Calcium in PDB 4r8n: Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature

Enzymatic activity of Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature

All present enzymatic activity of Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature:
3.1.31.1;

Protein crystallography data

The structure of Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature, PDB code: 4r8n was solved by J.A.Caro, E.Flores, J.L.Schlessman, A.Heroux, E.B.Garcia-Moreno, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

*Resolution Low / High (Å)*	47.60 / 1.65
*Space group*	P 4₁
*Cell size a, b, c (Å), α, β, γ (°)*	47.605, 47.605, 62.912, 90.00, 90.00, 90.00
*R / R_free (%)*	19.4 / 23.9

Calcium Binding Sites:

The binding sites of Calcium atom in the Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature (pdb code 4r8n). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature, PDB code: 4r8n:

Calcium binding site 1 out of 1 in 4r8n

Go back to

Calcium Binding Sites List in 4r8n

Calcium binding site 1 out of 1 in the Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature

Mono view

Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Crystal Structure of Staphylococcal Nuclease Variant V23I/V66I/I72V/I92V at Cryogenic Temperature within 5.0Å range:

probe	atom	residue	distance (Å)	B	Occ
A:Ca202 b:36.8 occ:1.00	OD1	A:ASP40	1.9	37.8	1.0
	O	A:HOH347	2.3	34.8	1.0
	O	A:HOH339	2.4	34.6	1.0
	OD1	A:ASP21	2.5	31.9	1.0
	O	A:THR41	2.7	42.3	1.0
	O	A:HOH346	2.8	41.2	1.0
	O4P	A:THP201	3.0	35.9	1.0
	CG	A:ASP40	3.1	39.3	1.0
	CG	A:ASP21	3.5	29.8	1.0
	O	A:HOH372	3.5	38.2	1.0
	OD2	A:ASP21	3.7	32.4	1.0
	NH2	A:ARG35	3.8	30.8	1.0
	C	A:THR41	3.8	39.2	1.0
	N	A:THR41	3.8	32.6	1.0
	OD2	A:ASP40	3.9	45.1	1.0
	P2	A:THP201	3.9	33.6	1.0
	OG1	A:THR41	4.1	33.3	1.0
	O5P	A:THP201	4.2	28.0	1.0
	CB	A:ASP40	4.2	37.3	1.0
	CA	A:ASP40	4.3	33.5	1.0
	C	A:ASP40	4.3	34.3	1.0
	CA	A:THR41	4.3	35.5	1.0
	OE1	A:GLU43	4.5	61.1	1.0
	CZ	A:ARG35	4.5	27.7	1.0
	O6P	A:THP201	4.5	38.9	1.0
	NE	A:ARG35	4.8	27.7	1.0
	OD1	A:ASP19	4.8	42.6	1.0
	CB	A:ASP21	4.8	29.0	1.0
	O	A:PRO42	4.9	49.0	1.0
	CB	A:THR41	4.9	33.7	1.0
	C	A:PRO42	4.9	50.4	1.0
	N	A:PRO42	4.9	41.0	1.0

Reference:

J.A.Caro, J.L.Schlessman, E.B.Garcia-Moreno. Cavities in Proteins To Be Published.

Page generated: Sun Jul 14 12:38:44 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0

	© Copyright 2008-2020 by atomistry.com
Home \| Site Map \| Copyright \| Contact us \| Privacy