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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S7XAS3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.565 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.503 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.575 |
DOC_CYCLIN_RxL_1 | 297 | 307 | PF00134 | 0.502 |
DOC_CYCLIN_RxL_1 | 319 | 326 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 225 | 234 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 330 | 337 | PF00069 | 0.545 |
DOC_PP4_FxxP_1 | 162 | 165 | PF00568 | 0.542 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.498 |
DOC_USP7_UBL2_3 | 472 | 476 | PF12436 | 0.551 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 22 | 26 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 319 | 325 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.483 |
LIG_Actin_WH2_2 | 7 | 24 | PF00022 | 0.532 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 385 | 389 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.583 |
LIG_CaM_IQ_9 | 348 | 364 | PF13499 | 0.515 |
LIG_eIF4E_1 | 290 | 296 | PF01652 | 0.487 |
LIG_FAT_LD_1 | 175 | 183 | PF03623 | 0.403 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.455 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.530 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.624 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.655 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.510 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.525 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.347 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.416 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.694 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.546 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.599 |
LIG_Integrin_RGD_1 | 220 | 222 | PF01839 | 0.485 |
LIG_LIR_Apic_2 | 159 | 165 | PF02991 | 0.547 |
LIG_LIR_Apic_2 | 422 | 426 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 277 | 287 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 306 | 317 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 386 | 396 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 463 | 471 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.494 |
LIG_LYPXL_yS_3 | 273 | 276 | PF13949 | 0.505 |
LIG_Pex14_1 | 461 | 465 | PF04695 | 0.582 |
LIG_Pex14_2 | 280 | 284 | PF04695 | 0.407 |
LIG_SH2_CRK | 465 | 469 | PF00017 | 0.555 |
LIG_SH2_PTP2 | 423 | 426 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 465 | 469 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.502 |
LIG_SH2_STAT6 | 409 | 413 | PF00017 | 0.541 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.609 |
LIG_SUMO_SIM_par_1 | 331 | 336 | PF11976 | 0.567 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.545 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.490 |
LIG_UBA3_1 | 178 | 185 | PF00899 | 0.401 |
LIG_UBA3_1 | 324 | 330 | PF00899 | 0.472 |
LIG_UBA3_1 | 53 | 60 | PF00899 | 0.540 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.616 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.511 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.454 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.539 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.509 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.418 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.363 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.412 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.749 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.568 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.614 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.581 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.497 |
MOD_Cter_Amidation | 483 | 486 | PF01082 | 0.602 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.590 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.531 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.598 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.398 |
MOD_GlcNHglycan | 49 | 53 | PF01048 | 0.572 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.525 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.683 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.483 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.752 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.517 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.620 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.563 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.589 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.433 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.555 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.591 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.461 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.431 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.530 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.377 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.352 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.664 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.522 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.537 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.657 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.452 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.535 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.467 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.541 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.717 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.405 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.669 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.516 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.598 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.491 |
MOD_Plk_2-3 | 478 | 484 | PF00069 | 0.608 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.435 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.472 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.465 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.471 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.616 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.594 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.612 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 475 | 478 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 159 | 167 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 226 | 232 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 442 | 450 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 466 | 474 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 65 | 74 | PF00179 | 0.701 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 123 | 127 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCT1 | Leptomonas seymouri | 62% | 97% |
A0A1X0P7R8 | Trypanosomatidae | 32% | 97% |
A0A422MV92 | Trypanosoma rangeli | 30% | 100% |
A4HP57 | Leishmania braziliensis | 76% | 100% |
A4IDG3 | Leishmania infantum | 100% | 100% |
D0A343 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ASW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q1N2 | Leishmania major | 92% | 100% |
V5DKS4 | Trypanosoma cruzi | 30% | 100% |