Structure of PDB 6mke Chain C Binding Site BS01
Receptor Information
>6mke Chain C (length=117) Species:
5763
(Naegleria fowleri) [
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TDWIPISQDQRLKKKIITAGSSDEQPPIGSKVSVHYTGTLTSGKKFDSSL
DRGQPFVFTLGKGEVIRGWDLGVKSMKKGEKSYFEIPSDYAYGNNAIPGL
IPANSTLMFEIELLSWK
Ligand information
Ligand ID
FK5
InChI
InChI=1S/C44H69NO12/c1-10-13-31-19-25(2)18-26(3)20-37(54-8)40-38(55-9)22-28(5)44(52,57-40)41(49)42(50)45-17-12-11-14-32(45)43(51)56-39(29(6)34(47)24-35(31)48)27(4)21-30-15-16-33(46)36(23-30)53-7/h10,19,21,26,28-34,36-40,46-47,52H,1,11-18,20,22-24H2,2-9H3/b25-19+,27-21+/t26-,28+,29+,30-,31+,32-,33+,34-,36+,37-,38-,39+,40+,44+/m0/s1
InChIKey
QJJXYPPXXYFBGM-LFZNUXCKSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC1CC(C2C(CC(C(O2)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C(CC(=O)C(C=C(C1)C)CC=C)O)C)C(=CC4CCC(C(C4)OC)O)C)O)C)OC)OC
CACTVS 3.341
CO[C@@H]1C[C@@H](CC[C@H]1O)/C=C(C)/[C@H]2OC(=O)[C@@H]3CCCCN3C(=O)C(=O)[C@]4(O)O[C@H]([C@H](C[C@@H](C)C\C(=C\[C@@H](CC=C)C(=O)C[C@H](O)[C@H]2C)C)OC)[C@H](C[C@H]4C)OC
ACDLabs 10.04
O=C3C(=O)N1CCCCC1C(=O)OC(C(=C/C2CCC(O)C(OC)C2)/C)C(C)C(O)CC(=O)C(C=C(CC(CC(OC)C4OC3(O)C(C)CC4OC)C)C)C\C=C
OpenEye OEToolkits 1.5.0
C[C@@H]1C[C@@H]([C@@H]2[C@H](C[C@H]([C@@](O2)(C(=O)C(=O)N3CCCC[C@H]3C(=O)O[C@@H]([C@@H]([C@H](CC(=O)[C@@H](\C=C(\C1)/C)CC=C)O)C)/C(=C/[C@@H]4CC[C@H]([C@@H](C4)OC)O)/C)O)C)OC)OC
CACTVS 3.341
CO[CH]1C[CH](CC[CH]1O)C=C(C)[CH]2OC(=O)[CH]3CCCCN3C(=O)C(=O)[C]4(O)O[CH]([CH](C[CH](C)CC(=C[CH](CC=C)C(=O)C[CH](O)[CH]2C)C)OC)[CH](C[CH]4C)OC
Formula
C44 H69 N O12
Name
8-DEETHYL-8-[BUT-3-ENYL]-ASCOMYCIN;
K506
ChEMBL
CHEMBL269732
DrugBank
DB00864
ZINC
ZINC000169289411
PDB chain
6mke Chain C Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
6mke
Crystal Structure of Peptidylprolyl Isomerase from Naegleria fowleri with bound FK506
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
D49 R54 F58 V67 W71 Y94 F111
Binding residue
(residue number reindexed from 1)
D47 R52 F56 V65 W69 Y92 F109
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y38 F48 D49 I68 Y94 F111
Catalytic site (residue number reindexed from 1)
Y36 F46 D47 I66 Y92 F109
Enzyme Commision number
5.2.1.8
: peptidylprolyl isomerase.
Gene Ontology
Molecular Function
GO:0003755
peptidyl-prolyl cis-trans isomerase activity
GO:0016853
isomerase activity
Biological Process
GO:0000413
protein peptidyl-prolyl isomerization
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6mke
,
PDBe:6mke
,
PDBj:6mke
PDBsum
6mke
PubMed
UniProt
A0A2H4A315
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