Structure of PDB 5zgb Chain B Binding Site BS22
Receptor Information
>5zgb Chain B (length=731) Species:
280699
(Cyanidioschyzon merolae strain 10D) [
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ATKFPKFSQALASDPTTRRIWYGIATAHDFESHDGMTEENLYQKIFASHF
GHLAIIFLWTSGNLFHVAWQGNFEQWVANPLKTKPLAHAIWDPHFGQAAL
KAFTRGDTVANISYSGVYHWWYTIGIRNNVELYTGALGLLVLSAVFLLAG
WLHIQPKFKPSLSWFKNNESRLNHHLAGLFGVSSLAWTGHLVHVAIPASR
GQHVGWDNFIMTPPHPAGLQPFFTGNWSVYAQSPDSMQHVFGTSQGAGTA
ILTFLGGFHPQTQSLWLTDMAHHHLAIAVIFIVAGHMYRTNFGIGHNLKT
ILEAHRPPSGRLGKGHIGIYQTLTNSLHFQLGLALASLSVVTSLVAQHMY
AMPPYAYMAFDYVTQSALYTHHQYIAGLLIVGAFAHGAIFFIRDYDPEQN
QDNVLARMLAHKEAVISHLSWVSLFLGFHTLGLYVHNDVVVAFGNPEKQI
LIEPIFAQWIQATSGKMLYGFQVLLSSSTSNASVAAQQLWLPGWLEAVNN
ESNSLFLTIGPGDFLVHHAIALGLHTTTLILVKGALDARGSKLMPDKKDF
GYSFPCDGPGRGGTCDISAWDAFYLAMFWMLNTIGWVTFYWHWKHLSLWQ
GNVAQFNESSTYLMGWLRDYLWLNSSPLINGYNPYGMNSLAVWSWMFLFA
HLVWATGFMFLISWRGYWQELIETLAWAHERTPLANLIRWKDKPVALSIV
QARLVGLVHFTVGYILTYAAFVIASTAGKFS
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
5zgb Chain B Residue 818 [
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Receptor-Ligand Complex Structure
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PDB
5zgb
Unique organization of photosystem I-light-harvesting supercomplex revealed by cryo-EM from a red alga
Resolution
3.63 Å
Binding residue
(original residue number in PDB)
T189 G190 V193 H194 I211 P214 G219 L220 Y231
Binding residue
(residue number reindexed from 1)
T188 G189 V192 H193 I210 P213 G218 L219 Y230
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:0009507
chloroplast
GO:0009522
photosystem I
GO:0009535
chloroplast thylakoid membrane
GO:0009579
thylakoid
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5zgb
,
PDBe:5zgb
,
PDBj:5zgb
PDBsum
5zgb
PubMed
29632169
UniProt
Q85FY6
|PSAB_CYAM1 Photosystem I P700 chlorophyll a apoprotein A2 (Gene Name=psaB)
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