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5N1P

Crystal structure of the polysaccharide deacetylase Bc1974 from Bacillus cereus in complex with N-hydroxynaphthalene-1-carboxamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0005975biological_processcarbohydrate metabolic process
A0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
B0005975biological_processcarbohydrate metabolic process
B0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
C0005975biological_processcarbohydrate metabolic process
C0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
D0005975biological_processcarbohydrate metabolic process
D0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
Functional Information from PDB Data
site_idAC1
Number of Residues13
Detailsbinding site for residue 8GK A 301
ChainResidue
AASP76
AHOH407
DPHE267
DTRP268
DHIS269
AASP77
AHIS126
AHIS130
APRO166
ATYR167
ATRP191
AHIS230
AZN302

site_idAC2
Number of Residues5
Detailsbinding site for residue ZN A 302
ChainResidue
AASP77
AHIS126
AHIS130
A8GK301
AHOH407

site_idAC3
Number of Residues10
Detailsbinding site for residue 8GK B 301
ChainResidue
BASP76
BASP77
BHIS126
BHIS130
BPRO166
BTYR167
BTRP191
BHIS230
BZN303
BHOH419

site_idAC4
Number of Residues5
Detailsbinding site for residue EDO B 302
ChainResidue
BTHR192
BASN219
BTHR221
BLYS222
BGLU225

site_idAC5
Number of Residues5
Detailsbinding site for residue ZN B 303
ChainResidue
BASP77
BHIS126
BHIS130
B8GK301
BHOH419

site_idAC6
Number of Residues12
Detailsbinding site for residue 8GK C 301
ChainResidue
BPHE267
BHIS269
CASP76
CASP77
CHIS126
CHIS130
CPRO166
CTYR167
CTRP191
CHIS230
CZN303
CHOH407

site_idAC7
Number of Residues6
Detailsbinding site for residue NA C 302
ChainResidue
ALYS81
ATYR82
AALA84
AGLU85
AHOH459
CHOH464

site_idAC8
Number of Residues5
Detailsbinding site for residue ZN C 303
ChainResidue
CASP77
CHIS126
CHIS130
C8GK301
CHOH407

site_idAC9
Number of Residues10
Detailsbinding site for residue 8GK D 301
ChainResidue
DASP76
DASP77
DHIS126
DHIS130
DPRO166
DTYR167
DTRP191
DHIS230
DZN304
DHOH408

site_idAD1
Number of Residues10
Detailsbinding site for residue PGE D 302
ChainResidue
BARG199
BTYR200
BASN201
BLYS202
BMET203
DARG199
DTYR200
DASN201
DLYS202
DMET203

site_idAD2
Number of Residues7
Detailsbinding site for residue NA D 303
ChainResidue
DPHE132
DGLY168
DSER169
DMET170
DPRO171
DGLY172
DHOH509

site_idAD3
Number of Residues5
Detailsbinding site for residue ZN D 304
ChainResidue
DASP77
DHIS126
DHIS130
D8GK301
DHOH408

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
AASP77
DASP77
DHIS126
DHIS130
AHIS126
AHIS130
BASP77
BHIS126
BHIS130
CASP77
CHIS126
CHIS130

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PDB entries from 2024-09-04

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