Structure of PDB 2okl Chain B Binding Site BS02
Receptor Information
>2okl Chain B (length=184) Species:
226900
(Bacillus cereus ATCC 14579) [
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MLTMKDVIREGDPILRNVAEEVSLPASEEDTTTLKEMIEFVINSQDPEMA
EKYSLRPGIGLAAPQIGVSKKMIAVHVTDADGTLYSHALFNPKIISHSVE
RTYLQGGEGCLSVDREVPGYVPRYTRITVKATSINGEEVKLRLKGLPAIV
FQHEIDHLNGVMFYDHINKENPFAAPDDSKPLER
Ligand information
Ligand ID
BB2
InChI
InChI=1S/C19H35N3O5/c1-4-5-6-8-14(11-16(24)21-27)18(25)20-17(13(2)3)19(26)22-10-7-9-15(22)12-23/h13-15,17,23,27H,4-12H2,1-3H3,(H,20,25)(H,21,24)/t14-,15+,17+/m1/s1
InChIKey
XJLATMLVMSFZBN-VYDXJSESSA-N
SMILES
Software
SMILES
CACTVS 3.341
CCCCC[CH](CC(=O)NO)C(=O)N[CH](C(C)C)C(=O)N1CCC[CH]1CO
OpenEye OEToolkits 1.5.0
CCCCCC(CC(=O)NO)C(=O)NC(C(C)C)C(=O)N1CCCC1CO
ACDLabs 10.04
O=C(N1C(CO)CCC1)C(NC(=O)C(CC(=O)NO)CCCCC)C(C)C
CACTVS 3.341
OpenEye OEToolkits 1.5.0
CCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1CO
Formula
C19 H35 N3 O5
Name
ACTINONIN;
2-[(FORMYL-HYDROXY-AMINO)-METHYL]-HEPTANOIC ACID [1-(2-HYDROXYMETHYL-PYRROLIDINE-1-CARBONYL)-2-METHYL-PROPYL]-AMIDE
ChEMBL
CHEMBL308333
DrugBank
DB04310
ZINC
ZINC000003979014
PDB chain
2okl Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
2okl
Characterization of Peptide Deformylase2 from B. cereus
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
Q105 R184
Binding residue
(residue number reindexed from 1)
Q105 R184
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G60 Q65 C110 L111 H153 E154 H157
Catalytic site (residue number reindexed from 1)
G60 Q65 C110 L111 H153 E154 H157
Enzyme Commision number
3.5.1.88
: peptide deformylase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0042586
peptide deformylase activity
GO:0046872
metal ion binding
Biological Process
GO:0006412
translation
GO:0043686
co-translational protein modification
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:2okl
,
PDBe:2okl
,
PDBj:2okl
PDBsum
2okl
PubMed
18047803
UniProt
Q819K2
|DEF2_BACCR Peptide deformylase 2 (Gene Name=def2)
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