eF-site ID 4q1w-B
PDB Code 4q1w
Chain B

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Title Mutations Outside the Active Site of HIV-1 Protease Alter Enzyme Structure and Dynamic Ensemble of the Active Site to Confer Drug Resistance
Classification hydrolase/hydrolase inhibitor
Compound ASPARTYL PROTEASE
Source (V5Y949_9HIV1)
Sequence B:  PQITLWKRPLVTIRIGGQLKEALLDTGADDTVLEEMNLPG
KWKPKMIGGIGGFIKVRQYDQIPIEICGHKAIGTVLVGPT
PVNIIGRNLMTQIGCTLNF
Description


Functional site

1) chain B
residue 16
type
sequence G
description BINDING SITE FOR RESIDUE PO4 A 101
source : AC1

2) chain B
residue 39
type
sequence P
description BINDING SITE FOR RESIDUE PO4 A 103
source : AC3

3) chain B
residue 40
type
sequence G
description BINDING SITE FOR RESIDUE PO4 A 103
source : AC3

4) chain B
residue 25
type
sequence D
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

5) chain B
residue 27
type
sequence G
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

6) chain B
residue 28
type
sequence A
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

7) chain B
residue 30
type
sequence D
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

8) chain B
residue 48
type
sequence G
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

9) chain B
residue 49
type
sequence G
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

10) chain B
residue 81
type
sequence P
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

11) chain B
residue 82
type
sequence V
description BINDING SITE FOR RESIDUE 017 A 104
source : AC4

12) chain B
residue 6
type
sequence W
description BINDING SITE FOR RESIDUE PO4 B 101
source : AC5

13) chain B
residue 7
type
sequence K
description BINDING SITE FOR RESIDUE PO4 B 101
source : AC5

14) chain B
residue 8
type
sequence R
description BINDING SITE FOR RESIDUE PO4 B 101
source : AC5

15) chain B
residue 91
type
sequence T
description BINDING SITE FOR RESIDUE ACT B 102
source : AC6

16) chain B
residue 92
type
sequence Q
description BINDING SITE FOR RESIDUE ACT B 102
source : AC6

17) chain B
residue 25
type catalytic
sequence D
description 175
source MCSA : MCSA2

18) chain B
residue 26
type catalytic
sequence T
description 175
source MCSA : MCSA2

19) chain B
residue 27
type catalytic
sequence G
description 175
source MCSA : MCSA2

20) chain B
residue 25
type ACT_SITE
sequence D
description For protease activity; shared with dimeric partner => ECO:0000255|PROSITE-ProRule:PRU10094, ECO:0000305|PubMed:33542150
source Swiss-Prot : SWS_FT_FI1

21) chain B
residue 99
type SITE
sequence F
description Cleavage; by viral protease => ECO:0000250
source Swiss-Prot : SWS_FT_FI2


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