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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E8NHS4
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.367 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.308 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.414 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.360 |
CLV_PCSK_PC1ET2_1 | 514 | 516 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 548 | 550 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.415 |
CLV_Separin_Metazoa | 447 | 451 | PF03568 | 0.378 |
CLV_Separin_Metazoa | 453 | 457 | PF03568 | 0.337 |
CLV_Separin_Metazoa | 66 | 70 | PF03568 | 0.349 |
DEG_APCC_DBOX_1 | 488 | 496 | PF00400 | 0.349 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.371 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.395 |
DOC_CDC14_PxL_1 | 27 | 35 | PF14671 | 0.294 |
DOC_CDC14_PxL_1 | 649 | 657 | PF14671 | 0.435 |
DOC_CYCLIN_RxL_1 | 346 | 358 | PF00134 | 0.416 |
DOC_MAPK_DCC_7 | 100 | 108 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 100 | 108 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 148 | 157 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 100 | 108 | PF00069 | 0.342 |
DOC_PP2B_LxvP_1 | 426 | 429 | PF13499 | 0.321 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.354 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.367 |
LIG_14-3-3_CanoR_1 | 555 | 561 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 601 | 605 | PF00244 | 0.360 |
LIG_Actin_WH2_1 | 515 | 532 | PF00022 | 0.362 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.391 |
LIG_APCC_ABBA_1 | 6 | 11 | PF00400 | 0.331 |
LIG_APCC_ABBA_1 | 628 | 633 | PF00400 | 0.419 |
LIG_APCC_ABBAyCdc20_2 | 504 | 510 | PF00400 | 0.347 |
LIG_deltaCOP1_diTrp_1 | 119 | 124 | PF00928 | 0.296 |
LIG_EH_1 | 336 | 340 | PF12763 | 0.379 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.580 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.304 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.631 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.549 |
LIG_LIR_Gen_1 | 123 | 131 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 277 | 288 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 505 | 512 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 591 | 602 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 591 | 597 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 650 | 655 | PF02991 | 0.429 |
LIG_LYPXL_yS_3 | 257 | 260 | PF13949 | 0.375 |
LIG_LYPXL_yS_3 | 30 | 33 | PF13949 | 0.401 |
LIG_LYPXL_yS_3 | 652 | 655 | PF13949 | 0.449 |
LIG_RPA_C_Fungi | 14 | 26 | PF08784 | 0.299 |
LIG_RPA_C_Fungi | 460 | 472 | PF08784 | 0.333 |
LIG_RPA_C_Fungi | 636 | 648 | PF08784 | 0.426 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.306 |
LIG_SH2_PTP2 | 497 | 500 | PF00017 | 0.352 |
LIG_SH2_SRC | 163 | 166 | PF00017 | 0.305 |
LIG_SH2_SRC | 497 | 500 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.306 |
LIG_SH2_STAP1 | 612 | 616 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.352 |
LIG_SH3_1 | 497 | 503 | PF00018 | 0.340 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.350 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.336 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.337 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.290 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.422 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.332 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.397 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.452 |
LIG_SH3_3 | 650 | 656 | PF00018 | 0.433 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.417 |
LIG_TRAF2_1 | 531 | 534 | PF00917 | 0.355 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.362 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.392 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.410 |
LIG_UBA3_1 | 127 | 136 | PF00899 | 0.372 |
LIG_UBA3_1 | 507 | 514 | PF00899 | 0.339 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.336 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.385 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.481 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.502 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.532 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.358 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.523 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.545 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.463 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.385 |
MOD_NEK2_2 | 474 | 479 | PF00069 | 0.353 |
MOD_NEK2_2 | 612 | 617 | PF00069 | 0.390 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.312 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.329 |
MOD_PKA_1 | 548 | 554 | PF00069 | 0.497 |
MOD_PKA_1 | 555 | 561 | PF00069 | 0.517 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.394 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.712 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.508 |
MOD_PKA_2 | 600 | 606 | PF00069 | 0.370 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.360 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.392 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.364 |
TRG_AP2beta_CARGO_1 | 277 | 287 | PF09066 | 0.347 |
TRG_AP2beta_CARGO_1 | 505 | 515 | PF09066 | 0.336 |
TRG_DiLeu_BaEn_1 | 123 | 128 | PF01217 | 0.324 |
TRG_DiLeu_BaEn_2 | 100 | 106 | PF01217 | 0.370 |
TRG_DiLeu_BaEn_2 | 180 | 186 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_2 | 27 | 33 | PF01217 | 0.288 |
TRG_DiLeu_BaEn_2 | 649 | 655 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 286 | 291 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 418 | 423 | PF01217 | 0.334 |
TRG_DiLeu_BaLyEn_6 | 579 | 584 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 549 | 552 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 60 | 63 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 609 | 611 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.365 |
TRG_NLS_MonoExtC_3 | 547 | 552 | PF00514 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 208 | 213 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 485 | 490 | PF00026 | 0.358 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NYQ1 | Trypanosomatidae | 34% | 70% |
A0A3R7KIM7 | Trypanosoma rangeli | 36% | 100% |
A4H817 | Leishmania braziliensis | 52% | 100% |
A4I2N7 | Leishmania infantum | 27% | 100% |
E8NHH1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 93% |
E8NHP1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
V5BG02 | Trypanosoma cruzi | 29% | 100% |