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: E9B1K1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.617 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.436 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 468 | 470 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.324 |
DEG_APCC_DBOX_1 | 530 | 538 | PF00400 | 0.612 |
DEG_COP1_1 | 354 | 363 | PF00400 | 0.740 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.509 |
DEG_SCF_FBW7_1 | 243 | 250 | PF00400 | 0.687 |
DOC_CKS1_1 | 438 | 443 | PF01111 | 0.468 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 414 | 420 | PF00134 | 0.590 |
DOC_CYCLIN_yCln2_LP_2 | 380 | 386 | PF00134 | 0.612 |
DOC_MAPK_gen_1 | 547 | 556 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 529 | 536 | PF00149 | 0.589 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.730 |
DOC_USP7_UBL2_3 | 227 | 231 | PF12436 | 0.646 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.754 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 397 | 413 | PF00022 | 0.553 |
LIG_APCC_ABBA_1 | 313 | 318 | PF00400 | 0.467 |
LIG_Clathr_ClatBox_1 | 532 | 536 | PF01394 | 0.603 |
LIG_deltaCOP1_diTrp_1 | 192 | 202 | PF00928 | 0.581 |
LIG_deltaCOP1_diTrp_1 | 472 | 478 | PF00928 | 0.662 |
LIG_deltaCOP1_diTrp_1 | 5 | 11 | PF00928 | 0.166 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.466 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.594 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.793 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.593 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.484 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.751 |
LIG_GBD_Chelix_1 | 412 | 420 | PF00786 | 0.352 |
LIG_LIR_Gen_1 | 209 | 215 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 348 | 352 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.702 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.609 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.500 |
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 | 0.682 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.553 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.546 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.477 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.759 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.739 |
LIG_SUMO_SIM_anti_2 | 552 | 558 | PF11976 | 0.624 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.669 |
LIG_TRAF2_1 | 558 | 561 | PF00917 | 0.632 |
MOD_CDK_SPxxK_3 | 537 | 544 | PF00069 | 0.634 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.667 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.774 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.573 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.601 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.638 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.648 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.659 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.669 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.540 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.742 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.475 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.815 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.614 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.468 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.575 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.592 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.414 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.428 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.579 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.440 |
MOD_GlcNHglycan | 51 | 55 | PF01048 | 0.517 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.559 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.583 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.679 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.652 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.731 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.785 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.465 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.544 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.619 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.581 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.580 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.693 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.756 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.619 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.345 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.652 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.571 |
MOD_NEK2_2 | 324 | 329 | PF00069 | 0.509 |
MOD_PKA_1 | 233 | 239 | PF00069 | 0.608 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.699 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.713 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.563 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.614 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.704 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.523 |
MOD_Plk_1 | 535 | 541 | PF00069 | 0.548 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.543 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.698 |
MOD_Plk_2-3 | 35 | 41 | PF00069 | 0.671 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.780 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.552 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.632 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.673 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.585 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.642 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.748 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.466 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.637 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.774 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.744 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.515 |
TRG_NES_CRM1_1 | 378 | 391 | PF08389 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 503 | 507 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBU7 | Leptomonas seymouri | 60% | 99% |
A0A0S4JJ62 | Bodo saltans | 30% | 100% |
A0A1X0NJF9 | Trypanosomatidae | 41% | 100% |
A0A1X0NZV2 | Trypanosomatidae | 42% | 100% |
A0A3S7X455 | Leishmania donovani | 93% | 100% |
A0A422NZZ9 | Trypanosoma rangeli | 40% | 100% |
A4HJ29 | Leishmania braziliensis | 80% | 98% |
A4I6K8 | Leishmania infantum | 93% | 100% |
C9ZN58 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZWY2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
Q4Q6L2 | Leishmania major | 90% | 99% |
V5BN17 | Trypanosoma cruzi | 39% | 100% |