Crystal Structure of human RhoGAP mutated in its arginin finger (R85A) in complex with RhoA.GDP.AlF4- human. Determined by X-ray diffraction at 2.2 Å resolution. Released 17 May 2017.
Explore 5M70 in 3D Show helices and sheets RCSB PDB PDBe
5M70 contains 55 α-helices and 14 β-strands across 4 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 | 49-55 | 7 | |
| α-helix | 64-76 | 13 | |
| α-helix | 90-101 | 12 | |
| α-helix | 104-106 | 3 | |
| α-helix | 108-110 | 3 | |
| α-helix | 115-126 | 12 | |
| α-helix | 135-137 | 3 | |
| α-helix | 138-142 | 5 | |
| α-helix | 144-146 | 3 | |
| α-helix | 149-151 | 3 | |
| α-helix | 152-160 | 9 | |
| α-helix | 165-183 | 19 | |
| α-helix | 185-188 | 4 | |
| α-helix | 192-203 | 12 | |
| α-helix | 209-214 | 6 | |
| α-helix | 216-228 | 13 | |
| α-helix | 230-233 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 6-12 | 7 | 1 |
| α-helix | 18-26 | 9 | |
| β-strand | 39-46 | 8 | 1 |
| β-strand | 53-60 | 8 | 1 |
| α-helix | 64-66 | 3 | |
| α-helix | 70-73 | 4 | |
| β-strand | 79-85 | 7 | 1 |
| α-helix | 89-94 | 6 | |
| α-helix | 95-99 | 5 | |
| α-helix | 100-106 | 7 | |
| β-strand | 112-117 | 6 | 1 |
| α-helix | 119-121 | 3 | |
| α-helix | 125-132 | 8 | |
| α-helix | 138-140 | 3 | |
| α-helix | 141-151 | 11 | |
| β-strand | 155-158 | 4 | 1 |
| β-strand | 160 | 1 | 2 |
| β-strand | 165 | 1 | 2 |
| α-helix | 167-178 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 49-55 | 7 | |
| α-helix | 64-76 | 13 | |
| α-helix | 90-102 | 13 | |
| α-helix | 104-106 | 3 | |
| α-helix | 108-110 | 3 | |
| α-helix | 115-126 | 12 | |
| α-helix | 135-137 | 3 | |
| α-helix | 138-142 | 5 | |
| α-helix | 144-146 | 3 | |
| α-helix | 152-161 | 10 | |
| α-helix | 165-183 | 19 | |
| α-helix | 185-188 | 4 | |
| α-helix | 192-203 | 12 | |
| α-helix | 209-214 | 6 | |
| α-helix | 216-228 | 13 | |
| α-helix | 230-233 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 6-12 | 7 | 1 |
| α-helix | 18-27 | 10 | |
| β-strand | 39-46 | 8 | 1 |
| β-strand | 53-60 | 8 | 1 |
| α-helix | 64-66 | 3 | |
| α-helix | 70-73 | 4 | |
| β-strand | 79-85 | 7 | 1 |
| α-helix | 89-94 | 6 | |
| α-helix | 95-99 | 5 | |
| α-helix | 100-106 | 7 | |
| β-strand | 112-117 | 6 | 1 |
| α-helix | 119-122 | 4 | |
| α-helix | 125-132 | 8 | |
| α-helix | 138-140 | 3 | |
| α-helix | 141-151 | 11 | |
| β-strand | 155-158 | 4 | 1 |
| α-helix | 167-178 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Rho GTPase-activating protein 1 | A, F | protein | 240 | Homo sapiens | Q07960 (AlphaFold model) |
| Transforming protein RhoA | B, G | protein | 192 | Homo sapiens | P61586 (AlphaFold model) |
>5M70_1 Rho GTPase-activating protein 1 (chains A, F) HVKLEQLGIPRQVLKYDDFLKSTQKSPATAPKPMPPRPPLPNQQFGVSLQHLQEKNPEQE PIPIVLRETVAYLQAHALTTEGIFARSANTQVVREVQQKYNMGLPVDFDQYNELHLPAVI LKTFLRELPEPLLTFDLYPHVVGFLNIDESQRVPATLQVLQTLPEENYQVLRFLTAFLVQ ISAHSDQNKMTNTNLAVVFGPNLLWAKDAAITLKAINPINTFTKFLLDHQGELFPSPDPS
>5M70_2 Transforming protein RhoA (chains B, G) AAIRKKLVIVGDGACGKTCLLIVNSKDQFPEVYVPTVFENYVADIEVDGKQVELALWDTA GQEDYDRLRPLSYPDTDVILMCFSIDSPDSLENIPEKWTPEVKHFCPNVPIILVGNKKDL RNDEHTRRELAKMKQEPVKPEEGRDMANRIGAFGYMECSAKTKDGVREVFEMATRAALQA RRGKKKSGCLVL
| ID | Name | Formula | Copies |
|---|---|---|---|
| ALF | Tetrafluoroaluminate ion | Al F4 | 2 |
| GDP | Guanosine-5'-diphosphate | C10 H15 N5 O11 P2 | 2 |
| MG | Magnesium ion | Mg | 2 |
Assessing the Influence of Mutation on GTPase Transition States by Using X-ray Crystallography, (19) F NMR, and DFT Approaches. Jin, Y., Molt, R.W., Pellegrini, E. et al. Angew Chem Int Ed Engl (2017) 56:9732-9735. DOI 10.1002/anie.201703074 · PubMed
Other PDB entries of the same protein (UniProt Q07960 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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