Structure of PDB 4ni0 Chain B Binding Site BS03

Receptor Information
>4ni0 Chain B (length=146) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
VHLTPEEKSAVTALWGKVNVDEVGGEALGRLLVVYPWTQRFFESFGDLST
PDAVMGNPKVKAHGKKVLGAFSDGLAHLDNLKGTFATLSELHCDKLHVDP
ENFRLLGNVLVCVLAHHFGKEFTPPVQAAYQKVVAGVANALAHKYH
Ligand information
Ligand ID2P3
InChIInChI=1S/C10H9N3O2S/c16-10-11-9(12-13-10)8-5-14-6-3-1-2-4-7(6)15-8/h1-4,8H,5H2,(H2,11,12,13,16)/t8-/m1/s1
InChIKeyWDUGNJIRKJHDNF-MRVPVSSYSA-N
SMILES
SoftwareSMILES
CACTVS 3.385S=C1NN=C(N1)[CH]2COc3ccccc3O2
ACDLabs 12.01S=C1NN=C(N1)C2Oc3ccccc3OC2
OpenEye OEToolkits 1.7.6c1ccc2c(c1)OC[C@@H](O2)C3=NNC(=S)N3
CACTVS 3.385S=C1NN=C(N1)[C@H]2COc3ccccc3O2
OpenEye OEToolkits 1.7.6c1ccc2c(c1)OCC(O2)C3=NNC(=S)N3
FormulaC10 H9 N3 O2 S
Name5-[(2S)-2,3-dihydro-1,4-benzodioxin-2-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione
ChEMBL
DrugBank
ZINCZINC000013556315
PDB chain4ni0 Chain B Residue 204 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB4ni0 Identification of a Small Molecule that Increases Hemoglobin Oxygen Affinity and Reduces SS Erythrocyte Sickling.
Resolution2.15 Å
Binding residue
(original residue number in PDB)
Y35 E101 R104 L105 N108 V109 C112
Binding residue
(residue number reindexed from 1)
Y35 E101 R104 L105 N108 V109 C112
Annotation score1
Enzymatic activity
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0004601 peroxidase activity
GO:0005344 oxygen carrier activity
GO:0005515 protein binding
GO:0019825 oxygen binding
GO:0020037 heme binding
GO:0030492 hemoglobin binding
GO:0031720 haptoglobin binding
GO:0031721 hemoglobin alpha binding
GO:0043177 organic acid binding
GO:0046872 metal ion binding
Biological Process
GO:0008217 regulation of blood pressure
GO:0015670 carbon dioxide transport
GO:0015671 oxygen transport
GO:0030185 nitric oxide transport
GO:0042542 response to hydrogen peroxide
GO:0042744 hydrogen peroxide catabolic process
GO:0045429 positive regulation of nitric oxide biosynthetic process
GO:0070293 renal absorption
GO:0070527 platelet aggregation
GO:0097746 blood vessel diameter maintenance
GO:0098869 cellular oxidant detoxification
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005829 cytosol
GO:0005833 hemoglobin complex
GO:0031838 haptoglobin-hemoglobin complex
GO:0070062 extracellular exosome
GO:0071682 endocytic vesicle lumen
GO:0072562 blood microparticle
GO:1904724 tertiary granule lumen
GO:1904813 ficolin-1-rich granule lumen

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:4ni0, PDBe:4ni0, PDBj:4ni0
PDBsum4ni0
PubMed25061917
UniProtP68871|HBB_HUMAN Hemoglobin subunit beta (Gene Name=HBB)

[Back to BioLiP]