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3K35

Crystal Structure of Human SIRT6

Functional Information from GO Data
ChainGOidnamespacecontents
A0070403molecular_functionNAD+ binding
B0070403molecular_functionNAD+ binding
C0070403molecular_functionNAD+ binding
D0070403molecular_functionNAD+ binding
E0070403molecular_functionNAD+ binding
F0070403molecular_functionNAD+ binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 317
ChainResidue
ACYS139
ACYS142
ACYS164
ACYS175

site_idAC2
Number of Residues25
DetailsBINDING SITE FOR RESIDUE APR A 1001
ChainResidue
APHE62
AARG63
ATRP69
AGLN111
AHIS131
AGLY212
ATHR213
ASER214
AILE217
AASN238
ALEU239
AGLN240
AGLY254
ATYR255
AVAL256
AHOH326
AHOH356
AHOH374
AHOH487
AHOH500
AGLY50
AALA51
AGLY52
ATHR55
AASP61

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 318
ChainResidue
ALYS31
AARG251
AHIS253
AHOH534

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 319
ChainResidue
AHIS66
AARG74
AHOH740

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 320
ChainResidue
AHIS66
ALYS79
AHOH626

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 321
ChainResidue
AARG203
AARG229
AARG230
AHOH526
BARG106

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 317
ChainResidue
BCYS139
BCYS142
BCYS164
BCYS175

site_idAC8
Number of Residues25
DetailsBINDING SITE FOR RESIDUE APR B 2001
ChainResidue
BGLY50
BALA51
BGLY52
BTHR55
BASP61
BPHE62
BARG63
BTRP69
BGLN111
BHIS131
BGLY212
BTHR213
BSER214
BILE217
BASN238
BLEU239
BGLN240
BGLY254
BTYR255
BVAL256
BHOH326
BHOH327
BHOH371
BHOH388
BHOH902

site_idAC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 B 318
ChainResidue
BLYS31
BARG251
BHIS253

site_idBC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 B 319
ChainResidue
BVAL152
BGLY153
BTHR160
BARG162
DLYS294

site_idBC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN C 317
ChainResidue
CCYS139
CCYS142
CCYS164
CCYS175

site_idBC3
Number of Residues26
DetailsBINDING SITE FOR RESIDUE APR C 3001
ChainResidue
CASN238
CLEU239
CGLN240
CGLY254
CTYR255
CVAL256
CHOH326
CHOH354
CHOH372
CHOH472
CHOH612
CHOH618
CGLY50
CALA51
CGLY52
CTHR55
CASP61
CPHE62
CARG63
CTRP69
CGLN111
CHIS131
CGLY212
CTHR213
CSER214
CILE217

site_idBC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 C 318
ChainResidue
CARG218
CPRO219
CASN222
CHOH366

site_idBC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN D 317
ChainResidue
DCYS139
DCYS142
DCYS164
DCYS175

site_idBC6
Number of Residues24
DetailsBINDING SITE FOR RESIDUE APR D 4001
ChainResidue
DGLY50
DALA51
DGLY52
DTHR55
DASP61
DPHE62
DARG63
DTRP69
DGLN111
DHIS131
DGLY212
DTHR213
DSER214
DILE217
DASN238
DLEU239
DGLN240
DGLY254
DTYR255
DVAL256
DHOH323
DHOH333
DHOH374
DHOH1005

site_idBC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 D 318
ChainResidue
DLYS31
DARG251
DHIS253
DHOH376
DHOH778

site_idBC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 D 319
ChainResidue
DHIS66
DLYS79
DHOH335
DHOH499
DHOH682
DHOH734

site_idBC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN E 317
ChainResidue
ECYS139
ECYS142
ECYS164
ECYS175

site_idCC1
Number of Residues24
DetailsBINDING SITE FOR RESIDUE APR E 5001
ChainResidue
EGLY50
EALA51
EGLY52
ETHR55
EASP61
EPHE62
EARG63
ETRP69
EGLN111
EHIS131
EGLY212
ETHR213
ESER214
EILE217
EASN238
ELEU239
EGLN240
EGLY254
ETYR255
EVAL256
EHOH326
EHOH343
EHOH345
EHOH468

site_idCC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 E 318
ChainResidue
EHIS66
ELYS79
EHOH337
EHOH341
EHOH419

site_idCC3
Number of Residues1
DetailsBINDING SITE FOR RESIDUE SO4 E 319
ChainResidue
EHIS66

site_idCC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN F 317
ChainResidue
FCYS139
FCYS142
FCYS164
FCYS175

site_idCC5
Number of Residues22
DetailsBINDING SITE FOR RESIDUE APR F 6001
ChainResidue
FGLY50
FALA51
FGLY52
FTHR55
FASP61
FPHE62
FARG63
FTRP69
FGLN111
FHIS131
FGLY212
FTHR213
FSER214
FILE217
FASN238
FLEU239
FGLN240
FGLY254
FTYR255
FVAL256
FHOH333
FHOH381

site_idCC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 F 318
ChainResidue
FLYS31
FARG251
FHIS253

site_idCC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 F 319
ChainResidue
BLYS294
DARG74
FVAL152
FGLY153
FARG162

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU00236, ECO:0000269|PubMed:18337721, ECO:0000305|PubMed:23552949, ECO:0000305|PubMed:23892288, ECO:0000305|PubMed:27322069, ECO:0000305|PubMed:28406396
ChainResidueDetails
AHIS131
BHIS131
CHIS131
DHIS131
EHIS131
FHIS131

site_idSWS_FT_FI2
Number of Residues6
DetailsBINDING: BINDING => ECO:0000305|PubMed:21362626, ECO:0007744|PDB:3K35, ECO:0007744|PDB:3ZG6
ChainResidueDetails
AALA51
BALA51
CALA51
DALA51
EALA51
FALA51

site_idSWS_FT_FI3
Number of Residues66
DetailsBINDING: BINDING => ECO:0000269|PubMed:23552949, ECO:0000305|PubMed:21362626, ECO:0007744|PDB:3K35, ECO:0007744|PDB:3ZG6
ChainResidueDetails
ATHR55
AGLN240
AVAL256
BTHR55
BPHE62
BARG63
BTRP69
BGLN111
BHIS131
BGLY212
BSER214
APHE62
BASN238
BGLN240
BVAL256
CTHR55
CPHE62
CARG63
CTRP69
CGLN111
CHIS131
CGLY212
AARG63
CSER214
CASN238
CGLN240
CVAL256
DTHR55
DPHE62
DARG63
DTRP69
DGLN111
DHIS131
ATRP69
DGLY212
DSER214
DASN238
DGLN240
DVAL256
ETHR55
EPHE62
EARG63
ETRP69
EGLN111
AGLN111
EHIS131
EGLY212
ESER214
EASN238
EGLN240
EVAL256
FTHR55
FPHE62
FARG63
FTRP69
AHIS131
FGLN111
FHIS131
FGLY212
FSER214
FASN238
FGLN240
FVAL256
AGLY212
ASER214
AASN238

site_idSWS_FT_FI4
Number of Residues24
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00236, ECO:0000269|PubMed:21362626, ECO:0000269|PubMed:23552949, ECO:0000269|PubMed:27990725, ECO:0007744|PDB:3K35, ECO:0007744|PDB:3PKI, ECO:0007744|PDB:3PKJ, ECO:0007744|PDB:3ZG6, ECO:0007744|PDB:5MF6, ECO:0007744|PDB:5MFP, ECO:0007744|PDB:5MFZ, ECO:0007744|PDB:5MGN
ChainResidueDetails
ACYS139
CCYS142
CCYS164
CCYS175
DCYS139
DCYS142
DCYS164
DCYS175
ECYS139
ECYS142
ECYS164
ACYS142
ECYS175
FCYS139
FCYS142
FCYS164
FCYS175
ACYS164
ACYS175
BCYS139
BCYS142
BCYS164
BCYS175
CCYS139

site_idSWS_FT_FI5
Number of Residues6
DetailsSITE: Formation of an covalent adduct with nitro-fatty acid activators => ECO:0000269|PubMed:33122195
ChainResidueDetails
ACYS16
BCYS16
CCYS16
DCYS16
ECYS16
FCYS16

site_idSWS_FT_FI6
Number of Residues6
DetailsMOD_RES: Phosphoserine; by MAPK8 => ECO:0000269|PubMed:27568560, ECO:0007744|PubMed:23186163
ChainResidueDetails
ASER8
BSER8
CSER8
DSER8
ESER8
FSER8

site_idSWS_FT_FI7
Number of Residues6
DetailsMOD_RES: N6-acetyllysine => ECO:0000269|PubMed:32538779
ChainResidueDetails
ALYS31
BLYS31
CLYS31
DLYS31
ELYS31
FLYS31

site_idSWS_FT_FI8
Number of Residues6
DetailsMOD_RES: Phosphothreonine => ECO:0007744|PubMed:24275569
ChainResidueDetails
ATHR292
BTHR292
CTHR292
DTHR292
ETHR292
FTHR292

site_idSWS_FT_FI9
Number of Residues6
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:23186163
ChainResidueDetails
ASER301
BSER301
CSER301
DSER301
ESER301
FSER301

site_idSWS_FT_FI10
Number of Residues12
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin) => ECO:0000269|PubMed:24043303
ChainResidueDetails
ALYS168
FLYS168
BLYS168
CLYS168
DLYS168
ELYS168

223166

PDB entries from 2024-07-31

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