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: A0A3S7X455
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.621 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.425 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 468 | 470 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.399 |
DEG_APCC_DBOX_1 | 530 | 538 | PF00400 | 0.612 |
DEG_COP1_1 | 354 | 363 | PF00400 | 0.730 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.512 |
DEG_SCF_FBW7_1 | 243 | 250 | PF00400 | 0.678 |
DEG_SPOP_SBC_1 | 592 | 596 | PF00917 | 0.639 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 414 | 420 | PF00134 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 380 | 386 | PF00134 | 0.610 |
DOC_MAPK_gen_1 | 547 | 556 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 529 | 536 | PF00149 | 0.588 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.709 |
DOC_USP7_UBL2_3 | 227 | 231 | PF12436 | 0.644 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.577 |
LIG_Actin_WH2_2 | 397 | 413 | PF00022 | 0.556 |
LIG_APCC_ABBA_1 | 313 | 318 | PF00400 | 0.467 |
LIG_Clathr_ClatBox_1 | 532 | 536 | PF01394 | 0.602 |
LIG_deltaCOP1_diTrp_1 | 192 | 202 | PF00928 | 0.577 |
LIG_deltaCOP1_diTrp_1 | 472 | 478 | PF00928 | 0.650 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.757 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.594 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.775 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.482 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.729 |
LIG_LIR_Gen_1 | 210 | 216 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 348 | 352 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.699 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.414 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.599 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.400 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.484 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.559 |
LIG_SH3_1 | 65 | 71 | PF00018 | 0.669 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.546 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.776 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.641 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.757 |
LIG_SUMO_SIM_anti_2 | 552 | 558 | PF11976 | 0.622 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.661 |
MOD_CDK_SPxxK_3 | 537 | 544 | PF00069 | 0.635 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.650 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.788 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.518 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.571 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.572 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.701 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.638 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.766 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.666 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.493 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.632 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.490 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.566 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.554 |
MOD_GlcNHglycan | 423 | 427 | PF01048 | 0.434 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.427 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.406 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.563 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.587 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.653 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.667 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.728 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.806 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.464 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.548 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.632 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.566 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.783 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.623 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.574 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.361 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.654 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.467 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.571 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.560 |
MOD_NEK2_2 | 324 | 329 | PF00069 | 0.502 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.685 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.699 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.560 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.523 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.549 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.541 |
MOD_Plk_1 | 592 | 598 | PF00069 | 0.640 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.695 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.547 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.620 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.652 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.582 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.628 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.717 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.638 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.751 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.757 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.647 |
MOD_SUMO_rev_2 | 275 | 282 | PF00179 | 0.715 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.521 |
TRG_NES_CRM1_1 | 378 | 391 | PF08389 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 503 | 507 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBU7 | Leptomonas seymouri | 61% | 99% |
A0A0S4JJ62 | Bodo saltans | 31% | 100% |
A0A1X0NJF9 | Trypanosomatidae | 42% | 100% |
A0A1X0NZV2 | Trypanosomatidae | 42% | 100% |
A0A422NZZ9 | Trypanosoma rangeli | 40% | 100% |
A4HJ29 | Leishmania braziliensis | 79% | 98% |
A4I6K8 | Leishmania infantum | 100% | 100% |
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) | 93% | 100% |
Q4Q6L2 | Leishmania major | 93% | 99% |
V5BN17 | Trypanosoma cruzi | 39% | 100% |