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5N8I

Serial Cu nitrite reductase structures at elevated cryogenic temperature, 100K reference dataset.

Functional Information from GO Data
ChainGOidnamespacecontents
A0005507molecular_functioncopper ion binding
A0016491molecular_functionoxidoreductase activity
A0019333biological_processdenitrification pathway
A0042128biological_processnitrate assimilation
A0042597cellular_componentperiplasmic space
A0046872molecular_functionmetal ion binding
A0050421molecular_functionnitrite reductase (NO-forming) activity
Functional Information from PDB Data
site_idAC1
Number of Residues4
Detailsbinding site for residue CU A 501
ChainResidue
AHIS95
ACYS136
AHIS145
AMET150

site_idAC2
Number of Residues5
Detailsbinding site for residue CU A 502
ChainResidue
AHIS100
AHIS135
AHIS306
AHOH611
AHOH781

site_idAC3
Number of Residues8
Detailsbinding site for residue MLI A 503
ChainResidue
AGLY225
APHE312
AHIS319
AHOH633
AHOH656
AHOH668
AHOH707
AHOH835

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBINDING: type 1 copper site
ChainResidueDetails
AHIS95
ACYS136
AHIS145
AMET150

site_idSWS_FT_FI2
Number of Residues3
DetailsBINDING: type 2 copper site
ChainResidueDetails
AHIS100
AHIS135
AHIS306

Catalytic Information from CSA
site_idMCSA1
Number of Residues11
DetailsM-CSA 4
ChainResidueDetails
AHIS95metal ligand
ATHR280electrostatic stabiliser, modifies pKa
AHIS306metal ligand
AASP98activator, hydrogen bond acceptor, proton acceptor, proton donor
AHIS100metal ligand
AHIS135metal ligand, single electron acceptor, single electron donor, single electron relay
ACYS136metal ligand, single electron acceptor, single electron donor, single electron relay
AHIS145metal ligand
AMET150metal ligand
AHIS255hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AGLU279electrostatic stabiliser, modifies pKa

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PDB entries from 2024-07-10

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