Protease domain of HGFA with inhibitor Fab58. Determined by X-ray diffraction at 3.51 Å resolution. Released 25 Dec 2007.
Explore 2R0K in 3D Show helices and sheets RCSB PDB PDBe
2R0K contains 20 α-helices and 71 β-strands across 3 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 |
|---|---|---|---|
| β-strand | 17 | 1 | 1 |
| β-strand | 20-21 | 2 | 2 |
| β-strand | 30-35 | 6 | 3 |
| β-strand | 40-46 | 7 | 3 |
| β-strand | 51-54 | 4 | 3 |
| α-helix | 56-58 | 3 | |
| α-helix | 61-63 | 3 | |
| β-strand | 64-68 | 5 | 3 |
| β-strand | 72 | 1 | 4 |
| β-strand | 81-83 | 3 | 3 |
| β-strand | 85-90 | 6 | 3 |
| β-strand | 104-108 | 5 | 3 |
| α-helix | 109-110 | 2 | |
| β-strand | 115 | 1 | 5 |
| β-strand | 118 | 1 | 5 |
| α-helix | 120-121 | 2 | |
| β-strand | 122 | 1 | 2 |
| α-helix | 123-125 | 3 | |
| β-strand | 135-140 | 6 | 2 |
| β-strand | 154 | 1 | 4 |
| β-strand | 156-162 | 7 | 2 |
| α-helix | 163-164 | 2 | |
| α-helix | 165-169 | 5 | |
| α-helix | 173-175 | 3 | |
| β-strand | 182-183 | 2 | 2 |
| β-strand | 189 | 1 | 1 |
| β-strand | 198-203 | 6 | 2 |
| β-strand | 206-215 | 10 | 2 |
| β-strand | 221 | 1 | 6 |
| β-strand | 224 | 1 | 6 |
| β-strand | 226-230 | 5 | 2 |
| α-helix | 231-234 | 4 | |
| α-helix | 235-239 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-7 | 5 | 12 |
| β-strand | 11-12 | 2 | 13 |
| β-strand | 17-25 | 9 | 12 |
| β-strand | 33-39 | 7 | 14 |
| β-strand | 45-52 | 8 | 14 |
| β-strand | 56-59 | 4 | 14 |
| β-strand | 67-72 | 6 | 12 |
| β-strand | 77-82A | 7 | 12 |
| α-helix | 84-86 | 3 | |
| β-strand | 88-95 | 8 | 14 |
| β-strand | 100-103 | 4 | 14 |
| β-strand | 107-109 | 3 | 14 |
| β-strand | 110-111 | 2 | 13 |
| β-strand | 117 | 1 | 15 |
| α-helix | 118-119 | 2 | |
| β-strand | 120 | 1 | 16 |
| β-strand | 123-124 | 2 | 17 |
| β-strand | 135-140 | 6 | 17 |
| β-strand | 143-145 | 3 | 16 |
| β-strand | 146 | 1 | 15 |
| β-strand | 151-154 | 4 | 18 |
| β-strand | 163-165 | 3 | 17 |
| α-helix | 166-168 | 3 | |
| β-strand | 169-171 | 3 | 16 |
| β-strand | 175-177 | 3 | 16 |
| β-strand | 180-185 | 6 | 17 |
| β-strand | 189 | 1 | 19 |
| β-strand | 192 | 1 | 19 |
| β-strand | 194-200 | 7 | 18 |
| α-helix | 201-203 | 3 | |
| β-strand | 205-211 | 7 | 18 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 7 |
| β-strand | 10-14 | 5 | 8 |
| β-strand | 19-25 | 7 | 7 |
| β-strand | 33-38 | 6 | 8 |
| β-strand | 45-49 | 5 | 8 |
| β-strand | 53-54 | 2 | 8 |
| β-strand | 62-66 | 5 | 7 |
| β-strand | 70-75 | 6 | 7 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-90 | 7 | 8 |
| α-helix | 96 | 1 | |
| β-strand | 98 | 1 | 8 |
| β-strand | 103-107 | 5 | 8 |
| β-strand | 111 | 1 | 9 |
| β-strand | 114-118 | 5 | 10 |
| α-helix | 119-121 | 3 | |
| α-helix | 122-126 | 5 | |
| β-strand | 130-139 | 10 | 10 |
| β-strand | 140 | 1 | 9 |
| β-strand | 145-150 | 6 | 11 |
| β-strand | 153-154 | 2 | 11 |
| β-strand | 161-163 | 3 | 10 |
| α-helix | 164-167 | 4 | |
| β-strand | 173-181 | 9 | 10 |
| α-helix | 183-187 | 5 | |
| β-strand | 191-197 | 7 | 11 |
| β-strand | 205-210 | 6 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Hepatocyte growth factor activator | A | protein | 283 | Homo sapiens | Q04756 (AlphaFold model) |
| antibody light chain of Fab58 | L | protein | 214 | Homo sapiens | |
| antibody heavy chain of Fab58, Fab portion only | H | protein | 225 | Homo sapiens |
>2R0K_1 Hepatocyte growth factor activator (chains A) VQLSPDLLATLPEPASPGRQACGRRHKKRTFLRPRIIGGSSSLPGSHPWLAAIYIGDSFC AGSLVHTCWVVSAAHCFSHSPPRDSVSVVLGQHFFNRTTDVTQTFGIEKYIPYTLYSVFN PSDHDLVLIRLKKKGDRCATRSQFVQPICLPEPGSTFPAGHKCQIAGWGHLDENVSGYSS SLREALVPLVADHKCSSPEVYGADISPNMLCAGYFDCKSDACQGDSGGPLACEKNGVAYL YGIISWGDGCGRLHKPGVYTRVANYVDWINDRIRPPRRLVAPS
>2R0K_2 antibody light chain of Fab58 (chains L) DIQMTQSPSSLSASVGDRVTITCRASQDVSTAVAWYQQKPGKAPKLLIYSASFLYSGVPS RFSGSGSGTDFTLTISSLQPEDFATYYCQQSYTTPPTFGQGTKVEIKRTVAAPSVFIFPP SDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLT LSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
>2R0K_3 antibody heavy chain of Fab58, Fab portion only (chains H) EVQLVESGGGLVQPGGSLRLSCAASGFTITGSAIHWVRQAPGKGLEWVAIINPNGGYTYY ADSVKGRFTISADTSKNTAYLQMNSLRAEDTAVYYCARSARFSFDYWGQGTLVTVSSAST KGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLY SLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHT
Structural insight into distinct mechanisms of protease inhibition by antibodies. Wu, Y., Eigenbrot, C., Liang, W.C. et al. Proc Natl Acad Sci U S A (2007) 104:19784-19789. DOI 10.1073/pnas.0708251104 · PubMed
Other PDB entries of the same protein (UniProt Q04756 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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