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3KI8

Crystal structure of hyperthermophilic nitrilase

Functional Information from GO Data
ChainGOidnamespacecontents
A0000257molecular_functionnitrilase activity
A0003837molecular_functionbeta-ureidopropionase activity
A0006807biological_processobsolete nitrogen compound metabolic process
A0016787molecular_functionhydrolase activity
A0033388biological_processputrescine biosynthetic process from arginine
A0033396biological_processbeta-alanine biosynthetic process via 3-ureidopropionate
A0050126molecular_functionN-carbamoylputrescine amidase activity
A0080061molecular_functionindole-3-acetonitrile nitrilase activity
B0000257molecular_functionnitrilase activity
B0003837molecular_functionbeta-ureidopropionase activity
B0006807biological_processobsolete nitrogen compound metabolic process
B0016787molecular_functionhydrolase activity
B0033388biological_processputrescine biosynthetic process from arginine
B0033396biological_processbeta-alanine biosynthetic process via 3-ureidopropionate
B0050126molecular_functionN-carbamoylputrescine amidase activity
B0080061molecular_functionindole-3-acetonitrile nitrilase activity
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ACY A 3001
ChainResidue
ACSD146
ATRP149
ALEU172
AVAL173
AMET174
AHOH289

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE ACY A 3004
ChainResidue
AARG132
AVAL133
AHOH314

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 263
ChainResidue
AHOH372
AHOH380
AHOH428
AHOH429
AHOH430
AHOH431

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ACY B 3002
ChainResidue
BCSD146
BTRP149
BLEU172
BVAL173
BMET174
BHOH267

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ACY B 3003
ChainResidue
BTYR118
BLEU204
BHOH289
BHOH322
BHOH398

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG B 263
ChainResidue
BASN49
BHOH264
BHOH322
BHOH323
BHOH324
BHOH398

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000305|PubMed:21095228
ChainResidueDetails
AGLU42
BGLU42

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: Proton donor => ECO:0000305|PubMed:21095228
ChainResidueDetails
ALYS113
BLYS113

site_idSWS_FT_FI3
Number of Residues2
DetailsACT_SITE: Nucleophile => ECO:0000255|PROSITE-ProRule:PRU00054, ECO:0000269|PubMed:21095228
ChainResidueDetails
ACSD146
BCSD146

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255
ChainResidueDetails
AVAL173
BVAL173

222036

PDB entries from 2024-07-03

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