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: Q4Q0A3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.698 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.578 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.542 |
DEG_APCC_DBOX_1 | 415 | 423 | PF00400 | 0.637 |
DEG_SPOP_SBC_1 | 145 | 149 | PF00917 | 0.654 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.423 |
DOC_CDC14_PxL_1 | 391 | 399 | PF14671 | 0.543 |
DOC_CKS1_1 | 536 | 541 | PF01111 | 0.625 |
DOC_CYCLIN_yCln2_LP_2 | 218 | 224 | PF00134 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 537 | 543 | PF00134 | 0.631 |
DOC_MAPK_DCC_7 | 507 | 517 | PF00069 | 0.641 |
DOC_MAPK_gen_1 | 524 | 530 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 583 | 590 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.616 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.393 |
DOC_PP2B_LxvP_1 | 537 | 540 | PF13499 | 0.626 |
DOC_PP4_FxxP_1 | 242 | 245 | PF00568 | 0.567 |
DOC_PP4_FxxP_1 | 363 | 366 | PF00568 | 0.622 |
DOC_SPAK_OSR1_1 | 362 | 366 | PF12202 | 0.560 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.618 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 175 | 183 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 210 | 219 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 304 | 309 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 428 | 432 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 525 | 529 | PF00244 | 0.742 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.522 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.628 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 358 | 363 | PF00928 | 0.563 |
LIG_DLG_GKlike_1 | 33 | 41 | PF00625 | 0.473 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.703 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.561 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.415 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.626 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.693 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.684 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.503 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.502 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.609 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.409 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.409 |
LIG_LIR_Apic_2 | 239 | 245 | PF02991 | 0.634 |
LIG_LIR_Apic_2 | 360 | 366 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 178 | 188 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 234 | 245 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 349 | 357 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.540 |
LIG_NRBOX | 54 | 60 | PF00104 | 0.562 |
LIG_PCNA_PIPBox_1 | 436 | 445 | PF02747 | 0.558 |
LIG_Pex14_1 | 359 | 363 | PF04695 | 0.564 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.712 |
LIG_SH3_1 | 258 | 264 | PF00018 | 0.468 |
LIG_SH3_1 | 429 | 435 | PF00018 | 0.571 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.624 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.570 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.463 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.571 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.697 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.698 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.510 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.642 |
LIG_SUMO_SIM_anti_2 | 311 | 318 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 572 | 578 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 395 | 402 | PF11976 | 0.555 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.478 |
LIG_WRC_WIRS_1 | 343 | 348 | PF05994 | 0.432 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.607 |
MOD_CDK_SPK_2 | 156 | 161 | PF00069 | 0.559 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.724 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.619 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.580 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.631 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.679 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.602 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.573 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.707 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.652 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.644 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.654 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.546 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.387 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.483 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.460 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.771 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.571 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.560 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.634 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.412 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.503 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.605 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.432 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.689 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.608 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.679 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.582 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.696 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.651 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.799 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.579 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.538 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.671 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.338 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.719 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.498 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.642 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.393 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.550 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.495 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.496 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.606 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.540 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.570 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.580 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.744 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.757 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.605 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.382 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.681 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.709 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.495 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.489 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.393 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.477 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.440 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.546 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.439 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.508 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.540 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.713 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.561 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.524 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.747 |
MOD_NEK2_2 | 435 | 440 | PF00069 | 0.580 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.537 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.517 |
MOD_PK_1 | 297 | 303 | PF00069 | 0.432 |
MOD_PKA_1 | 524 | 530 | PF00069 | 0.631 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.676 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.594 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.721 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.632 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.709 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.460 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.697 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.741 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.595 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.528 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.432 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.516 |
MOD_Plk_1 | 590 | 596 | PF00069 | 0.636 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.384 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.551 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.522 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.386 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.556 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.746 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.621 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.480 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.642 |
MOD_SUMO_rev_2 | 380 | 388 | PF00179 | 0.615 |
MOD_SUMO_rev_2 | 500 | 509 | PF00179 | 0.645 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 68 | 74 | PF01217 | 0.608 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.645 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 582 | 584 | PF00400 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.619 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2K6 | Leptomonas seymouri | 53% | 98% |
A0A1X0NLK5 | Trypanosomatidae | 35% | 100% |
A0A3R7NFJ5 | Trypanosoma rangeli | 34% | 100% |
A0A3S7XCD6 | Leishmania donovani | 93% | 100% |
A4HQH5 | Leishmania braziliensis | 76% | 100% |
A4ICB1 | Leishmania infantum | 93% | 88% |
D0A3M4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AU88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DDT5 | Trypanosoma cruzi | 33% | 100% |