Structure of PDB 1oah Chain B Binding Site BS04
Receptor Information
>1oah Chain B (length=482) Species:
876
(Desulfovibrio desulfuricans) [
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TGIAETETKMSAFKGQFPQQYASYMKNNEDRIMTDYKGSVPYHKNDNVNP
LPKGFKHAQPYLKNLWLGYPFMYEYNETRGHTYAIDDFLNIDRINRFAAD
GKGNLPATCWNCKTPKMMEWVSQYGDKFWSMDVNEFRAKDKINAHDETIG
CANCHDPATMELRLYSEPLKDWLKRSGKDWQKMSRNEKRTLVCAQCHVEY
YFTHKDNGPAAKPVFPWDNGFNPEDMYQYYKGHGAKGPDGKPGPFVDWVH
AASKVPMIKMQHPEYETFQDGPHGAAGVSCADCHMQYVREDGKKISSHWM
TSPMKDPEMRACRQCHADKTGEYLRQRVLYTQQKTFDQLLKAQEMSVKAH
EAVRLANAYEGHRAANYEALMAEAREMVRKGQLFWDYVSAENSVGFHNPA
KALDTLMTSMECSQKAVDLATEATDFGIAPALAGDIKKLVPPILTLSRKL
QQDPEFLKQNPWTRLLPALPKAEQVWEGQDRA
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
1oah Chain B Residue 1522 [
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Receptor-Ligand Complex Structure
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PDB
1oah
Cytochrome C Nitrite Reductase from Desulfovibrio Desulfuricans Atcc 27774. The Relevance of the Two Calcium Sites in the Structure of the Catalytic Subunit (Nrfa)
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
S76 T115 R116 H118 Y120 A121 D124 C149 K150 I186 Y202 C230 C233 H234 M337 T338
Binding residue
(residue number reindexed from 1)
S39 T78 R79 H81 Y83 A84 D87 C112 K113 I149 Y165 C193 C196 H197 M300 T301
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.7.2.2
: nitrite reductase (cytochrome; ammonia-forming).
Gene Ontology
Molecular Function
GO:0042279
nitrite reductase (cytochrome, ammonia-forming) activity
Cellular Component
GO:0042597
periplasmic space
View graph for
Molecular Function
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Cellular Component
External links
PDB
RCSB:1oah
,
PDBe:1oah
,
PDBj:1oah
PDBsum
1oah
PubMed
12618432
UniProt
Q8VNU2
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