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1DOB

THE MOBIL FLAVIN OF 4-OH BENZOATE HYDROXYLASE: MOTION OF A PROSTHETIC GROUP REGULATES CATALYSIS

Functional Information from GO Data
ChainGOidnamespacecontents
A0004497molecular_functionmonooxygenase activity
A0009056biological_processcatabolic process
A0016491molecular_functionoxidoreductase activity
A0016709molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen
A0018659molecular_function4-hydroxybenzoate 3-monooxygenase activity
A0043639biological_processbenzoate catabolic process
A0043640biological_processbenzoate catabolic process via hydroxylation
A0050660molecular_functionflavin adenine dinucleotide binding
A0071949molecular_functionFAD binding
A0106356molecular_function4-hydroxybenzoate 3-monooxygenase (NADPH) activity
Functional Information from PDB Data
site_idAC1
Number of Residues33
DetailsBINDING SITE FOR RESIDUE FAD A 395
ChainResidue
AILE8
AARG44
AALA45
AGLY46
AGLN102
ACYS158
AASP159
AGLY160
AGLY285
AASP286
APRO293
AGLY9
AALA296
ALYS297
AGLY298
ALEU299
AASN300
APHB396
AHOH413
AHOH446
AHOH464
AHOH483
AGLY11
AHOH550
AHOH551
AHOH552
AHOH557
APRO12
ASER13
ALEU31
AGLU32
AARG33
AARG42

site_idAC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PHB A 396
ChainResidue
AARG44
ATRP185
ATYR201
ASER212
AARG214
AARG220
APRO293
ATHR294
AALA296
AFAD395

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues9
DetailsBINDING: BINDING => ECO:0000269|PubMed:10600126, ECO:0000269|PubMed:11805318, ECO:0000269|PubMed:15924424, ECO:0000269|PubMed:7939628, ECO:0000269|PubMed:8312276, ECO:0000269|PubMed:8555229
ChainResidueDetails
ASER13
AGLU32
AARG42
AGLN102
ATYR201
ASER212
APHE222
APRO293
ALEU299

site_idSWS_FT_FI2
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:10600126, ECO:0000269|PubMed:15924424, ECO:0000269|PubMed:7939628, ECO:0000269|PubMed:8312276, ECO:0000269|PubMed:8555229
ChainResidueDetails
AASP286

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: Important for catalytic activity => ECO:0000269|PubMed:8312276
ChainResidueDetails
ATYR201
ATYR385

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1dod
ChainResidueDetails
ATYR201
ATYR385

site_idMCSA1
Number of Residues5
DetailsM-CSA 131
ChainResidueDetails
AHIS72hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, proton relay
ATYR201hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, proton relay
APRO293electrostatic stabiliser, hydrogen bond acceptor
ALYS297attractive charge-charge interaction, electrostatic stabiliser, steric role
ATYR385hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, proton relay

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PDB entries from 2024-07-24

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