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: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 4 |
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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HLV5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 488 | 492 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.588 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.819 |
CLV_Separin_Metazoa | 133 | 137 | PF03568 | 0.442 |
DEG_APCC_DBOX_1 | 127 | 135 | PF00400 | 0.439 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.623 |
DOC_CYCLIN_RxL_1 | 299 | 310 | PF00134 | 0.464 |
DOC_MAPK_DCC_7 | 399 | 408 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 399 | 408 | PF00069 | 0.602 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 231 | 235 | PF12436 | 0.590 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.725 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.840 |
LIG_14-3-3_CanoR_1 | 273 | 279 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 432 | 441 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 202 | 220 | PF00022 | 0.552 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.670 |
LIG_BIR_III_2 | 491 | 495 | PF00653 | 0.611 |
LIG_BRCT_BRCA1_1 | 478 | 482 | PF00533 | 0.582 |
LIG_Clathr_ClatBox_1 | 118 | 122 | PF01394 | 0.487 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.639 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.683 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.598 |
LIG_HP1_1 | 404 | 408 | PF01393 | 0.609 |
LIG_LIR_Apic_2 | 367 | 371 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 263 | 272 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.574 |
LIG_PCNA_yPIPBox_3 | 192 | 206 | PF02747 | 0.615 |
LIG_SH2_GRB2like | 178 | 181 | PF00017 | 0.415 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.541 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.644 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.880 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.649 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.617 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.698 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.625 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.660 |
LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.601 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.687 |
LIG_TRAF2_1 | 87 | 90 | PF00917 | 0.461 |
MOD_CDC14_SPxK_1 | 396 | 399 | PF00782 | 0.618 |
MOD_CDK_SPxK_1 | 393 | 399 | PF00069 | 0.622 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.739 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.712 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.481 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.760 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.715 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.679 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.717 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.798 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.803 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.603 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.668 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.584 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.544 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.609 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.866 |
MOD_GlcNHglycan | 378 | 382 | PF01048 | 0.706 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.660 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.620 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.758 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.630 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.420 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.618 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.752 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.724 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.759 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.746 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.784 |
MOD_LATS_1 | 101 | 107 | PF00433 | 0.485 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.414 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.753 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.776 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.767 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.406 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.698 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.626 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.598 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.613 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.650 |
MOD_PK_1 | 474 | 480 | PF00069 | 0.577 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.429 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.470 |
MOD_PKA_1 | 432 | 438 | PF00069 | 0.739 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.429 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.701 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.780 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.745 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.781 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.600 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.702 |
MOD_Plk_2-3 | 12 | 18 | PF00069 | 0.627 |
MOD_Plk_2-3 | 50 | 56 | PF00069 | 0.700 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.521 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.477 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.599 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.684 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.622 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.628 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.839 |
MOD_SUMO_for_1 | 252 | 255 | PF00179 | 0.647 |
MOD_SUMO_for_1 | 87 | 90 | PF00179 | 0.584 |
MOD_SUMO_rev_2 | 284 | 293 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 49 | 59 | PF00179 | 0.634 |
TRG_DiLeu_BaEn_4 | 263 | 269 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.680 |
TRG_NES_CRM1_1 | 298 | 310 | PF08389 | 0.463 |
TRG_NLS_Bipartite_1 | 212 | 234 | PF00514 | 0.606 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.595 |
TRG_NLS_MonoExtN_4 | 229 | 234 | PF00514 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 305 | 310 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.685 |
TRG_Pf-PMV_PEXEL_1 | 467 | 471 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMH4 | Leptomonas seymouri | 55% | 100% |
A0A1X0P3T7 | Trypanosomatidae | 40% | 100% |
A0A3S7X729 | Leishmania donovani | 56% | 100% |
E9AHR2 | Leishmania infantum | 56% | 100% |
E9B483 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
Q4Q3U3 | Leishmania major | 57% | 100% |