Structure of PDB 5j3x Chain F Binding Site BS02
Receptor Information
>5j3x Chain F (length=384) Species:
9606
(Homo sapiens) [
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TVDKKMVEKCWKLMDKVVRLCQNPKLALKNSPPYILDLLPDTYQHLRTIL
SRYEGKMETLGENEYFRVFMENLMKKTKQTISLFKEGKERMYEENSQPRR
NLTKLSLIFSHMLAELKGIFPSGLFQGDTFRITKADAAEFWRKAFGEKTI
VPWKSFRQALHEVHPISSGLEAMALKSTIDLTCNDYISVFEFDIFTRLFQ
PWSSLLRNWNSLAVTHPGYMAFLTYDEVKARLQKFIHKPGSYIFRLSCTR
LGQWAIGYVTADGNILQTIPHNKPLFQALIDGFREGFYLFPDGRNQNPDL
TGLCEPTDHIKVTQEQYELFCEMGSTFQLCKICAENDKDVKIEPCGHLMC
TSCLTSWQESEGQGCPFCRCEIKGTEPIVVDPFD
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
5j3x Chain F Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
5j3x
Casitas B-lineage lymphoma linker helix mutations found in myeloproliferative neoplasms affect conformation.
Resolution
2.822 Å
Binding residue
(original residue number in PDB)
C396 H398 C416 C419
Binding residue
(residue number reindexed from 1)
C345 H347 C365 C368
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.3.2.27
: RING-type E3 ubiquitin transferase.
Gene Ontology
Molecular Function
GO:0001784
phosphotyrosine residue binding
GO:0004842
ubiquitin-protein transferase activity
GO:0005509
calcium ion binding
GO:0046872
metal ion binding
Biological Process
GO:0007166
cell surface receptor signaling pathway
GO:0023051
regulation of signaling
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5j3x
,
PDBe:5j3x
,
PDBj:5j3x
PDBsum
5j3x
PubMed
27609087
UniProt
P22681
|CBL_HUMAN E3 ubiquitin-protein ligase CBL (Gene Name=CBL)
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