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5NC6

Crystal structure of the polysaccharide deacetylase Bc1974 from Bacillus cereus in complex with (E)-N-hydroxy-3-(naphthalen-1-yl)prop-2-enamide

Functional Information from GO Data
ChainGOidnamespacecontents
A0005975biological_processcarbohydrate metabolic process
A0016810molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
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 Residues10
Detailsbinding site for residue ACT A 301
ChainResidue
AASP76
DHIS269
AASP77
AHIS126
AHIS130
APRO166
ATYR167
AHIS230
AZN302
AHOH403

site_idAC2
Number of Residues6
Detailsbinding site for residue ZN A 302
ChainResidue
AASP76
AASP77
AHIS126
AHIS130
AACT301
AHOH403

site_idAC3
Number of Residues3
Detailsbinding site for residue EDO A 303
ChainResidue
AASP270
AHOH402
BGLU85

site_idAC4
Number of Residues10
Detailsbinding site for residue 8SQ B 301
ChainResidue
BASP76
BASP77
BHIS126
BHIS130
BPRO166
BTYR167
BTRP198
BHIS230
BZN302
BHOH410

site_idAC5
Number of Residues5
Detailsbinding site for residue ZN B 302
ChainResidue
BASP77
BHIS126
BHIS130
B8SQ301
BHOH410

site_idAC6
Number of Residues10
Detailsbinding site for residue ACT C 301
ChainResidue
BHIS269
CASP76
CASP77
CHIS126
CHIS130
CPRO166
CTYR167
CHIS230
CZN302
CHOH408

site_idAC7
Number of Residues5
Detailsbinding site for residue ZN C 302
ChainResidue
CASP77
CHIS126
CHIS130
CACT301
CHOH408

site_idAC8
Number of Residues12
Detailsbinding site for residue 8SQ D 301
ChainResidue
DASP76
DASP77
DHIS126
DHIS130
DPRO166
DTYR167
DASP194
DTRP198
DARG199
DHIS230
DZN302
DHOH401

site_idAC9
Number of Residues5
Detailsbinding site for residue ZN D 302
ChainResidue
DASP77
DHIS126
DHIS130
D8SQ301
DHOH401

site_idAD1
Number of Residues7
Detailsbinding site for residue PGE D 303
ChainResidue
BARG199
BTYR200
DARG199
DTYR200
DASN201
DLYS202
DMET203

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues60
DetailsTRANSMEM: Helical => ECO:0000255
ChainResidueDetails
BILE10-ILE30
CILE10-ILE30
DILE10-ILE30

site_idSWS_FT_FI2
Number of Residues3
DetailsACT_SITE: Proton acceptor => ECO:0000305|PubMed:29257674
ChainResidueDetails
BASP76
CASP76
DASP76

site_idSWS_FT_FI3
Number of Residues3
DetailsACT_SITE: Proton donor => ECO:0000305|PubMed:29257674
ChainResidueDetails
BHIS230
CHIS230
DHIS230

site_idSWS_FT_FI4
Number of Residues9
DetailsBINDING: BINDING => ECO:0000269|PubMed:29257674
ChainResidueDetails
BASP77
BHIS126
BHIS130
CASP77
CHIS126
CHIS130
DASP77
DHIS126
DHIS130

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PDB entries from 2024-07-10

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