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1YHC

Crystal structure of Aquifex aeolicus LpxC deacetylase complexed with cacodylate

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0005737cellular_componentcytoplasm
A0006629biological_processlipid metabolic process
A0006796biological_processphosphate-containing compound metabolic process
A0009245biological_processlipid A biosynthetic process
A0016020cellular_componentmembrane
A0016787molecular_functionhydrolase activity
A0019637biological_processorganophosphate metabolic process
A0046872molecular_functionmetal ion binding
A0103117molecular_functionUDP-3-O-acyl-N-acetylglucosamine deacetylase activity
A1901135biological_processcarbohydrate derivative metabolic process
B0003824molecular_functioncatalytic activity
B0005737cellular_componentcytoplasm
B0006629biological_processlipid metabolic process
B0006796biological_processphosphate-containing compound metabolic process
B0009245biological_processlipid A biosynthetic process
B0016020cellular_componentmembrane
B0016787molecular_functionhydrolase activity
B0019637biological_processorganophosphate metabolic process
B0046872molecular_functionmetal ion binding
B0103117molecular_functionUDP-3-O-acyl-N-acetylglucosamine deacetylase activity
B1901135biological_processcarbohydrate derivative metabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ZN A 601
ChainResidue
AHIS79
ATHR191
AHIS238
AASP242
ACAC401

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ZN B 602
ChainResidue
BCAC402
BHIS79
BTHR191
BHIS238
BASP242

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ZN A 603
ChainResidue
AGLY2
AGLU126
BILE27
BHIS29
BGLU95

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 606
ChainResidue
AHIS58
AHIS200
ACL334
ACL336

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 607
ChainResidue
BHIS58
BHIS200
BCL335
BHOH947

site_idAC6
Number of Residues10
DetailsBINDING SITE FOR RESIDUE CAC A 401
ChainResidue
AHIS58
AGLU78
AHIS79
ATHR191
AHIS238
AASP242
AHIS265
ASO4404
AZN601
APAM802

site_idAC7
Number of Residues10
DetailsBINDING SITE FOR RESIDUE CAC B 402
ChainResidue
BHIS58
BGLU78
BHIS79
BTHR191
BHIS238
BASP242
BHIS265
BSO4403
BZN602
BPAM801

site_idAC8
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 B 403
ChainResidue
BTHR56
BHIS58
BLYS239
BGLY264
BHIS265
BCAC402
BPAM801
BHOH881
BHOH946

site_idAC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SO4 A 404
ChainResidue
AHIS58
ALYS239
AGLY264
AHIS265
ACAC401
APAM802
AHOH931
AHOH969

site_idBC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CL A 334
ChainResidue
AASN57
AHIS58
APHE167
AHIS200
ACL336
AZN606

site_idBC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL B 335
ChainResidue
BHIS58
BHIS200
BZN607

site_idBC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL A 336
ChainResidue
AHIS58
AHIS200
ACL334
AZN606

site_idBC4
Number of Residues16
DetailsBINDING SITE FOR RESIDUE PAM B 801
ChainResidue
ATYR224
APAM802
BILE18
BHIS58
BPHE192
BALA193
BGLU197
BILE198
BILE201
BGLY210
BVAL217
BCAC402
BSO4403
BHOH827
BHOH939
BHOH940

site_idBC5
Number of Residues13
DetailsBINDING SITE FOR RESIDUE PAM A 802
ChainResidue
ACAC401
ASO4404
BPAM801
AHIS19
AHIS58
APHE192
AGLU197
AILE198
AILE201
AGLY210
ASER211
ALEU212
AVAL217

site_idBC6
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 701
ChainResidue
AVAL53
ATHR56
AGLU158
AARG170
AGLN171
ALYS172
ALYS273
AHOH888

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton donor => ECO:0000255|HAMAP-Rule:MF_00388, ECO:0000305|PubMed:15705580
ChainResidueDetails
AHIS265
BHIS265

site_idSWS_FT_FI2
Number of Residues6
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00388, ECO:0000269|PubMed:12819349, ECO:0000269|PubMed:15705580, ECO:0007744|PDB:1P42, ECO:0007744|PDB:1YH8, ECO:0007744|PDB:1YHC
ChainResidueDetails
AHIS79
AHIS238
AASP242
BHIS79
BHIS238
BASP242

238268

PDB entries from 2025-07-02

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