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2XQF

X-ray Structure of human butyrylcholinesterase inhibited by racemic VX

Entity
Entity IDChain IDDescriptionTypeChain lengthFormula weightNumber of moleculesDB Name (Accession)Biological sourceDescriptive keywords
1A
(A)
CHOLINESTERASEpolymer52759469.31UniProt (P06276)
Pfam (PF00135)
HOMO SAPIENS (HUMAN)ACYLCHOLINE ACYLHYDROLASE, CHOLINE ESTERASE II, BUTYRYLCHOLINE ESTERASE, PSEUDOCHOLINESTERASE
2B, C
(B, C)
2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[beta-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranosebranched570.52In PDB
GlyTouCan (G28454KX)
3D
(A)
GLYCINEnon-polymer75.11Chemie (GLY)
4AA, BA, CA, DA, E...
(A)
UNKNOWN ATOM OR IONnon-polymer36Chemie (UNX)
5OA
(A)
O-ETHYLMETHYLPHOSPHONIC ACID ESTER GROUPnon-polymer124.11Chemie (VX)
6PA
(A)
SODIUM IONnon-polymer23.01Chemie (NA)
7QA, RA
(A)
CHLORIDE IONnon-polymer35.52Chemie (CL)
8SA
(A)
POTASSIUM IONnon-polymer39.11Chemie (K)
9TA, UA
(A)
SULFATE IONnon-polymer96.12Chemie (SO4)
10VA, WA, XA, YA
(A)
2-acetamido-2-deoxy-beta-D-glucopyranosenon-polymer221.24Chemie (NAG)
11ZA
(A)
waterwater18.0432Chemie (HOH)
Sequence modifications
A: 3 - 529 (UniProt: P06276)
PDBExternal DatabaseDetails
Gln 17Asn 45engineered mutation
Gln 455Asn 483engineered mutation
Gln 481Asn 509engineered mutation
Gln 486Asn 514engineered mutation
Sequence viewer
Contents of the asymmetric unit
PolymersNumber of chains1
Total formula weight59469.3
BranchedNumber of molecules2
Total formula weight1141.1
Non-Polymers*Number of molecules48
Total formula weight1409.1
All*Total formula weight62019.5
*Water molecules are not included.

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PDB entries from 2025-08-06

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