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1ZN3

Crystal structure of Glu335Ala mutant of Clostridium botulinum neurotoxin type E

Functional Information from GO Data
ChainGOidnamespacecontents
A0004222molecular_functionmetalloendopeptidase activity
A0006508biological_processproteolysis
A0008270molecular_functionzinc ion binding
B0004222molecular_functionmetalloendopeptidase activity
B0006508biological_processproteolysis
B0008270molecular_functionzinc ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ZN A 422
ChainResidue
AHIS211
AGLU212
AHIS215
AGLU250
AHOH505

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 822
ChainResidue
BHIS211
BHIS215
BGLU250
BHOH823

site_idAC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL A 501
ChainResidue
AARG401
AHOH656

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 502
ChainResidue
AHIS124
AGLY126
AARG167

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 503
ChainResidue
AARG384
AHOH689
BASN319

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CL A 504
ChainResidue
AGLN203
AHIS211
AALA335
AARG347
AHOH568

site_idAC7
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL B 505
ChainResidue
BGLN203
BHIS211

Functional Information from PROSITE/UniProt
site_idPS00142
Number of Residues10
DetailsZINC_PROTEASE Neutral zinc metallopeptidases, zinc-binding region signature. TLMHELIHSL
ChainResidueDetails
ATHR208-LEU217

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"description":"Proton acceptor","evidences":[{"source":"PROSITE-ProRule","id":"PRU10095","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"15157097","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU10095","evidenceCode":"ECO:0000255"},{"source":"PDB","id":"1T3A","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1T3C","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZKW","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZKX","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZL6","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZN3","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3FFZ","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PDB","id":"1T3A","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1T3C","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZKW","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZKX","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZL6","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1ZN3","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3FFZ","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1i1e
ChainResidueDetails
ATYR350
AARG347
AGLU250

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1i1e
ChainResidueDetails
BTYR350
BARG347
BGLU250

250835

PDB entries from 2026-03-18

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