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Structure of PDB 6ph4 Chain B Binding Site BS03

Receptor Information
>6ph4 Chain B (length=460) Species: 224914 (Brucella melitensis bv. 1 str. 16M) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
QATDPFRAAVEFTLMPMLITNPHLPDNPIVFANPAFLKLTGYEADEVMGR
NCRFLQGHGTDPAHVRAIKSAIAAEKPIDIDIINYKKSGEAFWNRLHISP
VHNANGRLQHFVSSQLDVTLELSRLVELEKERKTLSIETARSKDQLDYIV
EVANIGFWTREFYSGKMTCSAECRRIYGFTPDEPVHFDTILDLVVLEDRM
TVVQKAHQAVTGEPYSIEYRIVTRLGETRWLETRAKALTGENPLVLGIVQ
DVTERKKAEANKALVSREIAHRFKNSMAMVQSIANQTLRNTYDPEQANRL
FSERLRALSQAHDMLLKENWAGATIQQICATALAPFNSTFANRIHMSGPH
LLVSDRVTVALSLAFYELATNAVKYGALSNEKGVINITWAIMEDKGEKKF
HMRWAESRGPEVMQPARRGFGQRLLHSVLAEELKAKCDVEFAASGLLIDV
LAPITPEVFP
Ligand information
Ligand IDACP
InChIInChI=1S/C11H18N5O12P3/c12-9-6-10(14-2-13-9)16(3-15-6)11-8(18)7(17)5(27-11)1-26-31(24,25)28-30(22,23)4-29(19,20)21/h2-3,5,7-8,11,17-18H,1,4H2,(H,22,23)(H,24,25)(H2,12,13,14)(H2,19,20,21)/t5-,7-,8-,11-/m1/s1
InChIKeyUFZTZBNSLXELAL-IOSLPCCCSA-N
SMILES
SoftwareSMILES
CACTVS 3.341Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)C[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04O=P(O)(O)CP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(CP(=O)(O)O)O)O)O)N
OpenEye OEToolkits 1.5.0c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(CP(=O)(O)O)O)O)O)N
CACTVS 3.341Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@](O)(=O)C[P](O)(O)=O)[C@@H](O)[C@H]3O
FormulaC11 H18 N5 O12 P3
NamePHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER;
ADENOSINE-5'-[BETA, GAMMA-METHYLENE]TRIPHOSPHATE
ChEMBLCHEMBL133463
DrugBankDB03909
ZINCZINC000008295124
PDB chain6ph4 Chain B Residue 505 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB6ph4 Dimer Asymmetry and Light Activation Mechanism in Brucella Blue-Light Sensor Histidine Kinase.
Resolution3.25 Å
Binding residue
(original residue number in PDB)
R321 N388 K391 Y392 E423 P432 G436 F437 G438 L463
Binding residue
(residue number reindexed from 1)
R304 N371 K374 Y375 E406 P415 G419 F420 G421 L446
Annotation score1
Enzymatic activity
Enzyme Commision number 2.7.13.3: histidine kinase.
Gene Ontology
Molecular Function
GO:0004673 protein histidine kinase activity
GO:0005524 ATP binding
GO:0009881 photoreceptor activity
GO:0016301 kinase activity
Biological Process
GO:0016310 phosphorylation
GO:0018106 peptidyl-histidine phosphorylation

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:6ph4, PDBe:6ph4, PDBj:6ph4
PDBsum6ph4
PubMed33879593
UniProtQ8YC53|LOVHK_BRUME Blue-light-activated histidine kinase (Gene Name=BMEII0679)

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