Structure of PDB 5c1z Chain B Binding Site BS01
Receptor Information
>5c1z Chain B (length=384) Species:
9606
(Homo sapiens) [
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MIVFVRFNSSHGFPVEVDSDTSIFQLKEVVAKRQGVPADQLRVIFAGKEL
RNDWTVQNCDLDQQSIVHIVQRPWRKGQEMNATNSFYVYCKGPCQRVQPG
KLRVQCSTCRQATLTLTQGPSCWDDVLIPNRMSGECQSPHCPGTSAEFFF
KCGAHPTSDKETSVALHLIATNSRNITCITCTDVRSPVLVFQCNSRHVIC
LDCFHLYCVTRLNDRQFVHDPQLGYSLPCVAGCPNSLIKELHHFRILGEE
QYNRYQQYGAEECVLQMGGVLCPRPGCGAGLLPEPDQRKVTCEGNGFAFC
RECKEAYHEGECSAVFEYRVDERAAEQARWEATTKPCPRCHVPVEKNGGC
MHMKCPQPQCRLEWCWNCGCEWNRVCMGDHWFDV
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
5c1z Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5c1z
Disruption of the autoinhibited state primes the E3 ligase parkin for activation and catalysis.
Resolution
1.79 Å
Binding residue
(original residue number in PDB)
C150 C154 C212 H215
Binding residue
(residue number reindexed from 1)
C90 C94 C152 H155
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.3.2.31
: RBR-type E3 ubiquitin transferase.
Gene Ontology
Molecular Function
GO:0004842
ubiquitin-protein transferase activity
GO:0008270
zinc ion binding
Biological Process
GO:0016567
protein ubiquitination
Cellular Component
GO:0005739
mitochondrion
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5c1z
,
PDBe:5c1z
,
PDBj:5c1z
PDBsum
5c1z
PubMed
26254304
UniProt
O60260
|PRKN_HUMAN E3 ubiquitin-protein ligase parkin (Gene Name=PRKN)
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