Structure of PDB 1u6r Chain B Binding Site BS01
Receptor Information
>1u6r Chain B (length=380) Species:
9986
(Oryctolagus cuniculus) [
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PFGNTHNKYKLNYKSEEEYPDLSKHNNHMAKVLTPDLYKKLRDKETPSGF
TLDDVIQTGVDNPGHPFIMTVGCVAGDEESYTVFKDLFDPIIQDRHGGFK
PTDKHKTDLNHENLKGGDDLDPHYVLSSRVRTGKSIKGYTLPPHCSRGER
RAVEKLSVEALNSLTGEFKGKYYPLKSMTEQEQQQLIDDHFLFDKPVSPL
LLASGMARDWPDARGIWHNDNKSFLVWVNEEDHLRVISMEKGGNMKEVFR
RFCVGLQKIEEIFKKAGHPFMWNEHLGYVLTCPSNLGTGLRGGVHVKLAH
LSKHPKFEEILTRLRLQKRGTGGVDTAAVGSVFDISNADRLGSSEVEQVQ
LVVDGVKLMVEMEKKLEKGQSIDDMIPAQK
Ligand information
Ligand ID
NO3
InChI
InChI=1S/NO3/c2-1(3)4/q-1
InChIKey
NHNBFGGVMKEFGY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
[O-][N+]([O-])=O
OpenEye OEToolkits 1.5.0
[N+](=O)([O-])[O-]
Formula
N O3
Name
NITRATE ION
ChEMBL
CHEMBL186200
DrugBank
DB14049
ZINC
PDB chain
1u6r Chain B Residue 1701 [
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Receptor-Ligand Complex Structure
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PDB
1u6r
Structural asymmetry and intersubunit communication in muscle creatine kinase
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
R131 E231 R235 R319
Binding residue
(residue number reindexed from 1)
R131 E231 R235 R319
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R131 E231 R235 C282 S284 R291 R319 V324
Catalytic site (residue number reindexed from 1)
R131 E231 R235 C282 S284 R291 R319 V324
Enzyme Commision number
2.7.3.2
: creatine kinase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004111
creatine kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016772
transferase activity, transferring phosphorus-containing groups
Biological Process
GO:0009408
response to heat
GO:0016310
phosphorylation
GO:0046314
phosphocreatine biosynthetic process
Cellular Component
GO:0005615
extracellular space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1u6r
,
PDBe:1u6r
,
PDBj:1u6r
PDBsum
1u6r
PubMed
17327675
UniProt
P00563
|KCRM_RABIT Creatine kinase M-type (Gene Name=CKM)
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