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6HGE

Crystal structure of Alpha1-antichymotrypsin variant NewBG-I in the uncleaved S-conformation

Entity
Entity IDChain IDDescriptionTypeChain lengthFormula weightNumber of moleculesDB Name (Accession)Biological sourceDescriptive keywords
1A
(A)
Alpha-1-antichymotrypsinpolymer40946893.51UniProt (P01011)
Pfam (PF00079)
Homo sapiens (Human)ACT,Cell growth-inhibiting gene 24/25 protein,Serpin A3
2B
(B)
Alpha-1-antichymotrypsinpolymer40946947.61UniProt (P01011)
Pfam (PF00079)
Homo sapiens (Human)ACT,Cell growth-inhibiting gene 24/25 protein,Serpin A3
3C
(C)
Alpha-1-antichymotrypsinpolymer40946893.51UniProt (P01011)
Pfam (PF00079)
Homo sapiens (Human)ACT,Cell growth-inhibiting gene 24/25 protein,Serpin A3
4D
(D)
Alpha-1-antichymotrypsinpolymer40946974.61UniProt (P01011)
Pfam (PF00079)
Homo sapiens (Human)ACT,Cell growth-inhibiting gene 24/25 protein,Serpin A3
5E, F, G, H
(A, B, C, D)
waterwater18.058Chemie (HOH)
Sequence modifications
A: 3 - 400 (UniProt: P01011)
PDBExternal DatabaseDetails
Met -8-initiating methionine
Lys -7-expression tag
His -6-expression tag
His -5-expression tag
His -4-expression tag
His -3-expression tag
His -2-expression tag
His -1-expression tag
Met 0-expression tag
Lys 1-expression tag
Gln 2-expression tag
Arg 24Leu 47engineered mutation
Gln 242Glu 265engineered mutation
Asn 244Lys 267engineered mutation
Ser 269Leu 292engineered mutation
Arg 270Pro 293engineered mutation
Asn 274Lys 297engineered mutation
Gly 277Arg 300engineered mutation
Asp 382Pro 405engineered mutation
His 383Thr 406engineered mutation
Phe 384Asp 407engineered mutation
Trp 386Gln 409engineered mutation
Ser 387Asn 410engineered mutation
B: 3 - 400 (UniProt: P01011)
PDBExternal DatabaseDetails
Met -8-initiating methionine
Lys -7-expression tag
His -6-expression tag
His -5-expression tag
His -4-expression tag
His -3-expression tag
His -2-expression tag
His -1-expression tag
Met 0-expression tag
Lys 1-expression tag
Gln 2-expression tag
Arg 24Leu 47engineered mutation
Gln 242Glu 265engineered mutation
Asn 244Lys 267engineered mutation
Ser 269Leu 292engineered mutation
Arg 270Pro 293engineered mutation
Asn 274Lys 297engineered mutation
Gly 277Arg 300engineered mutation
Asp 382Pro 405engineered mutation
His 383Thr 406engineered mutation
Phe 384Asp 407engineered mutation
Trp 386Gln 409engineered mutation
Ser 387Asn 410engineered mutation
C: 3 - 400 (UniProt: P01011)
PDBExternal DatabaseDetails
Met -8-initiating methionine
Lys -7-expression tag
His -6-expression tag
His -5-expression tag
His -4-expression tag
His -3-expression tag
His -2-expression tag
His -1-expression tag
Met 0-expression tag
Lys 1-expression tag
Gln 2-expression tag
Arg 24Leu 47engineered mutation
Gln 242Glu 265engineered mutation
Asn 244Lys 267engineered mutation
Ser 269Leu 292engineered mutation
Arg 270Pro 293engineered mutation
Asn 274Lys 297engineered mutation
Gly 277Arg 300engineered mutation
Asp 382Pro 405engineered mutation
His 383Thr 406engineered mutation
Phe 384Asp 407engineered mutation
Trp 386Gln 409engineered mutation
Ser 387Asn 410engineered mutation
D: 3 - 400 (UniProt: P01011)
PDBExternal DatabaseDetails
Met -8-initiating methionine
Lys -7-expression tag
His -6-expression tag
His -5-expression tag
His -4-expression tag
His -3-expression tag
His -2-expression tag
His -1-expression tag
Met 0-expression tag
Lys 1-expression tag
Gln 2-expression tag
Arg 24Leu 47engineered mutation
Gln 242Glu 265engineered mutation
Asn 244Lys 267engineered mutation
Ser 269Leu 292engineered mutation
Arg 270Pro 293engineered mutation
Asn 274Lys 297engineered mutation
Gly 277Arg 300engineered mutation
Asp 382Pro 405engineered mutation
His 383Thr 406engineered mutation
Phe 384Asp 407engineered mutation
Trp 386Gln 409engineered mutation
Ser 387Asn 410engineered mutation
Sequence viewer
Contents of the asymmetric unit
PolymersNumber of chains4
Total formula weight187709.2
All*Total formula weight187709.2
*Water molecules are not included.

226707

PDB entries from 2024-10-30

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