9F2F | pdb_00009f2f

Carbonic anhydrase II variant with bound iron complex in space group R3 (ArPase)


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.52 Å
  • R-Value Free: 
    0.167 (Depositor), 0.169 (DCC) 
  • R-Value Work: 
    0.146 (Depositor), 0.150 (DCC) 
  • R-Value Observed: 
    0.148 (Depositor) 

Starting Model: experimental
View more details

wwPDB Validation   3D Report Full Report


Ligand Structure Quality Assessment 


This is version 1.0 of the entry. See complete history


Literature

Directed Evolution of an Artificial Hydroxylase Based on a Thermostable Human Carbonic Anhydrase Protein

Morita, I.Faraone, A.Salvisberg, E.Zhang, K.Jakob, R.P.Maier, T.Ward, T.R.

(2024) ACS Catal 14: 17171-17179


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Carbonic anhydrase 2
A, B, C, D
260Homo sapiensMutation(s): 0 
Gene Names: CA2
EC: 4.2.1.1 (PDB Primary Data), 4.2.1.69 (PDB Primary Data)
UniProt & NIH Common Fund Data Resources
Find proteins for P00918 (Homo sapiens)
Explore P00918 
Go to UniProtKB:  P00918
PHAROS:  P00918
GTEx:  ENSG00000104267 
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupP00918
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Ligands 3 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
A1H9O (Subject of Investigation/LOI)
Query on A1H9O

Download Ideal Coordinates CCD File 
BA [auth D],
E [auth A],
L [auth B],
T [auth C]
4,4,7,10,10-pentamethyl-3,6,8,11-tetrakis(oxidanylidene)-N-[2-(4-sulfamoylphenyl)ethyl]-2,5,7,9,12-pentazabicyclo[11.4.0]heptadeca-1(13),14,16-triene-15-carboxamide containing iron
C26 H29 Fe N7 O7 S
FCEFGHWAAWIBFW-UHFFFAOYSA-J
ZN
Query on ZN

Download Ideal Coordinates CCD File 
AA [auth C]
CA [auth D]
EA [auth D]
F [auth A]
FA [auth D]
AA [auth C],
CA [auth D],
EA [auth D],
F [auth A],
FA [auth D],
GA [auth D],
I [auth A],
J [auth A],
K [auth A],
M [auth B],
Q [auth B],
R [auth B],
S [auth B],
U [auth C]
ZINC ION
Zn
PTFCDOFLOPIGGS-UHFFFAOYSA-N
EDO
Query on EDO

Download Ideal Coordinates CCD File 
DA [auth D]
G [auth A]
H [auth A]
N [auth B]
O [auth B]
DA [auth D],
G [auth A],
H [auth A],
N [auth B],
O [auth B],
P [auth B],
V [auth C],
W [auth C],
X [auth C],
Y [auth C],
Z [auth C]
1,2-ETHANEDIOL
C2 H6 O2
LYCAIKOWRPUZTN-UHFFFAOYSA-N
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.52 Å
  • R-Value Free:  0.167 (Depositor), 0.169 (DCC) 
  • R-Value Work:  0.146 (Depositor), 0.150 (DCC) 
  • R-Value Observed: 0.148 (Depositor) 
Space Group: H 3
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 179.167α = 90
b = 179.167β = 90
c = 109.705γ = 120
Software Package:
Software NamePurpose
PHENIXrefinement
XDSdata reduction
Aimlessdata scaling
PHASERphasing

Structure Validation

View Full Validation Report



Ligand Structure Quality Assessment 


Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
Swiss National Science FoundationSwitzerland180544

Revision History  (Full details and data files)

  • Version 1.0: 2025-03-05
    Type: Initial release