Structure of PDB 1iyk Chain A Binding Site BS02
Receptor Information
>1iyk Chain A (length=392) Species:
5476
(Candida albicans) [
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EGPIDKLKTPEDVPNDPLPLISDFEWSTLDIDDNLQLDELYKLLYDNYVE
DIDATFRFKYSHEFFQWALKPPGWRKDWHVGVRVKSTGKLVAFIAATPVT
FKLNKSNKVIDSVEINFLCIHKKLRNKRLAPVLIKEITRRVNKQNIWQAL
YTGGSILPTPLTTCRYQHRPINWSKLHDVGFSHLPPNQTKSSMVASYTLP
NNPKLKGLRPMTGKDVSTVLSLLYKYQERFDIVQLFTEEEFKHWMLGHDE
NSDSNVVKSYVVEDENGIITDYFSYYLLPFTVLDNAQHDELGIAYLFYYA
SDSFEKPNYKKRLNELITDALITSKKFGVDVFNCLTCQDNTYFLKDCKFG
SGDGFLNYYLFNYRTFPMDGGIDKKTKEVVEDQTSGIGVVLL
Ligand information
Ligand ID
MIM
InChI
InChI=1S/C33H52N6O4/c1-25-35-20-22-39(25)21-8-6-11-27-13-15-28(16-14-27)23-31(41)37-30(24-40)33(43)38-29(12-5-7-18-34)32(42)36-19-17-26-9-3-2-4-10-26/h13-16,20,22,26,29-30,40H,2-12,17-19,21,23-24,34H2,1H3,(H,36,42)(H,37,41)(H,38,43)/t29-,30-/m0/s1
InChIKey
WHLPIOSHBKQGHA-KYJUHHDHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
Cc1nccn1CCCCc2ccc(cc2)CC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)NCCC3CCCCC3
CACTVS 3.341
Cc1nccn1CCCCc2ccc(CC(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)NCCC3CCCCC3)cc2
ACDLabs 10.04
O=C(NCCC1CCCCC1)C(NC(=O)C(NC(=O)Cc2ccc(cc2)CCCCn3ccnc3C)CO)CCCCN
OpenEye OEToolkits 1.5.0
Cc1nccn1CCCCc2ccc(cc2)CC(=O)NC(CO)C(=O)NC(CCCCN)C(=O)NCCC3CCCCC3
CACTVS 3.341
Cc1nccn1CCCCc2ccc(CC(=O)N[CH](CO)C(=O)N[CH](CCCCN)C(=O)NCCC3CCCCC3)cc2
Formula
C33 H52 N6 O4
Name
[CYCLOHEXYLETHYL]-[[[[4-[2-METHYL-1-IMIDAZOLYL-BUTYL]PHENYL]ACETYL]-SERYL]-LYSINYL]-AMINE
ChEMBL
CHEMBL6269
DrugBank
DB02477
ZINC
ZINC000014880363
PDB chain
1iyk Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
1iyk
Crystal Structures of Candida albicans N-Myristoyltransferase with Two Distinct Inhibitors
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
V108 D110 D112 F117 T211 Y225 H227 P229 F240 G409 G411 D412 G413 L451
Binding residue
(residue number reindexed from 1)
V49 D51 D53 F58 T152 Y166 H168 P170 F181 G350 G352 D353 G354 L392
Annotation score
1
Binding affinity
MOAD
: Ki=0.25uM
BindingDB: Ki=31nM
Enzymatic activity
Catalytic site (original residue number in PDB)
N175 F176 L177 T211 L451
Catalytic site (residue number reindexed from 1)
N116 F117 L118 T152 L392
Enzyme Commision number
2.3.1.97
: glycylpeptide N-tetradecanoyltransferase.
Gene Ontology
Molecular Function
GO:0004379
glycylpeptide N-tetradecanoyltransferase activity
Biological Process
GO:0006499
N-terminal protein myristoylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1iyk
,
PDBe:1iyk
,
PDBj:1iyk
PDBsum
1iyk
PubMed
12401496
UniProt
P30418
|NMT_CANAL Glycylpeptide N-tetradecanoyltransferase (Gene Name=NMT1)
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