Structure of PDB 3mfv Chain B Binding Site BS03

Receptor Information
>3mfv Chain B (length=313) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
RTIGIIGAPFSKGQPRGGVEEGPTVLRKAGLLEKLKEQECDVKDYGDLPF
ADIPNDSPFQIVKNPRSVGKASEQLAGKVAEVKKNGRISLVLGGDHSLAI
GSISGHARVHPDLGVIWVDAHTDINTPLTTTSGNLHGQPVSFLLKELKGK
IPDVPGFSWVTPCISAKDIVYIGLRDVDPGEHYILKTLGIKYFSMTEVDR
LGIGKVMEETLSYLLGRKKRPIHLSFDVDGLDPSFTPATGTPVVGGLTYR
EGLYITEEIYKTGLLSGLDIMEVNPSLGKTPEEVTRTVNTAVAITLACFG
LAREGNHKPIDYL
Ligand information
Ligand IDZ70
InChIInChI=1S/C7H12N4O2/c8-5(6(12)13)2-1-4-3-10-7(9)11-4/h3,5H,1-2,8H2,(H,12,13)(H3,9,10,11)/t5-/m0/s1
InChIKeyFXIIKDXCDODGRI-YFKPBYRVSA-N
SMILES
SoftwareSMILES
CACTVS 3.370N[C@@H](CCc1[nH]c(N)nc1)C(O)=O
ACDLabs 12.01O=C(O)C(N)CCc1cnc(N)n1
OpenEye OEToolkits 1.7.0c1c([nH]c(n1)N)CC[C@@H](C(=O)O)N
CACTVS 3.370N[CH](CCc1[nH]c(N)nc1)C(O)=O
OpenEye OEToolkits 1.7.0c1c([nH]c(n1)N)CCC(C(=O)O)N
FormulaC7 H12 N4 O2
Name(2S)-2-amino-4-(2-amino-1H-imidazol-5-yl)butanoic acid;
2-aminohomohistidine
ChEMBLCHEMBL1099168
DrugBank
ZINCZINC000049089469
PDB chain3mfv Chain B Residue 323 [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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PDB3mfv 2-aminoimidazole amino acids as inhibitors of the binuclear manganese metalloenzyme human arginase I.
Resolution1.9 Å
Binding residue
(original residue number in PDB)		H126 D128 N130 S137 H141 D183 D232 D234 T246
Binding residue
(residue number reindexed from 1)		H121 D123 N125 S132 H136 D178 D227 D229 T241
Annotation score1
Binding affinityMOAD: Ki=3000uM
BindingDB: Ki=3000000nM
Enzymatic activity
Catalytic site (original residue number in PDB) H101 D124 H126 D128 H141 D232 D234 E277
Catalytic site (residue number reindexed from 1) H96 D119 H121 D123 H136 D227 D229 E272
Enzyme Commision number 3.5.3.1: arginase.
Gene Ontology
Molecular Function
GO:0004053 arginase activity
GO:0005515 protein binding
GO:0016787 hydrolase activity
GO:0016813 hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines
GO:0030145 manganese ion binding
GO:0046872 metal ion binding
Biological Process
GO:0000050 urea cycle
GO:0002250 adaptive immune response
GO:0006525 arginine metabolic process
GO:0006527 arginine catabolic process
GO:0009624 response to nematode
GO:0019547 arginine catabolic process to ornithine
GO:0042130 negative regulation of T cell proliferation
GO:0042832 defense response to protozoan
GO:0045087 innate immune response
GO:0046007 negative regulation of activated T cell proliferation
GO:0060336 negative regulation of type II interferon-mediated signaling pathway
GO:0070965 positive regulation of neutrophil mediated killing of fungus
GO:2000552 negative regulation of T-helper 2 cell cytokine production
Cellular Component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0035578 azurophil granule lumen
GO:0035580 specific granule lumen

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Molecular Function
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Biological Process
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Cellular Component
External links
PDB RCSB:3mfv, PDBe:3mfv, PDBj:3mfv
PDBsum3mfv
PubMed20441173
UniProtP05089|ARGI1_HUMAN Arginase-1 (Gene Name=ARG1)

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