Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

4WNA

Structure of the Nitrogenase MoFe Protein from Azotobacter vinelandii Pressurized with Xenon

Functional Information from GO Data
ChainGOidnamespacecontents
A0005524molecular_functionATP binding
A0009399biological_processnitrogen fixation
A0016163molecular_functionnitrogenase activity
A0016491molecular_functionoxidoreductase activity
A0016612cellular_componentmolybdenum-iron nitrogenase complex
A0018697molecular_functioncarbonyl sulfide nitrogenase activity
A0046872molecular_functionmetal ion binding
A0051536molecular_functioniron-sulfur cluster binding
B0005524molecular_functionATP binding
B0009399biological_processnitrogen fixation
B0016163molecular_functionnitrogenase activity
B0016491molecular_functionoxidoreductase activity
B0016612cellular_componentmolybdenum-iron nitrogenase complex
B0018697molecular_functioncarbonyl sulfide nitrogenase activity
B0046872molecular_functionmetal ion binding
B0051536molecular_functioniron-sulfur cluster binding
C0005524molecular_functionATP binding
C0009399biological_processnitrogen fixation
C0016163molecular_functionnitrogenase activity
C0016491molecular_functionoxidoreductase activity
C0016612cellular_componentmolybdenum-iron nitrogenase complex
C0018697molecular_functioncarbonyl sulfide nitrogenase activity
C0046872molecular_functionmetal ion binding
C0051536molecular_functioniron-sulfur cluster binding
D0005524molecular_functionATP binding
D0009399biological_processnitrogen fixation
D0016163molecular_functionnitrogenase activity
D0016491molecular_functionoxidoreductase activity
D0016612cellular_componentmolybdenum-iron nitrogenase complex
D0018697molecular_functioncarbonyl sulfide nitrogenase activity
D0046872molecular_functionmetal ion binding
D0051536molecular_functioniron-sulfur cluster binding
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue HCA A 501
ChainResidue
AALA65
AHOH675
AHOH699
AHOH731
AHOH755
AHOH834
BHOH772
BHOH1066
AGLN191
AGLY424
AILE425
AHIS442
AICS502
AHOH629
AHOH633
AHOH652

site_idAC2
Number of Residues13
Detailsbinding site for residue ICS A 502
ChainResidue
AVAL70
AARG96
AHIS195
ATYR229
ACYS275
ASER278
AGLY356
AGLY357
ALEU358
AARG359
APHE381
AHIS442
AHCA501

site_idAC3
Number of Residues14
Detailsbinding site for residue CLF A 503
ChainResidue
ACYS62
ATYR64
APRO85
AGLY87
ACYS88
ATYR91
ACYS154
AGLY185
BCYS70
BSER92
BCYS95
BTYR98
BCYS153
BSER188

site_idAC4
Number of Residues2
Detailsbinding site for residue XE A 504
ChainResidue
AILE75
AVAL202

site_idAC5
Number of Residues1
Detailsbinding site for residue XE A 505
ChainResidue
AASP200

site_idAC6
Number of Residues6
Detailsbinding site for residue FE B 601
ChainResidue
BASP353
BASP357
BHOH1022
DARG108
DGLU109
DHOH720

site_idAC7
Number of Residues6
Detailsbinding site for residue FE B 603
ChainResidue
BARG108
BGLU109
DASP353
DASP357
DHOH715
DHOH877

site_idAC8
Number of Residues16
Detailsbinding site for residue HCA C 501
ChainResidue
CALA65
CGLN191
CGLY424
CILE425
CHIS442
CICS502
CHOH624
CHOH628
CHOH638
CHOH694
CHOH717
CHOH718
CHOH729
CHOH829
DHOH757
DHOH785

site_idAC9
Number of Residues12
Detailsbinding site for residue ICS C 502
ChainResidue
CVAL70
CARG96
CHIS195
CTYR229
CCYS275
CGLY356
CGLY357
CLEU358
CARG359
CPHE381
CHIS442
CHCA501

site_idAD1
Number of Residues14
Detailsbinding site for residue CLF C 503
ChainResidue
DSER188
CCYS62
CTYR64
CPRO85
CGLY87
CCYS88
CTYR91
CCYS154
CGLY185
DCYS70
DSER92
DCYS95
DTYR98
DCYS153

site_idAD2
Number of Residues1
Detailsbinding site for residue XE C 504
ChainResidue
CVAL202

site_idAD3
Number of Residues1
Detailsbinding site for residue XE C 505
ChainResidue
CASP200

Functional Information from PROSITE/UniProt
site_idPS00699
Number of Residues8
DetailsNITROGENASE_1_1 Nitrogenases component 1 alpha and beta subunits signature 1. YVHGSQGC
ChainResidueDetails
BTYR88-CYS95
AILE81-CYS88

site_idPS00090
Number of Residues15
DetailsNITROGENASE_1_2 Nitrogenases component 1 alpha and beta subunits signature 2. TTCmaeviGDDLnAF
ChainResidueDetails
BTHR151-PHE165
ASER152-VAL166

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING:
ChainResidueDetails
BCYS70
CHIS442
BCYS95
BCYS153
BSER188
DCYS70
DCYS95
DCYS153
DSER188
CCYS275

Catalytic Information from CSA
site_idMCSA1
Number of Residues2
DetailsM-CSA 212
ChainResidueDetails
BCYS153metal ligand
BVAL157polar interaction, single electron acceptor, single electron donor, single electron relay
AARG96activator, hydrogen bond donor
AHIS195activator, polar interaction

site_idMCSA2
Number of Residues2
DetailsM-CSA 212
ChainResidueDetails
DCYS153metal ligand
DVAL157polar interaction, single electron acceptor, single electron donor, single electron relay
CARG96activator, hydrogen bond donor
CHIS195activator, polar interaction

219140

PDB entries from 2024-05-01

PDB statisticsPDBj update infoContact PDBjnumon