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: Q4QJ72
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.458 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.393 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.476 |
DEG_APCC_DBOX_1 | 307 | 315 | PF00400 | 0.374 |
DEG_APCC_DBOX_1 | 444 | 452 | PF00400 | 0.317 |
DOC_CDC14_PxL_1 | 277 | 285 | PF14671 | 0.380 |
DOC_CDC14_PxL_1 | 293 | 301 | PF14671 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 348 | 354 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 305 | 313 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 132 | 140 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 413 | 420 | PF00149 | 0.592 |
DOC_PP2B_LxvP_1 | 161 | 164 | PF13499 | 0.490 |
DOC_PP2B_LxvP_1 | 348 | 351 | PF13499 | 0.495 |
DOC_PP4_FxxP_1 | 176 | 179 | PF00568 | 0.516 |
DOC_PP4_FxxP_1 | 324 | 327 | PF00568 | 0.313 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 233 | 237 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 366 | 372 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 376 | 384 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 40 | 47 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.372 |
LIG_CSL_BTD_1 | 351 | 354 | PF09270 | 0.491 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.315 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.431 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.374 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.572 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.571 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.441 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.327 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.437 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.529 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.766 |
LIG_LIR_Apic_2 | 175 | 179 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 276 | 281 | PF02991 | 0.273 |
LIG_LIR_Apic_2 | 323 | 327 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 368 | 379 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 430 | 441 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.474 |
LIG_LIR_LC3C_4 | 6 | 11 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.473 |
LIG_Pex14_1 | 208 | 212 | PF04695 | 0.379 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.452 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.292 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.363 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.456 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.500 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.510 |
LIG_SH3_4 | 209 | 216 | PF00018 | 0.302 |
LIG_SUMO_SIM_anti_2 | 6 | 12 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 326 | 331 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 440 | 447 | PF11976 | 0.409 |
LIG_TYR_ITIM | 85 | 90 | PF00017 | 0.507 |
LIG_TYR_ITSM | 300 | 307 | PF00017 | 0.306 |
LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.352 |
LIG_WRC_WIRS_1 | 267 | 272 | PF05994 | 0.331 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.336 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.441 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.456 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.408 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.547 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.568 |
MOD_DYRK1A_RPxSP_1 | 132 | 136 | PF00069 | 0.386 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.416 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.482 |
MOD_GlcNHglycan | 167 | 171 | PF01048 | 0.408 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.574 |
MOD_GlcNHglycan | 329 | 333 | PF01048 | 0.486 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.612 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.450 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.551 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.388 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.593 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.339 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.398 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.381 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.472 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.385 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.502 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.288 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.467 |
MOD_LATS_1 | 222 | 228 | PF00433 | 0.328 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.523 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.524 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.462 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.368 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.335 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.322 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.565 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.556 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.344 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.397 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.454 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.308 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.386 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.489 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.467 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.382 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.565 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.358 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.551 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.398 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.305 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.416 |
MOD_Plk_2-3 | 393 | 399 | PF00069 | 0.370 |
MOD_Plk_2-3 | 54 | 60 | PF00069 | 0.525 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.409 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.445 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.359 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.364 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.462 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.435 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.419 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.379 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.423 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.665 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.543 |
TRG_DiLeu_BaEn_2 | 308 | 314 | PF01217 | 0.288 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.502 |
TRG_NES_CRM1_1 | 309 | 323 | PF08389 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.347 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NL12 | Trypanosomatidae | 28% | 100% |
A4H4H5 | Leishmania braziliensis | 74% | 100% |
C9ZT97 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AKN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5B4P7 | Trypanosoma cruzi | 30% | 100% |