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1F8W

CRYSTAL STRUCTURE OF NADH PEROXIDASE MUTANT: R303M

Functional Information from GO Data
ChainGOidnamespacecontents
A0004601molecular_functionperoxidase activity
A0016491molecular_functionoxidoreductase activity
A0016692molecular_functionNADH peroxidase activity
A0098869biological_processcellular oxidant detoxification
Functional Information from PDB Data
site_idAC1
Number of Residues32
DetailsBINDING SITE FOR RESIDUE FAD A 448
ChainResidue
ALEU6
ATHR77
AGLU78
AILE79
ASER110
APRO111
AGLY112
AALA113
AMET131
AARG132
ATYR159
AGLY7
AASN247
AGLY280
AASP281
AALA297
ALEU298
AALA299
ATHR300
APHE424
AGLN425
AHOH451
ASER9
AHOH492
AHOH506
AHOH567
AHIS10
AGLY11
AGLU32
ALYS33
ASER41
ACSX42

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor => ECO:0000269|PubMed:8756456
ChainResidueDetails
AHIS10

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Redox-active => ECO:0000269|PubMed:8756456
ChainResidueDetails
ACSX42

site_idSWS_FT_FI3
Number of Residues7
DetailsBINDING: BINDING => ECO:0000269|PubMed:8425532, ECO:0000269|PubMed:8756456
ChainResidueDetails
AGLY7
AGLU32
ACSX42
ASER110
AARG132
AASP281
AALA299

site_idSWS_FT_FI4
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:8425532
ChainResidueDetails
AILE160
AASP179
ATYR188
AGLY243
AALA297
AGLY328

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: Cysteine sulfenic acid (-SOH) => ECO:0000269|PubMed:8756456
ChainResidueDetails
ACSX42

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 895
ChainResidueDetails
AHIS10proton shuttle (general acid/base)
ASER41electrostatic stabiliser
ACSX42covalent catalysis, proton shuttle (general acid/base)
AMET303proton shuttle (general acid/base)

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PDB entries from 2024-07-24

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