Structure of PDB 2d5x Chain B Binding Site BS02
Receptor Information
>2d5x Chain B (length=146) Species:
9796
(Equus caballus) [
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VQLSGEEKAAVLALWDKVNEEEVGGEALGRLLVVYPWTQRFFDSFGDLSN
PGAVMGNPKVKAHGKKVLHSFGEGVHHLDNLKGTFAALSELHCDKLHVDP
ENFRLLGNVLVVVLARHFGKDFTPELQASYQKVVAGVANALAHKYH
Ligand information
Ligand ID
L35
InChI
InChI=1S/C17H16Cl2N2O4/c1-17(2,15(22)23)25-14-5-3-12(4-6-14)20-16(24)21-13-8-10(18)7-11(19)9-13/h3-9H,1-2H3,(H,22,23)(H2,20,21,24)
InChIKey
OYJPTSMWFKGZJM-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC(C)(Oc1ccc(NC(=O)Nc2cc(Cl)cc(Cl)c2)cc1)C(O)=O
OpenEye OEToolkits 1.5.0
CC(C)(C(=O)O)Oc1ccc(cc1)NC(=O)Nc2cc(cc(c2)Cl)Cl
ACDLabs 10.04
Clc2cc(NC(=O)Nc1ccc(OC(C(=O)O)(C)C)cc1)cc(Cl)c2
Formula
C17 H16 Cl2 N2 O4
Name
2-[4-({[(3,5-DICHLOROPHENYL)AMINO]CARBONYL}AMINO)PHENOXY]-2-METHYLPROPANOIC ACID
ChEMBL
CHEMBL76029
DrugBank
DB08077
ZINC
ZINC000003646141
PDB chain
2d5x Chain B Residue 1201 [
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Receptor-Ligand Complex Structure
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PDB
2d5x
R-state haemoglobin with low oxygen affinity: crystal structures of deoxy human and carbonmonoxy horse haemoglobin bound to the effector molecule L35
Resolution
1.45 Å
Binding residue
(original residue number in PDB)
Y35 W37 L105 N108
Binding residue
(residue number reindexed from 1)
Y35 W37 L105 N108
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0005344
oxygen carrier activity
GO:0019825
oxygen binding
GO:0020037
heme binding
GO:0031720
haptoglobin binding
GO:0031721
hemoglobin alpha binding
GO:0043177
organic acid binding
GO:0046872
metal ion binding
Biological Process
GO:0015671
oxygen transport
GO:0042744
hydrogen peroxide catabolic process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005833
hemoglobin complex
GO:0031838
haptoglobin-hemoglobin complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2d5x
,
PDBe:2d5x
,
PDBj:2d5x
PDBsum
2d5x
PubMed
16403522
UniProt
P02062
|HBB_HORSE Hemoglobin subunit beta (Gene Name=HBB)
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