eF-site ID 6h4o-ABC
PDB Code 6h4o
Chain A, B, C

click to enlarge
Title Crystal structure of human KDM4A in complex with compound 18a
Classification OXIDOREDUCTASE
Compound Lysine-specific demethylase 4A
Source (KDM4A_HUMAN)
Sequence A:  LNPSARIMTFYPTMEEFRNFSRYIAYIESQGAHRAGLAKV
VPPKEWKPRASYDDIDDLVIPAPIQQLVTGQSGLFTQYNI
QKKAMTVREFRKIANSDKYCTPRYSEFEELERKYWKNLTF
NPPIYGADVNGTLYEKHVDEWNIGRLRTILDLVEGVNTPY
LYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPPEH
GKRLERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKYGI
PFDKVTQEAGEFMITFPYGYHAGFNHGFNCAESTNFATRR
WIEYGKQAVLCSCRKMVKISMDVFVRKFQPERYKLWKAGK
DNTVIDHTLPTPEAAEFL
B:  TLNPSARIMTFYPTMEEFRNFSRYIAYIESQGAHRAGLAK
VVPPKEWKPRASYDDIDDLVIPAPIQQLVTGQSGLFTQYN
IQKKAMTVREFRKIANSDKYCTPRYSEFEELERKYWKNLT
FNPPIYGADVNGTLYEKHVDEWNIGRLRTILDLVEEGVNT
PYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPP
EHGKRLERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKY
GIPFDKVTQEAGEFMITFPYGYHAGFNHGFNCAESTNFAT
RRWIEYGKQAVLCSCRMVKISMDVFVRKFQPERYKLWKAG
KDNTVIDHTLPTPEAAEFL
C:  SARIMTFYPTMEEFRNFSRYIAYIESQGAHRAGLAKVVPP
KEWKPRASYDDIDDLVIPAPIQQLVTGQSGLFTQYNIQKK
AMTVREFRKIANSDKYCTPRYSEFEELERKYWKNLTFNPP
IYGADVNGTLYEKHVDEWNIGRLRTILDLVEKESGITIEG
VNTPYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYS
VPPEHGKRLERLAKGFFPGSAQSCEAFLRHKMTLISPLML
KKYGIPFDKVTQEAGEFMITFPYGYHAGFNHGFNCAESTN
FATRRWIEYGKQAVLCSCMVKISMDVFVRKFQPERYKLWK
AGKDNTVIDHTLPTPEAAEFL
Description


Functional site

1) chain A
residue 188
type
sequence H
description binding site for residue ZN A 401
source : AC1

2) chain A
residue 190
type
sequence E
description binding site for residue ZN A 401
source : AC1

3) chain A
residue 276
type
sequence H
description binding site for residue ZN A 401
source : AC1

4) chain A
residue 234
type
sequence C
description binding site for residue ZN A 402
source : AC2

5) chain A
residue 240
type
sequence H
description binding site for residue ZN A 402
source : AC2

6) chain A
residue 306
type
sequence C
description binding site for residue ZN A 402
source : AC2

7) chain A
residue 308
type
sequence C
description binding site for residue ZN A 402
source : AC2

8) chain A
residue 132
type
sequence Y
description binding site for residue FQH A 403
source : AC3

9) chain A
residue 177
type
sequence Y
description binding site for residue FQH A 403
source : AC3

10) chain A
residue 185
type
sequence F
description binding site for residue FQH A 403
source : AC3

11) chain A
residue 188
type
sequence H
description binding site for residue FQH A 403
source : AC3

12) chain A
residue 190
type
sequence E
description binding site for residue FQH A 403
source : AC3

13) chain A
residue 191
type
sequence D
description binding site for residue FQH A 403
source : AC3

14) chain A
residue 206
type
sequence K
description binding site for residue FQH A 403
source : AC3

15) chain A
residue 208
type
sequence W
description binding site for residue FQH A 403
source : AC3

16) chain A
residue 276
type
sequence H
description binding site for residue FQH A 403
source : AC3

17) chain A
residue 75
type
sequence V
description binding site for residue GOL A 404
source : AC4

18) chain A
residue 76
type
sequence T
description binding site for residue GOL A 404
source : AC4

19) chain A
residue 77
type
sequence G
description binding site for residue GOL A 404
source : AC4

20) chain A
residue 126
type
sequence T
description binding site for residue GOL A 404
source : AC4

21) chain A
residue 127
type
sequence F
description binding site for residue GOL A 404
source : AC4

22) chain C
residue 75
type
sequence V
description binding site for residue GOL A 404
source : AC4

23) chain C
residue 76
type
sequence T
description binding site for residue GOL A 404
source : AC4

24) chain C
residue 77
type
sequence G
description binding site for residue GOL A 404
source : AC4

25) chain C
residue 126
type
sequence T
description binding site for residue GOL A 404
source : AC4

26) chain C
residue 127
type
sequence F
description binding site for residue GOL A 404
source : AC4

27) chain A
residue 59
type
sequence Y
description binding site for residue CL A 405
source : AC5

28) chain B
residue 188
type
sequence H
description binding site for residue ZN B 401
source : AC6

29) chain B
residue 190
type
sequence E
description binding site for residue ZN B 401
source : AC6

30) chain B
residue 276
type
sequence H
description binding site for residue ZN B 401
source : AC6

31) chain B
residue 234
type
sequence C
description binding site for residue ZN B 402
source : AC7

32) chain B
residue 240
type
sequence H
description binding site for residue ZN B 402
source : AC7

33) chain B
residue 306
type
sequence C
description binding site for residue ZN B 402
source : AC7

34) chain B
residue 308
type
sequence C
description binding site for residue ZN B 402
source : AC7

35) chain B
residue 132
type
sequence Y
description binding site for residue FQH B 403
source : AC8

36) chain B
residue 175
type
sequence Y
description binding site for residue FQH B 403
source : AC8

37) chain B
residue 177
type
sequence Y
description binding site for residue FQH B 403
source : AC8

38) chain B
residue 185
type
sequence F
description binding site for residue FQH B 403
source : AC8

39) chain B
residue 188
type
sequence H
description binding site for residue FQH B 403
source : AC8

40) chain B
residue 190
type
sequence E
description binding site for residue FQH B 403
source : AC8

41) chain B
residue 206
type
sequence K
description binding site for residue FQH B 403
source : AC8

42) chain B
residue 208
type
sequence W
description binding site for residue FQH B 403
source : AC8

43) chain B
residue 276
type
sequence H
description binding site for residue FQH B 403
source : AC8

44) chain B
residue 75
type
sequence V
description binding site for residue GOL B 404
source : AC9

45) chain B
residue 76
type
sequence T
description binding site for residue GOL B 404
source : AC9

46) chain B
residue 77
type
sequence G
description binding site for residue GOL B 404
source : AC9

47) chain B
residue 126
type
sequence T
description binding site for residue GOL B 404
source : AC9

48) chain B
residue 127
type
sequence F
description binding site for residue GOL B 404
source : AC9

49) chain C
residue 188
type
sequence H
description binding site for residue ZN C 401
source : AD1

50) chain C
residue 190
type
sequence E
description binding site for residue ZN C 401
source : AD1

51) chain C
residue 276
type
sequence H
description binding site for residue ZN C 401
source : AD1

52) chain C
residue 234
type
sequence C
description binding site for residue ZN C 402
source : AD2

53) chain C
residue 240
type
sequence H
description binding site for residue ZN C 402
source : AD2

54) chain C
residue 306
type
sequence C
description binding site for residue ZN C 402
source : AD2

55) chain C
residue 308
type
sequence C
description binding site for residue ZN C 402
source : AD2

56) chain C
residue 132
type
sequence Y
description binding site for residue FQH C 403
source : AD3

57) chain C
residue 135
type
sequence D
description binding site for residue FQH C 403
source : AD3

58) chain C
residue 169
type
sequence E
description binding site for residue FQH C 403
source : AD3

59) chain C
residue 175
type
sequence Y
description binding site for residue FQH C 403
source : AD3

60) chain C
residue 177
type
sequence Y
description binding site for residue FQH C 403
source : AD3

61) chain C
residue 185
type
sequence F
description binding site for residue FQH C 403
source : AD3

62) chain C
residue 188
type
sequence H
description binding site for residue FQH C 403
source : AD3

63) chain C
residue 190
type
sequence E
description binding site for residue FQH C 403
source : AD3

64) chain C
residue 191
type
sequence D
description binding site for residue FQH C 403
source : AD3

65) chain C
residue 206
type
sequence K
description binding site for residue FQH C 403
source : AD3

66) chain C
residue 208
type
sequence W
description binding site for residue FQH C 403
source : AD3

67) chain C
residue 276
type
sequence H
description binding site for residue FQH C 403
source : AD3

68) chain C
residue 12
type
sequence A
description binding site for residue DMS C 404
source : AD4

69) chain C
residue 13
type
sequence R
description binding site for residue DMS C 404
source : AD4

70) chain C
residue 257
type
sequence F
description binding site for residue DMS C 404
source : AD4

71) chain C
residue 294
type
sequence R
description binding site for residue DMS C 405
source : AD5

72) chain C
residue 324
type
sequence F
description binding site for residue DMS C 405
source : AD5

73) chain A
residue 170
type catalytic
sequence G
description 370
source MCSA : MCSA1

74) chain A
residue 177
type catalytic
sequence Y
description 370
source MCSA : MCSA1

75) chain A
residue 188
type catalytic
sequence H
description 370
source MCSA : MCSA1

76) chain A
residue 190
type catalytic
sequence E
description 370
source MCSA : MCSA1

77) chain A
residue 276
type catalytic
sequence H
description 370
source MCSA : MCSA1

78) chain A
residue 288
type catalytic
sequence S
description 370
source MCSA : MCSA1

79) chain B
residue 170
type catalytic
sequence G
description 370
source MCSA : MCSA2

80) chain B
residue 177
type catalytic
sequence Y
description 370
source MCSA : MCSA2

81) chain B
residue 188
type catalytic
sequence H
description 370
source MCSA : MCSA2

82) chain B
residue 190
type catalytic
sequence E
description 370
source MCSA : MCSA2

83) chain B
residue 276
type catalytic
sequence H
description 370
source MCSA : MCSA2

84) chain B
residue 288
type catalytic
sequence S
description 370
source MCSA : MCSA2

85) chain C
residue 170
type catalytic
sequence G
description 370
source MCSA : MCSA3

86) chain C
residue 177
type catalytic
sequence Y
description 370
source MCSA : MCSA3

87) chain C
residue 188
type catalytic
sequence H
description 370
source MCSA : MCSA3

88) chain C
residue 190
type catalytic
sequence E
description 370
source MCSA : MCSA3

89) chain C
residue 276
type catalytic
sequence H
description 370
source MCSA : MCSA3

90) chain C
residue 288
type catalytic
sequence S
description 370
source MCSA : MCSA3

91) chain C
residue 206
type BINDING
sequence K
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

92) chain B
residue 198
type BINDING
sequence N
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

93) chain B
residue 206
type BINDING
sequence K
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

94) chain C
residue 132
type BINDING
sequence Y
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

95) chain C
residue 198
type BINDING
sequence N
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

96) chain A
residue 132
type BINDING
sequence Y
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

97) chain A
residue 198
type BINDING
sequence N
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

98) chain A
residue 206
type BINDING
sequence K
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

99) chain B
residue 132
type BINDING
sequence Y
description BINDING => ECO:0000269|PubMed:16677698
source Swiss-Prot : SWS_FT_FI1

100) chain C
residue 188
type BINDING
sequence H
description BINDING => ECO:0000255|PROSITE-ProRule:PRU00538, ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI2

101) chain C
residue 276
type BINDING
sequence H
description BINDING => ECO:0000255|PROSITE-ProRule:PRU00538, ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI2

102) chain A
residue 188
type BINDING
sequence H
description BINDING => ECO:0000255|PROSITE-ProRule:PRU00538, ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI2

103) chain A
residue 276
type BINDING
sequence H
description BINDING => ECO:0000255|PROSITE-ProRule:PRU00538, ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI2

104) chain B
residue 188
type BINDING
sequence H
description BINDING => ECO:0000255|PROSITE-ProRule:PRU00538, ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI2

105) chain B
residue 276
type BINDING
sequence H
description BINDING => ECO:0000255|PROSITE-ProRule:PRU00538, ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI2

106) chain A
residue 190
type BINDING
sequence E
description BINDING => ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI3

107) chain B
residue 190
type BINDING
sequence E
description BINDING => ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI3

108) chain C
residue 190
type BINDING
sequence E
description BINDING => ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
source Swiss-Prot : SWS_FT_FI3

109) chain C
residue 240
type BINDING
sequence H
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

110) chain C
residue 306
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

111) chain C
residue 308
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

112) chain B
residue 234
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

113) chain B
residue 240
type BINDING
sequence H
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

114) chain B
residue 306
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

115) chain B
residue 308
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

116) chain C
residue 234
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

117) chain A
residue 308
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

118) chain A
residue 234
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

119) chain A
residue 240
type BINDING
sequence H
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

120) chain A
residue 306
type BINDING
sequence C
description BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
source Swiss-Prot : SWS_FT_FI4

121) chain A
residue 241
type BINDING
sequence K
description BINDING => ECO:0000250|UniProtKB:B2RXH2
source Swiss-Prot : SWS_FT_FI5

122) chain B
residue 241
type BINDING
sequence K
description BINDING => ECO:0000250|UniProtKB:B2RXH2
source Swiss-Prot : SWS_FT_FI5

123) chain C
residue 241
type BINDING
sequence K
description BINDING => ECO:0000250|UniProtKB:B2RXH2
source Swiss-Prot : SWS_FT_FI5


Display surface

Download
Links