Structure of PDB 4i4z Chain B Binding Site BS03
Receptor Information
>4i4z Chain B (length=274) Species:
1111708
(Synechocystis sp. PCC 6803 substr. Kazusa) [
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DWHIAKHYDDILYYKAGGIAKIVINRPHKRNAFRPQTVFELYDAFCNARE
DNRIGVVLLTGAGPHSDGKYAFCSGGDQSVRGEGGYIDDQGTPRLNVLDL
QRLIRSMPKVVIALVAGYAIGGGHVLHLVCDLTIAADNAIFGQTGPKVGS
FDGGFGSSYLARIVGQKKAREIWYLCRQYSAQEAERMGMVNTVVPVDRLE
EEGIQWAKEILSKSPLAIRCLKAAFNADCDGQAGLQELAGNATLLYYMTE
EGSEGKQAFLEKRPPDFSQYPWLP
Ligand information
Ligand ID
2NE
InChI
InChI=1S/C28H40N7O18P3S/c1-28(2,22(39)25(40)31-8-7-18(37)30-9-10-57-27(41)15-5-3-4-6-16(15)36)12-50-56(47,48)53-55(45,46)49-11-17-21(52-54(42,43)44)20(38)26(51-17)35-14-34-19-23(29)32-13-33-24(19)35/h3-6,13-14,17,20-22,26,36,38-39H,7-12H2,1-2H3,(H,30,37)(H,31,40)(H,45,46)(H,47,48)(H2,29,32,33)(H2,42,43,44)/t17-,20-,21-,22+,26-/m1/s1
InChIKey
YTKKDFTVSNSVEE-TYHXJLICSA-N
SMILES
Software
SMILES
CACTVS 3.370
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCSC(=O)c4ccccc4O
ACDLabs 12.01
O=C(SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O)c4ccccc4O
OpenEye OEToolkits 1.7.6
CC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCSC(=O)c4ccccc4O)O
OpenEye OEToolkits 1.7.6
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)c4ccccc4O)O
CACTVS 3.370
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)c4ccccc4O
Formula
C28 H40 N7 O18 P3 S
Name
Salicylyl CoA
ChEMBL
DrugBank
ZINC
ZINC000096068394
PDB chain
4i4z Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4i4z
Structural basis of the induced-fit mechanism of 1,4-dihydroxy-2-naphthoyl coenzyme a synthase from the crotonase fold superfamily
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
F260 K263
Binding residue
(residue number reindexed from 1)
F259 K262
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
G77 R82 Y87 R95 L99 G123 V126 G146 S151 D153 G154 A240 Y248
Catalytic site (residue number reindexed from 1)
G76 R81 Y86 R94 L98 G122 V125 G145 S150 D152 G153 A239 Y247
Enzyme Commision number
4.1.3.36
: 1,4-dihydroxy-2-naphthoyl-CoA synthase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008935
1,4-dihydroxy-2-naphthoyl-CoA synthase activity
GO:0016829
lyase activity
Biological Process
GO:0009234
menaquinone biosynthetic process
GO:0042372
phylloquinone biosynthetic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4i4z
,
PDBe:4i4z
,
PDBj:4i4z
PDBsum
4i4z
PubMed
23658663
UniProt
P73495
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