Structure of PDB 3kaf Chain A Binding Site BS01
Receptor Information
>3kaf Chain A (length=145) Species:
9606
(Homo sapiens) [
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LPPGWEKAMSRSSGRVYYFNHITNASQWERPSEPARVRCSHLLVKHSQSR
RPSSWRQEKITRTKEEALELINGYIQKIKSGEEDFESLASQFSDCSSAKA
RGDLGAFSRGQMAKPFEDASFALRTGEMSGPVFTDSGIHIILRTE
Ligand information
Ligand ID
4D9
InChI
InChI=1S/C19H15N3O3S/c23-18(16-9-11-5-1-4-8-15(11)26-16)22-14(19(24)25)10-17-20-12-6-2-3-7-13(12)21-17/h1-9,14H,10H2,(H,20,21)(H,22,23)(H,24,25)/t14-/m1/s1
InChIKey
OEMQUBXYMQNIGH-CQSZACIVSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
c1ccc2c(c1)cc(s2)C(=O)NC(Cc3[nH]c4ccccc4n3)C(=O)O
CACTVS 3.352
OC(=O)[C@@H](Cc1[nH]c2ccccc2n1)NC(=O)c3sc4ccccc4c3
OpenEye OEToolkits 1.7.0
c1ccc2c(c1)cc(s2)C(=O)N[C@H](Cc3[nH]c4ccccc4n3)C(=O)O
CACTVS 3.352
OC(=O)[CH](Cc1[nH]c2ccccc2n1)NC(=O)c3sc4ccccc4c3
ACDLabs 11.02
O=C(O)C(NC(=O)c2sc1ccccc1c2)Cc4nc3ccccc3n4
Formula
C19 H15 N3 O3 S
Name
3-(1H-benzimidazol-2-yl)-N-(1-benzothiophen-2-ylcarbonyl)-D-alanine;
(R)-2-[(Benzo[b]thiophene-2-carbonyl)-amino]-3-(1H-benzoimidazol-2-yl)-propionic acid
ChEMBL
CHEMBL609887
DrugBank
ZINC
ZINC000044460290
PDB chain
3kaf Chain A Residue 164 [
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Receptor-Ligand Complex Structure
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PDB
3kaf
Structure-guided design of alpha-amino acid-derived Pin1 inhibitors
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
H59 K63 C113 S114 L122 M130 F134 S154 H157
Binding residue
(residue number reindexed from 1)
H41 K45 C95 S96 L104 M112 F116 S136 H139
Annotation score
1
Binding affinity
MOAD
: ic50=0.83uM
PDBbind-CN
: -logKd/Ki=6.08,IC50=0.83uM
BindingDB: IC50=830nM,Kd=10000nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H59 C113 A131 S154 H157
Catalytic site (residue number reindexed from 1)
H41 C95 A113 S136 H139
Enzyme Commision number
5.2.1.8
: peptidylprolyl isomerase.
Gene Ontology
Molecular Function
GO:0003755
peptidyl-prolyl cis-trans isomerase activity
GO:0003774
cytoskeletal motor activity
GO:0005515
protein binding
GO:0008013
beta-catenin binding
GO:0016859
cis-trans isomerase activity
GO:0031434
mitogen-activated protein kinase kinase binding
GO:0032794
GTPase activating protein binding
GO:0048156
tau protein binding
GO:0050815
phosphoserine residue binding
GO:0050816
phosphothreonine residue binding
GO:0051219
phosphoprotein binding
GO:1990757
ubiquitin ligase activator activity
Biological Process
GO:0000413
protein peptidyl-prolyl isomerization
GO:0001666
response to hypoxia
GO:0001932
regulation of protein phosphorylation
GO:0001934
positive regulation of protein phosphorylation
GO:0007088
regulation of mitotic nuclear division
GO:0010468
regulation of gene expression
GO:0030182
neuron differentiation
GO:0030512
negative regulation of transforming growth factor beta receptor signaling pathway
GO:0031647
regulation of protein stability
GO:0032091
negative regulation of protein binding
GO:0032092
positive regulation of protein binding
GO:0032465
regulation of cytokinesis
GO:0042177
negative regulation of protein catabolic process
GO:0043547
positive regulation of GTPase activity
GO:0045944
positive regulation of transcription by RNA polymerase II
GO:0046785
microtubule polymerization
GO:0050808
synapse organization
GO:0050821
protein stabilization
GO:0060255
regulation of macromolecule metabolic process
GO:0060392
negative regulation of SMAD protein signal transduction
GO:0070373
negative regulation of ERK1 and ERK2 cascade
GO:0080090
regulation of primary metabolic process
GO:0090263
positive regulation of canonical Wnt signaling pathway
GO:1900180
regulation of protein localization to nucleus
GO:1902430
negative regulation of amyloid-beta formation
GO:2000146
negative regulation of cell motility
Cellular Component
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016607
nuclear speck
GO:0030496
midbody
GO:0036064
ciliary basal body
GO:0098978
glutamatergic synapse
GO:0099524
postsynaptic cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3kaf
,
PDBe:3kaf
,
PDBj:3kaf
PDBsum
3kaf
PubMed
19969456
UniProt
Q13526
|PIN1_HUMAN Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (Gene Name=PIN1)
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