Structure of PDB 3sxq Chain A Binding Site BS02
Receptor Information
>3sxq Chain A (length=519) Species:
108010
(Thioalkalivibrio paradoxus) [
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QLKPVDALQCYDCHTQIEDMHVVGKHATVNCVHCHDATEHVETASARRMG
ERPVTHTSPEACASCHTAQFNSFASVRHESHPREEKANPRSRSPKFDTLI
GAHGFSLEHAEPRSHAFMLVDHFIVDRAYGGRFQYKSWQNVTDGLGAVRG
AWTVIEDMDPTTSDQRRFLAQTATAANPVCLNCKTQDHILDWAYMGDEHD
AAKWARTSKVVDFARDLHHPVNCYMCHDPHSTEPRVVRDALIHAVVDQGL
GTYPYDEAKSEHVTLTPVTFQRGGEDFRKIGLLNVADSNLMCGQCHVEYN
CNPGFQQSDGAPVGMDDRRTNHFFWANVFDYAEAAKEIDFFDFTHVTTGA
PLPKLQHPELETFWGSTHERNGVTCADCHMPRVKLENGKEYTMHSPRTPR
DMMNRACLNCHDGWTEAEAEYAIDYIKNYTHGKIMKAEFWLARMIDLFPV
AKRAGVSEDVLNEVRALHYDAHLHWEWWTAENSVGFHNPDQARESLMKSI
TKSKEGVGKLDAAIDAAVA
Ligand information
Ligand ID
HEC
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,9-12H2,1-6H3,(H,39,40)(H,41,42);/q-4;+4/b21-7?,22-8?,26-13-,29-14-,30-15-,31-16-;
InChIKey
HXQIYSLZKNYNMH-LJNAALQVSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)CCC1=C(C2=CC6=C(C(=C/C)\C5=CC4=C(C(\C3=Cc7c(c(c8C=C1N2[Fe](N34)(N56)n78)CCC(=O)O)C)=C/C)C)C)C
OpenEye OEToolkits 1.5.0
CC=C1C(=C2C=C3C(=CC)C(=C4N3[Fe]56N2C1=Cc7n5c(c(c7C)CCC(=O)O)C=C8N6C(=C4)C(=C8CCC(=O)O)C)C)C
CACTVS 3.341
C\C=C1/C(=C2C=C3N4C(=Cc5n6c(C=C7N8C(=C(C)\C7=C/C)C=C1N2[Fe@@]468)c(C)c5CCC(O)=O)C(=C3C)CCC(O)=O)C
CACTVS 3.341
CC=C1C(=C2C=C3N4C(=Cc5n6c(C=C7N8C(=C(C)C7=CC)C=C1N2[Fe]468)c(C)c5CCC(O)=O)C(=C3C)CCC(O)=O)C
Formula
C34 H34 Fe N4 O4
Name
HEME C
ChEMBL
DrugBank
ZINC
PDB chain
3sxq Chain A Residue 1005 [
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Receptor-Ligand Complex Structure
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PDB
3sxq
Comparative structural and functional analysis of two octaheme nitrite reductases from closely related Thioalkalivibrio species.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
H70 Q73 F77 C227 C230 H231 M295 Y395 T396 H398
Binding residue
(residue number reindexed from 1)
H66 Q69 F73 C223 C226 H227 M291 Y391 T392 H394
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.7.2.2
: nitrite reductase (cytochrome; ammonia-forming).
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0042279
nitrite reductase (cytochrome, ammonia-forming) activity
GO:0046872
metal ion binding
Biological Process
GO:0019645
anaerobic electron transport chain
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3sxq
,
PDBe:3sxq
,
PDBj:3sxq
PDBsum
3sxq
PubMed
22935005
UniProt
E7EDQ7
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