Structure of PDB 2wpn Chain A Binding Site BS03
Receptor Information
>2wpn Chain A (length=277) Species:
882
(Nitratidesulfovibrio vulgaris str. Hildenborough) [
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RPPVFWLQGQGCTGCSVTLLNSVHPSIADVLLKVISLEFHPTVMAWEGEH
AIEHMRKVAEKFKGKFFLVIEGSVPVEADGKYCIIGEANHHEISMVDALK
EFGPNAAAVLAVGTCAAYGGIPAAEGSETGATAVSKFLGDNGIKTPVVNI
PGCPPHPDWIVGTVVLALDAIKKNGLEGGLAEVVKVLDSDGRPTPFFGRN
IHENCPYLDKYDEGVMSATFTDKVGCRYDLGCKGPMTMADCFERKWNGGV
NWCVQNAVCIGCVEPDFPDGKSPFYQA
Ligand information
Ligand ID
SF4
InChI
InChI=1S/4Fe.4S
InChIKey
LJBDFODJNLIPKO-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
[S]12[Fe]3[S]4[Fe]1[S]5[Fe]2[S]3[Fe]45
CACTVS 3.385
S1[Fe]S[Fe]1.S2[Fe]S[Fe]2
Formula
Fe4 S4
Name
IRON/SULFUR CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
2wpn Chain A Residue 1286 [
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Receptor-Ligand Complex Structure
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PDB
2wpn
The three-dimensional structure of [NiFeSe] hydrogenase from Desulfovibrio vulgaris Hildenborough: a hydrogenase without a bridging ligand in the active site in its oxidised, "as-isolated" state.
Resolution
2.04 Å
Binding residue
(original residue number in PDB)
C18 C21 G119 C121 C159 P160
Binding residue
(residue number reindexed from 1)
C12 C15 G113 C115 C153 P154
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C18 C21 C121 C159 H208 C211 C232 C238 C247 C259 C265 C268
Catalytic site (residue number reindexed from 1)
C12 C15 C115 C153 H202 C205 C226 C232 C241 C253 C259 C262
Enzyme Commision number
1.12.2.1
: cytochrome-c3 hydrogenase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008901
ferredoxin hydrogenase activity
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0047806
cytochrome-c3 hydrogenase activity
GO:0051536
iron-sulfur cluster binding
GO:0051538
3 iron, 4 sulfur cluster binding
GO:0051539
4 iron, 4 sulfur cluster binding
Biological Process
GO:0009061
anaerobic respiration
Cellular Component
GO:0009375
ferredoxin hydrogenase complex
GO:0016020
membrane
GO:0042597
periplasmic space
GO:0044569
[Ni-Fe] hydrogenase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2wpn
,
PDBe:2wpn
,
PDBj:2wpn
PDBsum
2wpn
PubMed
20026074
UniProt
Q72AS4
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