Structure of PDB 7lx0 Chain b Binding Site BS21
Receptor Information
>7lx0 Chain b (length=739) Species:
98439
(Fischerella thermalis PCC 7521) [
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ATKFPKFSQDLANDPTTRRIFYAIATAHDFESHDGMTEENLYQRIFASHF
GHLAIIFLWASGILFHVAWQGNFEVWIKDPVHVRPIAHAIWDAQFGPGAI
KAFTQAGARNPVDICYSGVYHWWYTIGLRTNTELYVGALFLILLAAVFLF
AGWLHLQPRYRPNLGWFKNSEARLNHHLAGLFGVSSLAWAGHLVHVAIPE
SRGQHVGWDNFLSTPPHPAGLWAFFTGNWGAYAQNPDTAEHVFSTSQGAG
TAILTFLGGFHPQTQSLWLTDMAHHHLAIAVVLIIAGHMYRTNWRIGHSI
KEMMDSKTFFGRKVEGPFNLPHQGLYETVNNSLHFQLSLALACLGVASSL
TAQHMYSMPPYAFIAKDFTTMAALYTHHQYIAGFLMVGAFSHAAIFWIKD
YDPEQNKGNVLERVLKHKEAIIAHLSWVSLFLGFHTLGLYVHNDVEVAFG
AADKQILIEPVFAQFIQSANGKILYGFHTLLSNPDSIAFTAWPNHANVWL
PGWLDAINNGTNSLFLTIGPGDFYVHHAIALGLHVTTLILVKGALDARGS
KLMPDKKDFGYAFPCDGPGRGGTCDISAWDASYLAVFWMLNTLGWVTFYW
HWKHLSIWQGNVAQFNESSTYLMGWFRDYLWANSAQLINGYNPYGTNNLA
VWAWMFLFGHLAWAVSFMFLITWRGYWQELIETLAWAHEQTPLSFGYWRD
KPVALSIVQARLVGLTHFTVGYIATYGAFLIASTASKFG
Ligand information
Ligand ID
CLA
InChI
InChI=1S/C55H73N4O5.Mg/c1-13-39-35(8)42-28-44-37(10)41(24-25-48(60)64-27-26-34(7)23-17-22-33(6)21-16-20-32(5)19-15-18-31(3)4)52(58-44)50-51(55(62)63-12)54(61)49-38(11)45(59-53(49)50)30-47-40(14-2)36(9)43(57-47)29-46(39)56-42;/h13,26,28-33,37,41,51H,1,14-25,27H2,2-12H3,(H-,56,57,58,59,61);/q-1;+2/p-1/b34-26+;/t32-,33-,37+,41+,51-;/m1./s1
InChIKey
ATNHDLDRLWWWCB-AENOIHSZSA-M
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
CCC1=C(C2=Cc3c(c(c4n3[Mg]56[N]2=C1C=C7N5C8=C(C(C(=O)C8=C7C)C(=O)OC)C9=[N]6C(=C4)C(C9CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C
CACTVS 3.385
CCC1=C(C)C2=Cc3n4[Mg][N]5C(=CC1=N2)C(=C6C(=O)[CH](C(=O)OC)C(=C56)C7=NC(=Cc4c(C)c3C=C)[CH](C)[CH]7CCC(=O)OCC=C(C)CCC[CH](C)CCC[CH](C)CCCC(C)C)C
ACDLabs 12.01
O=C(OC)C1C(=O)C2=C(C)C3=CC=4C(CC)=C(C)C5=Cc6c(C=C)c(C)c7C=C8C(C)C(CCC(=O)OC\C=C(/C)CCCC(C)CCCC(C)CCCC(C)C)C=9C1=C2N3[Mg](n76)(N5=4)N8=9
OpenEye OEToolkits 2.0.7
CCC1=C(C2=Cc3c(c(c4n3[Mg]56[N]2=C1C=C7N5C8=C([C@H](C(=O)C8=C7C)C(=O)OC)C9=[N]6C(=C4)[C@H]([C@@H]9CCC(=O)OC/C=C(\C)/CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C)C)C=C)C
CACTVS 3.385
CCC1=C(C)C2=Cc3n4[Mg][N@@]5C(=CC1=N2)C(=C6C(=O)[C@H](C(=O)OC)C(=C56)C7=NC(=Cc4c(C)c3C=C)[C@@H](C)[C@@H]7CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C
Formula
C55 H72 Mg N4 O5
Name
CHLOROPHYLL A
ChEMBL
DrugBank
DB02133
ZINC
PDB chain
7lx0 Chain b Residue 1212 [
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Receptor-Ligand Complex Structure
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PDB
7lx0
Quantitative assessment of chlorophyll types in cryo-EM maps of photosystem I acclimated to far-red light
Resolution
2.96 Å
Binding residue
(original residue number in PDB)
L188 A189 A191 V195 H196 T215 P216 P217 G221 L222 L255 L278
Binding residue
(residue number reindexed from 1)
L187 A188 A190 V194 H195 T214 P215 P216 G220 L221 L254 L277
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.97.1.12
: photosystem I.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0009055
electron transfer activity
GO:0016168
chlorophyll binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0051539
4 iron, 4 sulfur cluster binding
Biological Process
GO:0015979
photosynthesis
Cellular Component
GO:0009522
photosystem I
GO:0009579
thylakoid
GO:0016020
membrane
GO:0031676
plasma membrane-derived thylakoid membrane
GO:0042651
thylakoid membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7lx0
,
PDBe:7lx0
,
PDBj:7lx0
PDBsum
7lx0
PubMed
UniProt
G6FMF0
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