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5NEL

Crystal structure of the polysaccharide deacetylase Bc1974 from Bacillus cereus in complex with ThiametG

Functional Information from GO Data
ChainGOidnamespacecontents
A0005886cellular_componentplasma membrane
A0005975biological_processcarbohydrate metabolic process
A0016787molecular_functionhydrolase activity
A0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
A0046872molecular_functionmetal ion binding
B0005886cellular_componentplasma membrane
B0005975biological_processcarbohydrate metabolic process
B0016787molecular_functionhydrolase activity
B0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
B0046872molecular_functionmetal ion binding
C0005886cellular_componentplasma membrane
C0005975biological_processcarbohydrate metabolic process
C0016787molecular_functionhydrolase activity
C0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
C0046872molecular_functionmetal ion binding
D0005886cellular_componentplasma membrane
D0005975biological_processcarbohydrate metabolic process
D0016787molecular_functionhydrolase activity
D0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
D0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues6
Detailsbinding site for residue ZN A 301
ChainResidue
AASP76
AASP77
AHIS126
AHIS130
AACT302
AHOH402

site_idAC2
Number of Residues8
Detailsbinding site for residue ACT A 302
ChainResidue
ATYR167
AHIS230
AZN301
AHOH402
DHIS269
AASP76
AHIS130
APRO166

site_idAC3
Number of Residues4
Detailsbinding site for residue ZN B 301
ChainResidue
BASP77
BHIS126
BHIS130
BNHT302

site_idAC4
Number of Residues6
Detailsbinding site for residue NHT B 302
ChainResidue
BASP76
BHIS126
BHIS130
BTYR167
BHIS230
BZN301

site_idAC5
Number of Residues10
Detailsbinding site for residue PGE B 303
ChainResidue
BARG199
BTYR200
BASN201
BLYS202
BMET203
DARG199
DTYR200
DASN201
DLYS202
DMET203

site_idAC6
Number of Residues3
Detailsbinding site for residue EDO B 304
ChainResidue
BTHR192
BASP194
BASN219

site_idAC7
Number of Residues5
Detailsbinding site for residue ZN C 301
ChainResidue
CASP77
CHIS126
CHIS130
CACT302
CHOH403

site_idAC8
Number of Residues8
Detailsbinding site for residue ACT C 302
ChainResidue
BHIS269
CASP76
CHIS126
CHIS130
CTYR167
CHIS230
CZN301
CHOH403

site_idAC9
Number of Residues4
Detailsbinding site for residue ZN D 301
ChainResidue
DASP77
DHIS126
DHIS130
DNHT302

site_idAD1
Number of Residues8
Detailsbinding site for residue NHT D 302
ChainResidue
DASP76
DASP77
DHIS126
DHIS130
DTYR167
DTRP198
DHIS230
DZN301

site_idAD2
Number of Residues5
Detailsbinding site for residue CIT D 303
ChainResidue
AMET170
BLYS202
DTHR192
DASP194
DASN219

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000305|PubMed:29257674
ChainResidueDetails
AASP76
BASP76
CASP76
DASP76

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Proton donor => ECO:0000305|PubMed:29257674
ChainResidueDetails
AHIS230
BHIS230
CHIS230
DHIS230

site_idSWS_FT_FI3
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:29257674
ChainResidueDetails
BHIS126
BHIS130
CASP77
CHIS126
CHIS130
DASP77
DHIS126
DHIS130
AASP77
AHIS126
AHIS130
BASP77

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PDB entries from 2024-06-12

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