Structure of PDB 2iae Chain F Binding Site BS02
Receptor Information
>2iae Chain F (length=291) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
KVFTKELDQWIEQLNECKQLSESQVKSLCEKAKEILTKESNVQEVRCPVT
VCGDVHGQFHDLMELFRIGGKSPDTNYLFMGDYVNRGYYSVETVTLLVAL
KVRYRERITILRGNHESRQITQVYGFYDECLRKYGNANVWKYFTDLFDYL
PLTALVDGQIFCLHGGLSPSIDTLDHIRALDRLQEVPHEGPMCDLLWSDP
DDRGGWGISPRGAGYTFGQDISETFNHANGLTLVSRAHQLVMEGYNWCHD
RNVVTIFSAPNYCYRCGNQAAIMELDDTLKYSFLQFDPAPR
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
2iae Chain F Residue 310 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
2iae
Crystal structure of a protein phosphatase 2A heterotrimeric holoenzyme.
Resolution
3.5 Å
Binding residue
(original residue number in PDB)
D57 H59 D85 H118
Binding residue
(residue number reindexed from 1)
D54 H56 D82 H115
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D57 H59 D85 N88 R89 N117 H118 H167 R214 H241
Catalytic site (residue number reindexed from 1)
D54 H56 D82 N85 R86 N114 H115 H164 R211 H238
Enzyme Commision number
3.1.3.16
: protein-serine/threonine phosphatase.
Gene Ontology
Molecular Function
GO:0004721
phosphoprotein phosphatase activity
GO:0004722
protein serine/threonine phosphatase activity
GO:0004725
protein tyrosine phosphatase activity
GO:0005515
protein binding
GO:0016787
hydrolase activity
GO:0017018
myosin phosphatase activity
GO:0046872
metal ion binding
GO:0046982
protein heterodimerization activity
GO:0048156
tau protein binding
GO:0050811
GABA receptor binding
Biological Process
GO:0000278
mitotic cell cycle
GO:0001932
regulation of protein phosphorylation
GO:0006470
protein dephosphorylation
GO:0007498
mesoderm development
GO:0010288
response to lead ion
GO:0010719
negative regulation of epithelial to mesenchymal transition
GO:0035331
negative regulation of hippo signaling
GO:0035556
intracellular signal transduction
GO:0035970
peptidyl-threonine dephosphorylation
GO:0040008
regulation of growth
GO:0043029
T cell homeostasis
GO:0045595
regulation of cell differentiation
GO:0051321
meiotic cell cycle
GO:0051898
negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
GO:0070262
peptidyl-serine dephosphorylation
GO:0071902
positive regulation of protein serine/threonine kinase activity
GO:1900227
positive regulation of NLRP3 inflammasome complex assembly
GO:1904526
regulation of microtubule binding
GO:1904528
positive regulation of microtubule binding
GO:1904539
negative regulation of glycolytic process through fructose-6-phosphate
GO:2000045
regulation of G1/S transition of mitotic cell cycle
Cellular Component
GO:0000159
protein phosphatase type 2A complex
GO:0000775
chromosome, centromeric region
GO:0000922
spindle pole
GO:0005634
nucleus
GO:0005694
chromosome
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0005856
cytoskeleton
GO:0005886
plasma membrane
GO:0008287
protein serine/threonine phosphatase complex
GO:0015630
microtubule cytoskeleton
GO:0016020
membrane
GO:0045121
membrane raft
GO:0045202
synapse
GO:0070062
extracellular exosome
GO:0090443
FAR/SIN/STRIPAK complex
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2iae
,
PDBe:2iae
,
PDBj:2iae
PDBsum
2iae
PubMed
17086192
UniProt
P67775
|PP2AA_HUMAN Serine/threonine-protein phosphatase 2A catalytic subunit alpha isoform (Gene Name=PPP2CA)
[
Back to BioLiP
]