PDBsum entry 4nvc

Oxidoreductase

PDB id: 4nvc

Contents

Protein chain

289 a.a.

Ligands

BEN

HEM

Waters ×387

PDB id:

4nvc

Name:

Oxidoreductase

Title:

Predicting protein conformational response in prospective ligand discovery

Structure:

CytochromE C peroxidase. Chain: a. Fragment: unp residues 72-362. Engineered: yes. Mutation: yes

Source:

Saccharomyces cerevisiae. Baker's yeast. Organism_taxid: 285006. Strain: rm11-1a. Gene: ccp1 ccp cpo ykr066c, scrg_04081. Expressed in: escherichia coli. Expression_system_taxid: 469008.

Resolution:

1.60Å R-factor: 0.144 R-free: 0.185

Authors:

M.Fischer,J.S.Fraser

Key ref:

M.Fischer et al. (2014). Incorporation of protein flexibility and conformational energy penalties in docking screens to improve ligand discovery. Nat Chem, 6, 575-583. PubMed id: 24950326 DOI: 10.1038/nchem.1954

Date:

05-Dec-13 Release date: 18-Dec-13

Protein chain

B3LRE1  (B3LRE1_YEAS1) -  Peroxidase from Saccharomyces cerevisiae (strain RM11-1a)

Seq: 362 a.a.

Struc: 289 a.a.*

* PDB and UniProt seqs differ at 1 residue position (black cross)

Enzyme reactions

• Enzyme class: E.C.1.11.1.- - ?????

DOI no: 10.1038/nchem.1954

Nat Chem 6:575-583 (2014)

PubMed id: 24950326

Incorporation of protein flexibility and conformational energy penalties in docking screens to improve ligand discovery.

M.Fischer, R.G.Coleman, J.S.Fraser, B.K.Shoichet.

ABSTRACT

Proteins fluctuate between alternative conformations, which presents a challenge for ligand discovery because such flexibility is difficult to treat computationally owing to problems with conformational sampling and energy weighting. Here we describe a flexible docking method that samples and weights protein conformations using experimentally derived conformations as a guide. The crystallographically refined occupancies of these conformations, which are observable in an apo receptor structure, define energy penalties for docking. In a large prospective library screen, we identified new ligands that target specific receptor conformations of a cavity in cytochrome c peroxidase, and we confirm both ligand pose and associated receptor conformation predictions by crystallography. The inclusion of receptor flexibility led to ligands with new chemotypes and physical properties. By exploiting experimental measures of loop and side-chain flexibility, this method can be extended to the discovery of new ligands for hundreds of targets in the Protein Data Bank for which similar experimental information is available.