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: A4H8G6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.804 |
CLV_MEL_PAP_1 | 500 | 506 | PF00089 | 0.593 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.666 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.822 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 228 | 230 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 433 | 435 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.781 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.822 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.651 |
DEG_APCC_DBOX_1 | 391 | 399 | PF00400 | 0.317 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.526 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.508 |
DEG_SPOP_SBC_1 | 409 | 413 | PF00917 | 0.566 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.602 |
DOC_CKS1_1 | 347 | 352 | PF01111 | 0.541 |
DOC_CYCLIN_RxL_1 | 300 | 311 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 347 | 353 | PF00134 | 0.599 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 141 | 150 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 261 | 268 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.399 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.234 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.336 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.510 |
DOC_PP2B_PxIxI_1 | 145 | 151 | PF00149 | 0.246 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 440 | 444 | PF12436 | 0.746 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 207 | 216 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 282 | 290 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 488 | 496 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 501 | 510 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 536 | 545 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 57 | 67 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 87 | 93 | PF00244 | 0.686 |
LIG_Actin_WH2_2 | 493 | 510 | PF00022 | 0.639 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.454 |
LIG_CaM_IQ_9 | 507 | 522 | PF13499 | 0.449 |
LIG_deltaCOP1_diTrp_1 | 239 | 245 | PF00928 | 0.441 |
LIG_eIF4E_1 | 336 | 342 | PF01652 | 0.332 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.442 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.438 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.490 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.542 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.363 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.526 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.492 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.621 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.593 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.445 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.642 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.603 |
LIG_Integrin_isoDGR_2 | 298 | 300 | PF01839 | 0.412 |
LIG_LIR_Gen_1 | 239 | 250 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 333 | 344 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.607 |
LIG_MAD2 | 129 | 137 | PF02301 | 0.498 |
LIG_NRBOX | 138 | 144 | PF00104 | 0.386 |
LIG_NRP_CendR_1 | 543 | 546 | PF00754 | 0.538 |
LIG_Pex14_1 | 386 | 390 | PF04695 | 0.409 |
LIG_RPA_C_Fungi | 225 | 237 | PF08784 | 0.441 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.441 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.517 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.610 |
LIG_SUMO_SIM_anti_2 | 149 | 155 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.603 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.498 |
LIG_TRAF2_1 | 519 | 522 | PF00917 | 0.605 |
LIG_TYR_ITIM | 334 | 339 | PF00017 | 0.349 |
LIG_WRC_WIRS_1 | 29 | 34 | PF05994 | 0.440 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.365 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.648 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.574 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.520 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.640 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.673 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.564 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.609 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.461 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.490 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.667 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.477 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.664 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.452 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.650 |
MOD_Cter_Amidation | 226 | 229 | PF01082 | 0.525 |
MOD_Cter_Amidation | 442 | 445 | PF01082 | 0.689 |
MOD_Cter_Amidation | 69 | 72 | PF01082 | 0.469 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.493 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.740 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.586 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.506 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.587 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.512 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.712 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.598 |
MOD_GlcNHglycan | 469 | 473 | PF01048 | 0.460 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.643 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.693 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.527 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.498 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.707 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.755 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.699 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.550 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.532 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.407 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.387 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.684 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.600 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.783 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.461 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.606 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.318 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.320 |
MOD_N-GLC_2 | 16 | 18 | PF02516 | 0.463 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.690 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.480 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.443 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.415 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.543 |
MOD_PKA_1 | 281 | 287 | PF00069 | 0.544 |
MOD_PKA_1 | 433 | 439 | PF00069 | 0.739 |
MOD_PKA_1 | 516 | 522 | PF00069 | 0.595 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.563 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.519 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.434 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.589 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.410 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.507 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.763 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.726 |
MOD_PKB_1 | 314 | 322 | PF00069 | 0.405 |
MOD_PKB_1 | 40 | 48 | PF00069 | 0.620 |
MOD_PKB_1 | 514 | 522 | PF00069 | 0.621 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.607 |
MOD_Plk_2-3 | 78 | 84 | PF00069 | 0.567 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.439 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.535 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.527 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.574 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.291 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.759 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.544 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.512 |
TRG_DiLeu_BaEn_1 | 313 | 318 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.674 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.572 |
TRG_NES_CRM1_1 | 262 | 278 | PF08389 | 0.327 |
TRG_NLS_Bipartite_1 | 433 | 448 | PF00514 | 0.684 |
TRG_NLS_MonoExtC_3 | 515 | 520 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 441 | 448 | PF00514 | 0.530 |
TRG_NLS_MonoExtN_4 | 514 | 520 | PF00514 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 270 | 275 | PF00026 | 0.316 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7X8 | Leptomonas seymouri | 59% | 82% |
A0A1X0NZC8 | Trypanosomatidae | 40% | 90% |
A0A3S7WTU1 | Leishmania donovani | 85% | 95% |
A0A422N971 | Trypanosoma rangeli | 40% | 91% |
A4HWT9 | Leishmania infantum | 85% | 95% |
C9ZPR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 95% |
E9AQJ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 95% |
Q4QEX9 | Leishmania major | 83% | 100% |
V5B948 | Trypanosoma cruzi | 41% | 97% |