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Iron in PDB 4fwz: Aquoferric Cub Myoglobin (L29H F43H Sperm Whale Myoglobin)

Protein crystallography data

The structure of Aquoferric Cub Myoglobin (L29H F43H Sperm Whale Myoglobin), PDB code: 4fwz was solved by Y.-G.Gao, H.Robinson, I.D.Petrik, K.D.Miner, Y.Lu, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.00 / 1.90
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 39.737, 47.682, 77.543, 90.00, 90.00, 90.00
R / Rfree (%) 20.4 / n/a

Iron Binding Sites:

The binding sites of Iron atom in the Aquoferric Cub Myoglobin (L29H F43H Sperm Whale Myoglobin) (pdb code 4fwz). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total only one binding site of Iron was determined in the Aquoferric Cub Myoglobin (L29H F43H Sperm Whale Myoglobin), PDB code: 4fwz:

Iron binding site 1 out of 1 in 4fwz

Go back to Iron Binding Sites List in 4fwz
Iron binding site 1 out of 1 in the Aquoferric Cub Myoglobin (L29H F43H Sperm Whale Myoglobin)


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Aquoferric Cub Myoglobin (L29H F43H Sperm Whale Myoglobin) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe201

b:18.2
occ:1.00
FE A:HEM201 0.0 18.2 1.0
ND A:HEM201 2.0 9.9 1.0
NC A:HEM201 2.0 13.9 1.0
NB A:HEM201 2.0 19.0 1.0
NA A:HEM201 2.0 12.7 1.0
NE2 A:HIS93 2.3 23.2 1.0
O A:HOH1144 2.3 24.1 1.0
C1C A:HEM201 3.0 18.9 1.0
C4D A:HEM201 3.0 11.5 1.0
C1D A:HEM201 3.0 15.0 1.0
C1B A:HEM201 3.0 14.7 1.0
C4A A:HEM201 3.0 22.8 1.0
C4B A:HEM201 3.1 16.2 1.0
C1A A:HEM201 3.1 16.3 1.0
C4C A:HEM201 3.1 9.9 1.0
CE1 A:HIS93 3.2 16.7 1.0
CD2 A:HIS93 3.3 24.5 1.0
CHC A:HEM201 3.4 14.3 1.0
CHA A:HEM201 3.4 17.1 1.0
CHB A:HEM201 3.4 15.9 1.0
CHD A:HEM201 3.4 13.1 1.0
C3D A:HEM201 4.2 17.2 1.0
C2D A:HEM201 4.2 17.3 1.0
C3B A:HEM201 4.3 14.9 1.0
C3A A:HEM201 4.3 13.8 1.0
C2C A:HEM201 4.3 14.8 1.0
C2A A:HEM201 4.3 8.2 1.0
C3C A:HEM201 4.3 17.8 1.0
C2B A:HEM201 4.3 12.0 1.0
O A:HOH1011 4.3 14.9 1.0
ND1 A:HIS93 4.3 21.9 1.0
CG2 A:VAL68 4.4 11.4 1.0
CG A:HIS93 4.4 20.7 1.0
NE2 A:HIS64 4.5 27.8 1.0
CE1 A:HIS64 4.8 27.8 1.0

Reference:

K.D.Miner, A.Mukherjee, Y.G.Gao, E.L.Null, I.D.Petrik, X.Zhao, N.Yeung, H.Robinson, Y.Lu. A Designed Functional Metalloenzyme That Reduces O(2) to H(2) O with Over One Thousand Turnovers. Angew.Chem.Int.Ed.Engl. V. 51 5589 2012.
ISSN: ISSN 1433-7851
PubMed: 22539151
DOI: 10.1002/ANIE.201201981
Page generated: Mon Aug 5 02:30:32 2024

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