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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S7X2F4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.682 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 593 | 595 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 593 | 595 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 599 | 601 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.514 |
CLV_PCSK_PC7_1 | 125 | 131 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.524 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.688 |
DEG_SPOP_SBC_1 | 147 | 151 | PF00917 | 0.686 |
DOC_CDC14_PxL_1 | 188 | 196 | PF14671 | 0.670 |
DOC_MAPK_DCC_7 | 406 | 416 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 240 | 250 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 283 | 293 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 370 | 376 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.622 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.356 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.735 |
LIG_14-3-3_CanoR_1 | 199 | 209 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 217 | 223 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 276 | 284 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 354 | 363 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 401 | 407 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 498 | 507 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.608 |
LIG_Actin_WH2_2 | 392 | 410 | PF00022 | 0.535 |
LIG_Actin_WH2_2 | 484 | 500 | PF00022 | 0.598 |
LIG_APCC_ABBA_1 | 570 | 575 | PF00400 | 0.569 |
LIG_BIR_III_4 | 34 | 38 | PF00653 | 0.714 |
LIG_BRCT_BRCA1_1 | 311 | 315 | PF00533 | 0.490 |
LIG_CaM_IQ_9 | 290 | 305 | PF13499 | 0.371 |
LIG_eIF4E_1 | 202 | 208 | PF01652 | 0.533 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.618 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.656 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.379 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.392 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.548 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.197 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.579 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.624 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.648 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.664 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.533 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.543 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.653 |
LIG_Integrin_RGD_1 | 32 | 34 | PF01839 | 0.592 |
LIG_LIR_Apic_2 | 60 | 65 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 257 | 268 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 485 | 495 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 504 | 515 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 567 | 577 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 616 | 622 | PF02991 | 0.779 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 616 | 621 | PF02991 | 0.781 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.469 |
LIG_LYPXL_yS_3 | 66 | 69 | PF13949 | 0.665 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.426 |
LIG_Pex14_1 | 289 | 293 | PF04695 | 0.366 |
LIG_Pex14_1 | 62 | 66 | PF04695 | 0.550 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.465 |
LIG_PTB_Apo_2 | 406 | 413 | PF02174 | 0.540 |
LIG_PTB_Phospho_1 | 406 | 412 | PF10480 | 0.547 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.622 |
LIG_SH2_CRK | 546 | 550 | PF00017 | 0.481 |
LIG_SH2_GRB2like | 390 | 393 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 202 | 206 | PF00017 | 0.618 |
LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 546 | 550 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 359 | 363 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.484 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.596 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.668 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.467 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.510 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.513 |
LIG_SUMO_SIM_par_1 | 346 | 351 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 4 | 11 | PF11976 | 0.700 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.630 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.710 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.708 |
LIG_TRFH_1 | 114 | 118 | PF08558 | 0.553 |
LIG_TYR_ITIM | 111 | 116 | PF00017 | 0.543 |
LIG_TYR_ITIM | 544 | 549 | PF00017 | 0.584 |
LIG_TYR_ITIM | 64 | 69 | PF00017 | 0.633 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.699 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.671 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.342 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.449 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.578 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.655 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.520 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.698 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.736 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.636 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.446 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.713 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.540 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.652 |
MOD_GlcNHglycan | 9 | 13 | PF01048 | 0.719 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.607 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.551 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.481 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.377 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.421 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.602 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.704 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.512 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.644 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.661 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.580 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.494 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.471 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.432 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.326 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.592 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.567 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.507 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.557 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.713 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.607 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.618 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.676 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.578 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.508 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.511 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.586 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.607 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.605 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.456 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.568 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.472 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.566 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.532 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.523 |
MOD_SUMO_for_1 | 598 | 601 | PF00179 | 0.658 |
MOD_SUMO_rev_2 | 394 | 400 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 79 | 84 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_2 | 440 | 446 | PF01217 | 0.582 |
TRG_DiLeu_BaEn_4 | 441 | 447 | PF01217 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 593 | 595 | PF00400 | 0.762 |
TRG_Pf-PMV_PEXEL_1 | 199 | 204 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 346 | 351 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHI1 | Leptomonas seymouri | 67% | 100% |
A0A0S4JMH1 | Bodo saltans | 29% | 100% |
A0A1X0P058 | Trypanosomatidae | 34% | 96% |
A0A3R7M9T5 | Trypanosoma rangeli | 33% | 98% |
A4HHC1 | Leishmania braziliensis | 88% | 100% |
C9ZLL7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 97% |
E9ADW9 | Leishmania major | 95% | 100% |
E9AHI6 | Leishmania infantum | 100% | 100% |
E9ALW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5DI43 | Trypanosoma cruzi | 34% | 99% |