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5NX8

Crystal structure of Neanderthal Adenylosuccinate Lyase (ADSL)

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0003824molecular_functioncatalytic activity
A0004018molecular_functionN6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity
A0005829cellular_componentcytosol
A0006164biological_processpurine nucleotide biosynthetic process
A0006167biological_processAMP biosynthetic process
A0006189biological_process'de novo' IMP biosynthetic process
A0009152biological_processpurine ribonucleotide biosynthetic process
A0016829molecular_functionlyase activity
A0044208biological_process'de novo' AMP biosynthetic process
A0070626molecular_function(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity
B0000166molecular_functionnucleotide binding
B0003824molecular_functioncatalytic activity
B0004018molecular_functionN6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity
B0005829cellular_componentcytosol
B0006164biological_processpurine nucleotide biosynthetic process
B0006167biological_processAMP biosynthetic process
B0006189biological_process'de novo' IMP biosynthetic process
B0009152biological_processpurine ribonucleotide biosynthetic process
B0016829molecular_functionlyase activity
B0044208biological_process'de novo' AMP biosynthetic process
B0070626molecular_function(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity
C0000166molecular_functionnucleotide binding
C0003824molecular_functioncatalytic activity
C0004018molecular_functionN6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity
C0005829cellular_componentcytosol
C0006164biological_processpurine nucleotide biosynthetic process
C0006167biological_processAMP biosynthetic process
C0006189biological_process'de novo' IMP biosynthetic process
C0009152biological_processpurine ribonucleotide biosynthetic process
C0016829molecular_functionlyase activity
C0044208biological_process'de novo' AMP biosynthetic process
C0070626molecular_function(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity
D0000166molecular_functionnucleotide binding
D0003824molecular_functioncatalytic activity
D0004018molecular_functionN6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity
D0005829cellular_componentcytosol
D0006164biological_processpurine nucleotide biosynthetic process
D0006167biological_processAMP biosynthetic process
D0006189biological_process'de novo' IMP biosynthetic process
D0009152biological_processpurine ribonucleotide biosynthetic process
D0016829molecular_functionlyase activity
D0044208biological_process'de novo' AMP biosynthetic process
D0070626molecular_function(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity
Functional Information from PDB Data
site_idAC1
Number of Residues4
Detailsbinding site for residue PEG A 501
ChainResidue
ALEU55
APRO56
AHOH699
AHOH835

site_idAC2
Number of Residues10
Detailsbinding site for residue PEG A 502
ChainResidue
AVAL247
AGLU250
AHOH604
AHOH669
BMET181
ALEU121
AASP192
ALEU193
AARG194
APHE236

site_idAC3
Number of Residues8
Detailsbinding site for residue GOL A 503
ChainResidue
AASP120
AARG337
AARG338
ALEU341
AALA342
AHOH635
AHOH640
AHOH643

site_idAC4
Number of Residues6
Detailsbinding site for residue GOL A 504
ChainResidue
AASP216
AHOH657
BGLY451
BARG452
BGLN455
BHOH668

site_idAC5
Number of Residues4
Detailsbinding site for residue CL A 505
ChainResidue
AGLY200
ATHR201
ASER207
AHOH778

site_idAC6
Number of Residues5
Detailsbinding site for residue CL A 506
ChainResidue
ATHR111
ATYR114
AARG196
ALYS199
AGLY200

site_idAC7
Number of Residues8
Detailsbinding site for residue GOL B 501
ChainResidue
BASP120
BARG337
BARG338
BLEU341
BALA342
BHOH638
BHOH644
BHOH659

site_idAC8
Number of Residues4
Detailsbinding site for residue CL B 502
ChainResidue
BTHR111
BARG196
BLYS199
BGLY200

site_idAC9
Number of Residues5
Detailsbinding site for residue CL B 503
ChainResidue
BGLY200
BTHR201
BALA206
BSER207
BHOH763

site_idAD1
Number of Residues6
Detailsbinding site for residue PEG C 501
ChainResidue
AGLN51
AHOH630
CHIS217
CLYS218
CGLN221
CHOH602

site_idAD2
Number of Residues10
Detailsbinding site for residue PEG C 502
ChainResidue
CLEU121
CASP192
CLEU193
CARG194
CPHE236
CVAL247
CGLU250
CHOH601
CHOH633
DMET181

site_idAD3
Number of Residues8
Detailsbinding site for residue GOL C 503
ChainResidue
CASP120
CARG337
CARG338
CLEU341
CALA342
CHOH648
CHOH662
CHOH691

site_idAD4
Number of Residues4
Detailsbinding site for residue GOL C 504
ChainResidue
CASP216
CHOH635
DGLY451
DGLN455

site_idAD5
Number of Residues4
Detailsbinding site for residue CL C 505
ChainResidue
CGLY200
CTHR201
CSER207
CHOH728

site_idAD6
Number of Residues4
Detailsbinding site for residue CL C 506
ChainResidue
CTHR111
CARG196
CLYS199
CGLY200

site_idAD7
Number of Residues9
Detailsbinding site for residue GOL D 502
ChainResidue
DASP120
DILE123
DARG337
DARG338
DLEU341
DALA342
DHOH641
DHOH692
DHOH696

site_idAD8
Number of Residues5
Detailsbinding site for residue GOL D 503
ChainResidue
CGLY451
CGLN455
DARG83
DASP216
DHOH647

site_idAD9
Number of Residues5
Detailsbinding site for residue CL D 504
ChainResidue
DTHR111
DTYR114
DARG196
DLYS199
DGLY200

site_idAE1
Number of Residues4
Detailsbinding site for residue CL D 505
ChainResidue
DGLY200
DTHR201
DALA206
DSER207

Functional Information from PROSITE/UniProt
site_idPS00163
Number of Residues10
DetailsFUMARATE_LYASES Fumarate lyases signature. GSsaMpYKrN
ChainResidueDetails
AGLY288-ASN297

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PDB entries from 2025-06-18

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