9 A resolution, and a complex of PNP.Imm

50 The structure of IFT52C/IFT46C was solved at 2.3 A resolution, and we show that it is e

51 protease alpha-lytic protease (alphaLP) has been solved at 0.83 A resolution at pH 8.

52 nicotinamide adenine dinucleotide phosphate were solved at 2.5 A resolution before and after photoly

53 Mg(2+).SHCHC complex of the K133R mutant has been solved at 1.62 A resolution by molecular replacemen

54 rate analog N-phosphonacetyl-L-ornithine has been solved at 1.85-A resolution by molecular replacemen

55 structure of the B-DNA hexamer d(CTCGAG) has been solved at 1.9 A resolution by iterative single isom

56 ydratase from Pseudomonas putida (GlucD) has been solved at 2.3 A resolution by multiple isomorphous

57 ), a protein with potent antiviral activity, was solved at 1.5 A resolution by molecular replacement

58 The crystal structure of free BstYI was solved at 1.85A resolution by multi-wavelength anoma

59 The structure was solved at 1.8A resolution by isomorphous phasing wit

60 The structure of IVD was solved at 2.6 A resolution by the molecular replacem

61 Structures have recently been solved at 8 A resolution for both Ca2+-ATPase from

62 The structures have been solved at an unprecedented resolution for septins (

63 lactamase from an Aureobacterium species has been solved at 1.73A resolution in the cubic space group

64 etic bacterium Rhodovulum sulfidophilum have been solved at 1.75 A resolution in the oxidized state a

65 he full-length native form of T4 RNase H has been solved at 2.06 angstroms resolution in the presence

66 The crystal structure of the RPE was solved at 1.8 A resolution in the presence of d-xyli

67 zyme, a divergent member of the NadE family, was solved at 1.9-A resolution in complex with reaction

68 nal antibody to Cryptococcus neoformans, has been solved at 2.4 A resolution, in both its unbound for

69 crystal structure of one of the variants has been solved at a resolution of 1.9 A, and the backbone c

70 The crystal structure of BipD has been solved at a resolution of 2.1 A revealing the detai

71 This structure, which was solved at a resolution of 1.15 A, reveals specific r

72 The structure of the FixK2-DNA complex was solved at a resolution of 1.77 A, at which the prote

73 The crystal structure of PtmT2 was solved at a resolution of 1.80 A, and docking studie

74 al structure of the 5-FTrp-containing enzyme was solved at a resolution of 2.0 A by difference Fourie

75 1, in complex with the substrate methyl red, was solved at a resolution of 2.18 A by X-ray crystallog

76 The structure of the corresponding complex was solved at a resolution of 2.5 A using molecular repl

77 The structure was solved at a resolution of 2.6-2.1 A.

78 all biosynthesis.The X-ray structure of YPD1 was solved at a resolution of 2.7 A by conventional mult

79 the crystal structure of antigen 85A, which was solved at a resolution of 2.7 A.

80 ized, and the structure of the true racemate was solved at a resolution of 2.7-2.15 A.

81 The structure of the corresponding complex was solved at a resolution of 3.0 A using molecular repl

82 Crystal structures were solved at a resolution of 1.8-2.2 A for the various

83 y inhibitors that also block parasite growth were solved at a resolution of 2.6 A and 3.0 A.

84 The new X-ray structure of s3 was solved at 2.0-A resolution (R = 17.4%; R(free) = 23.

85 ontaining an Asp64 --> Asn substitution have been solved at atomic resolution ranging 1.02-1.42 A.

86 f the spin-labeled Q54R1/L173R1 R125A mutant was solved at 2.1 A resolution, revealing no significant

87 The structure of NreA with bound nitrate was solved at 2.35A resolution, revealing a GAF domain f

88 ure of the STAM VHS domain-ubiquitin complex was solved at 2.6 A resolution, revealing that determina

89 R2) complexes with the three inhibitors have been solved at 1.2-A resolution to analyze the molecular

90 The crystal structure of GerE has been solved at 2.05 A resolution using multi-wavelength

91 taining the sequence r(GGUAUUGC-GGUACC)2 has been solved at 2.1 A resolution using experimental phase

92 mite (Dermatophagoides sp.) Der p 2 allergen was solved at 2.15 A resolution using the MAD phasing te

93 The structure was solved at 2.5 A resolution using multiwavelength ano

94 ture of recombinant non-glycosylated apo-hTF was solved at 2.7-A resolution using a multiple waveleng

95 The structure has been solved at 2.6 A resolution, which reveals that the

96 and DNA containing 4'-thio-2'-deoxycytidine was solved at 2.05 A resolution with a crystallographic