37EL
Crystal Structure of Histone-lysine N-methyltransferase from Leishmania major in complex with S-ADENOSYL-L-HOMOCYSTEINE
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | NSLS-II BEAMLINE 19-ID |
| Synchrotron site | NSLS-II |
| Beamline | 19-ID |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2026-01-31 |
| Detector | DECTRIS EIGER2 XE 9M |
| Wavelength(s) | 0.9786 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 68.916, 92.340, 37.813 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.360 - 1.510 |
| R-factor | 0.169 |
| Rwork | 0.167 |
| R-free | 0.20000 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.008 |
| RMSD bond angle | 0.973 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (2.0_5936) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.170 | 1.550 |
| High resolution limit [Å] | 1.510 | 1.510 |
| Rmerge | 0.074 | 1.340 |
| Rmeas | 0.077 | 1.402 |
| Rpim | 0.021 | 0.404 |
| Total number of observations | 510737 | 31914 |
| Number of reflections | 38744 | 2767 |
| <I/σ(I)> | 20.8 | 1.6 |
| Completeness [%] | 100.0 | |
| Redundancy | 13.2 | 11.5 |
| CC(1/2) | 1.000 | 0.801 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 291 | 27.5% P3350, 0.1M BT 5.5, 0.2M NaCl. LemaA.18205.a.B2.PW39520 at 12.4 mg/mL. electron density in the active site was consistent with SAH acquired from the expression host, plate 20826 E12 drop 1, Puck: PSL-1301, Cryo: 33% P3350, 0.1M BT 5.5, 0.2M NaCl |






