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: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4IAV2
Term | Name | Level | Count |
---|---|---|---|
GO:0002218 | activation of innate immune response | 3 | 1 |
GO:0002221 | pattern recognition receptor signaling pathway | 5 | 1 |
GO:0002224 | toll-like receptor signaling pathway | 6 | 1 |
GO:0002253 | activation of immune response | 2 | 1 |
GO:0002376 | immune system process | 1 | 1 |
GO:0002682 | regulation of immune system process | 3 | 1 |
GO:0002684 | positive regulation of immune system process | 4 | 1 |
GO:0002757 | immune response-activating signaling pathway | 3 | 1 |
GO:0002758 | innate immune response-activating signaling pathway | 4 | 1 |
GO:0002764 | immune response-regulating signaling pathway | 3 | 1 |
GO:0002831 | regulation of response to biotic stimulus | 4 | 1 |
GO:0002833 | positive regulation of response to biotic stimulus | 5 | 1 |
GO:0006955 | immune response | 2 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0031347 | regulation of defense response | 5 | 1 |
GO:0031349 | positive regulation of defense response | 5 | 1 |
GO:0032101 | regulation of response to external stimulus | 4 | 1 |
GO:0032103 | positive regulation of response to external stimulus | 5 | 1 |
GO:0045088 | regulation of innate immune response | 5 | 1 |
GO:0045089 | positive regulation of innate immune response | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0048584 | positive regulation of response to stimulus | 4 | 1 |
GO:0050776 | regulation of immune response | 4 | 1 |
GO:0050778 | positive regulation of immune response | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080134 | regulation of response to stress | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0004888 | transmembrane signaling receptor activity | 3 | 1 |
GO:0038023 | signaling receptor activity | 2 | 1 |
GO:0060089 | molecular transducer activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 883 | 885 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 883 | 885 | PF00082 | 0.553 |
DEG_Nend_UBRbox_3 | 1 | 2 | PF02207 | 0.498 |
DOC_MAPK_MEF2A_6 | 123 | 132 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.470 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 153 | 158 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 303 | 308 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 378 | 383 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 468 | 473 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 483 | 488 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 498 | 503 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 528 | 533 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 588 | 593 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 693 | 698 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 723 | 728 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 78 | 83 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 883 | 887 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.500 |
LIG_Actin_WH2_2 | 122 | 140 | PF00022 | 0.704 |
LIG_Actin_WH2_2 | 152 | 170 | PF00022 | 0.607 |
LIG_Actin_WH2_2 | 182 | 200 | PF00022 | 0.576 |
LIG_Actin_WH2_2 | 2 | 20 | PF00022 | 0.586 |
LIG_Actin_WH2_2 | 212 | 230 | PF00022 | 0.558 |
LIG_Actin_WH2_2 | 242 | 260 | PF00022 | 0.559 |
LIG_Actin_WH2_2 | 272 | 290 | PF00022 | 0.568 |
LIG_Actin_WH2_2 | 302 | 320 | PF00022 | 0.581 |
LIG_Actin_WH2_2 | 32 | 50 | PF00022 | 0.711 |
LIG_Actin_WH2_2 | 332 | 350 | PF00022 | 0.578 |
LIG_Actin_WH2_2 | 362 | 380 | PF00022 | 0.614 |
LIG_Actin_WH2_2 | 392 | 410 | PF00022 | 0.612 |
LIG_Actin_WH2_2 | 422 | 440 | PF00022 | 0.600 |
LIG_Actin_WH2_2 | 452 | 470 | PF00022 | 0.614 |
LIG_Actin_WH2_2 | 482 | 500 | PF00022 | 0.626 |
LIG_Actin_WH2_2 | 512 | 530 | PF00022 | 0.605 |
LIG_Actin_WH2_2 | 542 | 560 | PF00022 | 0.594 |
LIG_Actin_WH2_2 | 572 | 590 | PF00022 | 0.594 |
LIG_Actin_WH2_2 | 602 | 620 | PF00022 | 0.578 |
LIG_Actin_WH2_2 | 62 | 80 | PF00022 | 0.746 |
LIG_Actin_WH2_2 | 632 | 650 | PF00022 | 0.568 |
LIG_Actin_WH2_2 | 677 | 695 | PF00022 | 0.483 |
LIG_Actin_WH2_2 | 707 | 725 | PF00022 | 0.661 |
LIG_Actin_WH2_2 | 737 | 755 | PF00022 | 0.485 |
LIG_Actin_WH2_2 | 782 | 800 | PF00022 | 0.543 |
LIG_Actin_WH2_2 | 812 | 830 | PF00022 | 0.542 |
LIG_Actin_WH2_2 | 842 | 860 | PF00022 | 0.553 |
LIG_Actin_WH2_2 | 92 | 110 | PF00022 | 0.756 |
LIG_APCC_ABBA_1 | 875 | 880 | PF00400 | 0.537 |
LIG_EH1_1 | 602 | 610 | PF00400 | 0.424 |
LIG_EH1_1 | 677 | 685 | PF00400 | 0.408 |
LIG_EH1_1 | 707 | 715 | PF00400 | 0.414 |
LIG_FHA_1 | 872 | 878 | PF00498 | 0.521 |
LIG_LIR_LC3C_4 | 156 | 160 | PF02991 | 0.489 |
LIG_LIR_LC3C_4 | 171 | 175 | PF02991 | 0.476 |
LIG_LIR_LC3C_4 | 306 | 310 | PF02991 | 0.435 |
LIG_LIR_LC3C_4 | 81 | 85 | PF02991 | 0.497 |
LIG_LIR_LC3C_4 | 96 | 100 | PF02991 | 0.476 |
LIG_PDZ_Class_2 | 901 | 906 | PF00595 | 0.526 |
LIG_SUMO_SIM_anti_2 | 141 | 146 | PF11976 | 0.588 |
LIG_SUMO_SIM_anti_2 | 156 | 161 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 171 | 176 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 306 | 311 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 381 | 386 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 471 | 476 | PF11976 | 0.440 |
LIG_SUMO_SIM_anti_2 | 486 | 491 | PF11976 | 0.357 |
LIG_SUMO_SIM_anti_2 | 501 | 506 | PF11976 | 0.352 |
LIG_SUMO_SIM_anti_2 | 531 | 536 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 591 | 596 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 696 | 701 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 726 | 731 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 81 | 86 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 96 | 101 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 606 | 612 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 681 | 687 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 711 | 717 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 756 | 762 | PF11976 | 0.647 |
LIG_SUMO_SIM_par_1 | 771 | 777 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 786 | 792 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 831 | 837 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 873 | 881 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 896 | 901 | PF11976 | 0.489 |
MOD_CK1_1 | 887 | 893 | PF00069 | 0.581 |
MOD_GlcNHglycan | 886 | 889 | PF01048 | 0.568 |
MOD_GlcNHglycan | 890 | 893 | PF01048 | 0.513 |
MOD_GlcNHglycan | 900 | 903 | PF01048 | 0.531 |
MOD_GSK3_1 | 884 | 891 | PF00069 | 0.585 |
MOD_PK_1 | 138 | 144 | PF00069 | 0.619 |
MOD_PK_1 | 153 | 159 | PF00069 | 0.431 |
MOD_PK_1 | 168 | 174 | PF00069 | 0.505 |
MOD_PK_1 | 303 | 309 | PF00069 | 0.467 |
MOD_PK_1 | 378 | 384 | PF00069 | 0.476 |
MOD_PK_1 | 468 | 474 | PF00069 | 0.471 |
MOD_PK_1 | 483 | 489 | PF00069 | 0.393 |
MOD_PK_1 | 498 | 504 | PF00069 | 0.384 |
MOD_PK_1 | 528 | 534 | PF00069 | 0.454 |
MOD_PK_1 | 588 | 594 | PF00069 | 0.445 |
MOD_PK_1 | 693 | 699 | PF00069 | 0.424 |
MOD_PK_1 | 723 | 729 | PF00069 | 0.425 |
MOD_PK_1 | 78 | 84 | PF00069 | 0.519 |
MOD_PK_1 | 93 | 99 | PF00069 | 0.494 |
MOD_PKA_2 | 882 | 888 | PF00069 | 0.549 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.619 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.431 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.505 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.467 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.476 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.471 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.393 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.384 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.454 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.445 |
MOD_Plk_4 | 693 | 699 | PF00069 | 0.424 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.425 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.519 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.494 |
TRG_ER_diArg_1 | 882 | 884 | PF00400 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
E9AHU2 | Leishmania infantum | 58% | 100% |