BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 9687375)

  • 41. Substitution studies of the second divalent metal cation requirement of protein tyrosine kinase CSK.
    Sun G; Budde RJ
    Biochemistry; 1999 Apr; 38(17):5659-65. PubMed ID: 10220355
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Dynamic structural changes are observed upon collagen and metal ion binding to the integrin α1 I domain.
    Weinreb PH; Li S; Gao SX; Liu T; Pepinsky RB; Caravella JA; Lee JH; Woods VL
    J Biol Chem; 2012 Sep; 287(39):32897-912. PubMed ID: 22847004
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Ionic interactions with parvalbumins. Crystal structure determination of pike 4.10 parvalbumin in four different ionic environments.
    Declercq JP; Tinant B; Parello J; Rambaud J
    J Mol Biol; 1991 Aug; 220(4):1017-39. PubMed ID: 1880797
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Occupancy of CD11b/CD18 (Mac-1) divalent ion binding site(s) induces leukocyte adhesion.
    Altieri DC
    J Immunol; 1991 Sep; 147(6):1891-8. PubMed ID: 1890307
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Crystal structure of a SLC11 (NRAMP) transporter reveals the basis for transition-metal ion transport.
    Ehrnstorfer IA; Geertsma ER; Pardon E; Steyaert J; Dutzler R
    Nat Struct Mol Biol; 2014 Nov; 21(11):990-6. PubMed ID: 25326704
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Metal binding studies and EPR spectroscopy of the manganese transport regulator MntR.
    Golynskiy MV; Gunderson WA; Hendrich MP; Cohen SM
    Biochemistry; 2006 Dec; 45(51):15359-72. PubMed ID: 17176058
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The I domain is a major recognition site on the leukocyte integrin Mac-1 (CD11b/CD18) for four distinct adhesion ligands.
    Diamond MS; Garcia-Aguilar J; Bickford JK; Corbi AL; Springer TA
    J Cell Biol; 1993 Feb; 120(4):1031-43. PubMed ID: 7679388
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Distinct roles of beta1 metal ion-dependent adhesion site (MIDAS), adjacent to MIDAS (ADMIDAS), and ligand-associated metal-binding site (LIMBS) cation-binding sites in ligand recognition by integrin alpha2beta1.
    Valdramidou D; Humphries MJ; Mould AP
    J Biol Chem; 2008 Nov; 283(47):32704-14. PubMed ID: 18820259
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Structures of rat cytosolic PEPCK: insight into the mechanism of phosphorylation and decarboxylation of oxaloacetic acid.
    Sullivan SM; Holyoak T
    Biochemistry; 2007 Sep; 46(35):10078-88. PubMed ID: 17685635
    [TBL] [Abstract][Full Text] [Related]  

  • 50. How can Ca2+ selectively activate recoverin in the presence of Mg2+? Surface plasmon resonance and FT-IR spectroscopic studies.
    Ozawa T; Fukuda M; Nara M; Nakamura A; Komine Y; Kohama K; Umezawa Y
    Biochemistry; 2000 Nov; 39(47):14495-503. PubMed ID: 11087403
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Determination of metal ion binding sites within the hairpin ribozyme domains by NMR.
    Butcher SE; Allain FH; Feigon J
    Biochemistry; 2000 Mar; 39(9):2174-82. PubMed ID: 10694382
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Metal ions and phosphate binding in the H-N-H motif: crystal structures of the nuclease domain of ColE7/Im7 in complex with a phosphate ion and different divalent metal ions.
    Sui MJ; Tsai LC; Hsia KC; Doudeva LG; Ku WY; Han GW; Yuan HS
    Protein Sci; 2002 Dec; 11(12):2947-57. PubMed ID: 12441392
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Structural studies of metal binding by inositol monophosphatase: evidence for two-metal ion catalysis.
    Bone R; Frank L; Springer JP; Atack JR
    Biochemistry; 1994 Aug; 33(32):9468-76. PubMed ID: 8068621
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Dual divalent cation requirement for activation of pyruvate kinase; essential roles of both enzyme- and nucleotide-bound metal ions.
    Gupta RK; Oesterling RM
    Biochemistry; 1976 Jun; 15(13):2881-7. PubMed ID: 7293
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The A-domain of beta 2 integrin CR3 (CD11b/CD18) is a receptor for the hookworm-derived neutrophil adhesion inhibitor NIF.
    Rieu P; Ueda T; Haruta I; Sharma CP; Arnaout MA
    J Cell Biol; 1994 Dec; 127(6 Pt 2):2081-91. PubMed ID: 7528750
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Integrin α
    Hu P; Luo BH
    J Cell Biochem; 2017 Aug; 118(8):2044-2052. PubMed ID: 27808427
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Raman spectroscopy of DNA-metal complexes. I. Interactions and conformational effects of the divalent cations: Mg, Ca, Sr, Ba, Mn, Co, Ni, Cu, Pd, and Cd.
    Duguid J; Bloomfield VA; Benevides J; Thomas GJ
    Biophys J; 1993 Nov; 65(5):1916-28. PubMed ID: 8298021
    [TBL] [Abstract][Full Text] [Related]  

  • 58. NMR and mutagenesis evidence for an I domain allosteric site that regulates lymphocyte function-associated antigen 1 ligand binding.
    Huth JR; Olejniczak ET; Mendoza R; Liang H; Harris EA; Lupher ML; Wilson AE; Fesik SW; Staunton DE
    Proc Natl Acad Sci U S A; 2000 May; 97(10):5231-6. PubMed ID: 10805782
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Affinities and selectivities of divalent cation binding sites within an RNA tertiary structure.
    Bukhman YV; Draper DE
    J Mol Biol; 1997 Nov; 273(5):1020-31. PubMed ID: 9367788
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A quantitative appraisal of the ambivalent metal ion binding properties of cytidine in aqueous solution and an estimation of the anti-syn energy barrier of cytidine derivatives.
    Knobloch B; Sigel H
    J Biol Inorg Chem; 2004 Apr; 9(3):365-73. PubMed ID: 15034770
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.