Structure of PDB 2isa Chain C Binding Site BS01
Receptor Information
>2isa Chain C (length=482) Species:
316275
(Aliivibrio salmonicida LFI1238) [
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SKKLTTAAGCPVAHNQNVQTAGKRGPQLLQDVWFLEKLAHFDREVIPERR
MHAKGSGAYGTFTVTHDITKYTKAKIFSDIGKKTDMFARFSTVAGERGAA
DAERDIRGFSLKFYTEEGNWDLAGNNTPVFFLRDPLKFPDLNHAVKRDPR
TNMRSAKNNWDFWTSLPEALHQVTIVMSDRGIPATYRHMHGFGSHTFSFI
NSDNERYWVKFHFVSQQGIKNLSDAEAGELVGNDRESHQRDLLDSIDNQD
FPKWTLKVQIMPEADAATVPYNPFDLTKVWPHKDYPLIEVGEFELNRNPQ
NYFAEVEQAAFNPANVVPGISFSPDKMLQGRLFAYGDAQRYRLGVNHQHI
PVNAPRCPVHSYHRDGAMRVDGNFGSTLGYEPNDQGQWAEQPDFSEPPLN
LDGAAAHWDHREDEDYFSQPGDLFGLMTAEKQAILFDNTARNLNGVPKEI
QLRHVTHCYKADPAYGEGIGKLLGFDISEYNS
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
2isa Chain C Residue 485 [
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Receptor-Ligand Complex Structure
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PDB
2isa
The first structure of a cold-active catalase from Vibrio salmonicida at 1.96A reveals structural aspects of cold adaptation
Resolution
1.97 Å
Binding residue
(original residue number in PDB)
R51 M53 H54 R91 S112 A125 G126 N127 P137 F140 S196 F313 M329 R333 Y337 Q341 R344
Binding residue
(residue number reindexed from 1)
R49 M51 H52 R89 S110 A123 G124 N125 P135 F138 S194 F311 M327 R331 Y335 Q339 R342
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H54 N127 N314
Catalytic site (residue number reindexed from 1)
H52 N125 N312
Enzyme Commision number
1.11.1.6
: catalase.
Gene Ontology
Molecular Function
GO:0004096
catalase activity
GO:0004601
peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0006979
response to oxidative stress
GO:0042542
response to hydrogen peroxide
GO:0042744
hydrogen peroxide catabolic process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005737
cytoplasm
GO:0042597
periplasmic space
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2isa
,
PDBe:2isa
,
PDBj:2isa
PDBsum
2isa
PubMed
17242507
UniProt
Q3LSM1
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