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3K1A

Insights into substrate binding at FeMo-cofactor in nitrogenase from the structure of an alpha-70Ile MoFe protein variant

Functional Information from GO Data
ChainGOidnamespacecontents
A0005524molecular_functionATP binding
A0009399biological_processnitrogen fixation
A0016163molecular_functionnitrogenase activity
A0016491molecular_functionoxidoreductase activity
A0016612cellular_componentmolybdenum-iron nitrogenase complex
A0018697molecular_functionobsolete carbonyl 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_functionobsolete carbonyl 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_functionobsolete carbonyl 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_functionobsolete carbonyl sulfide nitrogenase activity
D0046872molecular_functionmetal ion binding
D0051536molecular_functioniron-sulfur cluster binding
Functional Information from PDB Data
site_idAC1
Number of Residues13
DetailsBINDING SITE FOR RESIDUE HCA A 494
ChainResidue
AALA65
AHOH516
AHOH530
AHOH590
ACFN6496
AARG96
AGLN191
AGLY424
AILE425
AHIS442
AHOH497
AHOH498
AHOH505

site_idAC2
Number of Residues11
DetailsBINDING SITE FOR RESIDUE CFN A 6496
ChainResidue
AILE70
AARG96
AHIS195
ATYR229
ACYS275
AGLY356
AGLY357
AARG359
APHE381
AHIS442
AHCA494

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE CLF B 6498
ChainResidue
ACYS62
AGLY87
ACYS88
ACYS154
BCYS70
BSER92
BCYS95
BTYR98
BTHR152
BCYS153
BSER188

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CA B 524
ChainResidue
BASP353
BASP357
BHOH835
DARG108
DGLU109

site_idAC5
Number of Residues11
DetailsBINDING SITE FOR RESIDUE CFN C 7496
ChainResidue
CILE70
CARG96
CHIS195
CTYR229
CCYS275
CGLY356
CGLY357
CARG359
CPHE381
CHIS442
CHCA494

site_idAC6
Number of Residues15
DetailsBINDING SITE FOR RESIDUE HCA C 494
ChainResidue
CALA65
CARG96
CGLN191
CGLY424
CILE425
CHIS442
CHOH500
CHOH502
CHOH530
CHOH534
CHOH560
CHOH607
CHOH685
CHOH781
CCFN7496

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CA D 524
ChainResidue
BARG108
BGLU109
DASP353
DASP357
DHOH599

site_idAC8
Number of Residues12
DetailsBINDING SITE FOR RESIDUE CLF D 7498
ChainResidue
CCYS62
CGLY87
CCYS88
CCYS154
DCYS70
DSER92
DCYS95
DTYR98
DTHR152
DCYS153
DSER188
DHOH619

Functional Information from PROSITE/UniProt
site_idPS00090
Number of Residues15
DetailsNITROGENASE_1_2 Nitrogenases component 1 alpha and beta subunits signature 2. TTCmaeviGDDLnAF
ChainResidueDetails
BTHR151-PHE165
ASER152-VAL166

site_idPS00699
Number of Residues8
DetailsNITROGENASE_1_1 Nitrogenases component 1 alpha and beta subunits signature 1. YVHGSQGC
ChainResidueDetails
BTYR88-CYS95
AILE81-CYS88

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

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PDB entries from 2024-07-17

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