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1SZC

Structural basis for nicotinamide cleavage and ADP-ribose transfer by NAD+-dependent Sir2 histone/protein deacetylases

Functional Information from GO Data
ChainGOidnamespacecontents
A0017136molecular_functionhistone deacetylase activity, NAD-dependent
A0051287molecular_functionNAD binding
A0070403molecular_functionNAD+ binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 701
ChainResidue
ACYS143
ACYS146
ACYS170
ACYS173

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL A 702
ChainResidue
AARG204
AARG204
AHOH2136
AHOH2136

site_idAC3
Number of Residues29
DetailsBINDING SITE FOR RESIDUE CNA A 1001
ChainResidue
AALA33
AGLY34
ATHR37
AARG45
AGLN115
AASN116
AILE117
AASP118
APHE184
AGLY223
ATHR224
ASER225
AASN248
ALEU249
AGLN268
ATYR269
ASER270
AHOH2003
AHOH2005
AHOH2021
AHOH2029
AHOH2098
AHOH2100
AHOH2112
AHOH2133
AHOH2135
AHOH2202
BALY16
AGLY32

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 1989
ChainResidue
ASER193
ATRP196
AGLU237
BLYS12

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 1990
ChainResidue
ATHR49
AGLY50
AHOH2012
AHOH2115

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 1991
ChainResidue
ALYS84
AASN90
ALEU159
AALA160
AHOH2260

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 1992
ChainResidue
ALYS26
ALYS110
ATRP202
ALYS206
AHOH2164

Functional Information from PROSITE/UniProt
site_idPS00047
Number of Residues5
DetailsHISTONE_H4 Histone H4 signature. GAKRH
ChainResidueDetails
BGLY14-HIS18

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsDNA_BIND:
ChainResidueDetails
BARG17-ILE21

site_idSWS_FT_FI2
Number of Residues1
DetailsMOD_RES: N6-methyllysine; alternate => ECO:0000269|PubMed:22343720
ChainResidueDetails
BGLY13
AGLN115
AGLY223
AASN248
ASER270

site_idSWS_FT_FI3
Number of Residues1
DetailsMOD_RES: N6-acetyllysine => ECO:0000269|PubMed:11080160, ECO:0000269|PubMed:15150415, ECO:0000269|PubMed:17289592, ECO:0000269|PubMed:19113941
ChainResidueDetails
BARG17
ACYS146
ACYS170
ACYS173

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: N-acetylserine => ECO:0007744|PubMed:22814378
ChainResidueDetails
ASER2

Catalytic Information from CSA
site_idMCSA1
Number of Residues7
DetailsM-CSA 240
ChainResidueDetails
APRO42hydrogen bond acceptor, steric role
AASP43hydrogen bond acceptor, hydrogen bond donor, steric role
APHE44steric role, van der waals interaction
AARG45electrostatic stabiliser, hydrogen bond donor
AASN116activator, electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, increase nucleophilicity
AASP118activator, hydrogen bond acceptor
AHIS135hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor

237735

PDB entries from 2025-06-18

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