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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9B3P2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.409 |
DEG_COP1_1 | 354 | 364 | PF00400 | 0.394 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.547 |
DOC_CYCLIN_RxL_1 | 140 | 151 | PF00134 | 0.479 |
DOC_CYCLIN_RxL_1 | 27 | 37 | PF00134 | 0.420 |
DOC_CYCLIN_RxL_1 | 91 | 102 | PF00134 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 340 | 346 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 193 | 202 | PF00069 | 0.409 |
DOC_PP1_RVXF_1 | 418 | 425 | PF00149 | 0.477 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.462 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.473 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 294 | 303 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 373 | 379 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 412 | 422 | PF00244 | 0.388 |
LIG_Actin_WH2_2 | 114 | 129 | PF00022 | 0.342 |
LIG_BIR_III_2 | 137 | 141 | PF00653 | 0.436 |
LIG_EH1_1 | 220 | 228 | PF00400 | 0.449 |
LIG_eIF4E_1 | 221 | 227 | PF01652 | 0.443 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.379 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.509 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.455 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.236 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.537 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.346 |
LIG_GBD_Chelix_1 | 104 | 112 | PF00786 | 0.459 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.437 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.344 |
LIG_PTB_Apo_2 | 164 | 171 | PF02174 | 0.575 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.455 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.257 |
LIG_SUMO_SIM_par_1 | 37 | 42 | PF11976 | 0.427 |
LIG_TRAF2_1 | 172 | 175 | PF00917 | 0.412 |
LIG_UBA3_1 | 95 | 100 | PF00899 | 0.412 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.401 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.648 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.279 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.498 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.571 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.623 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.431 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.648 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.582 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.500 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.400 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.430 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.406 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.529 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.578 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.603 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.368 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.374 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.290 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.392 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.473 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.459 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.383 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.597 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.685 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.476 |
MOD_N-GLC_2 | 264 | 266 | PF02516 | 0.236 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.610 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.580 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.654 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.323 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.552 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.384 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.551 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.472 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.417 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.430 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.473 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.431 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.301 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.519 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.408 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.457 |
MOD_PK_1 | 310 | 316 | PF00069 | 0.330 |
MOD_PK_1 | 63 | 69 | PF00069 | 0.485 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.434 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.411 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.525 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.727 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.474 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.337 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.484 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.423 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.592 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.413 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.353 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.526 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.263 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.418 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.394 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.433 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.463 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.525 |
MOD_SUMO_rev_2 | 192 | 199 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 337 | 343 | PF00179 | 0.445 |
TRG_DiLeu_BaEn_1 | 317 | 322 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.527 |
TRG_NLS_MonoExtC_3 | 214 | 220 | PF00514 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 201 | 205 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 405 | 409 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3R7 | Leptomonas seymouri | 55% | 99% |
A0A1X0P0P1 | Trypanosomatidae | 29% | 98% |
A0A3Q8IHM8 | Leishmania donovani | 91% | 100% |
A0A3S5IQQ0 | Trypanosoma rangeli | 27% | 100% |
A4HLA0 | Leishmania braziliensis | 79% | 100% |
A4I8S6 | Leishmania infantum | 91% | 100% |
D0A4S2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 99% |
Q4Q4E5 | Leishmania major | 91% | 100% |
V5BFC5 | Trypanosoma cruzi | 27% | 98% |