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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q8E4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.513 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.683 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.661 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 467 | 469 | PF00082 | 0.636 |
CLV_PCSK_PC7_1 | 463 | 469 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.656 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.390 |
DEG_COP1_1 | 187 | 197 | PF00400 | 0.621 |
DEG_SPOP_SBC_1 | 447 | 451 | PF00917 | 0.756 |
DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.486 |
DOC_MAPK_gen_1 | 16 | 24 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 16 | 24 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 243 | 250 | PF00069 | 0.555 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.439 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.545 |
DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.463 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 366 | 370 | PF12436 | 0.462 |
DOC_USP7_UBL2_3 | 393 | 397 | PF12436 | 0.638 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 279 | 284 | PF00244 | 0.616 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.583 |
LIG_BIR_III_4 | 368 | 372 | PF00653 | 0.487 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.564 |
LIG_BRCT_BRCA1_2 | 360 | 366 | PF00533 | 0.575 |
LIG_CSL_BTD_1 | 58 | 61 | PF09270 | 0.412 |
LIG_CtBP_PxDLS_1 | 157 | 161 | PF00389 | 0.525 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.484 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.538 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.403 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.674 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.549 |
LIG_HCF-1_HBM_1 | 28 | 31 | PF13415 | 0.403 |
LIG_LIR_Apic_2 | 361 | 367 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 332 | 336 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.502 |
LIG_PCNA_yPIPBox_3 | 335 | 344 | PF02747 | 0.416 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.424 |
LIG_SH2_CRK | 336 | 340 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 65 | 68 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.387 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.420 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.542 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.524 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.541 |
LIG_SH3_4 | 366 | 373 | PF00018 | 0.444 |
LIG_SUMO_SIM_anti_2 | 53 | 59 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.601 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.388 |
MOD_CDK_SPK_2 | 449 | 454 | PF00069 | 0.579 |
MOD_CDK_SPxxK_3 | 78 | 85 | PF00069 | 0.581 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.714 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.773 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.604 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.637 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.649 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.654 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.473 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.614 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.655 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.637 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.444 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.647 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.668 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.488 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.480 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.531 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.694 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.600 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.615 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.558 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.469 |
MOD_GlcNHglycan | 444 | 448 | PF01048 | 0.816 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.597 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.576 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.564 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.538 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.739 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.668 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.607 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.587 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.487 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.564 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.635 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.654 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.768 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.664 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.684 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.598 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.485 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.573 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.448 |
MOD_NEK2_2 | 150 | 155 | PF00069 | 0.454 |
MOD_NEK2_2 | 163 | 168 | PF00069 | 0.421 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.554 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.678 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.646 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.466 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.584 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.482 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.608 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.598 |
MOD_Plk_2-3 | 208 | 214 | PF00069 | 0.652 |
MOD_Plk_2-3 | 428 | 434 | PF00069 | 0.641 |
MOD_Plk_2-3 | 435 | 441 | PF00069 | 0.655 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.424 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.530 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.773 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.664 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.623 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.548 |
MOD_SUMO_rev_2 | 208 | 218 | PF00179 | 0.677 |
MOD_SUMO_rev_2 | 318 | 328 | PF00179 | 0.540 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.675 |
TRG_NLS_MonoCore_2 | 465 | 470 | PF00514 | 0.637 |
TRG_NLS_MonoExtC_3 | 465 | 470 | PF00514 | 0.637 |
TRG_NLS_MonoExtN_4 | 463 | 470 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.567 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J3 | Leptomonas seymouri | 54% | 98% |
A0A3Q8IQI6 | Leishmania donovani | 87% | 100% |
A4HGG9 | Leishmania braziliensis | 73% | 100% |
A4I3K1 | Leishmania infantum | 87% | 100% |
E9AZU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |