Structure of PDB 7n9z Chain F Binding Site BS03
Receptor Information
>7n9z Chain F (length=658) Species:
562
(Escherichia coli) [
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MFGKLSLDAVPFHEPIVMVTIAGIILGGLALVGLITYFGKWTYLWKEWLT
SVDHKRLGIMYIIVAIVMLLRGFADAIMMRSQQALASAGEAGFLPPHHYD
QIFTAHGVIMIFFVAMPFVIGLMNLVVPLQIGARDVAFPFLNNLSFWFTV
VGVILVNVSLGVGEFAQTGWLAYPPLSGIEYSPGVGVDYWIWSLQLSGIG
TTLTGINFFVTILKMRAPGMTMFKMPVFTWASLCANVLIIASFPILTVTV
ALLTLDRYLGTHFFTNDMGGNMMMYINLIWAWGHPEVYILILPVFGVFSE
IAATFSRKRLFGYTSLVWATVCITVLSFIVWLHHFFTMGAGANVNAFFGI
TTMIIAIPTGVKIFNWLFTMYQGRIVFHSAMLWTIGFIVTFSVGGMTGVL
LAVPGADFVLHNSLFLIAHFHNVIIGGVVFGCFAGMTYWWPKAFGFKLNE
TWGKRAFWFWIIGFFVAFMPLYALGFMGMTRRLSQQIDPQFHTMLMIAAS
GAVLIALGILCLVIQMYVSIRDRDQNRDLTGDPWGGRTLEWATSSPPPFY
NFAVVPHVHERDAFWEMKEKGEAYKKPDHYEEIHMPKNSGAGIVIAAFST
IFGFAMIWHIWWLAIVGFAGMIITWIVKSFDEDVDYYVPVAEIEKLENQH
FDEITKAG
Ligand information
Ligand ID
HEM
InChI
InChI=1S/C34H34N4O4.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;
InChIKey
KABFMIBPWCXCRK-RGGAHWMASA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)C=C)C(=C(C7=C2)C)C=C)C)CCC(=O)O
CACTVS 3.385
CC1=C(CCC(O)=O)C2=Cc3n4[Fe]5|6|N2=C1C=c7n5c(=CC8=N|6C(=Cc4c(C)c3CCC(O)=O)C(=C8C=C)C)c(C)c7C=C
ACDLabs 12.01
C=1c3c(c(c4C=C5C(=C(C=6C=C7C(=C(C8=CC=2C(=C(C=1N=2[Fe](n34)(N5=6)N78)CCC(=O)O)C)\C=C)C)\C=C)C)C)CCC(=O)O
Formula
C34 H32 Fe N4 O4
Name
PROTOPORPHYRIN IX CONTAINING FE;
HEME
ChEMBL
DrugBank
DB18267
ZINC
PDB chain
7n9z Chain F Residue 711 [
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Receptor-Ligand Complex Structure
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PDB
7n9z
Cryo-EM structures of Escherichia coli cytochrome bo 3 reveal bound phospholipids and ubiquinone-8 in a dynamic substrate binding site.
Resolution
2.19 Å
Binding residue
(original residue number in PDB)
A76 M79 R80 F103 H106 G107 M110 I111 G169 W170 F420 H421 I424 F468 R481 R482
Binding residue
(residue number reindexed from 1)
A76 M79 R80 F103 H106 G107 M110 I111 G169 W170 F420 H421 I424 F468 R481 R482
Annotation score
1
Enzymatic activity
Enzyme Commision number
7.1.1.3
: ubiquinol oxidase (H(+)-transporting).
Gene Ontology
Molecular Function
GO:0004129
cytochrome-c oxidase activity
GO:0005507
copper ion binding
GO:0005515
protein binding
GO:0009055
electron transfer activity
GO:0009486
cytochrome bo3 ubiquinol oxidase activity
GO:0015078
proton transmembrane transporter activity
GO:0015453
oxidoreduction-driven active transmembrane transporter activity
GO:0016682
oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0048039
ubiquinone binding
Biological Process
GO:0009060
aerobic respiration
GO:0015990
electron transport coupled proton transport
GO:0019646
aerobic electron transport chain
GO:0022904
respiratory electron transport chain
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005886
plasma membrane
GO:0009319
cytochrome o ubiquinol oxidase complex
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:7n9z
,
PDBe:7n9z
,
PDBj:7n9z
PDBsum
7n9z
PubMed
34417297
UniProt
P0ABI8
|CYOB_ECOLI Cytochrome bo(3) ubiquinol oxidase subunit 1 (Gene Name=cyoB)
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