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4UE6

Structure of methylene blue-treated anaerobically purified D. fructosovorans NiFe-hydrogenase

Functional Information from GO Data
ChainGOidnamespacecontents
A0008901molecular_functionferredoxin hydrogenase activity
A0009055molecular_functionelectron transfer activity
A0009061biological_processanaerobic respiration
A0009375cellular_componentferredoxin hydrogenase complex
A0016020cellular_componentmembrane
A0016491molecular_functionoxidoreductase activity
A0042597cellular_componentperiplasmic space
A0044569cellular_component[Ni-Fe] hydrogenase complex
A0046872molecular_functionmetal ion binding
A0047806molecular_functioncytochrome-c3 hydrogenase activity
A0051536molecular_functioniron-sulfur cluster binding
A0051538molecular_function3 iron, 4 sulfur cluster binding
A0051539molecular_function4 iron, 4 sulfur cluster binding
B0008901molecular_functionferredoxin hydrogenase activity
B0009055molecular_functionelectron transfer activity
B0009061biological_processanaerobic respiration
B0009375cellular_componentferredoxin hydrogenase complex
B0016020cellular_componentmembrane
B0016491molecular_functionoxidoreductase activity
B0042597cellular_componentperiplasmic space
B0044569cellular_component[Ni-Fe] hydrogenase complex
B0046872molecular_functionmetal ion binding
B0047806molecular_functioncytochrome-c3 hydrogenase activity
B0051536molecular_functioniron-sulfur cluster binding
B0051538molecular_function3 iron, 4 sulfur cluster binding
B0051539molecular_function4 iron, 4 sulfur cluster binding
C0008901molecular_functionferredoxin hydrogenase activity
C0009055molecular_functionelectron transfer activity
C0009061biological_processanaerobic respiration
C0009375cellular_componentferredoxin hydrogenase complex
C0016020cellular_componentmembrane
C0016491molecular_functionoxidoreductase activity
C0042597cellular_componentperiplasmic space
C0044569cellular_component[Ni-Fe] hydrogenase complex
C0046872molecular_functionmetal ion binding
C0047806molecular_functioncytochrome-c3 hydrogenase activity
C0051536molecular_functioniron-sulfur cluster binding
C0051538molecular_function3 iron, 4 sulfur cluster binding
C0051539molecular_function4 iron, 4 sulfur cluster binding
Q0008901molecular_functionferredoxin hydrogenase activity
Q0016151molecular_functionnickel cation binding
Q0016491molecular_functionoxidoreductase activity
Q0042597cellular_componentperiplasmic space
Q0046872molecular_functionmetal ion binding
Q0047806molecular_functioncytochrome-c3 hydrogenase activity
R0008901molecular_functionferredoxin hydrogenase activity
R0016151molecular_functionnickel cation binding
R0016491molecular_functionoxidoreductase activity
R0042597cellular_componentperiplasmic space
R0046872molecular_functionmetal ion binding
R0047806molecular_functioncytochrome-c3 hydrogenase activity
S0008901molecular_functionferredoxin hydrogenase activity
S0016151molecular_functionnickel cation binding
S0016491molecular_functionoxidoreductase activity
S0042597cellular_componentperiplasmic space
S0046872molecular_functionmetal ion binding
S0047806molecular_functioncytochrome-c3 hydrogenase activity
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SF4 A 1265
ChainResidue
AHIS184
ACYS187
AARG189
ALEU190
ACYS212
ALEU213
ACYS218

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE F3S A 1266
ChainResidue
APHE232
ACYS245
ALEU246
ACYS248
QGLN230
AASN225
ACYS227

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SF4 A 1267
ChainResidue
AGLU16
ACYS17
ACYS20
ATHR113
ACYS114
AGLY146
ACYS147
APRO148
QARG70

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 1271
ChainResidue
AALA55
QASN181
QALA182
QTYR183
QLEU185
QARG529

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 1272
ChainResidue
ALYS4
AARG6
ALEU37
AHOH2185
QPHE170
QSER173

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SF4 B 1265
ChainResidue
BHIS184
BCYS187
BARG189
BLEU190
BCYS212
BLEU213
BCYS218

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE F3S B 1266
ChainResidue
BASN225
BCYS227
BCYS245
BLEU246
BCYS248
RLYS225
RGLN230

site_idAC8
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SF4 B 1267
ChainResidue
BGLU16
BCYS17
BCYS20
BTHR113
BCYS114
BGLY146
BCYS147
BPRO148
RARG70

site_idAC9
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SF4 C 1265
ChainResidue
CHIS184
CCYS187
CARG189
CLEU190
CCYS212
CLEU213
CCYS218

site_idBC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE F3S C 1266
ChainResidue
CTHR223
CASN225
CCYS227
CPHE232
CCYS245
CLEU246
CCYS248
SGLN230

site_idBC2
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SF4 C 1267
ChainResidue
CGLU16
CCYS17
CGLY19
CCYS20
CTHR113
CCYS114
CGLY146
CCYS147
CPRO148
SARG70
SHIS228

site_idBC3
Number of Residues13
DetailsBINDING SITE FOR RESIDUE FCO Q 1550
ChainResidue
QCYS75
QVAL78
QHIS79
QALA474
QPRO475
QARG476
QLEU479
QVAL497
QPRO498
QSER499
QCSO543
QCYS546
QNI1551

site_idBC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NI Q 1551
ChainResidue
QCSO543
QCYS546
QFCO1550
QCYS72
QCYS75

site_idBC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG Q 1553
ChainResidue
QGLU53
QLEU495
QHIS549
QHOH2029
QHOH2030
QHOH2168

site_idBC6
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL Q 1561
ChainResidue
QARG100
QASN104
QPHE295
QALA296
QTRP442
QGLU445
QHOH2064
QHOH2150
QHOH2234

site_idBC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL Q 1562
ChainResidue
ALYS140
ALEU169
AASP170
AHOH2114

site_idBC8
Number of Residues13
DetailsBINDING SITE FOR RESIDUE FCO R 1550
ChainResidue
RCYS75
RVAL78
RHIS79
RALA474
RPRO475
RARG476
RLEU479
RVAL497
RPRO498
RSER499
RCSO543
RCYS546
RNI1551

site_idBC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NI R 1551
ChainResidue
RCYS72
RCYS75
RCSO543
RCYS546
RFCO1550

site_idCC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG R 1553
ChainResidue
RGLU53
RLEU495
RHIS549
RHOH2034
RHOH2035
RHOH2144

site_idCC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL R 1561
ChainResidue
BALA55
RASN181
RALA182
RTYR183
RLEU185
RARG529

site_idCC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL R 1562
ChainResidue
RSER313
RVAL324
RASN326
RLYS395
RHOH2126

site_idCC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL R 1563
ChainResidue
RARG100
RASN104
RPHE295
RALA296
RTHR297
RGLU445
RHOH2205

site_idCC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL R 1564
ChainResidue
RGLU465
RSER466
RLYS467
RARG484
RILE485

site_idCC6
Number of Residues12
DetailsBINDING SITE FOR RESIDUE FCO S 1550
ChainResidue
SCYS75
SVAL78
SHIS79
SALA474
SPRO475
SARG476
SLEU479
SVAL497
SPRO498
SSER499
SCYS546
SNI1551

site_idCC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NI S 1551
ChainResidue
SCYS72
SCYS75
SCSO543
SCYS546
SFCO1550

site_idCC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG S 1553
ChainResidue
SGLU53
SLEU495
SHIS549
SHOH2019
SHOH2020
SHOH2101

site_idCC9
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL S 1561
ChainResidue
SARG100
SASN104
SPHE295
SALA296
STHR297
SGLU445
SHOH2159

Functional Information from PROSITE/UniProt
site_idPS00507
Number of Residues26
DetailsNI_HGENASE_L_1 Nickel-dependent hydrogenases large subunit signature 1. RGLEiilkgrdprdaqhftQRaCGVC
ChainResidueDetails
QARG50-CYS75

site_idPS00508
Number of Residues10
DetailsNI_HGENASE_L_2 Nickel-dependent hydrogenases large subunit signature 2. FDPCIACgv.H
ChainResidueDetails
QPHE540-HIS549

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues12
DetailsBINDING: BINDING => ECO:0000255
ChainResidueDetails
BCYS20
BCYS114
BCYS147
BHIS184
BCYS187
BCYS212
BCYS218
BCYS227
BCYS245
BCYS248
CCYS17
CCYS20
CCYS114
CCYS147
CHIS184
CCYS187
CCYS212
CCYS218
CCYS227
CCYS245
CCYS248
QCYS72
QCYS75
QCSO543
QCYS546
RCYS72
RCYS75
RCSO543
RCYS546
SCYS72
SCYS75
SCSO543
SCYS546

219869

PDB entries from 2024-05-15

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