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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H4H5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.481 |
CLV_PCSK_FUR_1 | 112 | 116 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.339 |
CLV_PCSK_PC7_1 | 302 | 308 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.511 |
DEG_APCC_DBOX_1 | 308 | 316 | PF00400 | 0.420 |
DOC_CDC14_PxL_1 | 278 | 286 | PF14671 | 0.432 |
DOC_CDC14_PxL_1 | 294 | 302 | PF14671 | 0.379 |
DOC_MAPK_gen_1 | 306 | 314 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 366 | 376 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.407 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.294 |
DOC_PP1_RVXF_1 | 403 | 410 | PF00149 | 0.455 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.533 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.563 |
DOC_PP4_FxxP_1 | 178 | 181 | PF00568 | 0.497 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.326 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 186 | 190 | PF12436 | 0.323 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 336 | 341 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 357 | 362 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 430 | 434 | PF00244 | 0.385 |
LIG_CaM_IQ_9 | 39 | 55 | PF13499 | 0.438 |
LIG_EVH1_1 | 347 | 351 | PF00568 | 0.510 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.496 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.340 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.450 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.455 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.439 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.504 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.727 |
LIG_LIR_Apic_2 | 177 | 181 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 324 | 328 | PF02991 | 0.340 |
LIG_LIR_Apic_2 | 380 | 385 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 143 | 151 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 358 | 365 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 420 | 431 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 88 | 96 | PF02991 | 0.437 |
LIG_LIR_LC3C_4 | 7 | 11 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.435 |
LIG_Pex14_1 | 210 | 214 | PF04695 | 0.421 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.468 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.283 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.388 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.371 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 144 | 148 | PF00017 | 0.281 |
LIG_SH2_NCK_1 | 382 | 386 | PF00017 | 0.292 |
LIG_SH2_SRC | 394 | 397 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.522 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.625 |
LIG_SUMO_SIM_anti_2 | 196 | 202 | PF11976 | 0.259 |
LIG_SUMO_SIM_anti_2 | 7 | 12 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 166 | 171 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 179 | 185 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 327 | 332 | PF11976 | 0.444 |
LIG_TYR_ITIM | 142 | 147 | PF00017 | 0.283 |
LIG_TYR_ITIM | 200 | 205 | PF00017 | 0.301 |
LIG_TYR_ITIM | 87 | 92 | PF00017 | 0.533 |
LIG_WRC_WIRS_1 | 175 | 180 | PF05994 | 0.395 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.466 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.485 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.375 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.546 |
MOD_DYRK1A_RPxSP_1 | 134 | 138 | PF00069 | 0.418 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.549 |
MOD_GlcNHglycan | 169 | 173 | PF01048 | 0.445 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.534 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.459 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.409 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.640 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.470 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.427 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.329 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.510 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.365 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.493 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.395 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.427 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.356 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.536 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.418 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.479 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.431 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.381 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.564 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.436 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.406 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.374 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.408 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.381 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.397 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.299 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.441 |
MOD_Plk_2-3 | 383 | 389 | PF00069 | 0.397 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.336 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.481 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.421 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.419 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.491 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.365 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.442 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.408 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.465 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.471 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.564 |
MOD_SUMO_for_1 | 258 | 261 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 255 | 260 | PF00179 | 0.634 |
MOD_SUMO_rev_2 | 69 | 78 | PF00179 | 0.387 |
TRG_DiLeu_BaEn_1 | 25 | 30 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_2 | 309 | 315 | PF01217 | 0.307 |
TRG_DiLeu_BaLyEn_6 | 178 | 183 | PF01217 | 0.297 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.288 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.522 |
TRG_NES_CRM1_1 | 266 | 279 | PF08389 | 0.285 |
TRG_NES_CRM1_1 | 310 | 324 | PF08389 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 306 | 310 | PF00026 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NL12 | Trypanosomatidae | 31% | 100% |
C9ZT97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AKN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 98% |
Q4QJ72 | Leishmania major | 74% | 100% |
V5B4P7 | Trypanosoma cruzi | 31% | 100% |