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4EWL

Crystal Structure of MshB with glycerol and Acetate bound in the active site

Functional Information from GO Data
ChainGOidnamespacecontents
A0005886cellular_componentplasma membrane
A0008270molecular_functionzinc ion binding
A0010125biological_processmycothiol biosynthetic process
A0016137biological_processglycoside metabolic process
A0016787molecular_functionhydrolase activity
A0016811molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides
A0019213molecular_functiondeacetylase activity
A0035595molecular_functionN-acetylglucosaminylinositol deacetylase activity
A0046872molecular_functionmetal ion binding
B0005886cellular_componentplasma membrane
B0008270molecular_functionzinc ion binding
B0010125biological_processmycothiol biosynthetic process
B0016137biological_processglycoside metabolic process
B0016787molecular_functionhydrolase activity
B0016811molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides
B0019213molecular_functiondeacetylase activity
B0035595molecular_functionN-acetylglucosaminylinositol deacetylase activity
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PE4 A 401
ChainResidue
ATYR67
BHOH769
AGLY70
AHOH615
AHOH786
BTYR67
BGLY70
BARG77
BPE4408
BHOH705

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 402
ChainResidue
AALA33
AGLN34
AVAL35
AHIS36
AGLY80
ASER82

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 403
ChainResidue
AHIS13
AASP16
AHIS147
AACT404

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ACT A 404
ChainResidue
AHIS13
AASP15
AASP16
ATYR142
AHIS147
AZN403

site_idAC5
Number of Residues10
DetailsBINDING SITE FOR RESIDUE GOL A 405
ChainResidue
AHIS13
AGLY43
AGLU45
AGLY46
AARG68
AASP95
AGLY97
AMET98
AHIS144
AHOH617

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 406
ChainResidue
AVAL177
APRO178
AGLY277
AGLY278
AHOH636

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 407
ChainResidue
AASP291
AALA294
AGLY295
ALEU296
AGLY297
AHOH694
AHOH697

site_idAC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 401
ChainResidue
BHIS13
BASP16
BHIS147
BACT402

site_idAC9
Number of Residues7
DetailsBINDING SITE FOR RESIDUE ACT B 402
ChainResidue
BHIS13
BASP15
BASP16
BTYR142
BHIS147
BZN401
BHOH770

site_idBC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL B 403
ChainResidue
BHIS13
BGLY43
BGLY46
BARG68
BASP95
BGLY97
BHIS144
BHOH770

site_idBC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL B 404
ChainResidue
BALA33
BGLN34
BVAL35
BHIS36
BGLY80
BVAL81
BSER82
BHOH535

site_idBC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL B 405
ChainResidue
BVAL158
BVAL177
BPRO178
BGLY277
BGLY278
BHOH702
BHOH709

site_idBC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL B 406
ChainResidue
BALA282
BALA294
BGLY295
BGLY297
BHOH654
BHOH720
BHOH746

site_idBC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL B 407
ChainResidue
BARG6
BGLU127
BARG129
BASP220
BARG286

site_idBC6
Number of Residues19
DetailsBINDING SITE FOR RESIDUE PE4 B 408
ChainResidue
BSER82
BALA83
BPRO84
BILE85
BTYR86
BGLY88
BGLY89
BGLU285
BHOH534
BHOH551
BHOH598
BHOH600
BHOH662
BHOH706
AARG52
ATRP53
APE4401
AHOH527
BARG77

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:12958317
ChainResidueDetails
AHIS13
AASP16
AHIS147
BHIS13
BASP16
BHIS147

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PDB entries from 2024-10-09

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