1AWZ
3D SOLUTION STRUCTURE OF HUMAN ANGIOGENIN DETERMINED BY 1H, 15N NMR SPECTROSCOPY, 30 STRUCTURES
Summary for 1AWZ
| Entry DOI | 10.2210/pdb1awz/pdb |
| Descriptor | ANGIOGENIN (1 entity in total) |
| Functional Keywords | hydrolase, endoribonuclease, angiogenesis |
| Biological source | Homo sapiens (human) |
| Cellular location | Secreted: P03950 |
| Total number of polymer chains | 1 |
| Total formula weight | 14169.04 |
| Authors | Lequin, O.,Thuring, H.,Robin, M.,Lallemand, J.-Y. (deposition date: 1997-10-07, release date: 1998-02-25, Last modification date: 2024-10-16) |
| Primary citation | Lequin, O.,Thuring, H.,Robin, M.,Lallemand, J.Y. Three-dimensional solution structure of human angiogenin determined by 1H,15N-NMR spectroscopy--characterization of histidine protonation states and pKa values. Eur.J.Biochem., 250:712-726, 1997 Cited by PubMed Abstract: Human angiogenin is a member of the pancreatic ribonuclease superfamily that induces blood vessel formation. Its three-dimensional solution structure has been determined to high resolution by heteronuclear NMR spectroscopy. 30 structures were calculated, based on a total of 1441 assigned NOE correlations, 64 coupling constants and 50 hydrogen bonds. The backbone atomic rms difference from the mean coordinates is 0.067 +/- 0.012 nm and 0.13 nm from the previously determined crystal structure. The side-chain of Gln117 was found to obstruct the active site as observed in the crystal state. There was no evidence of an alternative open form of angiogenin, although two sets of chemical shifts were observed for some residues, mainly around the active site and in the C-terminal segment. The topology of the ribonucleolytic active site is described with a particular emphasis on the conformation and protonation of active-site His residues. The side-chain of His114 adopts two main conformations in solution. In contrast to pancreatic ribonuclease A, His13 was shown to be more basic than His114, with pKa values of 6.65 and 6.05 respectively. The His47 residue is located in an environment very resistant to protonation with a pKa lower than 4. PubMed: 9461294DOI: 10.1111/j.1432-1033.1997.00712.x PDB entries with the same primary citation |
| Experimental method | SOLUTION NMR |
Structure validation
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