Structure of PDB 3ttb Chain B Binding Site BS06
Receptor Information
>3ttb Chain B (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
3ttb Chain B Residue 1008 [
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Receptor-Ligand Complex Structure
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PDB
3ttb
Comparative structural and functional analysis of two octaheme nitrite reductases from closely related Thioalkalivibrio species.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
T371 H372 P403 A410 C411 C414 H415 W418 F490
Binding residue
(residue number reindexed from 1)
T367 H368 P399 A406 C407 C410 H411 W414 F486
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:3ttb
,
PDBe:3ttb
,
PDBj:3ttb
PDBsum
3ttb
PubMed
22935005
UniProt
E7EDQ7
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