Crystal Structure of Human DNA polymerase kappa in complex with DNA containing the major cisplatin lesion. Determined by X-ray diffraction at 3.15 Å resolution. Released 22 Aug 2018.
Explore 6BS1 in 3D Show helices and sheets RCSB PDB PDBe
6BS1 contains 41 α-helices and 32 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 | 35-44 | 10 | |
| α-helix | 48-72 | 25 | |
| α-helix | 76-96 | 21 | |
| β-strand | 103-108 | 6 | 1 |
| α-helix | 111-118 | 8 | |
| α-helix | 121-123 | 3 | |
| β-strand | 128-131 | 4 | 2 |
| β-strand | 136-139 | 4 | 2 |
| α-helix | 141-144 | 4 | |
| α-helix | 154-160 | 7 | |
| β-strand | 165-167 | 3 | 2 |
| α-helix | 168-169 | 2 | |
| α-helix | 171-188 | 18 | |
| β-strand | 193-194 | 2 | 1 |
| β-strand | 199-203 | 5 | 1 |
| α-helix | 205-211 | 7 | |
| α-helix | 216-219 | 4 | |
| β-strand | 220-222 | 3 | 3 |
| β-strand | 283-285 | 3 | 3 |
| α-helix | 290-305 | 16 | |
| β-strand | 309-314 | 6 | 1 |
| α-helix | 317-326 | 10 | |
| β-strand | 334 | 1 | 1 |
| α-helix | 339-346 | 8 | |
| β-strand | 350 | 1 | 4 |
| α-helix | 351-353 | 3 | |
| α-helix | 359-366 | 8 | |
| β-strand | 372 | 1 | 4 |
| α-helix | 373-378 | 6 | |
| α-helix | 380-386 | 7 | |
| α-helix | 389-399 | 11 | |
| β-strand | 415-425 | 11 | 5 |
| α-helix | 428-449 | 22 | |
| β-strand | 453-462 | 10 | 5 |
| β-strand | 467-478 | 12 | 5 |
| α-helix | 481-499 | 19 | |
| α-helix | 503-504 | 2 | |
| β-strand | 506-514 | 9 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 33-42 | 10 | |
| α-helix | 48-72 | 25 | |
| α-helix | 76-95 | 20 | |
| β-strand | 103-108 | 6 | 6 |
| α-helix | 111-118 | 8 | |
| β-strand | 128-131 | 4 | 7 |
| β-strand | 136-139 | 4 | 7 |
| α-helix | 141-144 | 4 | |
| α-helix | 154-160 | 7 | |
| β-strand | 165-167 | 3 | 7 |
| α-helix | 168-169 | 2 | |
| α-helix | 171-188 | 18 | |
| β-strand | 193-194 | 2 | 6 |
| β-strand | 199-203 | 5 | 6 |
| α-helix | 205-211 | 7 | |
| β-strand | 220-221 | 2 | 8 |
| β-strand | 284-285 | 2 | 8 |
| α-helix | 290-305 | 16 | |
| β-strand | 309-314 | 6 | 6 |
| α-helix | 317-324 | 8 | |
| β-strand | 334 | 1 | 6 |
| α-helix | 339-346 | 8 | |
| β-strand | 350 | 1 | 9 |
| α-helix | 351-353 | 3 | |
| α-helix | 359-367 | 9 | |
| β-strand | 372 | 1 | 9 |
| α-helix | 373-378 | 6 | |
| α-helix | 380-386 | 7 | |
| α-helix | 389-399 | 11 | |
| β-strand | 415-425 | 11 | 10 |
| α-helix | 428-449 | 22 | |
| β-strand | 453-462 | 10 | 10 |
| β-strand | 467-478 | 12 | 10 |
| α-helix | 481-499 | 19 | |
| β-strand | 506-514 | 9 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| DNA polymerase kappa | A, B | protein | 551 | Homo sapiens | Q9UBT6 (AlphaFold model) |
| DNA (5'-d(p*ap*tp*ap*cp*ap*tp*ap*cp*c)-3') | C, P | DNA | 9 | synthetic construct | |
| DNA (5'-d(*tp*ap*cp*tp*gp*gp*tp*ap*tp*gp*tp*ap*t)-3') | D, T | DNA | 13 | synthetic construct |
>6BS1_1 DNA polymerase kappa (chains A, B) MSYYHHHHHHDYDIPTTENLYFQGAMDSTKEKCDSYKDDLLLRMGLNDNKAGMEGLDKEK INKIIMEATKGSRFYGNELKKEKQVNQRIENMMQQKAQITSQQLRKAQLQVDRFAMELEQ SRNLSNTIVHIDMDAFYAAVEMRDNPELKDKPIAVGSMSMLSTSNYHARRFGVRAAMPGF IAKRLCPQLIIVPPNFDKYRAVSKEVKEILADYDPNFMAMSLDEAYLNITKHLEERQNWP EDKRRYFIKMGSSVENDNPGKEVNKLSEHERSISPLLFEESPSDVQPPGDPFQVNFEEQN NPQILQNSVVFGTSAQEVVKEIRFRIEQKTTLTASAGIAPNTMLAKVCSDKNKPNGQYQI LPNRQAVMDFIKDLPIRKVSGIGKVTEKMLKALGIITCTELYQQRALLSLLFSETSWHYF LHISLGLGSTHLTRDGERKSMSVERTFSEINKAEEQYSLCQELCSELAQDLQKERLKGRT VTIKLKNVNFEVKTRASTVSSVVSTAEEIFAIAKELLKTEIDADFPHPLRLRLMGVRISS FPNEEDRKHQQ
>6BS1_2 DNA (5'-D(P*AP*TP*AP*CP*AP*TP*AP*CP*C)-3') (chains C, P) ATACATACC
>6BS1_3 DNA (5'-D(*TP*AP*CP*TP*GP*GP*TP*AP*TP*GP*TP*AP*T)-3') (chains D, T) TACTGGTATGTAT
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 6 |
| DZ4 | 2'-deoxy-5'-O-[(R)-hydroxy{[(R)-hydroxy(phosphonooxy)phosphoryl]amino}phosphory… | C10 H17 N6 O11 P3 | 2 |
| CPT | Cisplatin | Cl2 H6 N2 Pt | 2 |
Water and common crystallization additives (IOD) are not listed.
Structural Basis for Human DNA Polymerase Kappa to Bypass Cisplatin Intrastrand Cross-Link (Pt-GG) Lesion as an Efficient and Accurate Extender. Jha, V., Ling, H. J Mol Biol (2018) 430:1577-1589. DOI 10.1016/j.jmb.2018.04.023 · PubMed
Other PDB entries of the same protein (UniProt Q9UBT6 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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