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Calcium in PDB 5wdp: H-Ras Mutant L120A Bound to Gmp-Pnp at 277K

Enzymatic activity of H-Ras Mutant L120A Bound to Gmp-Pnp at 277K

All present enzymatic activity of H-Ras Mutant L120A Bound to Gmp-Pnp at 277K:
3.6.5.2;

Protein crystallography data

The structure of H-Ras Mutant L120A Bound to Gmp-Pnp at 277K, PDB code: 5wdp was solved by J.C.Cofsky, P.Bandaru, C.L.Gee, J.Kuriyan, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 45.32 / 1.35
Space group H 3 2
Cell size a, b, c (Å), α, β, γ (°) 89.988, 89.988, 135.969, 90.00, 90.00, 120.00
R / Rfree (%) 14.5 / 15.4

Other elements in 5wdp:

The structure of H-Ras Mutant L120A Bound to Gmp-Pnp at 277K also contains other interesting chemical elements:

Magnesium (Mg) 2 atoms

Calcium Binding Sites:

The binding sites of Calcium atom in the H-Ras Mutant L120A Bound to Gmp-Pnp at 277K (pdb code 5wdp). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the H-Ras Mutant L120A Bound to Gmp-Pnp at 277K, PDB code: 5wdp:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 5wdp

Go back to Calcium Binding Sites List in 5wdp
Calcium binding site 1 out of 2 in the H-Ras Mutant L120A Bound to Gmp-Pnp at 277K


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of H-Ras Mutant L120A Bound to Gmp-Pnp at 277K within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca201

b:17.0
occ:1.00
O A:PHE28 2.3 17.7 1.0
OD1 A:ASP30 2.4 20.2 1.0
H A:ASP30 3.4 19.1 1.0
C A:PHE28 3.5 15.7 1.0
CG A:ASP30 3.6 21.2 1.0
HA A:VAL29 3.7 17.1 1.0
N A:ASP30 4.1 15.9 1.0
HB3 A:PHE28 4.1 20.3 1.0
HB2 A:ASP30 4.1 21.6 1.0
H A:PHE28 4.3 20.1 1.0
O A:HOH359 4.3 40.7 1.0
CA A:VAL29 4.4 14.2 1.0
N A:VAL29 4.4 15.1 1.0
CB A:ASP30 4.4 18.0 1.0
OD2 A:ASP30 4.5 24.8 1.0
O A:HOH379 4.5 27.3 1.0
CA A:PHE28 4.5 15.1 1.0
HD2 A:PHE28 4.5 20.5 1.0
HB2 A:HIS27 4.6 22.3 1.0
N A:PHE28 4.7 16.7 1.0
C A:VAL29 4.7 17.3 1.0
O A:HOH410 4.8 49.8 1.0
CB A:PHE28 4.8 16.9 1.0
CA A:ASP30 4.9 16.7 1.0
ND1 A:HIS27 5.0 18.8 1.0

Calcium binding site 2 out of 2 in 5wdp

Go back to Calcium Binding Sites List in 5wdp
Calcium binding site 2 out of 2 in the H-Ras Mutant L120A Bound to Gmp-Pnp at 277K


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of H-Ras Mutant L120A Bound to Gmp-Pnp at 277K within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca203

b:15.1
occ:0.71
MG A:MG204 0.0 15.0 0.3
O3G A:GNP202 2.0 16.7 1.0
O2B A:GNP202 2.0 14.2 1.0
O A:HOH318 2.1 15.6 1.0
OG A:SER17 2.1 14.6 1.0
O A:HOH326 2.1 16.4 1.0
OG1 A:THR35 2.1 16.9 1.0
HB A:THR35 3.0 20.3 1.0
CB A:THR35 3.1 16.9 1.0
HB2 A:SER17 3.1 18.5 1.0
CB A:SER17 3.2 15.4 1.0
PG A:GNP202 3.2 15.5 1.0
PB A:GNP202 3.2 14.1 1.0
H A:THR35 3.3 20.4 1.0
H A:SER17 3.3 16.3 1.0
N3B A:GNP202 3.4 14.2 1.0
N A:THR35 3.8 17.0 1.0
HB3 A:SER17 3.8 18.5 1.0
N A:SER17 3.9 13.6 1.0
HB2 A:LYS16 3.9 17.1 1.0
HG21 A:THR35 4.0 22.5 1.0
O1G A:GNP202 4.0 17.2 1.0
OD2 A:ASP57 4.1 17.3 1.0
CA A:THR35 4.1 17.0 1.0
CA A:SER17 4.1 13.3 1.0
O2A A:GNP202 4.1 16.1 1.0
O A:HOH331 4.1 21.3 1.0
CG2 A:THR35 4.1 18.8 1.0
HE2 A:LYS16 4.2 20.1 1.0
OD1 A:ASP57 4.2 17.0 1.0
O3A A:GNP202 4.2 14.1 1.0
HNB3 A:GNP202 4.3 17.0 1.0
O1B A:GNP202 4.3 13.9 1.0
O2G A:GNP202 4.4 17.1 1.0
HA A:PRO34 4.4 20.5 1.0
HA A:SER17 4.4 16.0 1.0
O A:ASP33 4.5 17.0 0.4
O A:ASP33 4.5 17.1 0.6
PA A:GNP202 4.5 14.6 1.0
CG A:ASP57 4.5 15.6 1.0
O A:THR58 4.5 18.6 1.0
HA A:THR35 4.6 20.4 1.0
HG23 A:THR35 4.6 22.5 1.0
HE1 A:TYR32 4.6 24.7 1.0
O1A A:GNP202 4.7 15.1 1.0
HZ1 A:LYS16 4.7 18.4 1.0
C A:PRO34 4.8 17.3 1.0
CB A:LYS16 4.8 14.2 1.0
HZ3 A:LYS16 4.8 18.4 1.0
HG22 A:THR35 4.9 22.5 1.0
C A:LYS16 5.0 13.6 1.0

Reference:

P.Bandaru, N.H.Shah, M.Bhattacharyya, J.P.Barton, Y.Kondo, J.C.Cofsky, C.L.Gee, A.K.Chakraborty, T.Kortemme, R.Ranganathan, J.Kuriyan. Deconstruction of the Ras Switching Cycle Through Saturation Mutagenesis. Elife V. 6 2017.
ISSN: ESSN 2050-084X
PubMed: 28686159
DOI: 10.7554/ELIFE.27810
Page generated: Wed Jul 9 11:11:45 2025

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