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PDBsum entry 5edc

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protein ligands links
Lipid binding protein PDB id
5edc

 

 

 

 

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Contents
Protein chain
133 a.a.
Ligands
5M7
SO4 ×3
Waters ×126
PDB id:
5edc
Name: Lipid binding protein
Title: Human fabp4 in complex with 6-chloro-4-phenyl-2-piperidin-1-yl- quinoline-3-carboxylic acid at 1.29a
Structure: Fatty acid-binding protein, adipocyte. Chain: a. Fragment: soluble form, residues 3-132. Synonym: adipocyte lipid-binding protein,albp,adipocyte-type fatty acid-binding protein,afabp,fatty acid-binding protein 4. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: fabp4. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008.
Resolution:
1.29Å     R-factor:   0.157     R-free:   0.189
Authors: M.G.Rudolph,A.Ehler
Key ref: B.Kuhn et al. (2016). A Real-World Perspective on Molecular Design. J Med Chem, 59, 4087-4102. PubMed id: 26878596 DOI: 10.1021/acs.jmedchem.5b01875
Date:
21-Oct-15     Release date:   09-Mar-16    
PROCHECK
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 Headers
 References

Protein chain
P15090  (FABP4_HUMAN) -  Fatty acid-binding protein, adipocyte from Homo sapiens
Seq:
Struc:
132 a.a.
133 a.a.
Key:    Secondary structure  CATH domain

 

 
DOI no: 10.1021/acs.jmedchem.5b01875 J Med Chem 59:4087-4102 (2016)
PubMed id: 26878596  
 
 
A Real-World Perspective on Molecular Design.
B.Kuhn, W.Guba, J.Hert, D.Banner, C.Bissantz, S.Ceccarelli, W.Haap, M.Körner, A.Kuglstatter, C.Lerner, P.Mattei, W.Neidhart, E.Pinard, M.G.Rudolph, T.Schulz-Gasch, T.Woltering, M.Stahl.
 
  ABSTRACT  
 
We present a series of small molecule drug discovery case studies where computational methods were prospectively employed to impact Roche research projects, with the aim of highlighting those methods that provide real added value. Our brief accounts encompass a broad range of methods and techniques applied to a variety of enzymes and receptors. Most of these are based on judicious application of knowledge about molecular conformations and interactions: filling of lipophilic pockets to gain affinity or selectivity, addition of polar substituents, scaffold hopping, transfer of SAR, conformation analysis, and molecular overlays. A case study of sequence-driven focused screening is presented to illustrate how appropriate preprocessing of information enables effective exploitation of prior knowledge. We conclude that qualitative statements enabling chemists to focus on promising regions of chemical space are often more impactful than quantitative prediction.
 

 

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