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: A0A3S7X099
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.578 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.674 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.674 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.602 |
DEG_APCC_DBOX_1 | 547 | 555 | PF00400 | 0.621 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.542 |
DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.674 |
DOC_CKS1_1 | 541 | 546 | PF01111 | 0.571 |
DOC_MAPK_gen_1 | 476 | 485 | PF00069 | 0.675 |
DOC_MAPK_MEF2A_6 | 476 | 485 | PF00069 | 0.684 |
DOC_MAPK_MEF2A_6 | 68 | 75 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 77 | 84 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 566 | 572 | PF00149 | 0.516 |
DOC_PP2B_LxvP_1 | 459 | 462 | PF13499 | 0.682 |
DOC_PP4_FxxP_1 | 383 | 386 | PF00568 | 0.430 |
DOC_PP4_FxxP_1 | 532 | 535 | PF00568 | 0.403 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.820 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.642 |
DOC_USP7_MATH_2 | 544 | 550 | PF00917 | 0.579 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 212 | 217 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 313 | 320 | PF00244 | 0.764 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 441 | 450 | PF00244 | 0.649 |
LIG_Actin_WH2_2 | 90 | 108 | PF00022 | 0.529 |
LIG_APCC_ABBA_1 | 460 | 465 | PF00400 | 0.560 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.826 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.693 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.548 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.431 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.643 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.545 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.580 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.404 |
LIG_FHA_2 | 121 | 127 | PF00498 | 0.799 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.657 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.494 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.528 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.622 |
LIG_FXI_DFP_1 | 218 | 222 | PF00024 | 0.551 |
LIG_GBD_Chelix_1 | 38 | 46 | PF00786 | 0.581 |
LIG_Integrin_isoDGR_2 | 210 | 212 | PF01839 | 0.613 |
LIG_IRF3_LxIS_1 | 74 | 81 | PF10401 | 0.544 |
LIG_LIR_Apic_2 | 382 | 386 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 531 | 535 | PF02991 | 0.403 |
LIG_LIR_Apic_2 | 539 | 544 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 215 | 226 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 409 | 419 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 468 | 474 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.610 |
LIG_LYPXL_yS_3 | 508 | 511 | PF13949 | 0.473 |
LIG_LYPXL_yS_3 | 579 | 582 | PF13949 | 0.585 |
LIG_PCNA_yPIPBox_3 | 194 | 208 | PF02747 | 0.575 |
LIG_PROFILIN_1 | 149 | 155 | PF00235 | 0.613 |
LIG_SH2_NCK_1 | 541 | 545 | PF00017 | 0.608 |
LIG_SH2_SRC | 463 | 466 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.448 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.813 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.472 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.774 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.668 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 69 | 75 | PF11976 | 0.531 |
LIG_TRAF2_1 | 203 | 206 | PF00917 | 0.536 |
LIG_TRAF2_1 | 462 | 465 | PF00917 | 0.648 |
LIG_TRAF2_1 | 543 | 546 | PF00917 | 0.520 |
LIG_TRAF2_2 | 562 | 567 | PF00917 | 0.508 |
LIG_UBA3_1 | 480 | 486 | PF00899 | 0.621 |
LIG_WRC_WIRS_1 | 356 | 361 | PF05994 | 0.639 |
LIG_WW_2 | 152 | 155 | PF00397 | 0.503 |
MOD_CDK_SPxxK_3 | 306 | 313 | PF00069 | 0.733 |
MOD_CDK_SPxxK_3 | 540 | 547 | PF00069 | 0.577 |
MOD_CDK_SPxxK_3 | 61 | 68 | PF00069 | 0.626 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.753 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.566 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.772 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.690 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.677 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.481 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.665 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.529 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.481 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.583 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.725 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.575 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.552 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.648 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.465 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.477 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.525 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.704 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.649 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.732 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.592 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.559 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.507 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.593 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.557 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.669 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.715 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.693 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.617 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.627 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.606 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.590 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.624 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.391 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.645 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.520 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.613 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.582 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.598 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.557 |
MOD_N-GLC_2 | 118 | 120 | PF02516 | 0.748 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.621 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.430 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.529 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.593 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.587 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.501 |
MOD_NEK2_2 | 466 | 471 | PF00069 | 0.585 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.694 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.739 |
MOD_PK_1 | 430 | 436 | PF00069 | 0.536 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.651 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.687 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.664 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.770 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.607 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.692 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.638 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.518 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.576 |
MOD_Plk_2-3 | 355 | 361 | PF00069 | 0.646 |
MOD_Plk_2-3 | 507 | 513 | PF00069 | 0.568 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.746 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.580 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.728 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.498 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.538 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.531 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.774 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.582 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.576 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.488 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.521 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.676 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.574 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.536 |
MOD_SUMO_rev_2 | 512 | 520 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 9 | 15 | PF00179 | 0.657 |
TRG_DiLeu_BaEn_1 | 410 | 415 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_1 | 70 | 75 | PF01217 | 0.529 |
TRG_DiLeu_LyEn_5 | 410 | 415 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.585 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 441 | 445 | PF00026 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I848 | Leptomonas seymouri | 56% | 100% |
A0A1X0P7D0 | Trypanosomatidae | 32% | 100% |
A0A3R7MCE3 | Trypanosoma rangeli | 35% | 100% |
A4HFA9 | Leishmania braziliensis | 79% | 100% |
A4I2J1 | Leishmania infantum | 100% | 100% |
C9ZWZ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AYP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q8S6 | Leishmania major | 94% | 100% |
V5B7P2 | Trypanosoma cruzi | 35% | 100% |