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Calcium in PDB 1mmq: Matrilysin Complexed with Hydroxamate Inhibitor

Enzymatic activity of Matrilysin Complexed with Hydroxamate Inhibitor

All present enzymatic activity of Matrilysin Complexed with Hydroxamate Inhibitor:
3.4.24.23;

Protein crystallography data

The structure of Matrilysin Complexed with Hydroxamate Inhibitor, PDB code: 1mmq was solved by M.F.Browner, W.W.Smith, A.L.Castelhano, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 6.00 / 1.90
Space group P 31 2 1
Cell size a, b, c (Å), α, β, γ (°) 61.900, 61.900, 88.000, 90.00, 90.00, 120.00
R / Rfree (%) 17.9 / n/a

Other elements in 1mmq:

The structure of Matrilysin Complexed with Hydroxamate Inhibitor also contains other interesting chemical elements:

Zinc (Zn) 2 atoms

Calcium Binding Sites:

The binding sites of Calcium atom in the Matrilysin Complexed with Hydroxamate Inhibitor (pdb code 1mmq). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Matrilysin Complexed with Hydroxamate Inhibitor, PDB code: 1mmq:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 1mmq

Go back to Calcium Binding Sites List in 1mmq
Calcium binding site 1 out of 2 in the Matrilysin Complexed with Hydroxamate Inhibitor


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Matrilysin Complexed with Hydroxamate Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca3

b:11.2
occ:1.00
OE2 A:GLU201 2.0 13.4 1.0
O A:GLY176 2.0 14.6 1.0
OD2 A:ASP198 2.1 14.0 1.0
OD1 A:ASP175 2.1 15.9 1.0
O A:THR180 2.1 14.0 1.0
O A:GLY178 2.3 14.6 1.0
CG A:ASP198 3.2 12.3 1.0
CD A:GLU201 3.2 12.0 1.0
C A:GLY176 3.3 14.7 1.0
C A:THR180 3.3 12.5 1.0
CG A:ASP175 3.4 18.2 1.0
C A:GLY178 3.5 13.4 1.0
N A:GLY178 3.9 12.1 1.0
CB A:ASP198 3.9 13.8 1.0
OD2 A:ASP175 3.9 22.9 1.0
C A:PRO177 3.9 15.1 1.0
N A:GLY176 4.0 16.8 1.0
OE1 A:GLU201 4.0 16.6 1.0
N A:THR180 4.1 14.8 1.0
OD1 A:ASP198 4.1 12.1 1.0
N A:PRO177 4.2 17.8 1.0
C A:ASP175 4.2 17.5 1.0
CA A:GLY176 4.3 14.6 1.0
CA A:GLY178 4.3 14.9 1.0
CA A:PRO177 4.3 17.2 1.0
CG A:GLU201 4.3 9.9 1.0
CA A:THR180 4.3 14.3 1.0
N A:LEU181 4.3 11.4 1.0
C A:ASN179 4.4 14.8 1.0
O A:PRO177 4.4 13.7 1.0
N A:ASP175 4.4 19.2 1.0
CA A:LEU181 4.5 12.1 1.0
N A:ASN179 4.6 13.5 1.0
CB A:ASP175 4.6 17.2 1.0
CA A:ASP175 4.7 17.1 1.0
O A:ASP175 4.7 18.5 1.0
CD1 A:LEU181 4.8 16.6 1.0
CB A:THR180 4.9 17.2 1.0
CA A:ASN179 4.9 16.3 1.0
CB A:ASN179 4.9 21.0 1.0
O A:ASN179 4.9 13.0 1.0

Calcium binding site 2 out of 2 in 1mmq

Go back to Calcium Binding Sites List in 1mmq
Calcium binding site 2 out of 2 in the Matrilysin Complexed with Hydroxamate Inhibitor


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Matrilysin Complexed with Hydroxamate Inhibitor within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca4

b:10.9
occ:1.00
O A:HOH313 2.1 14.7 1.0
O A:GLY192 2.1 17.8 1.0
O A:HOH317 2.1 15.0 1.0
O A:GLY190 2.1 15.4 1.0
OD1 A:ASP194 2.1 14.0 1.0
O A:ASP158 2.2 14.7 1.0
CG A:ASP194 3.2 12.2 1.0
C A:GLY190 3.4 13.2 1.0
C A:GLY192 3.4 13.0 1.0
C A:ASP158 3.4 13.9 1.0
OD2 A:ASP194 3.6 11.8 1.0
C A:LEU191 4.0 14.2 1.0
N A:GLY192 4.0 14.1 1.0
O A:ALA157 4.1 13.2 1.0
N A:ASP194 4.2 12.0 1.0
O A:LEU191 4.2 14.2 1.0
O A:GLY188 4.2 14.6 1.0
CA A:GLY192 4.3 13.8 1.0
CA A:ASP158 4.3 14.4 1.0
N A:GLY190 4.3 15.9 1.0
CA A:GLY190 4.3 16.9 1.0
N A:LEU191 4.3 13.5 1.0
N A:GLY193 4.3 11.9 1.0
O A:HOH372 4.4 23.5 1.0
N A:ILE159 4.4 10.0 1.0
CA A:LEU191 4.5 15.9 1.0
CB A:ASP194 4.5 10.7 1.0
O A:HOH314 4.5 20.9 1.0
C A:GLY193 4.5 12.4 1.0
N A:MET160 4.6 9.0 1.0
CA A:GLY193 4.6 11.1 1.0
O A:HOH319 4.6 13.7 1.0
CG A:MET160 4.6 13.3 1.0
CA A:ILE159 4.7 11.2 1.0
C A:THR189 4.7 17.0 1.0
CA A:ASP194 4.8 11.7 1.0
O A:HOH315 4.8 21.6 1.0
CH2 A:TRP109 4.9 18.5 1.0

Reference:

M.F.Browner, W.W.Smith, A.L.Castelhano. Matrilysin-Inhibitor Complexes: Common Themes Among Metalloproteases. Biochemistry V. 34 6602 1995.
ISSN: ISSN 0006-2960
PubMed: 7756291
DOI: 10.1021/BI00020A004
Page generated: Thu Jul 11 12:33:45 2024

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