Publication identifier(s): 31356625
GPI-anchored cell surface protease. Broad-spectrum ectoenzyme involved in pathogenesis. Heavily expanded family in all parazitic species.. Localization: Cell surface (experimental)
by homology
Contact email: albert.descoteaux@iaf.inrs.ca
Publication title: The host cell secretory pathway mediates the export of Leishmania virulence factors out of the parasitophorous vacuole
Publication 1st author(s): Amandine Isnard
Publication Identifier(s): 25826301
Host organism: -1
Interaction detection method(s): protease assay
Interaction type: physical association
Identification method participant A: monoclonal antibody western blot
Identification method participant B: monoclonal antibody western blot
ID(s) interactor A: P05627
ID(s) interactor B: P08148
Taxid interactor A: Mus musculus
Taxid interactor B: Leishmania major
Biological role(s) interactor A: enzyme
Biological role(s) interactor B: enzyme target
Experimental role(s) interactor A: neutral component
Plasma membrane, GP63, leishmanolysin GP63-3
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 48 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 41, no: 6 |
NetGPI | no | yes: 0, no: 47 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 48 |
GO:0110165 | cellular anatomical entity | 1 | 48 |
GO:0005737 | cytoplasm | 2 | 4 |
GO:0018995 | host cellular component | 2 | 4 |
GO:0033643 | host cell part | 3 | 4 |
GO:0033646 | host intracellular part | 4 | 4 |
GO:0033647 | host intracellular organelle | 5 | 4 |
GO:0033648 | host intracellular membrane-bounded organelle | 6 | 4 |
GO:0042025 | host cell nucleus | 7 | 4 |
Related structures:
AlphaFold database: A4HUG0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 48 |
GO:0006807 | nitrogen compound metabolic process | 2 | 48 |
GO:0007155 | cell adhesion | 2 | 48 |
GO:0008152 | metabolic process | 1 | 48 |
GO:0009987 | cellular process | 1 | 48 |
GO:0019538 | protein metabolic process | 3 | 48 |
GO:0043170 | macromolecule metabolic process | 3 | 48 |
GO:0044238 | primary metabolic process | 2 | 48 |
GO:0071704 | organic substance metabolic process | 2 | 48 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 48 |
GO:0009966 | regulation of signal transduction | 4 | 4 |
GO:0010646 | regulation of cell communication | 4 | 4 |
GO:0010749 | regulation of nitric oxide mediated signal transduction | 6 | 4 |
GO:0023051 | regulation of signaling | 3 | 4 |
GO:0035821 | modulation of process of another organism | 2 | 4 |
GO:0044003 | modulation by symbiont of host process | 3 | 4 |
GO:0044068 | modulation by symbiont of host cellular process | 4 | 4 |
GO:0044081 | modulation by symbiont of host nitric oxide-mediated signal transduction | 5 | 4 |
GO:0044403 | biological process involved in symbiotic interaction | 2 | 4 |
GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 4 |
GO:0044501 | modulation of signal transduction in another organism | 3 | 4 |
GO:0048583 | regulation of response to stimulus | 3 | 4 |
GO:0050789 | regulation of biological process | 2 | 4 |
GO:0050794 | regulation of cellular process | 3 | 4 |
GO:0051701 | biological process involved in interaction with host | 3 | 4 |
GO:0052027 | modulation by symbiont of host signal transduction pathway | 4 | 4 |
GO:0065007 | biological regulation | 1 | 4 |
GO:0075130 | modulation by symbiont of host protein kinase-mediated signal transduction | 5 | 4 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 48 |
GO:0004175 | endopeptidase activity | 4 | 48 |
GO:0004222 | metalloendopeptidase activity | 5 | 48 |
GO:0005488 | binding | 1 | 48 |
GO:0008233 | peptidase activity | 3 | 48 |
GO:0008237 | metallopeptidase activity | 4 | 48 |
GO:0016787 | hydrolase activity | 2 | 48 |
GO:0043167 | ion binding | 2 | 48 |
GO:0043169 | cation binding | 3 | 48 |
GO:0046872 | metal ion binding | 4 | 48 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 48 |
GO:0008047 | enzyme activator activity | 3 | 4 |
GO:0008160 | protein tyrosine phosphatase activator activity | 6 | 4 |
GO:0019208 | phosphatase regulator activity | 3 | 4 |
GO:0019211 | phosphatase activator activity | 4 | 4 |
GO:0019888 | protein phosphatase regulator activity | 4 | 4 |
GO:0030234 | enzyme regulator activity | 2 | 4 |
GO:0072542 | protein phosphatase activator activity | 5 | 4 |
GO:0098772 | molecular function regulator activity | 1 | 4 |
GO:0140677 | molecular function activator activity | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 743 | 745 | PF00675 | 0.717 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 743 | 745 | PF00082 | 0.717 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.613 |
CLV_PCSK_PC7_1 | 44 | 50 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 700 | 708 | PF00400 | 0.373 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.661 |
DEG_SCF_TRCP1_1 | 297 | 302 | PF00400 | 0.234 |
DEG_SPOP_SBC_1 | 167 | 171 | PF00917 | 0.740 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.644 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.639 |
DOC_CYCLIN_yCln2_LP_2 | 279 | 285 | PF00134 | 0.334 |
DOC_CYCLIN_yCln2_LP_2 | 505 | 511 | PF00134 | 0.345 |
DOC_MAPK_gen_1 | 133 | 143 | PF00069 | 0.632 |
DOC_MAPK_gen_1 | 158 | 167 | PF00069 | 0.629 |
DOC_MAPK_gen_1 | 23 | 33 | PF00069 | 0.644 |
DOC_MAPK_gen_1 | 451 | 459 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 136 | 145 | PF00069 | 0.628 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.640 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.649 |
DOC_PP2B_LxvP_1 | 505 | 508 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.638 |
DOC_PP4_FxxP_1 | 355 | 358 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 601 | 604 | PF00568 | 0.317 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.649 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.647 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 163 | 168 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 227 | 232 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 271 | 279 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 34 | 41 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 451 | 460 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 48 | 53 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 580 | 584 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 630 | 638 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 656 | 664 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 681 | 686 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 69 | 76 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 747 | 755 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 8 | 15 | PF00244 | 0.643 |
LIG_APCC_ABBA_1 | 326 | 331 | PF00400 | 0.451 |
LIG_APCC_ABBA_1 | 520 | 525 | PF00400 | 0.424 |
LIG_APCC_ABBA_1 | 619 | 624 | PF00400 | 0.320 |
LIG_APCC_ABBA_1 | 641 | 646 | PF00400 | 0.451 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.638 |
LIG_BRCT_BRCA1_1 | 433 | 437 | PF00533 | 0.377 |
LIG_BRCT_BRCA1_1 | 67 | 71 | PF00533 | 0.624 |
LIG_BRCT_BRCA1_1 | 707 | 711 | PF00533 | 0.451 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.645 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.641 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.375 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.371 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.336 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.348 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.638 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.400 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.265 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.441 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.425 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.435 |
LIG_FHA_1 | 695 | 701 | PF00498 | 0.279 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.476 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.377 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.283 |
LIG_GBD_Chelix_1 | 141 | 149 | PF00786 | 0.420 |
LIG_GBD_Chelix_1 | 755 | 763 | PF00786 | 0.689 |
LIG_LIR_Apic_2 | 353 | 358 | PF02991 | 0.428 |
LIG_LIR_Apic_2 | 80 | 86 | PF02991 | 0.631 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 413 | 423 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 477 | 485 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 477 | 483 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 666 | 670 | PF02991 | 0.358 |
LIG_MYND_1 | 592 | 596 | PF01753 | 0.283 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.623 |
LIG_PCNA_yPIPBox_3 | 414 | 423 | PF02747 | 0.238 |
LIG_PDZ_Class_2 | 758 | 763 | PF00595 | 0.478 |
LIG_Pex14_1 | 562 | 566 | PF04695 | 0.439 |
LIG_Pex14_2 | 433 | 437 | PF04695 | 0.386 |
LIG_PTB_Apo_2 | 365 | 372 | PF02174 | 0.435 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.396 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.657 |
LIG_SH2_CRK | 515 | 519 | PF00017 | 0.451 |
LIG_SH2_CRK | 667 | 671 | PF00017 | 0.411 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.637 |
LIG_SH2_GRB2like | 693 | 696 | PF00017 | 0.338 |
LIG_SH2_NCK_1 | 83 | 87 | PF00017 | 0.637 |
LIG_SH2_PTP2 | 242 | 245 | PF00017 | 0.341 |
LIG_SH2_PTP2 | 722 | 725 | PF00017 | 0.447 |
LIG_SH2_SRC | 480 | 483 | PF00017 | 0.340 |
LIG_SH2_SRC | 722 | 725 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 683 | 687 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 683 | 686 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.633 |
LIG_SH3_2 | 153 | 158 | PF14604 | 0.615 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.630 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.657 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.618 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.338 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.254 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.296 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.314 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.625 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.644 |
LIG_Sin3_3 | 750 | 757 | PF02671 | 0.487 |
LIG_SxIP_EBH_1 | 32 | 45 | PF03271 | 0.604 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.322 |
LIG_TRAF2_1 | 710 | 713 | PF00917 | 0.300 |
LIG_TRFH_1 | 107 | 111 | PF08558 | 0.521 |
LIG_TYR_ITIM | 240 | 245 | PF00017 | 0.387 |
LIG_TYR_ITIM | 478 | 483 | PF00017 | 0.437 |
LIG_WW_2 | 125 | 128 | PF00397 | 0.529 |
MOD_CDK_SPxxK_3 | 694 | 701 | PF00069 | 0.464 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.510 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.696 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.397 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.237 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.527 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.471 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.338 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.354 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.414 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.503 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.524 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.541 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.360 |
MOD_Cter_Amidation | 741 | 744 | PF01082 | 0.632 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.525 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.511 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.365 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.248 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.472 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.412 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.405 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.471 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.261 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.506 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.527 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.521 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.527 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.375 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.244 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.524 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.531 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.433 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.329 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.554 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.390 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.500 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.390 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.404 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.507 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.535 |
MOD_N-GLC_1 | 557 | 562 | PF02516 | 0.455 |
MOD_N-GLC_1 | 694 | 699 | PF02516 | 0.385 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.531 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.533 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.454 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.505 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.517 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.524 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.501 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.536 |
MOD_PK_1 | 163 | 169 | PF00069 | 0.599 |
MOD_PK_1 | 174 | 180 | PF00069 | 0.676 |
MOD_PK_1 | 681 | 687 | PF00069 | 0.423 |
MOD_PKA_1 | 451 | 457 | PF00069 | 0.237 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.556 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.382 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.311 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.237 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.556 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.401 |
MOD_PKA_2 | 629 | 635 | PF00069 | 0.325 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.526 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.293 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.373 |
MOD_Plk_1 | 702 | 708 | PF00069 | 0.396 |
MOD_Plk_2-3 | 307 | 313 | PF00069 | 0.440 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.344 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.346 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.520 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.497 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.541 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.527 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.535 |
MOD_SUMO_rev_2 | 348 | 358 | PF00179 | 0.393 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 515 | 518 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 667 | 670 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 450 | 452 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 48 | 52 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL11 | Leptomonas seymouri | 35% | 100% |
A0A0S4IN60 | Bodo saltans | 32% | 85% |
A0A0S4IYM3 | Bodo saltans | 29% | 100% |
A0A1X0NDU8 | Trypanosomatidae | 27% | 100% |
A0A1X0NFL1 | Trypanosomatidae | 27% | 81% |
A0A1X0NFT1 | Trypanosomatidae | 26% | 83% |
A0A1X0NI38 | Trypanosomatidae | 27% | 87% |
A0A1X0NI74 | Trypanosomatidae | 27% | 100% |
A0A1X0NII4 | Trypanosomatidae | 28% | 91% |
A0A1X0NK29 | Trypanosomatidae | 30% | 83% |
A0A1X0NMK3 | Trypanosomatidae | 26% | 100% |
A0A1X0NRY8 | Trypanosomatidae | 33% | 100% |
A0A1X0NVC3 | Trypanosomatidae | 29% | 100% |
A0A1X0NX98 | Trypanosomatidae | 30% | 95% |
A0A1X0NXH6 | Trypanosomatidae | 32% | 100% |
A0A1X0NXR7 | Trypanosomatidae | 32% | 100% |
A0A1X0NYE3 | Trypanosomatidae | 29% | 100% |
A0A1X0NZN6 | Trypanosomatidae | 28% | 100% |
A0A1X0P3K0 | Trypanosomatidae | 28% | 100% |
A0A1X0P5J0 | Trypanosomatidae | 33% | 100% |
A0A1X0P7R3 | Trypanosomatidae | 35% | 100% |
A0A3Q8I8N3 | Leishmania donovani | 88% | 100% |
A0A3Q8I8P8 | Leishmania donovani | 94% | 100% |
A0A3Q8I8S6 | Leishmania donovani | 85% | 100% |
A0A3Q8I8S9 | Leishmania donovani | 94% | 100% |
A0A3Q8IAZ8 | Leishmania donovani | 88% | 100% |
A0A3Q8IC35 | Leishmania donovani | 88% | 100% |
A0A3Q8IC44 | Leishmania donovani | 90% | 100% |
A0A3Q8IH61 | Leishmania donovani | 92% | 100% |
A0A3Q8IIN4 | Leishmania donovani | 35% | 100% |
A0A3R7KLR6 | Trypanosoma rangeli | 32% | 100% |
A0A3R7KMY2 | Trypanosoma rangeli | 34% | 100% |
A0A3R7LFC4 | Trypanosoma rangeli | 34% | 100% |
A0A3R7LFZ4 | Trypanosoma rangeli | 33% | 100% |
A0A3R7LWG1 | Trypanosoma rangeli | 33% | 100% |
A0A3R7LX11 | Trypanosoma rangeli | 35% | 100% |
A0A3R7NTI8 | Trypanosoma rangeli | 33% | 100% |
A0A3R7R5R1 | Trypanosoma rangeli | 34% | 100% |
A0A3S5H6G0 | Leishmania donovani | 94% | 100% |
A0A3S5IQY2 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WR43 | Leishmania donovani | 88% | 100% |
A0A3S7WR46 | Leishmania donovani | 93% | 100% |
A0A3S7WR60 | Leishmania donovani | 95% | 100% |
A0A3S7X192 | Leishmania donovani | 36% | 100% |
A0A422MVF5 | Trypanosoma rangeli | 33% | 100% |
A0A422N361 | Trypanosoma rangeli | 33% | 100% |
A4H626 | Leishmania braziliensis | 59% | 100% |
A4H627 | Leishmania braziliensis | 57% | 100% |
A4H630 | Leishmania braziliensis | 63% | 100% |
A4H631 | Leishmania braziliensis | 59% | 100% |
A4H633 | Leishmania braziliensis | 59% | 100% |
A4H634 | Leishmania braziliensis | 62% | 100% |
A4H635 | Leishmania braziliensis | 62% | 100% |
A4H637 | Leishmania braziliensis | 63% | 100% |
A4H638 | Leishmania braziliensis | 70% | 100% |
A4H639 | Leishmania braziliensis | 66% | 100% |
A4H640 | Leishmania braziliensis | 62% | 100% |
A4H6D3 | Leishmania braziliensis | 58% | 100% |
A4H6D5 | Leishmania braziliensis | 59% | 100% |
A4H6D7 | Leishmania braziliensis | 57% | 100% |
A4H6D8 | Leishmania braziliensis | 57% | 100% |
A4H6D9 | Leishmania braziliensis | 57% | 100% |
A4H6E0 | Leishmania braziliensis | 57% | 100% |
A4H6E1 | Leishmania braziliensis | 57% | 100% |
A4H6E2 | Leishmania braziliensis | 59% | 100% |
A4H6E3 | Leishmania braziliensis | 61% | 100% |
A4H6E5 | Leishmania braziliensis | 68% | 100% |
A4HJI2 | Leishmania braziliensis | 35% | 100% |
A4HUF6 | Leishmania infantum | 88% | 100% |
A4HUF8 | Leishmania infantum | 95% | 100% |
A4HUF9 | Leishmania infantum | 85% | 100% |
A4I6X5 | Leishmania infantum | 35% | 100% |
E9AHH5 | Leishmania infantum | 36% | 100% |
E9AN53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9AN54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9AN55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9AN56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9AN57 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AZL8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
P08148 | Leishmania major | 83% | 100% |
P15706 | Leishmania chagasi | 95% | 100% |
P23223 | Leishmania donovani | 87% | 100% |
P43150 | Leishmania mexicana | 73% | 100% |
Q00689 | Leishmania guyanensis | 63% | 100% |
Q06031 | Crithidia fasciculata | 53% | 100% |
Q27673 | Leishmania amazonensis | 78% | 100% |
Q29AK2 | Drosophila pseudoobscura pseudoobscura | 24% | 100% |
Q4Q662 | Leishmania major | 35% | 100% |
Q4Q8L3 | Leishmania major | 39% | 100% |
Q4QHG9 | Leishmania major | 83% | 100% |
Q4QHH0 | Leishmania major | 81% | 100% |
Q4QHH1 | Leishmania major | 84% | 100% |
Q4QHH2 | Leishmania major | 84% | 100% |
Q6LA77 | Leishmania infantum | 95% | 100% |
Q8MNZ1 | Leishmania tropica | 81% | 100% |
Q9VH19 | Drosophila melanogaster | 23% | 100% |
V5AII7 | Trypanosoma cruzi | 37% | 100% |