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3ORT

Mycobacterium tuberculosis PknB kinase domain L33D mutant (crystal form 6)

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues19
DetailsBINDING SITE FOR RESIDUE AGS A 340
ChainResidue
AGLY18
AGLU93
AVAL95
ATHR99
ALYS140
AMET155
AASP156
AHOH341
AHOH368
AHOH372
AHOH381
APHE19
AGLY20
AGLY21
AMET22
ASER23
AVAL25
ALYS40
AVAL72

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE MES A 343
ChainResidue
AMET1
ATHR2
ATHR3
AGLU24
AHIS26
AASP45
ALEU54
AARG58

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues24
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGFGGMSEVHlArdlrdhrd..........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 Residues1
DetailsACT_SITE: Proton acceptor
ChainResidueDetails
AASP138

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00159, ECO:0000269|PubMed:12548283, ECO:0000269|PubMed:12551895
ChainResidueDetails
ALEU17
ALYS40
AGLU93
ALYS140

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING:
ChainResidueDetails
AASN143
AASP156

site_idSWS_FT_FI4
Number of Residues1
DetailsMOD_RES: N-acetylthreonine => ECO:0007744|PubMed:21969609
ChainResidueDetails
ATHR2

site_idSWS_FT_FI5
Number of Residues1
DetailsMOD_RES: Phosphoserine; by autocatalysis => ECO:0000269|PubMed:12548283, ECO:0000269|PubMed:15967413
ChainResidueDetails
ASER166

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: Phosphoserine; by autocatalysis => ECO:0000269|PubMed:12548283
ChainResidueDetails
ASER169
ASER295

site_idSWS_FT_FI7
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by autocatalysis => ECO:0000269|PubMed:12548283, ECO:0000269|PubMed:12950916, ECO:0000269|PubMed:15967413, ECO:0000269|PubMed:15985609, ECO:0000269|PubMed:19008858
ChainResidueDetails
ATHR171

site_idSWS_FT_FI8
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by autocatalysis => ECO:0000269|PubMed:12548283, ECO:0000269|PubMed:12950916, ECO:0000269|PubMed:15967413, ECO:0000269|PubMed:15985609
ChainResidueDetails
ATHR173

site_idSWS_FT_FI9
Number of Residues1
DetailsMOD_RES: Phosphothreonine; by autocatalysis => ECO:0000269|PubMed:12548283, ECO:0000269|PubMed:15967413
ChainResidueDetails
ATHR294

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PDB entries from 2024-11-13

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