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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HEJ9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.664 |
CLV_PCSK_FUR_1 | 305 | 309 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.590 |
DEG_Kelch_Keap1_1 | 527 | 532 | PF01344 | 0.571 |
DEG_ODPH_VHL_1 | 39 | 50 | PF01847 | 0.343 |
DEG_SCF_FBW7_1 | 390 | 395 | PF00400 | 0.481 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.516 |
DOC_ANK_TNKS_1 | 379 | 386 | PF00023 | 0.485 |
DOC_CKS1_1 | 448 | 453 | PF01111 | 0.476 |
DOC_CYCLIN_RxL_1 | 287 | 294 | PF00134 | 0.395 |
DOC_CYCLIN_RxL_1 | 330 | 344 | PF00134 | 0.589 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 416 | 422 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 173 | 182 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 396 | 404 | PF00069 | 0.562 |
DOC_PP1_RVXF_1 | 334 | 341 | PF00149 | 0.603 |
DOC_PP1_RVXF_1 | 560 | 567 | PF00149 | 0.580 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.437 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.626 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.554 |
DOC_USP7_UBL2_3 | 520 | 524 | PF12436 | 0.540 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 290 | 300 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 427 | 432 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 569 | 577 | PF00244 | 0.682 |
LIG_APCC_ABBA_1 | 178 | 183 | PF00400 | 0.330 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_BIR_III_2 | 19 | 23 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 562 | 566 | PF00533 | 0.437 |
LIG_EH_1 | 6 | 10 | PF12763 | 0.453 |
LIG_eIF4E_1 | 333 | 339 | PF01652 | 0.595 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.617 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.506 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.552 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.679 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.646 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.586 |
LIG_GBD_Chelix_1 | 471 | 479 | PF00786 | 0.620 |
LIG_LIR_Apic_2 | 133 | 138 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 13 | 23 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 565 | 574 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.482 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.428 |
LIG_Pex14_2 | 404 | 408 | PF04695 | 0.428 |
LIG_Rb_pABgroove_1 | 12 | 20 | PF01858 | 0.613 |
LIG_REV1ctd_RIR_1 | 564 | 573 | PF16727 | 0.645 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.513 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.676 |
LIG_SH2_PTP2 | 47 | 50 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 504 | 508 | PF00017 | 0.630 |
LIG_SH2_STAT3 | 109 | 112 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.699 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.578 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.568 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.589 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.481 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.753 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.702 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.507 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.538 |
LIG_TYR_ITIM | 45 | 50 | PF00017 | 0.571 |
LIG_TYR_ITIM | 474 | 479 | PF00017 | 0.641 |
LIG_UBA3_1 | 331 | 336 | PF00899 | 0.588 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.673 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.486 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.587 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.515 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.666 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.630 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.562 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.610 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.620 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.609 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.419 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.657 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.739 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.818 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.557 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.666 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.582 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.672 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.473 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.660 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.687 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.548 |
MOD_GlcNHglycan | 527 | 532 | PF01048 | 0.652 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.589 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.714 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.537 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.505 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.641 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.636 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.572 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.642 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.534 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.410 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.716 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.612 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.615 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.464 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.502 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.628 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.634 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.584 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.612 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.718 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.630 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.647 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.634 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.699 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.686 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.594 |
MOD_PKB_1 | 186 | 194 | PF00069 | 0.598 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.531 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.566 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.633 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.578 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.601 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.652 |
MOD_Plk_2-3 | 208 | 214 | PF00069 | 0.596 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.530 |
MOD_Plk_2-3 | 560 | 566 | PF00069 | 0.695 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.602 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.439 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.449 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.712 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.617 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.684 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.719 |
MOD_SUMO_rev_2 | 519 | 526 | PF00179 | 0.654 |
MOD_SUMO_rev_2 | 586 | 593 | PF00179 | 0.714 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.599 |
TRG_DiLeu_BaLyEn_6 | 475 | 480 | PF01217 | 0.622 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.671 |
TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 478 | 483 | PF00026 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZM0 | Leptomonas seymouri | 47% | 100% |
A0A1X0NY83 | Trypanosomatidae | 27% | 100% |
A0A3S7WZ73 | Leishmania donovani | 77% | 100% |
A0A422NL47 | Trypanosoma rangeli | 30% | 100% |
A4I1J9 | Leishmania infantum | 77% | 100% |
C9ZK33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AXN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 96% |
Q4Q9T8 | Leishmania major | 74% | 99% |