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: A0A3Q8IDD8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.433 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.657 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 318 | 320 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.427 |
DOC_CDC14_PxL_1 | 145 | 153 | PF14671 | 0.447 |
DOC_CYCLIN_RxL_1 | 346 | 357 | PF00134 | 0.310 |
DOC_CYCLIN_yCln2_LP_2 | 111 | 117 | PF00134 | 0.310 |
DOC_CYCLIN_yCln2_LP_2 | 120 | 126 | PF00134 | 0.310 |
DOC_CYCLIN_yCln2_LP_2 | 140 | 146 | PF00134 | 0.150 |
DOC_MAPK_gen_1 | 11 | 18 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.600 |
DOC_PP1_RVXF_1 | 13 | 19 | PF00149 | 0.576 |
DOC_PP1_RVXF_1 | 275 | 282 | PF00149 | 0.406 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.310 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.150 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.310 |
DOC_PP4_FxxP_1 | 280 | 283 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.310 |
DOC_PP4_FxxP_1 | 317 | 320 | PF00568 | 0.310 |
DOC_SPAK_OSR1_1 | 431 | 435 | PF12202 | 0.498 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.366 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.387 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 248 | 258 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 410 | 417 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 482 | 492 | PF00244 | 0.639 |
LIG_Actin_WH2_2 | 164 | 180 | PF00022 | 0.309 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.723 |
LIG_BIR_III_2 | 401 | 405 | PF00653 | 0.465 |
LIG_Clathr_ClatBox_1 | 352 | 356 | PF01394 | 0.330 |
LIG_eIF4E_1 | 347 | 353 | PF01652 | 0.330 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.340 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.360 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.457 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.463 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.324 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.433 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.714 |
LIG_LIR_Apic_2 | 278 | 283 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 295 | 300 | PF02991 | 0.206 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.257 |
LIG_LIR_Apic_2 | 315 | 320 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 17 | 21 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.609 |
LIG_Pex14_2 | 485 | 489 | PF04695 | 0.659 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.320 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.310 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.330 |
LIG_SH2_NCK_1 | 202 | 206 | PF00017 | 0.387 |
LIG_SH2_NCK_1 | 341 | 345 | PF00017 | 0.433 |
LIG_SH2_SRC | 202 | 205 | PF00017 | 0.426 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.387 |
LIG_SH2_SRC | 383 | 386 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.554 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.319 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.625 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.520 |
LIG_SH3_5 | 343 | 347 | PF00018 | 0.330 |
LIG_SUMO_SIM_anti_2 | 254 | 260 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 319 | 325 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 349 | 354 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 54 | 59 | PF11976 | 0.496 |
LIG_TYR_ITIM | 115 | 120 | PF00017 | 0.330 |
LIG_UBA3_1 | 440 | 447 | PF00899 | 0.418 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.387 |
LIG_WRC_WIRS_1 | 406 | 411 | PF05994 | 0.381 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.447 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.365 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.355 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.480 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.391 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.558 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.435 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.722 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.472 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.679 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.419 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.508 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.463 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.339 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.310 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.417 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.359 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.387 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.368 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.417 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.703 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.412 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.307 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.496 |
MOD_N-GLC_1 | 435 | 440 | PF02516 | 0.486 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.351 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.318 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.408 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.461 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.470 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.412 |
MOD_OFUCOSY | 419 | 425 | PF10250 | 0.458 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.430 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.504 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.373 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.388 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.480 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.466 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.694 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.505 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.413 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.429 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.576 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.577 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.473 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.410 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.608 |
TRG_NLS_MonoExtN_4 | 478 | 485 | PF00514 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 98 | 103 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWQ0 | Leptomonas seymouri | 72% | 96% |
A0A0S4J446 | Bodo saltans | 46% | 94% |
A0A1X0NQV6 | Trypanosomatidae | 59% | 96% |
A4HGY3 | Leishmania braziliensis | 89% | 100% |
A4I415 | Leishmania infantum | 100% | 100% |
D0A8Z4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9B0A2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q7Y2 | Leishmania major | 96% | 100% |
V5ATN3 | Trypanosoma cruzi | 58% | 100% |