Mercury in PDB 1fqm: X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant

Enzymatic activity of X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant

All present enzymatic activity of X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant:
4.2.1.1;

Protein crystallography data

The structure of X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant, PDB code: 1fqm was solved by J.D.Cox, J.A.Hunt, K.M.Compher, C.A.Fierke, D.W.Christianson, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

*Resolution Low / High (Å)*	20.00 / 2.00
*Space group*	P 1 2₁ 1
*Cell size a, b, c (Å), α, β, γ (°)*	41.800, 41.290, 72.350, 90.00, 103.75, 90.00
*R / R_free (%)*	18.5 / 26.8

Other elements in 1fqm:

The structure of X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant also contains other interesting chemical elements:

Zinc

(Zn)

1 atom

Mercury Binding Sites:

The binding sites of Mercury atom in the X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant (pdb code 1fqm). This binding sites where shown within 5.0 Angstroms radius around Mercury atom.
In total only one binding site of Mercury was determined in the X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant, PDB code: 1fqm:

Mercury binding site 1 out of 1 in 1fqm

Go back to

Mercury Binding Sites List in 1fqm

Mercury binding site 1 out of 1 in the X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant

Mono view

Stereo pair view

A full contact list of Mercury with other atoms in the Hg binding site number 1 of X-Ray Crystal Structure of Zinc-Bound F93I/F95M/W97V Carbonic Anhydrase (Caii) Variant within 5.0Å range:

probe	atom	residue	distance (Å)	B	Occ
A:Hg263 b:23.6 occ:1.00	SG	A:CYS206	2.1	16.4	1.0
	O	A:GLN137	3.0	15.2	1.0
	CB	A:CYS206	3.2	10.0	1.0
	O	A:GLU205	3.2	13.0	1.0
	C	A:GLN137	3.4	16.6	1.0
	C	A:GLU205	3.5	15.7	1.0
	CA	A:CYS206	3.5	13.1	1.0
	O	A:VAL135	3.5	16.8	1.0
	N	A:CYS206	3.6	12.6	1.0
	N	A:GLN137	3.7	18.9	1.0
	C	A:VAL135	3.9	16.4	1.0
	C	A:GLN136	4.0	21.7	1.0
	N	A:PRO138	4.0	16.6	1.0
	CA	A:GLN137	4.1	17.2	1.0
	CA	A:PRO138	4.3	14.0	1.0
	N	A:GLU205	4.3	14.2	1.0
	N	A:GLN136	4.3	17.9	1.0
	O	A:HOH397	4.3	23.2	1.0
	CA	A:GLN136	4.3	21.3	1.0
	CA	A:GLU205	4.4	15.0	1.0
	CB	A:LEU204	4.6	14.6	1.0
	CA	A:VAL135	4.6	15.3	1.0
	O	A:GLN136	4.6	22.4	1.0
	C	A:LEU204	4.7	14.2	1.0
	O	A:ALA134	4.8	14.4	1.0
	C	A:CYS206	5.0	11.9	1.0

Reference:

J.D.Cox, J.A.Hunt, K.M.Compher, C.A.Fierke, D.W.Christianson. Structural Influence of Hydrophobic Core Residues on Metal Binding and Specificity in Carbonic Anhydrase II. Biochemistry V. 39 13687 2000.
ISSN: ISSN 0006-2960
PubMed: 11076507
DOI: 10.1021/BI001649J

Page generated: Sat Aug 10 23:45:11 2024

Last articles

Zn in 2YRC
Zn in 2YQP
Zn in 2YR2
Zn in 2YQL
Zn in 2YPT
Zn in 2YPA
Zn in 2YPU
Zn in 2YNW
Zn in 2YNT
Zn in 2YNV

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