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: E9AEN4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.727 |
CLV_MEL_PAP_1 | 40 | 46 | PF00089 | 0.710 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 688 | 690 | PF00675 | 0.742 |
CLV_PCSK_FUR_1 | 302 | 306 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 688 | 690 | PF00082 | 0.742 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.680 |
CLV_PCSK_PC7_1 | 300 | 306 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.746 |
DEG_APCC_DBOX_1 | 157 | 165 | PF00400 | 0.690 |
DEG_APCC_DBOX_1 | 467 | 475 | PF00400 | 0.742 |
DEG_SCF_FBW7_1 | 508 | 515 | PF00400 | 0.727 |
DEG_SPOP_SBC_1 | 512 | 516 | PF00917 | 0.718 |
DOC_MAPK_gen_1 | 467 | 476 | PF00069 | 0.647 |
DOC_MAPK_MEF2A_6 | 695 | 704 | PF00069 | 0.712 |
DOC_MAPK_NFAT4_5 | 695 | 703 | PF00069 | 0.710 |
DOC_PP2B_LxvP_1 | 259 | 262 | PF13499 | 0.670 |
DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.655 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.677 |
DOC_PP4_MxPP_1 | 585 | 588 | PF00568 | 0.547 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.724 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.790 |
LIG_14-3-3_CanoR_1 | 219 | 228 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 232 | 240 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 336 | 344 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 43 | 53 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 490 | 500 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 580 | 586 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 605 | 615 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 67 | 77 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 681 | 685 | PF00244 | 0.598 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.677 |
LIG_Clathr_ClatBox_1 | 246 | 250 | PF01394 | 0.547 |
LIG_deltaCOP1_diTrp_1 | 153 | 157 | PF00928 | 0.626 |
LIG_deltaCOP1_diTrp_1 | 169 | 172 | PF00928 | 0.501 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.635 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.759 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.744 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.775 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.697 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.594 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.623 |
LIG_LIR_Gen_1 | 121 | 132 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 168 | 174 | PF02991 | 0.701 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 530 | 539 | PF02991 | 0.736 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 530 | 535 | PF02991 | 0.626 |
LIG_MLH1_MIPbox_1 | 208 | 212 | PF16413 | 0.677 |
LIG_MYND_3 | 29 | 33 | PF01753 | 0.717 |
LIG_NRBOX | 701 | 707 | PF00104 | 0.486 |
LIG_PCNA_PIPBox_1 | 205 | 214 | PF02747 | 0.580 |
LIG_Pex14_1 | 690 | 694 | PF04695 | 0.723 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.495 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.682 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.692 |
LIG_SH2_STAP1 | 422 | 426 | PF00017 | 0.683 |
LIG_SH2_STAT3 | 607 | 610 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.576 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.677 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.797 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.776 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.764 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.555 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.660 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.687 |
LIG_TRAF2_1 | 470 | 473 | PF00917 | 0.738 |
LIG_UBA3_1 | 363 | 367 | PF00899 | 0.744 |
LIG_ULM_U2AF65_1 | 302 | 309 | PF00076 | 0.690 |
LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.677 |
MOD_CDK_SPxxK_3 | 266 | 273 | PF00069 | 0.741 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.725 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.673 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.678 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.712 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.791 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.647 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.645 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.545 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.605 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.800 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.711 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.674 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.613 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.496 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.679 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.763 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.579 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.650 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.691 |
MOD_CMANNOS | 154 | 157 | PF00535 | 0.719 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.743 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.649 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.679 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.788 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.709 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.580 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.809 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.753 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.661 |
MOD_GlcNHglycan | 541 | 545 | PF01048 | 0.689 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.750 |
MOD_GlcNHglycan | 637 | 641 | PF01048 | 0.785 |
MOD_GlcNHglycan | 655 | 659 | PF01048 | 0.547 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.488 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.717 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.616 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.702 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.703 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.621 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.727 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.623 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.672 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.605 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.746 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.558 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.666 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.775 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.594 |
MOD_LATS_1 | 217 | 223 | PF00433 | 0.460 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.679 |
MOD_N-GLC_2 | 393 | 395 | PF02516 | 0.705 |
MOD_N-GLC_2 | 558 | 560 | PF02516 | 0.728 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.602 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.685 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.740 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.803 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.604 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.784 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.683 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.563 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.665 |
MOD_NEK2_2 | 207 | 212 | PF00069 | 0.683 |
MOD_NEK2_2 | 354 | 359 | PF00069 | 0.560 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.652 |
MOD_NEK2_2 | 680 | 685 | PF00069 | 0.676 |
MOD_OFUCOSY | 488 | 495 | PF10250 | 0.615 |
MOD_OFUCOSY | 672 | 677 | PF10250 | 0.698 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.642 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.712 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.789 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.693 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.651 |
MOD_PIKK_1 | 623 | 629 | PF00454 | 0.475 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.596 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.703 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.800 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.735 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.611 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.581 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.694 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.693 |
MOD_PKB_1 | 128 | 136 | PF00069 | 0.639 |
MOD_PKB_1 | 158 | 166 | PF00069 | 0.712 |
MOD_PKB_1 | 305 | 313 | PF00069 | 0.676 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.661 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.608 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.749 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.711 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.718 |
MOD_Plk_2-3 | 250 | 256 | PF00069 | 0.510 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.610 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.682 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.799 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.557 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.584 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.642 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.713 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.578 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.739 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.741 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.727 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.792 |
MOD_SUMO_for_1 | 195 | 198 | PF00179 | 0.754 |
TRG_DiLeu_LyEn_5 | 242 | 247 | PF01217 | 0.575 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.609 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.690 |
TRG_ER_diArg_1 | 319 | 322 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.701 |
TRG_ER_diArg_1 | 688 | 690 | PF00400 | 0.641 |
TRG_NLS_MonoCore_2 | 301 | 306 | PF00514 | 0.676 |
TRG_NLS_MonoExtC_3 | 301 | 306 | PF00514 | 0.681 |
TRG_NLS_MonoExtN_4 | 300 | 307 | PF00514 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 469 | 473 | PF00026 | 0.741 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3A3 | Leptomonas seymouri | 29% | 100% |
A0A3S7X8U8 | Leishmania donovani | 87% | 100% |
A4HM92 | Leishmania braziliensis | 64% | 100% |
A4IAV6 | Leishmania infantum | 88% | 100% |
E9B5U0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |