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: Q4QFE9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.749 |
CLV_PCSK_FUR_1 | 189 | 193 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.759 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.756 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.567 |
DEG_APCC_DBOX_1 | 633 | 641 | PF00400 | 0.647 |
DEG_ODPH_VHL_1 | 578 | 589 | PF01847 | 0.747 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.571 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.717 |
DOC_MAPK_gen_1 | 191 | 200 | PF00069 | 0.755 |
DOC_MAPK_gen_1 | 372 | 381 | PF00069 | 0.667 |
DOC_MAPK_MEF2A_6 | 346 | 355 | PF00069 | 0.608 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.665 |
DOC_PP1_RVXF_1 | 637 | 643 | PF00149 | 0.640 |
DOC_PP2B_LxvP_1 | 51 | 54 | PF13499 | 0.658 |
DOC_PP2B_LxvP_1 | 572 | 575 | PF13499 | 0.761 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.743 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.732 |
LIG_14-3-3_CanoR_1 | 232 | 240 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 266 | 274 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 346 | 351 | PF00244 | 0.838 |
LIG_14-3-3_CanoR_1 | 372 | 381 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 408 | 415 | PF00244 | 0.688 |
LIG_Actin_WH2_2 | 159 | 175 | PF00022 | 0.637 |
LIG_Actin_WH2_2 | 619 | 636 | PF00022 | 0.716 |
LIG_AP_GAE_1 | 523 | 529 | PF02883 | 0.635 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.751 |
LIG_BIR_III_2 | 137 | 141 | PF00653 | 0.577 |
LIG_BIR_III_4 | 213 | 217 | PF00653 | 0.671 |
LIG_BRCT_BRCA1_1 | 510 | 514 | PF00533 | 0.693 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.768 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.600 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.822 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.685 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.599 |
LIG_GBD_Chelix_1 | 629 | 637 | PF00786 | 0.571 |
LIG_LIR_Gen_1 | 523 | 533 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.664 |
LIG_Pex14_2 | 642 | 646 | PF04695 | 0.719 |
LIG_PTAP_UEV_1 | 193 | 198 | PF05743 | 0.727 |
LIG_RPA_C_Fungi | 527 | 539 | PF08784 | 0.657 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.649 |
LIG_SH2_NCK_1 | 240 | 244 | PF00017 | 0.707 |
LIG_SH2_SRC | 168 | 171 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.753 |
LIG_SH2_STAP1 | 322 | 326 | PF00017 | 0.730 |
LIG_SH2_STAP1 | 336 | 340 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 643 | 647 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.782 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.568 |
LIG_SH3_1 | 191 | 197 | PF00018 | 0.725 |
LIG_SH3_2 | 571 | 576 | PF14604 | 0.579 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.724 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.790 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.667 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.793 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.718 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.730 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.775 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.720 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.725 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.816 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.637 |
LIG_WW_3 | 343 | 347 | PF00397 | 0.828 |
LIG_WW_3 | 52 | 56 | PF00397 | 0.639 |
MOD_CDK_SPxK_1 | 468 | 474 | PF00069 | 0.734 |
MOD_CDK_SPxxK_3 | 347 | 354 | PF00069 | 0.611 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.709 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.712 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.732 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.711 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.755 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.671 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.763 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.813 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.782 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.832 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.703 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.685 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.742 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.705 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.740 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.759 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.721 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.595 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.502 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.594 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.787 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.716 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.711 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.587 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.796 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.588 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.730 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.821 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.779 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.710 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.714 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.776 |
MOD_GlcNHglycan | 597 | 601 | PF01048 | 0.690 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.747 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.604 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.688 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.693 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.692 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.718 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.734 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.666 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.712 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.685 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.676 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.651 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.623 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.588 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.663 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.791 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.667 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.537 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.655 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.719 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.705 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.679 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.642 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.551 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.558 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.635 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.720 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.541 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.670 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.670 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.710 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.759 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.663 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.752 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.652 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.627 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.647 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.648 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.756 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.766 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.656 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.688 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.744 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.824 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.734 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.734 |
MOD_SUMO_for_1 | 47 | 50 | PF00179 | 0.726 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.586 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.602 |
TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.749 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 393 | 397 | PF00026 | 0.762 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC10 | Leptomonas seymouri | 33% | 100% |
A0A3S7WTB9 | Leishmania donovani | 84% | 100% |
A4H805 | Leishmania braziliensis | 58% | 100% |
A4HWD3 | Leishmania infantum | 85% | 100% |
E9AQ33 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |