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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0012505 | endomembrane system | 2 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
Related structures:
AlphaFold database: E9AZN3
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0005509 | calcium ion binding | 5 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 141 | 145 | PF00656 | 0.346 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.468 |
CLV_PCSK_PC7_1 | 565 | 571 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.572 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.604 |
DEG_SPOP_SBC_1 | 487 | 491 | PF00917 | 0.477 |
DOC_CYCLIN_RxL_1 | 50 | 58 | PF00134 | 0.497 |
DOC_MAPK_FxFP_2 | 191 | 194 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 223 | 230 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 27 | 36 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 517 | 525 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 569 | 576 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 223 | 230 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 352 | 359 | PF00069 | 0.321 |
DOC_MAPK_MEF2A_6 | 517 | 525 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 540 | 548 | PF00069 | 0.435 |
DOC_PP4_FxxP_1 | 191 | 194 | PF00568 | 0.362 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.569 |
DOC_PP4_FxxP_1 | 337 | 340 | PF00568 | 0.258 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.641 |
DOC_USP7_UBL2_3 | 352 | 356 | PF12436 | 0.302 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.406 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 379 | 389 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 480 | 486 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 540 | 545 | PF00244 | 0.355 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.342 |
LIG_CaM_NSCaTE_8 | 314 | 321 | PF13499 | 0.346 |
LIG_deltaCOP1_diTrp_1 | 161 | 170 | PF00928 | 0.400 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.356 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.549 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.594 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.570 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.415 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.367 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.427 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.737 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.653 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.468 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.371 |
LIG_LIR_Apic_2 | 216 | 222 | PF02991 | 0.578 |
LIG_LIR_Apic_2 | 71 | 76 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 101 | 107 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 224 | 232 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.441 |
LIG_LYPXL_yS_3 | 518 | 521 | PF13949 | 0.587 |
LIG_MLH1_MIPbox_1 | 341 | 345 | PF16413 | 0.342 |
LIG_NRBOX | 545 | 551 | PF00104 | 0.388 |
LIG_PDZ_Class_2 | 580 | 585 | PF00595 | 0.440 |
LIG_Pex14_2 | 134 | 138 | PF04695 | 0.343 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.272 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.374 |
LIG_REV1ctd_RIR_1 | 389 | 397 | PF16727 | 0.547 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 46 | 50 | PF00017 | 0.640 |
LIG_SH2_PTP2 | 73 | 76 | PF00017 | 0.557 |
LIG_SH2_SRC | 46 | 49 | PF00017 | 0.533 |
LIG_SH2_SRC | 582 | 585 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 103 | 107 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 271 | 275 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.640 |
LIG_SH2_STAT3 | 38 | 41 | PF00017 | 0.637 |
LIG_SH2_STAT3 | 535 | 538 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.557 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.487 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.317 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.363 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.586 |
LIG_TYR_ITIM | 580 | 585 | PF00017 | 0.431 |
LIG_TYR_ITIM | 70 | 75 | PF00017 | 0.356 |
LIG_WRC_WIRS_1 | 341 | 346 | PF05994 | 0.258 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.657 |
LIG_WRC_WIRS_1 | 455 | 460 | PF05994 | 0.568 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.457 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.445 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.460 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.582 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.543 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.431 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.666 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.518 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.631 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.739 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.534 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.534 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.535 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.470 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.410 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.320 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.379 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.427 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.372 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.347 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.443 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.308 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.602 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.316 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.342 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.593 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.436 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.419 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.348 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.602 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.581 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.533 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.302 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.585 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.555 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.378 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.362 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.258 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.589 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.532 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.581 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.432 |
MOD_PKB_1 | 479 | 487 | PF00069 | 0.496 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.535 |
MOD_Plk_2-3 | 467 | 473 | PF00069 | 0.567 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.542 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.615 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.276 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.605 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.593 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.558 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.425 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.535 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.342 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.323 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.287 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.412 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.406 |
MOD_SUMO_rev_2 | 491 | 496 | PF00179 | 0.512 |
TRG_DiLeu_BaEn_1 | 430 | 435 | PF01217 | 0.651 |
TRG_DiLeu_BaLyEn_6 | 517 | 522 | PF01217 | 0.642 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.613 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 568 | 570 | PF00400 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 552 | 557 | PF00026 | 0.646 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7S3 | Leptomonas seymouri | 64% | 100% |
A0A1X0NYV6 | Trypanosomatidae | 47% | 100% |
A0A3Q8IAW4 | Leishmania donovani | 93% | 100% |
A0A422P1M7 | Trypanosoma rangeli | 47% | 100% |
A4HGB2 | Leishmania braziliensis | 82% | 100% |
A4I3E6 | Leishmania infantum | 93% | 100% |
D0A801 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
Q4Q8J8 | Leishmania major | 91% | 100% |
V5B0S4 | Trypanosoma cruzi | 45% | 100% |