Structure of PDB 1fkd Chain A Binding Site BS01
Receptor Information
>1fkd Chain A (length=107) Species:
9606
(Homo sapiens) [
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GVQVETISPGDGRTFPKRGQTCVVHYTGMLEDGKKFDSSRDRNKPFKFML
GKQEVIRGWEEGVAQMSVGQRAKLTISPDYAYGATGHPGIIPPHATLVFD
VELLKLE
Ligand information
Ligand ID
818
InChI
InChI=1S/C43H69NO13/c1-10-29-18-23(2)37(48)24(3)19-35(54-8)39-36(55-9)20-26(5)43(52,57-39)40(49)41(50)44-16-12-11-13-30(44)42(51)56-38(27(6)32(46)22-33(29)47)25(4)17-28-14-15-31(45)34(21-28)53-7/h17-18,24,26-32,34-39,45-46,48,52H,10-16,19-22H2,1-9H3/b23-18+,25-17+/t24-,26-,27-,28+,29-,30+,31-,32+,34-,35+,36+,37-,38-,39-,43-/m1/s1
InChIKey
NOQNPBXNHMZMTC-UGTSZWOVSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CCC1C=C(C(C(CC(C2C(CC(C(O2)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C(CC1=O)O)C)C(=CC4CCC(C(C4)OC)O)C)O)C)OC)OC)C)O)C
CACTVS 3.341
CC[C@@H]1/C=C(C)/[C@@H](O)[C@H](C)C[C@H](OC)[C@H]2O[C@](O)([C@H](C)C[C@@H]2OC)C(=O)C(=O)N3CCCC[C@H]3C(=O)O[C@@H]([C@H](C)[C@@H](O)CC1=O)\C(C)=C\[C@@H]4CC[C@@H](O)[C@@H](C4)OC
OpenEye OEToolkits 1.5.0
CC[C@@H]1\C=C(\[C@H]([C@@H](C[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](CC1=O)O)C)/C(=C/[C@@H]4CC[C@H]([C@@H](C4)OC)O)/C)O)C)OC)OC)C)O)/C
CACTVS 3.341
CC[CH]1C=C(C)[CH](O)[CH](C)C[CH](OC)[CH]2O[C](O)([CH](C)C[CH]2OC)C(=O)C(=O)N3CCCC[CH]3C(=O)O[CH]([CH](C)[CH](O)CC1=O)C(C)=C[CH]4CC[CH](O)[CH](C4)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(C(O)C(CC(OC)C4OC3(O)C(C)CC4OC)C)C)CC
Formula
C43 H69 N O13
Name
18-HYDROXYASCOMYCIN;
L-685,818
ChEMBL
DrugBank
ZINC
ZINC000169734975
PDB chain
1fkd Chain A Residue 108 [
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Receptor-Ligand Complex Structure
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PDB
1fkd
FK-506-binding protein: three-dimensional structure of the complex with the antagonist L-685,818.
Resolution
1.72 Å
Binding residue
(original residue number in PDB)
Y26 D37 F46 E54 V55 I56 W59 Y82 F99
Binding residue
(residue number reindexed from 1)
Y26 D37 F46 E54 V55 I56 W59 Y82 F99
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y26 F36 D37 I56 Y82 F99
Catalytic site (residue number reindexed from 1)
Y26 F36 D37 I56 Y82 F99
Enzyme Commision number
5.2.1.8
: peptidylprolyl isomerase.
Gene Ontology
Molecular Function
GO:0003755
peptidyl-prolyl cis-trans isomerase activity
GO:0005160
transforming growth factor beta receptor binding
GO:0005515
protein binding
GO:0005527
macrolide binding
GO:0005528
FK506 binding
GO:0016247
channel regulator activity
GO:0030547
signaling receptor inhibitor activity
GO:0034713
type I transforming growth factor beta receptor binding
GO:0044325
transmembrane transporter binding
GO:0070411
I-SMAD binding
GO:0070697
activin receptor binding
Biological Process
GO:0000413
protein peptidyl-prolyl isomerization
GO:0003007
heart morphogenesis
GO:0006457
protein folding
GO:0006458
'de novo' protein folding
GO:0014809
regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion
GO:0022417
protein maturation by protein folding
GO:0030512
negative regulation of transforming growth factor beta receptor signaling pathway
GO:0032092
positive regulation of protein binding
GO:0032880
regulation of protein localization
GO:0032926
negative regulation of activin receptor signaling pathway
GO:0042026
protein refolding
GO:0042110
T cell activation
GO:0043123
positive regulation of canonical NF-kappaB signal transduction
GO:0050776
regulation of immune response
GO:0055010
ventricular cardiac muscle tissue morphogenesis
GO:0060314
regulation of ryanodine-sensitive calcium-release channel activity
GO:0060347
heart trabecula formation
GO:0070588
calcium ion transmembrane transport
GO:0097435
supramolecular fiber organization
GO:1902991
regulation of amyloid precursor protein catabolic process
GO:1990000
amyloid fibril formation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0014802
terminal cisterna
GO:0016020
membrane
GO:0016529
sarcoplasmic reticulum
GO:0030018
Z disc
GO:0033017
sarcoplasmic reticulum membrane
GO:0098562
cytoplasmic side of membrane
GO:1990425
ryanodine receptor complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1fkd
,
PDBe:1fkd
,
PDBj:1fkd
PDBsum
1fkd
PubMed
7684380
UniProt
P62942
|FKB1A_HUMAN Peptidyl-prolyl cis-trans isomerase FKBP1A (Gene Name=FKBP1A)
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