Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: E9B241
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.505 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.642 |
DEG_SCF_FBW7_1 | 31 | 36 | PF00400 | 0.508 |
DEG_SPOP_SBC_1 | 125 | 129 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 136 | 140 | PF00917 | 0.521 |
DOC_CYCLIN_yClb3_PxF_3 | 83 | 89 | PF00134 | 0.637 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 84 | PF00134 | 0.683 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.620 |
DOC_PP4_FxxP_1 | 23 | 26 | PF00568 | 0.596 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.680 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.634 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.692 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.538 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.631 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.588 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.688 |
LIG_LIR_Gen_1 | 140 | 151 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 54 | 60 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.569 |
LIG_PDZ_Class_2 | 198 | 203 | PF00595 | 0.572 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.466 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.776 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.633 |
LIG_SH3_CIN85_PxpxPR_1 | 162 | 167 | PF14604 | 0.458 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.571 |
LIG_WW_3 | 73 | 77 | PF00397 | 0.678 |
MOD_CDC14_SPxK_1 | 73 | 76 | PF00782 | 0.675 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.683 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.654 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.741 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.639 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.725 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.779 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.571 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.647 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.621 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.539 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.610 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.649 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.610 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.538 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.673 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.733 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.668 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.692 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.691 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.730 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.606 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.592 |
MOD_NEK2_2 | 52 | 57 | PF00069 | 0.617 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.621 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.643 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.664 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.485 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.496 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.635 |
TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.663 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4V8 | Leishmania donovani | 85% | 100% |
A4HJM5 | Leishmania braziliensis | 62% | 99% |
A4I747 | Leishmania infantum | 84% | 100% |