Crystal Structure of Human Lysyl-tRNA Synthetase complexed with L-Lysylsulfamoyl Adenosine. Determined by X-ray diffraction at 2.5 Å resolution. Released 7 Mar 2018.
Explore 6CHD in 3D Show helices and sheets RCSB PDB PDBe
6CHD contains 61 α-helices and 54 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 73-89 | 17 | |
| α-helix | 105-112 | 8 | |
| α-helix | 115-116 | 2 | |
| β-strand | 120 | 1 | 1 |
| β-strand | 126-137 | 12 | 1 |
| β-strand | 142-149 | 8 | 1 |
| β-strand | 152-159 | 8 | 1 |
| α-helix | 166-175 | 10 | |
| β-strand | 181-190 | 10 | 1 |
| β-strand | 196-207 | 12 | 1 |
| α-helix | 212-215 | 4 | |
| α-helix | 223-228 | 6 | |
| α-helix | 230-236 | 7 | |
| α-helix | 238-260 | 23 | |
| α-helix | 263 | 1 | |
| β-strand | 264-265 | 2 | 2 |
| β-strand | 271-272 | 2 | 3 |
| α-helix | 281-283 | 3 | |
| β-strand | 284-287 | 4 | 3 |
| β-strand | 292-296 | 5 | 3 |
| α-helix | 301-309 | 9 | |
| β-strand | 314-322 | 9 | 2 |
| β-strand | 328 | 1 | 4 |
| β-strand | 331 | 1 | 4 |
| β-strand | 334-343 | 10 | 2 |
| α-helix | 347-366 | 20 | |
| β-strand | 370-373 | 4 | 5 |
| β-strand | 383-386 | 4 | 5 |
| α-helix | 388 | 1 | |
| α-helix | 391 | 1 | |
| β-strand | 392-395 | 4 | 2 |
| α-helix | 396-404 | 9 | |
| α-helix | 407-409 | 3 | |
| α-helix | 411-413 | 3 | |
| α-helix | 417-430 | 14 | |
| α-helix | 435 | 1 | |
| α-helix | 440-451 | 12 | |
| α-helix | 453-455 | 3 | |
| β-strand | 460-463 | 4 | 2 |
| β-strand | 466 | 1 | 6 |
| α-helix | 467-469 | 3 | |
| β-strand | 473 | 1 | 7 |
| α-helix | 474 | 1 | |
| β-strand | 475 | 1 | 8 |
| α-helix | 476 | 1 | |
| β-strand | 482 | 1 | 6 |
| β-strand | 483 | 1 | 8 |
| β-strand | 485-490 | 6 | 2 |
| β-strand | 493-500 | 8 | 2 |
| β-strand | 501 | 1 | 7 |
| α-helix | 502 | 1 | |
| α-helix | 505-520 | 16 | |
| α-helix | 526-528 | 3 | |
| α-helix | 531-537 | 7 | |
| β-strand | 544-550 | 7 | 2 |
| α-helix | 551-558 | 8 | |
| α-helix | 564-567 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 73-90 | 18 | |
| α-helix | 105-112 | 8 | |
| α-helix | 115-116 | 2 | |
| β-strand | 120 | 1 | 9 |
| β-strand | 126-137 | 12 | 9 |
| β-strand | 142-149 | 8 | 9 |
| β-strand | 152-159 | 8 | 9 |
| α-helix | 166-175 | 10 | |
| β-strand | 181-190 | 10 | 9 |
| β-strand | 196-207 | 12 | 9 |
| α-helix | 223-228 | 6 | |
| α-helix | 230-236 | 7 | |
| α-helix | 238-260 | 23 | |
| α-helix | 263 | 1 | |
| β-strand | 264-265 | 2 | 10 |
| β-strand | 271-272 | 2 | 11 |
| α-helix | 281-283 | 3 | |
| β-strand | 284-287 | 4 | 11 |
| β-strand | 292-296 | 5 | 11 |
| α-helix | 301-309 | 9 | |
| β-strand | 314-322 | 9 | 10 |
| β-strand | 328 | 1 | 12 |
| β-strand | 331 | 1 | 12 |
| β-strand | 334-343 | 10 | 10 |
| α-helix | 347-366 | 20 | |
| β-strand | 370-373 | 4 | 13 |
| β-strand | 383-386 | 4 | 13 |
| α-helix | 388 | 1 | |
| α-helix | 391 | 1 | |
| β-strand | 392-395 | 4 | 10 |
| α-helix | 396-404 | 9 | |
| α-helix | 407-410 | 4 | |
| α-helix | 411-413 | 3 | |
| α-helix | 417-429 | 13 | |
| α-helix | 435 | 1 | |
| α-helix | 437 | 1 | |
| α-helix | 440-451 | 12 | |
| α-helix | 453-455 | 3 | |
| β-strand | 460-463 | 4 | 10 |
| β-strand | 466 | 1 | 14 |
| α-helix | 467-469 | 3 | |
| β-strand | 473 | 1 | 15 |
| α-helix | 474 | 1 | |
| β-strand | 475 | 1 | 16 |
| α-helix | 476 | 1 | |
| β-strand | 482 | 1 | 14 |
| β-strand | 483 | 1 | 16 |
| β-strand | 485-490 | 6 | 10 |
| β-strand | 493-500 | 8 | 10 |
| β-strand | 501 | 1 | 15 |
| α-helix | 502 | 1 | |
| α-helix | 505-520 | 16 | |
| α-helix | 526-529 | 4 | |
| α-helix | 531-538 | 8 | |
| α-helix | 541-542 | 2 | |
| β-strand | 544-550 | 7 | 10 |
| α-helix | 551-558 | 8 | |
| α-helix | 564-567 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Lysine--tRNA ligase | A, B | protein | 597 | Homo sapiens | Q15046 (AlphaFold model) |
>6CHD_1 Lysine--tRNA ligase (chains A, B) MAAVQAAEVKVDGSEPKLSKNELKRRLKAEKKVAEKEAKQKELSEKQLSQATAAATNHTT DNGVGPEEESVDPNQYYKIRSQAIHQLKVNGEDPYPHKFHVDISLTDFIQKYSHLQPGDH LTDITLKVAGRIHAKRASGGKLIFYDLRGEGVKLQVMANSRNYKSEEEFIHINNKLRRGD IIGVQGNPGKTKKGELSIIPYEITLLSPCLHMLPHLHFGLKDKETRYRQRYLDLILNDFV RQKFIIRSKIITYIRSFLDELGFLEIETPMMNIIPGGAVAKPFITYHNELDMNLYMRIAP ELYHKMLVVGGIDRVYEIGRQFRNEGIDLTHNPEFTTCEFYMAYADYHDLMEITEKMVSG MVKHITGSYKVTYHPDGPEGQAYDVDFTPPFRRINMVEELEKALGMKLPETNLFETEETR KILDDICVAKAVECPPPRTTARLLDKLVGEFLEVTCINPTFICDHPQIMSPLAKWHRSKE GLTERFELFVMKKEICNAYTELNDPMRQRQLFEEQAKAKAAGDDEAMFIDENFCTALEYG LPPTAGWGMGIDRVAMFLTDSNNIKEVLLFPAMKPEDKKENVATTDTLESTTVGTSV
| ID | Name | Formula | Copies |
|---|---|---|---|
| KAA | 5'-O-[(L-lysylamino)sulfonyl]adenosine | C16 H26 N8 O7 S | 2 |
Water and common crystallization additives (SO4, EDO, GOL) are not listed.
Crystal Structure of Human Lysyl-tRNA Synthetase complexed with L-Lysylsulfamoyl Adenosine. Dranow, D.M., Abendroth, J., Baragana, B. et al. To be published.
Other PDB entries of the same protein (UniProt Q15046 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 6CHD directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.