Structure of PDB 7krz Chain F Binding Site BS01
Receptor Information
>7krz Chain F (length=512) Species:
9606
(Homo sapiens) [
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KFRERLKELVVPKHVMDVVDEELSKLGLLDNHSSEFNVTRNYLDWLTSIP
WGKYSNENLDLARAQAVLEEDHYGMEDVKKRILEFIAVSQLRGSTQGKIL
CFYGPPGVGKTSIARSIARALNREYFRFSVGAEIKGHRRTYVGAMPGKII
QCLKKTKTENPLILIDEVDKIGDPSSALLELLDPEQNANFLDHYLDVPVD
LSKVLFICTANVTDTIPEPLRDRMEMINVSGYVAQEKLAIAERYLVPQAR
ALCGLDESKAKLSSDVLTLLIKQYCRESGVRNLQKQVEKVLRKSAYKIVS
GEAESVEVTPENLQDFVGKPVFTVERMYDVTPPGVVMGLAWTAMGGSTLF
VETSLRRPQDKDGSLEVTGQLGEVMKESARIAYTFARAFLMQHAPANDYL
VTSHIHLHVPEGATPKDGPSAGCTIVTALLSLAMGRPVRQNLAMTGEVSL
TGKILPVGGIKEKTIAAKRAGVTCIVLPAENKKDFYDLAAFITEGLEVHF
VEHYREIFDIAF
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
7krz Chain F Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
7krz
Structures of the human LONP1 protease reveal regulatory steps involved in protease activation.
Resolution
3.2 Å
Binding residue
(original residue number in PDB)
H491 Y492 V527 G528 K529 T530 I669 Y673 V709
Binding residue
(residue number reindexed from 1)
H72 Y73 V108 G109 K110 T111 I240 Y244 V280
Annotation score
5
Enzymatic activity
Enzyme Commision number
3.4.21.53
: endopeptidase La.
Gene Ontology
Molecular Function
GO:0004176
ATP-dependent peptidase activity
GO:0004252
serine-type endopeptidase activity
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
Biological Process
GO:0006508
proteolysis
GO:0030163
protein catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:7krz
,
PDBe:7krz
,
PDBj:7krz
PDBsum
7krz
PubMed
34050165
UniProt
P36776
|LONM_HUMAN Lon protease homolog, mitochondrial (Gene Name=LONP1)
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