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3USE

Crystal Structure of E. coli hydrogenase-1 in its as-isolated form

Functional Information from GO Data
ChainGOidnamespacecontents
L0005515molecular_functionprotein binding
L0005886cellular_componentplasma membrane
L0006113biological_processfermentation
L0008901molecular_functionferredoxin hydrogenase activity
L0009055molecular_functionelectron transfer activity
L0009061biological_processanaerobic respiration
L0009267biological_processcellular response to starvation
L0016020cellular_componentmembrane
L0016151molecular_functionnickel cation binding
L0016491molecular_functionoxidoreductase activity
L0019645biological_processanaerobic electron transport chain
L0030288cellular_componentouter membrane-bounded periplasmic space
L0033748molecular_functionhydrogenase (acceptor) activity
L0044569cellular_component[Ni-Fe] hydrogenase complex
L0046872molecular_functionmetal ion binding
L0098567cellular_componentperiplasmic side of plasma membrane
L1902421biological_processhydrogen metabolic process
M0005515molecular_functionprotein binding
M0005886cellular_componentplasma membrane
M0006113biological_processfermentation
M0008901molecular_functionferredoxin hydrogenase activity
M0009055molecular_functionelectron transfer activity
M0009061biological_processanaerobic respiration
M0009267biological_processcellular response to starvation
M0016020cellular_componentmembrane
M0016151molecular_functionnickel cation binding
M0016491molecular_functionoxidoreductase activity
M0019645biological_processanaerobic electron transport chain
M0030288cellular_componentouter membrane-bounded periplasmic space
M0033748molecular_functionhydrogenase (acceptor) activity
M0044569cellular_component[Ni-Fe] hydrogenase complex
M0046872molecular_functionmetal ion binding
M0098567cellular_componentperiplasmic side of plasma membrane
M1902421biological_processhydrogen metabolic process
S0005515molecular_functionprotein binding
S0005886cellular_componentplasma membrane
S0006113biological_processfermentation
S0008901molecular_functionferredoxin hydrogenase activity
S0009055molecular_functionelectron transfer activity
S0009061biological_processanaerobic respiration
S0009267biological_processcellular response to starvation
S0009375cellular_componentferredoxin hydrogenase complex
S0016020cellular_componentmembrane
S0016491molecular_functionoxidoreductase activity
S0019645biological_processanaerobic electron transport chain
S0033748molecular_functionhydrogenase (acceptor) activity
S0044569cellular_component[Ni-Fe] hydrogenase complex
S0046872molecular_functionmetal ion binding
S0051536molecular_functioniron-sulfur cluster binding
S0051538molecular_function3 iron, 4 sulfur cluster binding
S0051539molecular_function4 iron, 4 sulfur cluster binding
S0098567cellular_componentperiplasmic side of plasma membrane
S1902421biological_processhydrogen metabolic process
T0005515molecular_functionprotein binding
T0005886cellular_componentplasma membrane
T0006113biological_processfermentation
T0008901molecular_functionferredoxin hydrogenase activity
T0009055molecular_functionelectron transfer activity
T0009061biological_processanaerobic respiration
T0009267biological_processcellular response to starvation
T0009375cellular_componentferredoxin hydrogenase complex
T0016020cellular_componentmembrane
T0016491molecular_functionoxidoreductase activity
T0019645biological_processanaerobic electron transport chain
T0033748molecular_functionhydrogenase (acceptor) activity
T0044569cellular_component[Ni-Fe] hydrogenase complex
T0046872molecular_functionmetal ion binding
T0051536molecular_functioniron-sulfur cluster binding
T0051538molecular_function3 iron, 4 sulfur cluster binding
T0051539molecular_function4 iron, 4 sulfur cluster binding
T0098567cellular_componentperiplasmic side of plasma membrane
T1902421biological_processhydrogen metabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SF4 S 401
ChainResidue
SHIS187
SCYS190
SARG193
SCYS215
SLEU216
SCYS221

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE F3S S 402
ChainResidue
SCYS230
STRP235
SPRO242
SCYS249
SLEU250
SCYS252
LLYS226
STHR226
SASN228

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE F4S S 403
ChainResidue
SGLU16
SCYS17
STHR18
SCYS19
SCYS20
SGLU76
STHR114
SCYS115
SCYS120
SGLY148
SCYS149

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SF3 S 404
ChainResidue
SGLU16
SCYS17
STHR18
SCYS19
SCYS20
SGLU76
STHR114
SCYS115
SCYS120
SGLY148
SCYS149

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE LMT S 405
ChainResidue
SILE7
SVAL9
STRP11
SILE72
SMET163
SASP167
SARG168

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 S 406
ChainResidue
LLEU482
LALA483
SARG211

site_idAC7
Number of Residues2
DetailsBINDING SITE FOR RESIDUE SO4 S 407
ChainResidue
SLYS218
SARG266

site_idAC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL S 408
ChainResidue
STRP118
SCYS120
SGLY256
SHOH550

site_idAC9
Number of Residues13
DetailsBINDING SITE FOR RESIDUE FCO L 601
ChainResidue
LCYS79
LVAL82
LHIS83
LALA507
LPRO508
LARG509
LLEU512
LVAL530
LPRO531
LTHR532
LCYS579
L3NI602
LHOH701

site_idBC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE 3NI L 602
ChainResidue
LCYS76
LCYS79
LCYS576
LCYS579
LFCO601
LHOH701
LHOH702

site_idBC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG L 603
ChainResidue
LGLU57
LCYS528
LHIS582
LHOH703
LHOH704
LHOH705

site_idBC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE LI L 604
ChainResidue
LASN390
LGLN392
LHOH927

site_idBC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL L 605
ChainResidue
LPHE331
LHIS421
LGLN446
LHOH1007
LHOH1036
LHOH1052
LHOH1071

site_idBC5
Number of Residues11
DetailsBINDING SITE FOR RESIDUE GOL L 606
ChainResidue
MHOH1134
LLEU135
LLEU179
LPHE182
LARG183
LASN184
LGLY185
LTRP187
LHOH1108
MLYS489
MHOH1082

site_idBC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SF4 T 401
ChainResidue
THIS187
TCYS190
TARG193
TCYS215
TLEU216
TTYR217
TCYS221

site_idBC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE F3S T 402
ChainResidue
MLYS226
TTHR226
TASN228
TCYS230
TTRP235
TCYS249
TLEU250
TCYS252

site_idBC8
Number of Residues11
DetailsBINDING SITE FOR RESIDUE F4S T 403
ChainResidue
TGLU16
TCYS17
TTHR18
TCYS19
TCYS20
TGLU76
TTHR114
TCYS115
TCYS120
TGLY148
TCYS149

site_idBC9
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SF3 T 404
ChainResidue
TGLU16
TCYS17
TTHR18
TCYS19
TCYS20
TGLU76
TTHR114
TCYS115
TCYS120
TGLY148
TCYS149

site_idCC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE LMT T 405
ChainResidue
TILE7
TVAL9
TTRP11
TMET163
TASP167
TARG168

site_idCC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 T 406
ChainResidue
LLYS171
MLEU482
MALA483
TARG211

site_idCC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 T 407
ChainResidue
TGLN203
TLYS218
TARG266

site_idCC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE SO4 T 408
ChainResidue
TASP173
TARG174

site_idCC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL T 409
ChainResidue
TTRP118
TCYS120
TGLY256
THOH547

site_idCC6
Number of Residues13
DetailsBINDING SITE FOR RESIDUE FCO M 601
ChainResidue
MCYS79
MVAL82
MHIS83
MALA507
MPRO508
MARG509
MLEU512
MVAL530
MPRO531
MTHR532
MCYS579
M3NI602
MHOH701

site_idCC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE 3NI M 602
ChainResidue
MCYS76
MCYS79
MCYS576
MCYS579
MFCO601
MHOH701
MHOH702

site_idCC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG M 603
ChainResidue
MGLU57
MCYS528
MHIS582
MHOH703
MHOH704
MHOH705

site_idCC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 M 604
ChainResidue
MASN375
MARG394
SARG125

site_idDC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE LI M 605
ChainResidue
MHOH780
MHOH820
MHOH868
MHOH885

site_idDC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CL M 606
ChainResidue
MTYR354
MARG355
MTYR356
MASP359
MHOH1153

Functional Information from PROSITE/UniProt
site_idPS00507
Number of Residues26
DetailsNI_HGENASE_L_1 Nickel-dependent hydrogenases large subunit signature 1. RGLEiilqgrdprdawafvERiCGVC
ChainResidueDetails
LARG54-CYS79

site_idPS00508
Number of Residues10
DetailsNI_HGENASE_L_2 Nickel-dependent hydrogenases large subunit signature 2. FDPCLACst.H
ChainResidueDetails
LPHE573-HIS582

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING: BINDING => ECO:0000255
ChainResidueDetails
LCYS76
LCYS79
LCYS576
LCYS579
MCYS76
MCYS79
MCYS576
MCYS579

site_idSWS_FT_FI2
Number of Residues44
DetailsTRANSMEM: Helical => ECO:0000255
ChainResidueDetails
STHR281-VAL303
TTHR281-VAL303

site_idSWS_FT_FI3
Number of Residues46
DetailsTOPO_DOM: Cytoplasmic => ECO:0000255
ChainResidueDetails
SASP304-ALA327
TASP304-ALA327

site_idSWS_FT_FI4
Number of Residues22
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P21853
ChainResidueDetails
SCYS17
SCYS249
SCYS252
TCYS17
TCYS20
TCYS115
TCYS149
THIS187
TCYS190
TCYS215
TCYS221
SCYS20
TCYS230
TCYS249
TCYS252
SCYS115
SCYS149
SHIS187
SCYS190
SCYS215
SCYS221
SCYS230

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PDB entries from 2024-07-24

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