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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AL46
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.787 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.364 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.764 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.787 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.764 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.530 |
DEG_COP1_1 | 288 | 298 | PF00400 | 0.534 |
DEG_SCF_FBW7_1 | 452 | 458 | PF00400 | 0.660 |
DOC_ANK_TNKS_1 | 533 | 540 | PF00023 | 0.719 |
DOC_CKS1_1 | 388 | 393 | PF01111 | 0.524 |
DOC_CKS1_1 | 433 | 438 | PF01111 | 0.722 |
DOC_CKS1_1 | 444 | 449 | PF01111 | 0.773 |
DOC_CKS1_1 | 452 | 457 | PF01111 | 0.633 |
DOC_CYCLIN_yCln2_LP_2 | 352 | 358 | PF00134 | 0.534 |
DOC_MAPK_gen_1 | 624 | 633 | PF00069 | 0.511 |
DOC_PP1_RVXF_1 | 41 | 47 | PF00149 | 0.701 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.534 |
DOC_PP4_FxxP_1 | 8 | 11 | PF00568 | 0.756 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.837 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.677 |
DOC_USP7_UBL2_3 | 188 | 192 | PF12436 | 0.839 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.681 |
DOC_USP7_UBL2_3 | 255 | 259 | PF12436 | 0.733 |
DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.736 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.825 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.815 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 383 | 387 | PF00244 | 0.817 |
LIG_14-3-3_CanoR_1 | 423 | 433 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 624 | 630 | PF00244 | 0.726 |
LIG_Actin_WH2_2 | 151 | 168 | PF00022 | 0.519 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 550 | 554 | PF00533 | 0.801 |
LIG_BRCT_BRCA1_1 | 621 | 625 | PF00533 | 0.794 |
LIG_BRCT_BRCA1_1 | 650 | 654 | PF00533 | 0.621 |
LIG_deltaCOP1_diTrp_1 | 33 | 39 | PF00928 | 0.716 |
LIG_deltaCOP1_diTrp_1 | 644 | 654 | PF00928 | 0.721 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.510 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.527 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.617 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.546 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.653 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.569 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.816 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.725 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.685 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.345 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.731 |
LIG_LIR_Apic_2 | 639 | 645 | PF02991 | 0.610 |
LIG_LIR_Apic_2 | 7 | 11 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 585 | 594 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.597 |
LIG_MYND_1 | 538 | 542 | PF01753 | 0.738 |
LIG_PCNA_yPIPBox_3 | 225 | 235 | PF02747 | 0.681 |
LIG_Pex14_1 | 35 | 39 | PF04695 | 0.718 |
LIG_Pex14_2 | 625 | 629 | PF04695 | 0.804 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.585 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.618 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.797 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.397 |
LIG_SH2_PTP2 | 61 | 64 | PF00017 | 0.726 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.726 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.770 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.726 |
LIG_SH3_1 | 306 | 312 | PF00018 | 0.632 |
LIG_SH3_1 | 449 | 455 | PF00018 | 0.783 |
LIG_SH3_2 | 301 | 306 | PF14604 | 0.548 |
LIG_SH3_2 | 444 | 449 | PF14604 | 0.858 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.824 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.699 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.582 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.517 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.483 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.846 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.728 |
LIG_TYR_ITIM | 130 | 135 | PF00017 | 0.571 |
LIG_UBA3_1 | 146 | 152 | PF00899 | 0.656 |
LIG_UBA3_1 | 235 | 244 | PF00899 | 0.701 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.766 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.648 |
LIG_WW_2 | 301 | 304 | PF00397 | 0.535 |
MOD_CDC14_SPxK_1 | 583 | 586 | PF00782 | 0.675 |
MOD_CDK_SPK_2 | 432 | 437 | PF00069 | 0.721 |
MOD_CDK_SPxK_1 | 443 | 449 | PF00069 | 0.857 |
MOD_CDK_SPxK_1 | 580 | 586 | PF00069 | 0.759 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.751 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.723 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.811 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.558 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.797 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.631 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.783 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.745 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.696 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.623 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.726 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.681 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.554 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.696 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.789 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.720 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.774 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.656 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.648 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.709 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.559 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.734 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.636 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.743 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.585 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.564 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.758 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.798 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.670 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.772 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.565 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.651 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.633 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.752 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.512 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.660 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.576 |
MOD_PIKK_1 | 602 | 608 | PF00454 | 0.405 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.590 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.615 |
MOD_PKA_1 | 280 | 286 | PF00069 | 0.721 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.811 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.405 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.511 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.687 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.669 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.729 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.523 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.764 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.729 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.592 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.824 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.816 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.759 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.796 |
MOD_SUMO_for_1 | 279 | 282 | PF00179 | 0.709 |
MOD_SUMO_for_1 | 591 | 594 | PF00179 | 0.620 |
MOD_SUMO_rev_2 | 541 | 548 | PF00179 | 0.726 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.799 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.692 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.787 |
TRG_ER_diArg_1 | 598 | 600 | PF00400 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 263 | 267 | PF00026 | 0.691 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5X4 | Leishmania donovani | 89% | 100% |
A4H4Y1 | Leishmania braziliensis | 69% | 97% |
A4HT32 | Leishmania infantum | 89% | 100% |
Q4QIQ8 | Leishmania major | 89% | 100% |