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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QGT6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.516 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.469 |
CLV_PCSK_FUR_1 | 356 | 360 | PF00082 | 0.525 |
CLV_PCSK_FUR_1 | 444 | 448 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 410 | 412 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.664 |
CLV_PCSK_PC7_1 | 206 | 212 | PF00082 | 0.470 |
CLV_PCSK_PC7_1 | 391 | 397 | PF00082 | 0.488 |
CLV_PCSK_PC7_1 | 505 | 511 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.601 |
DEG_APCC_DBOX_1 | 182 | 190 | PF00400 | 0.475 |
DOC_CYCLIN_RxL_1 | 180 | 188 | PF00134 | 0.510 |
DOC_CYCLIN_RxL_1 | 247 | 257 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 22 | 28 | PF00134 | 0.426 |
DOC_MAPK_DCC_7 | 474 | 484 | PF00069 | 0.491 |
DOC_MAPK_FxFP_2 | 165 | 168 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 124 | 131 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 318 | 326 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 473 | 482 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.531 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.560 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.476 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.710 |
DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.377 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 361 | 369 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 560 | 564 | PF00244 | 0.486 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.503 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.365 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.523 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.391 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.412 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.734 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.494 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.654 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.707 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.442 |
LIG_LIR_Apic_2 | 113 | 117 | PF02991 | 0.592 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 374 | 381 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 47 | 58 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 5 | 15 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.476 |
LIG_NRP_CendR_1 | 618 | 620 | PF00754 | 0.653 |
LIG_Pex14_2 | 13 | 17 | PF04695 | 0.476 |
LIG_RPA_C_Fungi | 337 | 349 | PF08784 | 0.595 |
LIG_RPA_C_Plants | 323 | 334 | PF08784 | 0.373 |
LIG_SH2_CRK | 598 | 602 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 114 | 118 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 428 | 432 | PF00017 | 0.492 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.459 |
LIG_SH2_STAP1 | 536 | 540 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.361 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.449 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.546 |
LIG_SUMO_SIM_par_1 | 167 | 173 | PF11976 | 0.452 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.579 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.536 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.639 |
LIG_WRC_WIRS_1 | 7 | 12 | PF05994 | 0.448 |
MOD_CDK_SPxxK_3 | 159 | 166 | PF00069 | 0.501 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.485 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.466 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.689 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.509 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.707 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.501 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.628 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.470 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.497 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.602 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.475 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.701 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.508 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.446 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.578 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.464 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.512 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.538 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.700 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.588 |
MOD_NEK2_2 | 373 | 378 | PF00069 | 0.632 |
MOD_OFUCOSY | 93 | 100 | PF10250 | 0.641 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.703 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.420 |
MOD_PK_1 | 475 | 481 | PF00069 | 0.489 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.479 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.476 |
MOD_PKB_1 | 359 | 367 | PF00069 | 0.437 |
MOD_PKB_1 | 473 | 481 | PF00069 | 0.575 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.378 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.618 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.562 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.629 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.446 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.528 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.490 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.573 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.471 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.447 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.566 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.600 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 302 | 310 | PF00179 | 0.572 |
MOD_SUMO_rev_2 | 543 | 552 | PF00179 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 478 | 483 | PF01217 | 0.524 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 358 | 360 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 559 | 561 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.500 |
TRG_NLS_MonoExtN_4 | 105 | 110 | PF00514 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 183 | 187 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 531 | 535 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 561 | 566 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK43 | Leptomonas seymouri | 48% | 100% |
A0A1X0NM25 | Trypanosomatidae | 27% | 100% |
A0A3Q8I971 | Leishmania donovani | 83% | 100% |
A0A422N6D2 | Trypanosoma rangeli | 29% | 100% |
A4H6S2 | Leishmania braziliensis | 70% | 100% |
A4HV51 | Leishmania infantum | 83% | 100% |
C9ZQD4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9ANT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |