| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 1 |
| Forrest at al. (metacyclic) | no | yes: 1 |
| Forrest at al. (procyclic) | no | yes: 1 |
| Silverman et al. | no | yes: 1 |
| Pissara et al. | yes | yes: 5 |
| 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: 4 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 10 |
| NetGPI | no | yes: 0, no: 10 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005856 | cytoskeleton | 5 | 11 |
| GO:0015629 | actin cytoskeleton | 6 | 11 |
| GO:0043226 | organelle | 2 | 11 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
| GO:0043229 | intracellular organelle | 3 | 11 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
| GO:0110165 | cellular anatomical entity | 1 | 11 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0031974 | membrane-enclosed lumen | 2 | 1 |
| GO:0031981 | nuclear lumen | 5 | 1 |
| GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
| GO:0043233 | organelle lumen | 3 | 1 |
| GO:0070013 | intracellular organelle lumen | 4 | 1 |
| GO:0097014 | ciliary plasm | 5 | 1 |
| GO:0099568 | cytoplasmic region | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0007015 | actin filament organization | 5 | 11 |
| GO:0008154 | actin polymerization or depolymerization | 6 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0016043 | cellular component organization | 3 | 11 |
| GO:0022411 | cellular component disassembly | 4 | 11 |
| GO:0030042 | actin filament depolymerization | 7 | 11 |
| GO:0032984 | protein-containing complex disassembly | 5 | 11 |
| GO:0043933 | protein-containing complex organization | 4 | 11 |
| GO:0051261 | protein depolymerization | 6 | 11 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
| GO:0097435 | supramolecular fiber organization | 4 | 11 |
| GO:0006810 | transport | 3 | 1 |
| GO:0046907 | intracellular transport | 3 | 1 |
| GO:0051179 | localization | 1 | 1 |
| GO:0051234 | establishment of localization | 2 | 1 |
| GO:0051301 | cell division | 2 | 1 |
| GO:0051641 | cellular localization | 2 | 1 |
| GO:0051649 | establishment of localization in cell | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003779 | actin binding | 4 | 11 |
| GO:0005488 | binding | 1 | 11 |
| GO:0005515 | protein binding | 2 | 11 |
| GO:0008092 | cytoskeletal protein binding | 3 | 11 |
| GO:0044877 | protein-containing complex binding | 2 | 1 |
| GO:0051015 | actin filament binding | 3 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.449 |
| CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.659 |
| CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.543 |
| CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.339 |
| CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.364 |
| CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.364 |
| CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.324 |
| CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.363 |
| CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.338 |
| CLV_Separin_Metazoa | 128 | 132 | PF03568 | 0.495 |
| DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.580 |
| DEG_APCC_DBOX_1 | 77 | 85 | PF00400 | 0.524 |
| DOC_MAPK_gen_1 | 22 | 31 | PF00069 | 0.528 |
| DOC_MAPK_gen_1 | 77 | 84 | PF00069 | 0.564 |
| DOC_USP7_UBL2_3 | 92 | 96 | PF12436 | 0.559 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 |
| LIG_FHA_2 | 5 | 11 | PF00498 | 0.562 |
| LIG_LIR_Gen_1 | 24 | 33 | PF02991 | 0.515 |
| LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.536 |
| LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.556 |
| LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.537 |
| LIG_SH2_NCK_1 | 71 | 75 | PF00017 | 0.564 |
| LIG_SH2_SRC | 113 | 116 | PF00017 | 0.664 |
| LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.589 |
| LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.525 |
| LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.609 |
| LIG_SH3_4 | 92 | 99 | PF00018 | 0.559 |
| LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.524 |
| LIG_TRAF2_2 | 115 | 120 | PF00917 | 0.556 |
| LIG_TYR_ITIM | 48 | 53 | PF00017 | 0.551 |
| LIG_UBA3_1 | 28 | 36 | PF00899 | 0.521 |
| LIG_UBA3_1 | 83 | 92 | PF00899 | 0.517 |
| MOD_CK1_1 | 107 | 113 | PF00069 | 0.632 |
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.488 |
| MOD_CK2_1 | 73 | 79 | PF00069 | 0.550 |
| MOD_Cter_Amidation | 34 | 37 | PF01082 | 0.404 |
| MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.393 |
| MOD_GlcNHglycan | 120 | 124 | PF01048 | 0.411 |
| MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.526 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.573 |
| MOD_NEK2_1 | 21 | 26 | PF00069 | 0.427 |
| MOD_NEK2_1 | 53 | 58 | PF00069 | 0.596 |
| MOD_NEK2_1 | 97 | 102 | PF00069 | 0.524 |
| MOD_Plk_1 | 44 | 50 | PF00069 | 0.575 |
| MOD_SUMO_rev_2 | 47 | 56 | PF00179 | 0.534 |
| TRG_DiLeu_BaEn_1 | 79 | 84 | PF01217 | 0.604 |
| TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.664 |
| TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.525 |
| TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.579 |
| TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.573 |
| TRG_NLS_MonoExtN_4 | 20 | 26 | PF00514 | 0.524 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I6H8 | Leptomonas seymouri | 78% | 100% |
| A0A0S4JEQ6 | Bodo saltans | 45% | 100% |
| A0A1X0NZK0 | Trypanosomatidae | 55% | 100% |
| A0A3R7NX89 | Trypanosoma rangeli | 53% | 100% |
| A0A3S7X2A7 | Leishmania donovani | 93% | 100% |
| A4HH52 | Leishmania braziliensis | 74% | 100% |
| A4I4A3 | Leishmania infantum | 92% | 100% |
| C9ZKM6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
| E9ADQ2 | Leishmania major | 91% | 100% |
| O49606 | Arabidopsis thaliana | 30% | 99% |
| P0CM06 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 32% | 100% |
| P0CM07 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 32% | 100% |
| P0DJ26 | Dictyostelium discoideum | 30% | 100% |
| P0DJ27 | Dictyostelium discoideum | 30% | 100% |
| P10668 | Sus scrofa | 30% | 84% |
| P18359 | Gallus gallus | 31% | 84% |
| P18760 | Mus musculus | 32% | 84% |
| P21566 | Gallus gallus | 32% | 84% |
| P23528 | Homo sapiens | 30% | 84% |
| P30174 | Brassica napus | 29% | 100% |
| P30175 | Lilium longiflorum | 27% | 100% |
| P37167 | Acanthamoeba castellanii | 29% | 100% |
| P45591 | Mus musculus | 31% | 84% |
| P45592 | Rattus norvegicus | 32% | 84% |
| P45593 | Xenopus laevis | 30% | 83% |
| P45594 | Drosophila melanogaster | 39% | 94% |
| P45695 | Xenopus laevis | 28% | 83% |
| P46251 | Zea mays | 27% | 100% |
| P60981 | Homo sapiens | 31% | 84% |
| P60982 | Sus scrofa | 31% | 84% |
| P78929 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 100% |
| Q03048 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 97% |
| Q07749 | Caenorhabditis elegans | 32% | 91% |
| Q0DLA3 | Oryza sativa subsp. japonica | 32% | 100% |
| Q10P87 | Oryza sativa subsp. japonica | 26% | 97% |
| Q148F1 | Bos taurus | 31% | 84% |
| Q2QLT8 | Oryza sativa subsp. japonica | 28% | 96% |
| Q337A5 | Oryza sativa subsp. japonica | 28% | 92% |
| Q39250 | Arabidopsis thaliana | 28% | 100% |
| Q39251 | Arabidopsis thaliana | 31% | 100% |
| Q41764 | Zea mays | 28% | 100% |
| Q43694 | Zea mays | 28% | 100% |
| Q4I963 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 32% | 91% |
| Q4P6E9 | Ustilago maydis (strain 521 / FGSC 9021) | 32% | 100% |
| Q4R5C0 | Macaca fascicularis | 30% | 84% |
| Q570Y6 | Arabidopsis thaliana | 25% | 99% |
| Q5E9D5 | Bos taurus | 31% | 84% |
| Q5E9F7 | Bos taurus | 30% | 84% |
| Q5G6V9 | Sus scrofa | 31% | 84% |
| Q5U4Y2 | Xenopus tropicalis | 33% | 83% |
| Q5XHH8 | Xenopus laevis | 33% | 83% |
| Q67ZM4 | Arabidopsis thaliana | 30% | 100% |
| Q6B7M7 | Ovis aries | 30% | 84% |
| Q6BWX4 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 33% | 97% |
| Q6C0Y0 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 35% | 91% |
| Q6CQ22 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 34% | 97% |
| Q6EUH7 | Oryza sativa subsp. japonica | 28% | 100% |
| Q6FV81 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 33% | 97% |
| Q6NX11 | Xenopus tropicalis | 28% | 83% |
| Q759P0 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 37% | 97% |
| Q7M0E3 | Rattus norvegicus | 31% | 84% |
| Q7XSN9 | Oryza sativa subsp. japonica | 29% | 100% |
| Q84TB3 | Oryza sativa subsp. japonica | 28% | 100% |
| Q84TB6 | Oryza sativa subsp. japonica | 24% | 93% |
| Q8H2P8 | Oryza sativa subsp. japonica | 27% | 100% |
| Q8LFH6 | Arabidopsis thaliana | 30% | 100% |
| Q8SAG3 | Vitis vinifera | 27% | 97% |
| Q96VU9 | Ogataea parapolymorpha (strain ATCC 26012 / BCRC 20466 / JCM 22074 / NRRL Y-7560 / DL-1) | 35% | 97% |
| Q9AY76 | Oryza sativa subsp. japonica | 31% | 96% |
| Q9FVI1 | Petunia hybrida | 30% | 97% |
| Q9FVI2 | Petunia hybrida | 30% | 100% |
| Q9HF97 | Zygosaccharomyces rouxii | 35% | 97% |
| Q9LQ81 | Arabidopsis thaliana | 24% | 99% |
| Q9R0P5 | Mus musculus | 30% | 84% |
| Q9Y281 | Homo sapiens | 31% | 84% |
| Q9ZNT3 | Arabidopsis thaliana | 32% | 97% |
| Q9ZSK2 | Arabidopsis thaliana | 30% | 95% |
| Q9ZSK3 | Arabidopsis thaliana | 29% | 100% |
| Q9ZSK4 | Arabidopsis thaliana | 30% | 100% |