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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AUT4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.461 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.563 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.607 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.489 |
DOC_CYCLIN_RxL_1 | 363 | 373 | PF00134 | 0.506 |
DOC_CYCLIN_RxL_1 | 43 | 54 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 76 | 86 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 273 | 280 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 57 | 66 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 99 | 106 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.356 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.472 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.464 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 179 | 186 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 191 | 197 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 214 | 221 | PF00244 | 0.754 |
LIG_APCC_ABBAyCdc20_2 | 69 | 75 | PF00400 | 0.499 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.708 |
LIG_BIR_III_4 | 266 | 270 | PF00653 | 0.593 |
LIG_BIR_III_4 | 29 | 33 | PF00653 | 0.461 |
LIG_CaM_IQ_9 | 335 | 351 | PF13499 | 0.462 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.534 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.412 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.394 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.462 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.519 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.387 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.567 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.460 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.621 |
LIG_LIR_Apic_2 | 224 | 230 | PF02991 | 0.637 |
LIG_LIR_Apic_2 | 282 | 287 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.346 |
LIG_NRBOX | 93 | 99 | PF00104 | 0.426 |
LIG_PCNA_PIPBox_1 | 49 | 58 | PF02747 | 0.455 |
LIG_PCNA_yPIPBox_3 | 46 | 56 | PF02747 | 0.450 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.624 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.646 |
LIG_SH2_NCK_1 | 284 | 288 | PF00017 | 0.624 |
LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.331 |
LIG_SH3_2 | 21 | 26 | PF14604 | 0.418 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.498 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.602 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.254 |
LIG_SH3_4 | 59 | 66 | PF00018 | 0.457 |
LIG_Sin3_3 | 377 | 384 | PF02671 | 0.455 |
LIG_SUMO_SIM_par_1 | 317 | 325 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 366 | 373 | PF11976 | 0.500 |
LIG_TYR_ITIM | 175 | 180 | PF00017 | 0.371 |
LIG_UBA3_1 | 367 | 375 | PF00899 | 0.467 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.703 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.626 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.624 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.393 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.710 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.639 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.627 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.569 |
MOD_DYRK1A_RPxSP_1 | 193 | 197 | PF00069 | 0.446 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.753 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.639 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.658 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.455 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.660 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.516 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.656 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.577 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.586 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.647 |
MOD_LATS_1 | 190 | 196 | PF00433 | 0.567 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.787 |
MOD_N-GLC_2 | 81 | 83 | PF02516 | 0.365 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.672 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.481 |
MOD_NEK2_2 | 74 | 79 | PF00069 | 0.410 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.538 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.584 |
MOD_PKA_1 | 151 | 157 | PF00069 | 0.518 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.703 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.518 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.416 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.652 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.546 |
MOD_PKB_1 | 229 | 237 | PF00069 | 0.479 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.662 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.561 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.381 |
MOD_Plk_2-3 | 121 | 127 | PF00069 | 0.441 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.402 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.381 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.587 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.479 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.637 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.671 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.616 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.629 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 121 | 131 | PF00179 | 0.440 |
TRG_DiLeu_BaEn_1 | 158 | 163 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_1 | 61 | 66 | PF01217 | 0.456 |
TRG_DiLeu_LyEn_5 | 158 | 163 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.524 |
TRG_NES_CRM1_1 | 158 | 171 | PF08389 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 329 | 334 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 366 | 371 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 76 | 80 | PF00026 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYV9 | Leptomonas seymouri | 56% | 96% |
A0A1X0NWT1 | Trypanosomatidae | 36% | 100% |
A0A3S7WW52 | Leishmania donovani | 92% | 100% |
A0A422N975 | Trypanosoma rangeli | 36% | 100% |
A4HYY8 | Leishmania infantum | 92% | 100% |
E9AIK2 | Leishmania braziliensis | 80% | 96% |
Q4QCP9 | Leishmania major | 93% | 100% |