Structure of PDB 6l3h Chain B Binding Site BS02
Receptor Information
>6l3h Chain B (length=741) Species:
662598
(Neisseria meningitidis alpha14) [
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GQYKKLWYLLFAVLAVCFTILGYMGSEVYKKAPPYPEQVVSASGKVLMAK
DDILAGQSAWQTTGGMEVGSVLGHGAYQAPDWTADWLHRELSAWLDLTAQ
QTYGKKFDEVSPEEQAVLKTRLADEYRNQSRIKEDGSVVISDTRVKAIES
ILPYYHGVYGDDPALQTTREHFAMKNNTLPSQEAREKLFDFFFWTSWSAS
TNRPDETFTYTNNWPHEPLINNVPTTENYMWSFTSVVLLLMGIGLLMWGY
SFLTKHEEVEVPTEDPISKVQLTPSQKALGKYVFLTVALFVVQVLLGGLT
AHYTVEGQGFEALGFEMSDWFPYALTRTWHIQSAIFWIATGFLTAGLFLA
PIVNGGKDPKFQRAGVNFLYIALFIVVGGSYAGNFFALTHILPPEFNFWF
GHQGYEYLDLGRFWQLLLMVGLLLWLFLMLRCTVSAFKEKGVDKNLLAIF
VASMVGVGVFYAPGLFYGEKSPIAVMEYWRWWVVHLWVEGFFEVFATAAF
AFVFYNMGFVRRSTATASTLAAAAIFMLGGVPGTLHHLYFSGSTSASMAI
GACFSALEVVPLVLLGREAYEHWSYQHLSEWAKRLRWPLMCFVAVAFWNM
IGAGVFGFLINPPISLFYIQGLNTSAVHAHAALFGVYGFLALGFVLLVAR
YLKPNVQFDDKLMTWGFWLLNGGLVGMIAISLLPVGVIQAYASITHGLWY
ARSEEFLQMEILDTLRWVRTAADLIFIGGAICVAIQATKIV
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
6l3h Chain B Residue 802 [
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Receptor-Ligand Complex Structure
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PDB
6l3h
The active form of quinol-dependent nitric oxide reductase fromNeisseria meningitidisis a dimer.
Resolution
3.06 Å
Binding residue
(original residue number in PDB)
Y412 W486 E494 H541 H542 A608 G612 I615 N616 S630 H633 A634 A637 L638 Y642
Binding residue
(residue number reindexed from 1)
Y407 W481 E489 H536 H537 A603 G607 I610 N611 S625 H628 A629 A632 L633 Y637
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.7.99.7
: Transferred entry: 1.7.2.5.
Gene Ontology
Molecular Function
GO:0004129
cytochrome-c oxidase activity
GO:0009486
cytochrome bo3 ubiquinol oxidase activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0009060
aerobic respiration
GO:0015990
electron transport coupled proton transport
GO:0022904
respiratory electron transport chain
Cellular Component
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:6l3h
,
PDBe:6l3h
,
PDBj:6l3h
PDBsum
6l3h
PubMed
32431824
UniProt
C6S880
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