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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4I1D5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.811 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.620 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.845 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.720 |
CLV_PCSK_FUR_1 | 464 | 468 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.850 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.831 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.841 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 466 | 468 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.727 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.755 |
CLV_PCSK_PC7_1 | 141 | 147 | PF00082 | 0.717 |
CLV_PCSK_PC7_1 | 464 | 470 | PF00082 | 0.702 |
CLV_PCSK_PC7_1 | 580 | 586 | PF00082 | 0.700 |
CLV_PCSK_PC7_1 | 82 | 88 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.755 |
CLV_Separin_Metazoa | 275 | 279 | PF03568 | 0.654 |
DEG_APCC_DBOX_1 | 264 | 272 | PF00400 | 0.553 |
DEG_COP1_1 | 508 | 515 | PF00400 | 0.781 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.660 |
DEG_SCF_FBW7_1 | 316 | 321 | PF00400 | 0.736 |
DEG_SPOP_SBC_1 | 500 | 504 | PF00917 | 0.577 |
DOC_ANK_TNKS_1 | 130 | 137 | PF00023 | 0.571 |
DOC_ANK_TNKS_1 | 393 | 400 | PF00023 | 0.751 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.695 |
DOC_CKS1_1 | 456 | 461 | PF01111 | 0.660 |
DOC_CKS1_1 | 542 | 547 | PF01111 | 0.686 |
DOC_MAPK_gen_1 | 262 | 271 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 327 | 336 | PF00069 | 0.597 |
DOC_PP1_RVXF_1 | 578 | 584 | PF00149 | 0.575 |
DOC_PP2B_LxvP_1 | 417 | 420 | PF13499 | 0.773 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.683 |
DOC_USP7_UBL2_3 | 378 | 382 | PF12436 | 0.690 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.815 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.770 |
LIG_14-3-3_CanoR_1 | 127 | 134 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 265 | 269 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 361 | 367 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 371 | 377 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 467 | 474 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 553 | 561 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 87 | 92 | PF00244 | 0.707 |
LIG_Actin_WH2_2 | 250 | 267 | PF00022 | 0.648 |
LIG_BIR_III_2 | 478 | 482 | PF00653 | 0.619 |
LIG_deltaCOP1_diTrp_1 | 421 | 431 | PF00928 | 0.810 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.785 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.818 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.699 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.616 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.601 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.709 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.620 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.580 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 567 | 576 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 496 | 501 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 567 | 572 | PF02991 | 0.562 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.592 |
LIG_Rb_LxCxE_1 | 514 | 529 | PF01857 | 0.706 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.547 |
LIG_SH2_SRC | 346 | 349 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 569 | 573 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.570 |
LIG_SH3_1 | 305 | 311 | PF00018 | 0.637 |
LIG_SH3_2 | 308 | 313 | PF14604 | 0.601 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.738 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.595 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.682 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.610 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.707 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.665 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.655 |
LIG_Sin3_3 | 536 | 543 | PF02671 | 0.746 |
LIG_SUMO_SIM_anti_2 | 534 | 541 | PF11976 | 0.650 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.740 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.741 |
LIG_TRAF2_1 | 544 | 547 | PF00917 | 0.679 |
LIG_UBA3_1 | 333 | 338 | PF00899 | 0.594 |
MOD_CDK_SPK_2 | 58 | 63 | PF00069 | 0.584 |
MOD_CDK_SPxK_1 | 455 | 461 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 541 | 548 | PF00069 | 0.691 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.756 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.800 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.602 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.772 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.730 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.713 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.731 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.624 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.615 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.608 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.754 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.615 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.539 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.791 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.705 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.618 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.747 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.821 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.593 |
MOD_CMANNOS | 457 | 460 | PF00535 | 0.658 |
MOD_Cter_Amidation | 379 | 382 | PF01082 | 0.794 |
MOD_Cter_Amidation | 96 | 99 | PF01082 | 0.726 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.703 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.666 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.595 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.774 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.660 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.586 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.736 |
MOD_GlcNHglycan | 401 | 407 | PF01048 | 0.670 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.793 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.632 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.780 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.731 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.753 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.646 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.606 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.771 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.588 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.755 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.768 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.793 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.519 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.789 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.768 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.743 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.724 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.740 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.575 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.725 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.833 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.717 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.578 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.578 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.704 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.696 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.538 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.811 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.604 |
MOD_PKA_1 | 145 | 151 | PF00069 | 0.723 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.732 |
MOD_PKA_1 | 467 | 473 | PF00069 | 0.718 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.773 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.642 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.724 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.722 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.559 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.632 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.600 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.718 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.747 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.820 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.821 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.692 |
MOD_Plk_2-3 | 47 | 53 | PF00069 | 0.782 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.821 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.581 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.633 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.756 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.689 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.546 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.661 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.753 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.675 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.817 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.770 |
MOD_SUMO_for_1 | 241 | 244 | PF00179 | 0.644 |
TRG_DiLeu_BaEn_1 | 106 | 111 | PF01217 | 0.822 |
TRG_DiLeu_BaLyEn_6 | 329 | 334 | PF01217 | 0.624 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.734 |
TRG_NLS_Bipartite_1 | 84 | 102 | PF00514 | 0.755 |
TRG_NLS_MonoCore_2 | 83 | 88 | PF00514 | 0.747 |
TRG_NLS_MonoExtC_3 | 368 | 373 | PF00514 | 0.621 |
TRG_NLS_MonoExtC_3 | 97 | 102 | PF00514 | 0.759 |
TRG_NLS_MonoExtN_4 | 369 | 374 | PF00514 | 0.627 |
TRG_NLS_MonoExtN_4 | 82 | 89 | PF00514 | 0.749 |
TRG_Pf-PMV_PEXEL_1 | 284 | 289 | PF00026 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 338 | 342 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P735 | Leptomonas seymouri | 43% | 100% |
A0A3Q8INB5 | Leishmania donovani | 99% | 100% |
A4HE29 | Leishmania braziliensis | 67% | 98% |
E9AXH2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QA00 | Leishmania major | 86% | 100% |