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5AO4

Crystal structure of in vitro phosphorylated human SAMHD1 (amino acid residues 115-626) bound to GTP

Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE FE A 1584
ChainResidue
AARG164
AHIS167
AASP207
AASP311

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE FE B 1582
ChainResidue
BHIS167
BASP207
BASP311

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE FE C 1581
ChainResidue
CASP207
CASP311
CARG164
CHIS167

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE FE D 1582
ChainResidue
DHIS167
DASP207
DASP311

site_idAC5
Number of Residues11
DetailsBINDING SITE FOR RESIDUE GTP A 1585
ChainResidue
ALYS116
AVAL117
AILE136
AASP137
AGLN142
AARG145
APHE165
BTYR155
BVAL156
BVAL378
BARG451

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE GTP A 1586
ChainResidue
ATYR155
AVAL156
AVAL378
AARG451
BLYS116
BVAL117
BILE118
BASP137
BGLN142
BARG145
BPHE165

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GTP D 1583
ChainResidue
CLYS116
CVAL117
CASP137
CARG145
CPHE165
DTYR155
DVAL156
DARG451

site_idAC8
Number of Residues11
DetailsBINDING SITE FOR RESIDUE GTP C 1582
ChainResidue
CTYR155
CVAL156
CVAL378
CARG451
CLEU453
DVAL117
DILE118
DILE136
DASP137
DGLN142
DPHE165

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: ACT_SITE => ECO:0000305|PubMed:22056990
ChainResidueDetails
AHIS233
BHIS233
CHIS233
DHIS233

site_idSWS_FT_FI2
Number of Residues24
DetailsBINDING: in other chain => ECO:0000269|PubMed:24141705, ECO:0000269|PubMed:24217394, ECO:0000269|PubMed:25267621, ECO:0000269|PubMed:25288794, ECO:0000269|PubMed:25760601, ECO:0000269|PubMed:26294762, ECO:0000269|PubMed:26431200
ChainResidueDetails
ALYS116
BARG352
BASN358
BLYS523
CLYS116
CASP137
CARG333
CARG352
CASN358
CLYS523
DLYS116
AASP137
DASP137
DARG333
DARG352
DASN358
DLYS523
AARG333
AARG352
AASN358
ALYS523
BLYS116
BASP137
BARG333

site_idSWS_FT_FI3
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:24141705, ECO:0000269|PubMed:24217394, ECO:0000269|PubMed:25267621, ECO:0000269|PubMed:25288794, ECO:0000269|PubMed:25760601, ECO:0000269|PubMed:26294762, ECO:0000269|PubMed:26431200
ChainResidueDetails
AASN119
BLYS455
CASN119
CHIS376
CLYS377
CARG451
CLYS455
DASN119
DHIS376
DLYS377
DARG451
AHIS376
DLYS455
ALYS377
AARG451
ALYS455
BASN119
BHIS376
BLYS377
BARG451

site_idSWS_FT_FI4
Number of Residues32
DetailsBINDING: BINDING => ECO:0000269|PubMed:24141705
ChainResidueDetails
AGLN149
BARG164
BHIS210
BASP309
BTYR315
BASP319
BARG366
BHIS370
CGLN149
CARG164
CHIS210
AARG164
CASP309
CTYR315
CASP319
CARG366
CHIS370
DGLN149
DARG164
DHIS210
DASP309
DTYR315
AHIS210
DASP319
DARG366
DHIS370
AASP309
ATYR315
AASP319
AARG366
AHIS370
BGLN149

site_idSWS_FT_FI5
Number of Residues16
DetailsBINDING: BINDING => ECO:0000269|PubMed:24141705, ECO:0000269|PubMed:24217394, ECO:0000269|PubMed:25288794, ECO:0000269|PubMed:25760601, ECO:0000269|PubMed:26431200
ChainResidueDetails
AHIS167
CHIS206
CASP207
CASP311
DHIS167
DHIS206
DASP207
DASP311
AHIS206
AASP207
AASP311
BHIS167
BHIS206
BASP207
BASP311
CHIS167

site_idSWS_FT_FI6
Number of Residues4
DetailsMOD_RES: Phosphothreonine; by CDK1 => ECO:0000269|PubMed:23601106, ECO:0000269|PubMed:23602554, ECO:0000269|PubMed:26294762, ECO:0000269|PubMed:26431200, ECO:0000269|PubMed:29610582, ECO:0000269|PubMed:29670289, ECO:0007744|PubMed:17081983, ECO:0007744|PubMed:18669648, ECO:0007744|PubMed:18691976, ECO:0007744|PubMed:19369195, ECO:0007744|PubMed:20068231, ECO:0007744|PubMed:23186163, ECO:0007744|PubMed:24275569
ChainResidueDetails
ATHR592
BTHR592
CTHR592
DTHR592

site_idSWS_FT_FI7
Number of Residues20
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2) => ECO:0007744|PubMed:28112733
ChainResidueDetails
ALYS467
BLYS622
CLYS467
CLYS469
CLYS492
CLYS622
DLYS467
DLYS469
DLYS492
DLYS622
ALYS469
ALYS492
ALYS622
BLYS467
BLYS469
BLYS492

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PDB entries from 2024-07-24

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