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2ZPH

Complex of Fe-type nitrile hydratase with tert-butylisonitrile, photo-activated for 340min at 293K

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0006807biological_processobsolete nitrogen compound metabolic process
A0016829molecular_functionlyase activity
A0018822molecular_functionnitrile hydratase activity
A0046872molecular_functionmetal ion binding
A0046914molecular_functiontransition metal ion binding
A0080109molecular_functionindole-3-acetonitrile nitrile hydratase activity
B0006807biological_processobsolete nitrogen compound metabolic process
B0016829molecular_functionlyase activity
B0018822molecular_functionnitrile hydratase activity
B0046914molecular_functiontransition metal ion binding
B0080109molecular_functionindole-3-acetonitrile nitrile hydratase activity
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FE A 300
ChainResidue
ACYS109
ACSD112
ASER113
ACSO114
ATB0301

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE TB0 A 301
ChainResidue
AHOH604
BTYR37
BTYR72
ACSD112
ASER113
ACSO114
AFE300

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 602
ChainResidue
AHOH605
AHOH606
AHOH607
AHOH608
AHOH609
AHOH610

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 603
ChainResidue
AHOH611
AHOH612
AHOH613
AHOH614
AHOH615
AHOH616

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG B 601
ChainResidue
BHOH1902
BHOH1903
BHOH1904
BHOH1905
BHOH1906
BHOH1907

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE TRS B1901
ChainResidue
AARG138
AGLU139
BGLN11
BPRO137
BASP193
BTHR194
BASP195
BHOH2009
BHOH2010
BHOH2012
BHOH2014

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:9586994, ECO:0007744|PDB:2AHJ
ChainResidueDetails
ACYS109
ACSD112
ASER113
ACSO114

site_idSWS_FT_FI2
Number of Residues1
DetailsMOD_RES: Cysteine sulfinic acid (-SO2H) => ECO:0000269|PubMed:9368004, ECO:0000269|PubMed:9586994
ChainResidueDetails
ACSD112

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: Cysteine sulfenic acid (-SOH) => ECO:0000269|PubMed:9586994
ChainResidueDetails
ACSO114

Catalytic Information from CSA
site_idMCSA1
Number of Residues3
DetailsM-CSA 57
ChainResidueDetails
BARG56electrostatic stabiliser, proton acceptor, proton donor
BTYR72proton acceptor, proton donor
BTYR76increase acidity, increase basicity
ACSO114electrofuge, metal ligand, nucleophile, proton acceptor, proton donor

218853

PDB entries from 2024-04-24

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