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 |
Related structures:
AlphaFold database: Q9U1E2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.276 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.526 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 210 | 212 | PF00082 | 0.319 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 536 | 538 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 569 | 571 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.475 |
DEG_APCC_DBOX_1 | 276 | 284 | PF00400 | 0.307 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.537 |
DEG_ODPH_VHL_1 | 257 | 270 | PF01847 | 0.224 |
DOC_CYCLIN_RxL_1 | 238 | 246 | PF00134 | 0.279 |
DOC_CYCLIN_RxL_1 | 274 | 282 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 20 | PF00134 | 0.669 |
DOC_CYCLIN_yCln2_LP_2 | 443 | 449 | PF00134 | 0.279 |
DOC_MAPK_DCC_7 | 10 | 20 | PF00069 | 0.588 |
DOC_MAPK_gen_1 | 167 | 176 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 440 | 449 | PF00069 | 0.271 |
DOC_MAPK_gen_1 | 465 | 472 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 536 | 543 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 75 | 83 | PF00069 | 0.531 |
DOC_MAPK_JIP1_4 | 598 | 604 | PF00069 | 0.682 |
DOC_MAPK_MEF2A_6 | 152 | 160 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 536 | 545 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 87 | 95 | PF00069 | 0.572 |
DOC_MAPK_RevD_3 | 93 | 107 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 508 | 515 | PF00149 | 0.465 |
DOC_PP1_SILK_1 | 223 | 228 | PF00149 | 0.349 |
DOC_PP1_SILK_1 | 431 | 436 | PF00149 | 0.292 |
DOC_PP2B_LxvP_1 | 410 | 413 | PF13499 | 0.515 |
DOC_PP4_FxxP_1 | 495 | 498 | PF00568 | 0.425 |
DOC_SPAK_OSR1_1 | 66 | 70 | PF12202 | 0.577 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.481 |
DOC_USP7_MATH_2 | 498 | 504 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.400 |
DOC_USP7_UBL2_3 | 167 | 171 | PF12436 | 0.348 |
DOC_USP7_UBL2_3 | 507 | 511 | PF12436 | 0.596 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.271 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 227 | 232 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 576 | 586 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 86 | 104 | PF00022 | 0.331 |
LIG_BIR_III_2 | 478 | 482 | PF00653 | 0.324 |
LIG_BIR_III_4 | 289 | 293 | PF00653 | 0.421 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.581 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.630 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.271 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.601 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.335 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.574 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.294 |
LIG_LIR_Apic_2 | 493 | 498 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 593 | 599 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 323 | 334 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 406 | 417 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.452 |
LIG_NRBOX | 140 | 146 | PF00104 | 0.408 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.432 |
LIG_PTB_Apo_2 | 40 | 47 | PF02174 | 0.514 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.289 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.496 |
LIG_SH2_CRK | 596 | 600 | PF00017 | 0.561 |
LIG_SH2_GRB2like | 242 | 245 | PF00017 | 0.404 |
LIG_SH2_GRB2like | 399 | 402 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 596 | 600 | PF00017 | 0.561 |
LIG_SH2_PTP2 | 469 | 472 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.649 |
LIG_SH2_STAT3 | 578 | 581 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.541 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.286 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.343 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.447 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.182 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.516 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.463 |
LIG_SUMO_SIM_anti_2 | 267 | 272 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 264 | 269 | PF11976 | 0.250 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.540 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.466 |
LIG_TRAF2_1 | 481 | 484 | PF00917 | 0.577 |
LIG_UBA3_1 | 501 | 507 | PF00899 | 0.482 |
LIG_WRC_WIRS_1 | 434 | 439 | PF05994 | 0.349 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.459 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.577 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.570 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.542 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.472 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.562 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.485 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.632 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.594 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.395 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.480 |
MOD_Cter_Amidation | 208 | 211 | PF01082 | 0.271 |
MOD_Cter_Amidation | 382 | 385 | PF01082 | 0.555 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.414 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.505 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.668 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.486 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.552 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.443 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.378 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.292 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.345 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.508 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.601 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.571 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.472 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.289 |
MOD_N-GLC_2 | 546 | 548 | PF02516 | 0.463 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.427 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.250 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.603 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.549 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.603 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.439 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.408 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.602 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.652 |
MOD_NEK2_2 | 531 | 536 | PF00069 | 0.514 |
MOD_NEK2_2 | 591 | 596 | PF00069 | 0.573 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.589 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.630 |
MOD_PK_1 | 429 | 435 | PF00069 | 0.292 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.424 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.504 |
MOD_PKB_1 | 568 | 576 | PF00069 | 0.696 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.537 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.384 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.467 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.553 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.572 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.384 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.451 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.556 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.570 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.271 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.467 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.271 |
MOD_SUMO_for_1 | 496 | 499 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 105 | 112 | PF00179 | 0.484 |
TRG_DiLeu_BaEn_3 | 150 | 156 | PF01217 | 0.484 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 421 | 426 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.493 |
TRG_NLS_MonoExtN_4 | 130 | 135 | PF00514 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 152 | 157 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.322 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBK1 | Leptomonas seymouri | 70% | 100% |
A0A1X0NRN7 | Trypanosomatidae | 58% | 99% |
A0A3R7NSK8 | Trypanosoma rangeli | 60% | 100% |
A0A3S7X5W5 | Leishmania donovani | 95% | 100% |
A4HKT6 | Leishmania braziliensis | 87% | 100% |
A4I8B5 | Leishmania infantum | 95% | 100% |
D0AAI7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 99% |
E9B374 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5DE73 | Trypanosoma cruzi | 57% | 100% |