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: A4H4L5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 504 | 508 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.538 |
DEG_APCC_DBOX_1 | 471 | 479 | PF00400 | 0.528 |
DEG_SCF_FBW7_1 | 206 | 213 | PF00400 | 0.487 |
DEG_SCF_FBW7_2 | 45 | 51 | PF00400 | 0.557 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.613 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.637 |
DOC_CKS1_1 | 207 | 212 | PF01111 | 0.491 |
DOC_CKS1_1 | 387 | 392 | PF01111 | 0.558 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.557 |
DOC_CKS1_1 | 471 | 476 | PF01111 | 0.549 |
DOC_CYCLIN_RxL_1 | 102 | 113 | PF00134 | 0.610 |
DOC_CYCLIN_RxL_1 | 229 | 237 | PF00134 | 0.508 |
DOC_CYCLIN_RxL_1 | 531 | 541 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 174 | 180 | PF00134 | 0.518 |
DOC_MAPK_DCC_7 | 324 | 334 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 355 | 364 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 355 | 364 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 405 | 414 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 230 | 237 | PF00149 | 0.509 |
DOC_PP1_RVXF_1 | 303 | 309 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 353 | 360 | PF00149 | 0.543 |
DOC_PP1_RVXF_1 | 427 | 433 | PF00149 | 0.660 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.603 |
DOC_PP2B_LxvP_1 | 412 | 415 | PF13499 | 0.700 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.590 |
DOC_USP7_UBL2_3 | 569 | 573 | PF12436 | 0.612 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 350 | 354 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 422 | 432 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 453 | 463 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 547 | 551 | PF00244 | 0.678 |
LIG_AP2alpha_1 | 511 | 515 | PF02296 | 0.529 |
LIG_BIR_III_4 | 507 | 511 | PF00653 | 0.507 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.493 |
LIG_Clathr_ClatBox_1 | 536 | 540 | PF01394 | 0.414 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.515 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.599 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.544 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.556 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.574 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.588 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 235 | 243 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 356 | 367 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 498 | 508 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 315 | 319 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 577 | 581 | PF02991 | 0.596 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.596 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.624 |
LIG_Pex14_2 | 511 | 515 | PF04695 | 0.529 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.534 |
LIG_SH2_PTP2 | 585 | 588 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.586 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.497 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.503 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.537 |
LIG_SUMO_SIM_anti_2 | 383 | 389 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 204 | 209 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 383 | 389 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 410 | 416 | PF11976 | 0.608 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.567 |
LIG_TYR_ITIM | 548 | 553 | PF00017 | 0.689 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.522 |
LIG_WW_2 | 365 | 368 | PF00397 | 0.536 |
MOD_CDK_SPK_2 | 386 | 391 | PF00069 | 0.547 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.685 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.520 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.628 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.565 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.605 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.673 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.521 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.660 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.661 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.612 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.744 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.552 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.765 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.754 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.570 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.690 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.504 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.503 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.478 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.656 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.585 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.599 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.729 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.507 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.526 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.717 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.659 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.569 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.656 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.600 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.637 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.747 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.606 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.605 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.513 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.602 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.681 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.688 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.576 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.520 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.686 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.575 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.580 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.541 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.574 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.556 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.640 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.570 |
MOD_NEK2_2 | 495 | 500 | PF00069 | 0.692 |
MOD_OFUCOSY | 276 | 283 | PF10250 | 0.459 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.545 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.604 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.362 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.547 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.611 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.770 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.583 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.509 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.699 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.572 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.673 |
MOD_PKB_1 | 305 | 313 | PF00069 | 0.451 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.523 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.549 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.601 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.756 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.515 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.509 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.499 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.487 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.436 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.572 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.547 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.643 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.489 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.503 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.566 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.552 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.574 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.535 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.629 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.648 |
MOD_SUMO_for_1 | 266 | 269 | PF00179 | 0.436 |
MOD_SUMO_rev_2 | 386 | 396 | PF00179 | 0.576 |
TRG_DiLeu_BaEn_1 | 533 | 538 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 532 | 537 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.691 |
TRG_ENDOCYTIC_2 | 585 | 588 | PF00928 | 0.586 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.518 |
TRG_NLS_MonoExtC_3 | 571 | 576 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 569 | 576 | PF00514 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 232 | 237 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 535 | 540 | PF00026 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 579 | 583 | PF00026 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I218 | Leptomonas seymouri | 85% | 100% |
A0A0S4KH91 | Bodo saltans | 71% | 100% |
A0A1X0NLE5 | Trypanosomatidae | 66% | 98% |
A0A3S5IR64 | Trypanosoma rangeli | 76% | 100% |
A0A3S7WPF9 | Leishmania donovani | 94% | 100% |
A4HSU1 | Leishmania infantum | 94% | 100% |
C9ZTF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 75% | 100% |
E9AKS8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QJ29 | Leishmania major | 95% | 100% |