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1E8H

STRUCTURE OF THE H61T MUTANT OF THE FLAVOENZYME VANILLYL-ALCOHOL OXIDASE IN THE APO FORM COMPLEXED BY ADP

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004458molecular_functionD-lactate dehydrogenase (cytochrome) activity
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005777cellular_componentperoxisome
A0008720molecular_functionD-lactate dehydrogenase activity
A0015945biological_processmethanol metabolic process
A0016491molecular_functionoxidoreductase activity
A0018465molecular_functionvanillyl-alcohol oxidase activity
A0050660molecular_functionflavin adenine dinucleotide binding
A0071949molecular_functionFAD binding
A1903457biological_processlactate catabolic process
B0003824molecular_functioncatalytic activity
B0004458molecular_functionD-lactate dehydrogenase (cytochrome) activity
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005777cellular_componentperoxisome
B0008720molecular_functionD-lactate dehydrogenase activity
B0015945biological_processmethanol metabolic process
B0016491molecular_functionoxidoreductase activity
B0018465molecular_functionvanillyl-alcohol oxidase activity
B0050660molecular_functionflavin adenine dinucleotide binding
B0071949molecular_functionFAD binding
B1903457biological_processlactate catabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues14
DetailsBINDING SITE FOR RESIDUE ADP A 600
ChainResidue
ATRP98
AGLY260
AILE261
AVAL262
ALYS545
AHOH2046
APRO99
ASER101
AILE102
AGLY103
AARG104
AASN105
ASER175
AGLU182

site_idAC2
Number of Residues15
DetailsBINDING SITE FOR RESIDUE ADP B 600
ChainResidue
BTRP98
BPRO99
BSER101
BILE102
BGLY103
BARG104
BASN105
BSER175
BGLU182
BGLY260
BILE261
BVAL262
BLYS545
BHOH2023
BHOH2043

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsACT_SITE:
ChainResidueDetails
ATYR108
ATYR503
AARG504
BTYR108
BTYR503
BARG504

site_idSWS_FT_FI2
Number of Residues2
DetailsSITE: Important for the catalytic mechanism; Involved in substrate deprotonation
ChainResidueDetails
AASP170
BASP170

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: Tele-8alpha-FAD histidine
ChainResidueDetails
AHIS422
BHIS422

Catalytic Information from CSA
site_idCSA1
Number of Residues5
DetailsAnnotated By Reference To The Literature 1vao
ChainResidueDetails
AARG504
AHIS422
ATYR503
AASP170
ATYR108

site_idCSA2
Number of Residues5
DetailsAnnotated By Reference To The Literature 1vao
ChainResidueDetails
BARG504
BHIS422
BTYR503
BASP170
BTYR108

site_idMCSA1
Number of Residues5
DetailsM-CSA 103
ChainResidueDetails
ATYR108electrostatic stabiliser, hydrogen bond donor
AASP170hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, proton relay
AHIS422activator, covalently attached, increase redox potential
ATYR503electrostatic stabiliser, hydrogen bond donor
AARG504activator, electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues5
DetailsM-CSA 103
ChainResidueDetails
BTYR108electrostatic stabiliser, hydrogen bond donor
BASP170hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, proton relay
BHIS422activator, covalently attached, increase redox potential
BTYR503electrostatic stabiliser, hydrogen bond donor
BARG504activator, electrostatic stabiliser, hydrogen bond donor

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PDB entries from 2024-10-09

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