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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AM75
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 121 | 125 | PF00082 | 0.588 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.489 |
CLV_PCSK_PC7_1 | 144 | 150 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.383 |
DOC_CYCLIN_RxL_1 | 112 | 119 | PF00134 | 0.574 |
DOC_CYCLIN_RxL_1 | 246 | 259 | PF00134 | 0.373 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.684 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.576 |
DOC_USP7_UBL2_3 | 186 | 190 | PF12436 | 0.592 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 183 | 192 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 268 | 285 | PF00022 | 0.484 |
LIG_Actin_WH2_2 | 91 | 109 | PF00022 | 0.375 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.434 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.343 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.558 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.455 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.456 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.397 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.483 |
LIG_LIR_Gen_1 | 83 | 91 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.323 |
LIG_NRBOX | 171 | 177 | PF00104 | 0.339 |
LIG_PCNA_yPIPBox_3 | 171 | 185 | PF02747 | 0.474 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.458 |
LIG_PTB_Apo_2 | 238 | 245 | PF02174 | 0.515 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.439 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.623 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.487 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.470 |
LIG_SUMO_SIM_anti_2 | 170 | 177 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 170 | 177 | PF11976 | 0.344 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.676 |
LIG_TRAF2_1 | 91 | 94 | PF00917 | 0.223 |
LIG_TYR_ITIM | 98 | 103 | PF00017 | 0.424 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.613 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.611 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.359 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.568 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.570 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.467 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.548 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.736 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.347 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.455 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.535 |
MOD_NEK2_2 | 142 | 147 | PF00069 | 0.612 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.422 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.476 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.350 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.405 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.460 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.598 |
MOD_Plk_2-3 | 76 | 82 | PF00069 | 0.629 |
MOD_SUMO_for_1 | 129 | 132 | PF00179 | 0.646 |
MOD_SUMO_rev_2 | 69 | 79 | PF00179 | 0.508 |
TRG_DiLeu_BaEn_4 | 75 | 81 | PF01217 | 0.740 |
TRG_DiLeu_BaLyEn_6 | 133 | 138 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.623 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.446 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 134 | 136 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 146 | 149 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.706 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 193 | 198 | PF00026 | 0.643 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIG8 | Leptomonas seymouri | 66% | 100% |
A0A0S4ITL7 | Bodo saltans | 34% | 100% |
A0A1X0NZE1 | Trypanosomatidae | 67% | 96% |
A0A3Q8IB97 | Leishmania donovani | 90% | 100% |
A0A3R7KKG3 | Trypanosoma rangeli | 65% | 100% |
A4HH12 | Leishmania braziliensis | 76% | 100% |
A4I441 | Leishmania infantum | 91% | 100% |
C9ZKS1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
E9ADK6 | Leishmania major | 91% | 100% |
V5BUH7 | Trypanosoma cruzi | 60% | 81% |