Structure of PDB 1xr1 Chain A Binding Site BS02
Receptor Information
>1xr1 Chain A (length=277) Species:
9606
(Homo sapiens) [
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EPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELP
NGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILERPEPVQDLFD
FITERGALQEELARSFFWQVLEAVRHCHNCGVLHRDIKDENILIDLNRGE
LKLIDFGSGALLKDTVYTDFDGTRVYSPPEWIRYHRYHGRSAAVWSLGIL
LYDMVCGDIPFEHDEEIIRGQVFFRQRVSSECQHLIRWCLALRPSDRPTF
EEIQNHPWMQDVLLPQETAEIHLHSLS
Ligand information
Ligand ID
ANP
InChI
InChI=1S/C10H17N6O12P3/c11-8-5-9(13-2-12-8)16(3-14-5)10-7(18)6(17)4(27-10)1-26-31(24,25)28-30(22,23)15-29(19,20)21/h2-4,6-7,10,17-18H,1H2,(H,24,25)(H2,11,12,13)(H4,15,19,20,21,22,23)/t4-,6-,7-,10-/m1/s1
InChIKey
PVKSNHVPLWYQGJ-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(NP(=O)(O)O)O)O)O)N
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)N[P](O)(O)=O)[CH](O)[CH]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(=O)N[P](O)(O)=O)[C@@H](O)[C@H]3O
ACDLabs 12.01
O=P(O)(O)NP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.7.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(NP(=O)(O)O)O)O)O)N
Formula
C10 H17 N6 O12 P3
Name
PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER
ChEMBL
CHEMBL1230989
DrugBank
ZINC
ZINC000008660410
PDB chain
1xr1 Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
1xr1
Structural Basis of Constitutive Activity and a Unique Nucleotide Binding Mode of Human Pim-1 Kinase.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
V52 A65 K67 R122 L174 D186
Binding residue
(residue number reindexed from 1)
V21 A34 K36 R91 L143 D155
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
D167 K169 N172 D186 L193 T204
Catalytic site (residue number reindexed from 1)
D136 K138 N141 D155 L162 T173
Enzyme Commision number
2.7.11.1
: non-specific serine/threonine protein kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004674
protein serine/threonine kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0008134
transcription factor binding
GO:0030145
manganese ion binding
GO:0043024
ribosomal small subunit binding
GO:0044024
histone H2AS1 kinase activity
GO:0046872
metal ion binding
GO:0106310
protein serine kinase activity
Biological Process
GO:0006338
chromatin remodeling
GO:0006468
protein phosphorylation
GO:0006915
apoptotic process
GO:0016310
phosphorylation
GO:0022898
regulation of transmembrane transporter activity
GO:0043066
negative regulation of apoptotic process
GO:0043433
negative regulation of DNA-binding transcription factor activity
GO:0045824
negative regulation of innate immune response
GO:0045893
positive regulation of DNA-templated transcription
GO:0046777
protein autophosphorylation
GO:0050821
protein stabilization
GO:0060045
positive regulation of cardiac muscle cell proliferation
GO:0070561
vitamin D receptor signaling pathway
GO:0071346
cellular response to type II interferon
GO:0090336
positive regulation of brown fat cell differentiation
GO:1902033
regulation of hematopoietic stem cell proliferation
GO:1904263
positive regulation of TORC1 signaling
GO:1905062
positive regulation of cardioblast proliferation
GO:1990748
cellular detoxification
Cellular Component
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005730
nucleolus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005886
plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1xr1
,
PDBe:1xr1
,
PDBj:1xr1
PDBsum
1xr1
PubMed
15525646
UniProt
P11309
|PIM1_HUMAN Serine/threonine-protein kinase pim-1 (Gene Name=PIM1)
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