Structure of PDB 4qii Chain A Binding Site BS01
Receptor Information
>4qii Chain A (length=300) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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LSDNPFDAKAWRLVDGFDDLTDITYHRHVDDATVRVAFNRPEVRNAFRPH
TVDELYRVLDHARMSPDVGVVLLTGNGPSPKDGGWAFCSGGDQRIRGRSG
YQYASGDTADTVDVARAGRLHILEVQRLIRFMPKVVICLVNGWAAGGGHS
LHVVCDLTLASREYARFKQTDADVGSFDGGYGSAYLARQVGQKFAREIFF
LGRTYTAEQMHQMGAVNAVAEHAELETVGLQWAAEINAKSPQAQRMLKFA
FNLLDDGLVGQQLFAGEATRLAYMTDEAVEGRDAFLQKRPPDWSPFPRYF
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
4qii Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4qii
Ligand-dependent active-site closure revealed in the crystal structure of Mycobacterium tuberculosis MenB complexed with product analogues
Resolution
1.64 Å
Binding residue
(original residue number in PDB)
V57 R58 A60 F61 S103 G104 G105 D106 Q107 I136 W157 G160 G161 T184 D185 V188 S190
Binding residue
(residue number reindexed from 1)
V43 R44 A46 F47 S89 G90 G91 D92 Q93 I122 W143 G146 G147 T170 D171 V174 S176
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
G105 R110 Y115 R130 H135 G161 S164 D185 S190 D192 G193 A279 Y287
Catalytic site (residue number reindexed from 1)
G91 R96 Y101 R116 H121 G147 S150 D171 S176 D178 G179 A265 Y273
Enzyme Commision number
4.1.3.36
: 1,4-dihydroxy-2-naphthoyl-CoA synthase.
Gene Ontology
Molecular Function
GO:0008935
1,4-dihydroxy-2-naphthoyl-CoA synthase activity
GO:0016829
lyase activity
Biological Process
GO:0009234
menaquinone biosynthetic process
GO:0034214
protein hexamerization
Cellular Component
GO:0005886
plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4qii
,
PDBe:4qii
,
PDBj:4qii
PDBsum
4qii
PubMed
25372686
UniProt
P9WNP5
|MENB_MYCTU 1,4-dihydroxy-2-naphthoyl-CoA synthase (Gene Name=menB)
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