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1ZO8

X-ray Structure of the haloalcohol dehalogenase HheC of Agrobacterium radiobacter AD1 in complex with (S)-para-nitrostyrene oxide, with a water molecule in the halide-binding site

Functional Information from GO Data
ChainGOidnamespacecontents
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
C0016491molecular_functionoxidoreductase activity
C0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
D0016491molecular_functionoxidoreductase activity
D0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
E0016491molecular_functionoxidoreductase activity
E0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
F0016491molecular_functionoxidoreductase activity
F0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
G0016491molecular_functionoxidoreductase activity
G0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
H0016491molecular_functionoxidoreductase activity
H0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
I0016491molecular_functionoxidoreductase activity
I0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
J0016491molecular_functionoxidoreductase activity
J0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
K0016491molecular_functionoxidoreductase activity
K0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
L0016491molecular_functionoxidoreductase activity
L0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
M0016491molecular_functionoxidoreductase activity
M0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
N0016491molecular_functionoxidoreductase activity
N0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
O0016491molecular_functionoxidoreductase activity
O0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
P0016491molecular_functionoxidoreductase activity
P0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Functional Information from PDB Data
site_idAC1
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SNO A 5002
ChainResidue
APRO84
AHOH5003
CTRP249
APHE86
ASER132
ATRP139
ATYR145
APRO175
AASN176
APHE186
ATYR187

site_idAC2
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SNO B 5001
ChainResidue
BPHE12
BPRO84
BPHE86
BSER132
BTRP139
BTYR145
BPRO175
BASN176
BPHE186
BTYR187
BHOH5002
DTRP249

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SNO C 5003
ChainResidue
ATRP249
CPRO84
CPHE86
CSER132
CTRP139
CTYR145
CPRO175
CASN176
CPHE186
CTYR187
CHOH5004

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SNO D 5004
ChainResidue
BTRP249
DPRO84
DPHE86
DSER132
DTRP139
DTYR145
DPRO175
DASN176
DPHE186
DTYR187
DHOH5005

site_idAC5
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SNO E 5006
ChainResidue
EPRO84
EPHE86
ESER132
ETRP139
ETYR145
EPRO175
EASN176
EPHE186
EHOH5007
GTRP249

site_idAC6
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SNO F 5005
ChainResidue
FPHE12
FPRO84
FPHE86
FSER132
FTRP139
FTYR145
FPRO175
FASN176
FPHE186
FTYR187
FHOH5006
HTRP249

site_idAC7
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SNO G 5007
ChainResidue
ETRP249
GPHE12
GPRO84
GPHE86
GSER132
GTRP139
GTYR145
GPRO175
GASN176
GPHE186
GTYR187
GHOH5008

site_idAC8
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SNO H 5008
ChainResidue
FTRP249
HPRO84
HPHE86
HSER132
HTRP139
HTYR145
HPRO175
HASN176
HPHE186
HTYR187
HHOH5009

site_idAC9
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SNO I 5010
ChainResidue
ITYR187
IHOH5011
KTRP249
IPHE12
IPRO84
IPHE86
ISER132
ITRP139
ITYR145
IPRO175
IASN176
IPHE186

site_idBC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SNO J 5009
ChainResidue
JPRO84
JPHE86
JSER132
JTRP139
JTYR145
JPRO175
JPHE186
JTYR187
JHOH5010
LTRP249

site_idBC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SNO K 5011
ChainResidue
ITRP249
KPRO84
KPHE86
KSER132
KTRP139
KTYR145
KPRO175
KASN176
KPHE186
KHOH5012

site_idBC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SNO L 5012
ChainResidue
JTRP249
LPHE12
LPRO84
LPHE86
LSER132
LTRP139
LTYR145
LPRO175
LASN176
LPHE186
LHOH5013

site_idBC4
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SNO M 5014
ChainResidue
MPHE12
MPRO84
MPHE86
MSER132
MTRP139
MTYR145
MPRO175
MASN176
MPHE186
MTYR187
MTRP249
MHOH5015

site_idBC5
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SNO N 5013
ChainResidue
NPHE12
NPRO84
NPHE86
NSER132
NTRP139
NTYR145
NPRO175
NASN176
NPHE186
NTYR187
NTRP249
NHOH5014

site_idBC6
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SNO O 5016
ChainResidue
OPHE12
OPRO84
OPHE86
OSER132
OTRP139
OTYR145
OPRO175
OASN176
OPHE186
OTYR187
OTRP249
OHOH5017

site_idBC7
Number of Residues10
DetailsBINDING SITE FOR RESIDUE SNO P 5015
ChainResidue
PPRO84
PPHE86
PSER132
PTRP139
PTYR145
PPRO175
PASN176
PPHE186
PTRP249
PHOH5016

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
ATYR145
AARG149

site_idCSA10
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
JTYR145
JARG149

site_idCSA11
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
KTYR145
KARG149

site_idCSA12
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
LTYR145
LARG149

site_idCSA13
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
MTYR145
MARG149

site_idCSA14
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
NTYR145
NARG149

site_idCSA15
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
OTYR145
OARG149

site_idCSA16
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
PTYR145
PARG149

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
BTYR145
BARG149

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
CTYR145
CARG149

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
DTYR145
DARG149

site_idCSA5
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
ETYR145
EARG149

site_idCSA6
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
FTYR145
FARG149

site_idCSA7
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
GTYR145
GARG149

site_idCSA8
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
HTYR145
HARG149

site_idCSA9
Number of Residues2
DetailsAnnotated By Reference To The Literature 1gz6
ChainResidueDetails
ITYR145
IARG149

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PDB entries from 2024-07-24

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