Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

1Q6N

THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 4

Functional Information from GO Data
ChainGOidnamespacecontents
A0004725molecular_functionprotein tyrosine phosphatase activity
A0006470biological_processprotein dephosphorylation
A0016311biological_processdephosphorylation
B0004725molecular_functionprotein tyrosine phosphatase activity
B0006470biological_processprotein dephosphorylation
B0016311biological_processdephosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG A 5000
ChainResidue
AHIS554
AHOH4001
AHOH4002
AHOH4006

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG A 5010
ChainResidue
AHOH2172
AHOH4012
AHOH4013
AHOH4015
AHOH4016

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG B 5020
ChainResidue
BHIS1054
BGLU1130
BHOH4021
BHOH4022
BHOH4023
BHOH4024
BHOH4026

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG B 5030
ChainResidue
AHOH4035
BGLU1026
BHOH4032
BHOH4033
BHOH4036

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 6001
ChainResidue
AARG524
AARG754
AGLN762

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL B 6002
ChainResidue
BARG1024
BARG1254
BGLN1262

site_idAC7
Number of Residues19
DetailsBINDING SITE FOR RESIDUE P90 A 801
ChainResidue
ATYR546
AARG547
AASP548
ASER618
APHE682
ACYS715
ASER716
AALA717
AGLY718
AILE719
AGLY720
AARG721
AGLN762
AHOH2001
AHOH2103
BALA1018
BASP1022
BHIS1025
BGLU1026

site_idAC8
Number of Residues18
DetailsBINDING SITE FOR RESIDUE P90 B 1301
ChainResidue
AGLY514
AALA518
AGLN521
BTYR1046
BARG1047
BASP1048
BLYS1120
BPHE1182
BCYS1215
BSER1216
BALA1217
BGLY1218
BILE1219
BGLY1220
BARG1221
BGLN1262
BHOH2002
BHOH2099

Functional Information from PROSITE/UniProt
site_idPS00383
Number of Residues11
DetailsTYR_PHOSPHATASE_1 Tyrosine specific protein phosphatases active site. VHCsaGigRSG
ChainResidueDetails
AVAL713-GLY723

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues548
DetailsDomain: {"description":"Tyrosine-protein phosphatase","evidences":[{"source":"PROSITE-ProRule","id":"PRU00160","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues2
DetailsActive site: {"description":"Phosphocysteine intermediate"}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues14
DetailsBinding site: {"evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsModified residue: {"description":"N-acetylmethionine","evidences":[{"source":"PubMed","id":"2546149","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues2
DetailsModified residue: {"description":"Phosphotyrosine","evidences":[{"source":"PubMed","id":"15592455","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues2
DetailsModified residue: {"description":"Phosphoserine; by PKB/AKT1, CLK1 and CLK2","evidences":[{"source":"PubMed","id":"10480872","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"11579209","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"23186163","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues2
DetailsModified residue: {"description":"Phosphotyrosine; by EGFR","evidences":[{"source":"PubMed","id":"9355745","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI9
Number of Residues2
DetailsModified residue: {"description":"S-nitrosocysteine; in reversibly inhibited form","evidences":[{"source":"PubMed","id":"22169477","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI10
Number of Residues4
DetailsModified residue: {"description":"Phosphoserine; by CLK1 and CLK2","evidences":[{"source":"PubMed","id":"10480872","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI11
Number of Residues4
DetailsCross-link: {"description":"N,N-(cysteine-1,S-diyl)serine (Cys-Ser); in inhibited form","evidences":[{"source":"PubMed","id":"12802338","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"12802339","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1d5r
ChainResidueDetails
AARG721
ACYS715
AASP681

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1d5r
ChainResidueDetails
BASP1181
BARG1221
BCYS1215

site_idCSA3
Number of Residues4
DetailsAnnotated By Reference To The Literature 1d5r
ChainResidueDetails
AARG721
ASER722
ACYS715
AASP681

site_idCSA4
Number of Residues4
DetailsAnnotated By Reference To The Literature 1d5r
ChainResidueDetails
BASP1181
BSER1222
BARG1221
BCYS1215

site_idMCSA1
Number of Residues5
DetailsM-CSA 469
ChainResidueDetails
AASP681proton shuttle (general acid/base)
ACYS715covalent catalysis
AARG721activator, electrostatic stabiliser
ASER722activator, electrostatic stabiliser
AGLN762steric role

site_idMCSA2
Number of Residues5
DetailsM-CSA 469
ChainResidueDetails
BASP1181proton shuttle (general acid/base)
BCYS1215covalent catalysis
BARG1221activator, electrostatic stabiliser
BSER1222activator, electrostatic stabiliser
BGLN1262steric role

251174

PDB entries from 2026-03-25

PDB statisticsPDBj update infoContact PDBjnumon