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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4Q6L2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.754 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.532 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.393 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.286 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.523 |
DEG_COP1_1 | 349 | 358 | PF00400 | 0.730 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.499 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 409 | 415 | PF00134 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 375 | 381 | PF00134 | 0.524 |
DOC_MAPK_gen_1 | 542 | 551 | PF00069 | 0.525 |
DOC_PP1_RVXF_1 | 524 | 531 | PF00149 | 0.572 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.553 |
DOC_USP7_UBL2_3 | 227 | 231 | PF12436 | 0.614 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 341 | 345 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 392 | 408 | PF00022 | 0.519 |
LIG_APCC_ABBA_1 | 308 | 313 | PF00400 | 0.430 |
LIG_Clathr_ClatBox_1 | 527 | 531 | PF01394 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 192 | 202 | PF00928 | 0.545 |
LIG_deltaCOP1_diTrp_1 | 467 | 473 | PF00928 | 0.640 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.688 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.552 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.704 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.447 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.668 |
LIG_GBD_Chelix_1 | 407 | 415 | PF00786 | 0.323 |
LIG_LIR_Gen_1 | 210 | 215 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 322 | 332 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.664 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.359 |
LIG_Pex14_2 | 381 | 385 | PF04695 | 0.574 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.355 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.447 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 470 | 474 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.531 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.554 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.746 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.730 |
LIG_SUMO_SIM_anti_2 | 547 | 553 | PF11976 | 0.606 |
MOD_CDK_SPxxK_3 | 532 | 539 | PF00069 | 0.617 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.661 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.756 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.518 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.572 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.577 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.699 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.724 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.651 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.459 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.785 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.603 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.425 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.526 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.550 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.283 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.404 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.420 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.615 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.405 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.550 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.561 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.619 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.652 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.796 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.538 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.630 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.613 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.548 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.627 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.560 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.344 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.440 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.620 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.391 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.598 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.793 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.548 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.562 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.482 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.588 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.623 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.563 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.514 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.512 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.573 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.674 |
MOD_Plk_2-3 | 35 | 41 | PF00069 | 0.610 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.757 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.455 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.517 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.626 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.645 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.575 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.415 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.620 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.675 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.731 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.747 |
MOD_SUMO_for_1 | 395 | 398 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 270 | 277 | PF00179 | 0.662 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.481 |
TRG_NES_CRM1_1 | 373 | 386 | PF08389 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 498 | 502 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBU7 | Leptomonas seymouri | 60% | 98% |
A0A0S4JJ62 | Bodo saltans | 31% | 100% |
A0A1X0NJF9 | Trypanosomatidae | 42% | 100% |
A0A1X0NZV2 | Trypanosomatidae | 43% | 100% |
A0A3S7X455 | Leishmania donovani | 93% | 99% |
A0A422NZZ9 | Trypanosoma rangeli | 40% | 100% |
A4HJ29 | Leishmania braziliensis | 79% | 100% |
A4I6K8 | Leishmania infantum | 93% | 99% |
C9ZN58 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZWY2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B1K1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
V5BN17 | Trypanosoma cruzi | 40% | 100% |