Structure of PDB 1vrp Chain B Binding Site BS01
Receptor Information
>1vrp Chain B (length=374) Species:
7787
(Tetronarce californica) [
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NKWKLNYSAAEEFPDLSKHNNHMAKALTLDIYKKLRDKETPSGFTLDDII
QTGVDNPGHPFIMTVGCVAGDEECYEVFKDLFDPVIEDRHGGYKPTDKHK
TDLNQENLKGGDDLDPNYVLSSRVRTGRSIKGIALPPHCSRGERRLVEKL
CIDGLATLTGEFQGKYYPLSSMSDAEQQQLIDDHFLFDKPISPLLLASGM
ARDWPDGRGIWHNNDKTFLVWVNEEDHLRVISMQKGGNMKEVFRRFCVGL
KKIEDIFVKAGRGFMWNEHLGYVLTCPSNLGTGLRGGVHVKIPHLCKHEK
FSEVLKRTRLQKRGTGGVDTAAVGSIYDISNADRLGFSEVEQVQMVVDGV
KLMVEMEKRLENGKSIDDLMPAQK
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
1vrp Chain B Residue 405 [
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Receptor-Ligand Complex Structure
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PDB
1vrp
The 2.1 A Structure of Torpedo californica Creatine Kinase Complexed with the ADP-Mg(2+)-NO3(-)-Creatine Transition-State Analogue Complex
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
R236 R320
Binding residue
(residue number reindexed from 1)
R229 R313
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R132 E232 R236 C283 S285 R292 R320 V325
Catalytic site (residue number reindexed from 1)
R125 E225 R229 C276 S278 R285 R313 V318
Enzyme Commision number
2.7.3.2
: creatine kinase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004111
creatine kinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016772
transferase activity, transferring phosphorus-containing groups
Biological Process
GO:0016310
phosphorylation
GO:0046314
phosphocreatine biosynthetic process
Cellular Component
GO:0005615
extracellular space
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1vrp
,
PDBe:1vrp
,
PDBj:1vrp
PDBsum
1vrp
PubMed
12437342
UniProt
P04414
|KCRM_TETCF Creatine kinase M-type
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