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1MRU

Intracellular Ser/Thr protein kinase domain of Mycobacterium tuberculosis PknB.

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
B0004672molecular_functionprotein kinase activity
B0005524molecular_functionATP binding
B0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE MG A 341
ChainResidue
AASP156
AAGS340

site_idAC2
Number of Residues1
DetailsBINDING SITE FOR RESIDUE MG A 342
ChainResidue
AAGS340

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE MG B 441
ChainResidue
BASP156
BGLY158
BAGS440

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE MG B 442
ChainResidue
BALA142
BASN143
BAGS440

site_idAC5
Number of Residues14
DetailsBINDING SITE FOR RESIDUE AGS A 340
ChainResidue
ALEU17
ASER23
AVAL25
AALA38
ALYS40
AGLU93
AVAL95
ATHR99
AASN143
AMET145
AMET155
AASP156
AMG341
AMG342

site_idAC6
Number of Residues16
DetailsBINDING SITE FOR RESIDUE AGS B 440
ChainResidue
BLEU17
BGLY20
BGLY21
BSER23
BVAL25
BALA38
BLYS40
BGLU93
BVAL95
BLYS140
BALA142
BASN143
BMET155
BASP156
BMG441
BMG442

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues24
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGFGGMSEVHlArdlrlhrd..........VAVK
ChainResidueDetails
ALEU17-LYS40

site_idPS00108
Number of Residues13
DetailsPROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. IiHrDVKpaNIMI
ChainResidueDetails
AILE134-ILE146

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"description":"Proton acceptor"}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues28
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"12548283","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"12551895","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues1
DetailsModified residue: {"description":"N-acetylthreonine","evidences":[{"source":"PubMed","id":"21969609","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
AALA142
AASP138

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
BALA142
BASP138

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
AASP138
ALYS140

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
BASP138
BLYS140

site_idCSA5
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
ATHR179
AASP138
ALYS140

site_idCSA6
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
BTHR179
BASP138
BLYS140

site_idCSA7
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
AASP138
AASN143
ALYS140

site_idCSA8
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ir3
ChainResidueDetails
BASP138
BASN143
BLYS140

249697

PDB entries from 2026-02-25

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