eF-site ID 2p5n-AB
PDB Code 2p5n
Chain A, B

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Title Crystal structure of mouse 17-alpha hydroxysteroid dehydrogenase in complex with coenzyme NADPH
Classification OXIDOREDUCTASE
Compound Aldo-keto reductase family 1, member C21
Source (Q6P8V0_MOUSE)
Sequence A:  MNSKCHCVILNDGNFIPVLGFGTALPLECPKSKAKELTKI
AIDAGFHHFDSASVYNTEDHVGEAIRSKIADGTVRREDIF
YTSKVWCTSLHPELVRASLERSLQKLQFDYVDLYLIHYPM
ALKPGEENFPVDEHGKLIFDRVDLCATWEAMEKCKDAGLT
KSIGVSNFNYRQLEMILNKPGLKYKPVCNQVECHPYLNQM
KLLDFCKSKDIVLVAYGVLGTQRYGGWVDQNSPVLLDEPV
LGSMAKKYNRTPALIALRYQLQRGIVVLNTSLKEERIKEN
MQVFEFQLSSEDMKVLDGLNRNMRYIPAAIFKGHPNWPFL
DEY
B:  MNSKCHCVILNDGNFIPVLGFGTALPLECPKSKAKELTKI
AIDAGFHHFDSASVYNTEDHVGEAIRSKIADGTVRREDIF
YTSKVWCTSLHPELVRASLERSLQKLQFDYVDLYLIHYPM
ALKPGEENFPVDEHGKLIFDRVDLCATWEAMEKCKDAGLT
KSIGVSNFNYRQLEMILNKPGLKYKPVCNQVECHPYLNQM
KLLDFCKSKDIVLVAYGVLGTQRYGGWVDQNSPVLLDEPV
LGSMAKKYNRTPALIALRYQLQRGIVVLNTSLKEERIKEN
MQVFEFQLSSEDMKVLDGLNRNMRYIPAAIFKGHPNWPFL
DEY
Description


Functional site

1) chain A
residue 22
type
sequence G
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

2) chain A
residue 23
type
sequence T
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

3) chain A
residue 24
type
sequence A
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

4) chain A
residue 50
type
sequence D
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

5) chain A
residue 55
type
sequence Y
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

6) chain A
residue 117
type
sequence H
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

7) chain A
residue 166
type
sequence S
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

8) chain A
residue 167
type
sequence N
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

9) chain A
residue 190
type
sequence Q
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

10) chain A
residue 216
type
sequence Y
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

11) chain A
residue 217
type
sequence G
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

12) chain A
residue 218
type
sequence V
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

13) chain A
residue 219
type
sequence L
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

14) chain A
residue 220
type
sequence G
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

15) chain A
residue 221
type
sequence T
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

16) chain A
residue 222
type
sequence Q
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

17) chain A
residue 224
type
sequence Y
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

18) chain A
residue 253
type
sequence A
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

19) chain A
residue 269
type
sequence N
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

20) chain A
residue 270
type
sequence T
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

21) chain A
residue 271
type
sequence S
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

22) chain A
residue 272
type
sequence L
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

23) chain A
residue 273
type
sequence K
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

24) chain A
residue 276
type
sequence R
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

25) chain A
residue 279
type
sequence E
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

26) chain A
residue 280
type
sequence N
description BINDING SITE FOR RESIDUE NDP A 1350
source : AC1

27) chain B
residue 22
type
sequence G
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

28) chain B
residue 23
type
sequence T
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

29) chain B
residue 24
type
sequence A
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

30) chain B
residue 50
type
sequence D
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

31) chain B
residue 55
type
sequence Y
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

32) chain B
residue 84
type
sequence K
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

33) chain B
residue 117
type
sequence H
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

34) chain B
residue 166
type
sequence S
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

35) chain B
residue 167
type
sequence N
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

36) chain B
residue 190
type
sequence Q
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

37) chain B
residue 216
type
sequence Y
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

38) chain B
residue 217
type
sequence G
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

39) chain B
residue 218
type
sequence V
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

40) chain B
residue 219
type
sequence L
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

41) chain B
residue 220
type
sequence G
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

42) chain B
residue 221
type
sequence T
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

43) chain B
residue 222
type
sequence Q
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

44) chain B
residue 224
type
sequence Y
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

45) chain B
residue 236
type
sequence L
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

46) chain B
residue 253
type
sequence A
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

47) chain B
residue 269
type
sequence N
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

48) chain B
residue 270
type
sequence T
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

49) chain B
residue 271
type
sequence S
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

50) chain B
residue 272
type
sequence L
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

51) chain B
residue 273
type
sequence K
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

52) chain B
residue 276
type
sequence R
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

53) chain B
residue 279
type
sequence E
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

54) chain B
residue 280
type
sequence N
description BINDING SITE FOR RESIDUE NDP B 2350
source : AC2

55) chain A
residue 55
type
sequence Y
description BINDING SITE FOR RESIDUE MPD A 1001
source : AC3

56) chain A
residue 224
type
sequence Y
description BINDING SITE FOR RESIDUE MPD A 1001
source : AC3

57) chain A
residue 227
type
sequence W
description BINDING SITE FOR RESIDUE MPD A 1001
source : AC3

58) chain B
residue 55
type
sequence Y
description BINDING SITE FOR RESIDUE MPD B 2001
source : AC4

59) chain B
residue 224
type
sequence Y
description BINDING SITE FOR RESIDUE MPD B 2001
source : AC4

60) chain B
residue 227
type
sequence W
description BINDING SITE FOR RESIDUE MPD B 2001
source : AC4

61) chain A
residue 151-168
type prosite
sequence MEKCKDAGLTKSIGVSNF
description ALDOKETO_REDUCTASE_2 Aldo/keto reductase family signature 2. MekckdaglTKSIGVSNF
source prosite : PS00062

62) chain A
residue 55
type ACT_SITE
sequence Y
description Proton donor
source Swiss-Prot : SWS_FT_FI1

63) chain B
residue 55
type ACT_SITE
sequence Y
description Proton donor
source Swiss-Prot : SWS_FT_FI1

64) chain A
residue 20
type BINDING
sequence G
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

65) chain B
residue 190
type BINDING
sequence Q
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

66) chain B
residue 216
type BINDING
sequence Y
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

67) chain B
residue 270
type BINDING
sequence T
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

68) chain A
residue 50
type BINDING
sequence D
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

69) chain A
residue 166
type BINDING
sequence S
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

70) chain A
residue 190
type BINDING
sequence Q
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

71) chain A
residue 216
type BINDING
sequence Y
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

72) chain A
residue 270
type BINDING
sequence T
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

73) chain B
residue 20
type BINDING
sequence G
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

74) chain B
residue 50
type BINDING
sequence D
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

75) chain B
residue 166
type BINDING
sequence S
description BINDING => ECO:0000269|PubMed:17034817, ECO:0000269|PubMed:17909281, ECO:0000269|PubMed:19237748
source Swiss-Prot : SWS_FT_FI2

76) chain A
residue 31
type BINDING
sequence K
description
source Swiss-Prot : SWS_FT_FI3

77) chain A
residue 117
type BINDING
sequence H
description
source Swiss-Prot : SWS_FT_FI3

78) chain B
residue 31
type BINDING
sequence K
description
source Swiss-Prot : SWS_FT_FI3

79) chain B
residue 117
type BINDING
sequence H
description
source Swiss-Prot : SWS_FT_FI3

80) chain A
residue 84
type SITE
sequence K
description Lowers pKa of active site Tyr => ECO:0000250
source Swiss-Prot : SWS_FT_FI4

81) chain B
residue 84
type SITE
sequence K
description Lowers pKa of active site Tyr => ECO:0000250
source Swiss-Prot : SWS_FT_FI4


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