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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AMQ2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.693 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.744 |
CLV_PCSK_PC7_1 | 104 | 110 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.749 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.623 |
DEG_ODPH_VHL_1 | 111 | 122 | PF01847 | 0.515 |
DOC_CYCLIN_RxL_1 | 133 | 143 | PF00134 | 0.475 |
DOC_MAPK_gen_1 | 55 | 63 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 81 | 88 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 19 | 26 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 56 | 65 | PF00069 | 0.412 |
DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.401 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.525 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.427 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.470 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.470 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.551 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.735 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.248 |
LIG_CtBP_PxDLS_1 | 237 | 241 | PF00389 | 0.675 |
LIG_EH_1 | 176 | 180 | PF12763 | 0.691 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.544 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.540 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.413 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.645 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.618 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.719 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.658 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.677 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.568 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.501 |
LIG_LIR_Apic_2 | 83 | 87 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.411 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.464 |
LIG_PTB_Apo_2 | 74 | 81 | PF02174 | 0.505 |
LIG_PTB_Phospho_1 | 74 | 80 | PF10480 | 0.501 |
LIG_REV1ctd_RIR_1 | 388 | 392 | PF16727 | 0.698 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.658 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.398 |
LIG_SH2_GRB2like | 175 | 178 | PF00017 | 0.654 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.555 |
LIG_SH2_NCK_1 | 175 | 179 | PF00017 | 0.736 |
LIG_SH2_NCK_1 | 307 | 311 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.513 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.632 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.503 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.565 |
LIG_SUMO_SIM_anti_2 | 2 | 9 | PF11976 | 0.512 |
LIG_SUMO_SIM_anti_2 | 356 | 362 | PF11976 | 0.574 |
LIG_SUMO_SIM_par_1 | 152 | 157 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 308 | 314 | PF11976 | 0.495 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.670 |
LIG_TRAF2_1 | 380 | 383 | PF00917 | 0.666 |
LIG_TYR_ITSM | 115 | 122 | PF00017 | 0.547 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.667 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.558 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.523 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.541 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.685 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.555 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.664 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.523 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.720 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.565 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.574 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.439 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.667 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.594 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.643 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.536 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.571 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.578 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.365 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.501 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.377 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.551 |
MOD_PK_1 | 82 | 88 | PF00069 | 0.254 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.670 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.597 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.579 |
MOD_PKB_1 | 196 | 204 | PF00069 | 0.668 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.562 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.419 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.515 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.371 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.424 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.419 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.465 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.443 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.750 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.567 |
MOD_SUMO_for_1 | 285 | 288 | PF00179 | 0.795 |
MOD_SUMO_for_1 | 330 | 333 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 382 | 390 | PF00179 | 0.666 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 16 | 21 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.563 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.613 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.682 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB46 | Leptomonas seymouri | 63% | 98% |
A0A1X0NNC7 | Trypanosomatidae | 33% | 100% |
A0A3Q8IAS3 | Leishmania donovani | 86% | 94% |
A4H5M8 | Leishmania braziliensis | 79% | 99% |
A4HTW5 | Leishmania infantum | 84% | 97% |
D0A9C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4QHX3 | Leishmania major | 85% | 100% |
V5DJG9 | Trypanosoma cruzi | 34% | 100% |