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1BG0

TRANSITION STATE STRUCTURE OF ARGININE KINASE

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0003824molecular_functioncatalytic activity
A0004054molecular_functionarginine kinase activity
A0004111molecular_functioncreatine kinase activity
A0005524molecular_functionATP binding
A0005615cellular_componentextracellular space
A0005737cellular_componentcytoplasm
A0016301molecular_functionkinase activity
A0016310biological_processphosphorylation
A0016740molecular_functiontransferase activity
A0016772molecular_functiontransferase activity, transferring phosphorus-containing groups
A0046314biological_processphosphocreatine biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE NO3 A 500
ChainResidue
AGLY112
ALEU113
AASP114
APRO115
AGLY191
AGLN196
AGLY237
AASP238
AHOH598

site_idAC2
Number of Residues12
DetailsBINDING SITE FOR RESIDUE NO3 A 401
ChainResidue
AARG126
AGLU225
AARG229
AASN274
AARG309
AGLU314
AADP400
AMG402
ADAR403
AHOH720
AHOH797
AHOH798

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG A 402
ChainResidue
AADP400
ANO3401
AHOH796
AHOH797
AHOH798

site_idAC4
Number of Residues26
DetailsBINDING SITE FOR RESIDUE ADP A 400
ChainResidue
ASER122
AARG124
AARG126
AHIS185
ATRP221
AARG229
AARG280
ASER282
AVAL283
AHIS284
AARG309
ATHR311
AARG312
AGLY313
AGLU314
AASP324
ANO3401
AMG402
AHOH709
AHOH710
AHOH713
AHOH715
AHOH730
AHOH796
AHOH797
AHOH798

site_idAC5
Number of Residues14
DetailsBINDING SITE FOR RESIDUE DAR A 403
ChainResidue
ASER63
AGLY64
AVAL65
AGLY66
ATYR68
AGLU225
ACYS271
ATHR273
AGLU314
AHIS315
ANO3401
AHOH724
AHOH727
AHOH740

Functional Information from PROSITE/UniProt
site_idPS00112
Number of Residues7
DetailsPHOSPHAGEN_KINASE Phosphagen kinase active site signature. CP.TNLGT
ChainResidueDetails
ACYS271-THR277

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues82
DetailsDomain: {"description":"Phosphagen kinase N-terminal","evidences":[{"source":"PROSITE-ProRule","id":"PRU00842","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues237
DetailsDomain: {"description":"Phosphagen kinase C-terminal","evidences":[{"source":"PROSITE-ProRule","id":"PRU00843","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues22
DetailsBinding site: {}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues5
Detailsa catalytic site defined by CSA, PubMed 10829032, 9671698, 9849893
ChainResidueDetails
AARG309
AARG280
AARG229
AARG126
AGLU225

site_idMCSA1
Number of Residues8
DetailsM-CSA 86
ChainResidueDetails
AARG126electrostatic stabiliser, hydrogen bond donor
AGLU225hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AARG229electrostatic stabiliser, hydrogen bond donor
ACYS271electrostatic stabiliser, hydrogen bond acceptor, steric role
ATHR273electrostatic stabiliser, hydrogen bond donor
AARG280electrostatic stabiliser, hydrogen bond donor
AARG309electrostatic stabiliser, hydrogen bond donor
AGLU314electrostatic stabiliser

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PDB entries from 2025-12-10

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