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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
DetailsActive site: {"description":"Proton acceptor","evidences":[{"source":"PubMed","id":"8756456","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues1
DetailsActive site: {"description":"Redox-active","evidences":[{"source":"PubMed","id":"8756456","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues12
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"8425532","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"8756456","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues6
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"8425532","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues1
DetailsModified residue: {"description":"Cysteine sulfenic acid (-SOH)","evidences":[{"source":"PubMed","id":"8756456","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idMCSA1
Number of Residues4
DetailsM-CSA 895
ChainResidueDetails
AHIS10proton shuttle (general acid/base)
ASER41electrostatic stabiliser
AGLY43covalent catalysis, proton shuttle (general acid/base)
AARG307proton shuttle (general acid/base)

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PDB entries from 2026-01-14

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