| 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: 13 |
| NetGPI | no | yes: 0, no: 13 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0031201 | SNARE complex | 3 | 14 |
| GO:0032991 | protein-containing complex | 1 | 14 |
| GO:0098796 | membrane protein complex | 2 | 14 |
| GO:0012505 | endomembrane system | 2 | 1 |
| GO:0016020 | membrane | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HN16
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 14 |
| GO:0006886 | intracellular protein transport | 4 | 14 |
| GO:0008104 | protein localization | 4 | 14 |
| GO:0009987 | cellular process | 1 | 14 |
| GO:0015031 | protein transport | 4 | 14 |
| GO:0016192 | vesicle-mediated transport | 4 | 13 |
| GO:0033036 | macromolecule localization | 2 | 14 |
| GO:0045184 | establishment of protein localization | 3 | 14 |
| GO:0046907 | intracellular transport | 3 | 14 |
| GO:0051179 | localization | 1 | 14 |
| GO:0051234 | establishment of localization | 2 | 14 |
| GO:0051641 | cellular localization | 2 | 14 |
| GO:0051649 | establishment of localization in cell | 3 | 14 |
| GO:0070727 | cellular macromolecule localization | 3 | 14 |
| GO:0071702 | organic substance transport | 4 | 14 |
| GO:0071705 | nitrogen compound transport | 4 | 14 |
| GO:0006906 | vesicle fusion | 6 | 1 |
| GO:0006996 | organelle organization | 4 | 1 |
| GO:0016043 | cellular component organization | 3 | 1 |
| GO:0016050 | vesicle organization | 5 | 1 |
| GO:0022406 | membrane docking | 2 | 1 |
| GO:0048278 | vesicle docking | 4 | 1 |
| GO:0048284 | organelle fusion | 5 | 1 |
| GO:0051640 | organelle localization | 2 | 1 |
| GO:0061024 | membrane organization | 4 | 1 |
| GO:0061025 | membrane fusion | 5 | 1 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
| GO:0090174 | organelle membrane fusion | 6 | 1 |
| GO:0140056 | organelle localization by membrane tethering | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000149 | SNARE binding | 3 | 1 |
| GO:0005484 | SNAP receptor activity | 3 | 3 |
| GO:0005488 | binding | 1 | 1 |
| GO:0005515 | protein binding | 2 | 1 |
| GO:0030674 | protein-macromolecule adaptor activity | 2 | 3 |
| GO:0060090 | molecular adaptor activity | 1 | 3 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.478 |
| CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.598 |
| CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.276 |
| CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.363 |
| CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.472 |
| CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.453 |
| CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.363 |
| CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.546 |
| CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.499 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.637 |
| DOC_CKS1_1 | 31 | 36 | PF01111 | 0.704 |
| DOC_CYCLIN_RxL_1 | 135 | 146 | PF00134 | 0.502 |
| DOC_MAPK_gen_1 | 136 | 144 | PF00069 | 0.484 |
| DOC_MAPK_gen_1 | 280 | 286 | PF00069 | 0.325 |
| DOC_MAPK_MEF2A_6 | 136 | 144 | PF00069 | 0.497 |
| DOC_PP1_RVXF_1 | 6 | 13 | PF00149 | 0.354 |
| DOC_PP4_FxxP_1 | 39 | 42 | PF00568 | 0.617 |
| DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.446 |
| DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.580 |
| DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.463 |
| DOC_USP7_UBL2_3 | 264 | 268 | PF12436 | 0.381 |
| DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.609 |
| DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.422 |
| DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.593 |
| LIG_14-3-3_CanoR_1 | 15 | 23 | PF00244 | 0.629 |
| LIG_14-3-3_CanoR_1 | 270 | 276 | PF00244 | 0.614 |
| LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.572 |
| LIG_Actin_WH2_2 | 101 | 117 | PF00022 | 0.557 |
| LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.439 |
| LIG_FHA_1 | 105 | 111 | PF00498 | 0.508 |
| LIG_FHA_1 | 230 | 236 | PF00498 | 0.544 |
| LIG_FHA_1 | 33 | 39 | PF00498 | 0.693 |
| LIG_FHA_1 | 66 | 72 | PF00498 | 0.401 |
| LIG_FHA_1 | 92 | 98 | PF00498 | 0.475 |
| LIG_FHA_2 | 115 | 121 | PF00498 | 0.505 |
| LIG_FHA_2 | 190 | 196 | PF00498 | 0.462 |
| LIG_FHA_2 | 207 | 213 | PF00498 | 0.407 |
| LIG_FHA_2 | 31 | 37 | PF00498 | 0.459 |
| LIG_FHA_2 | 86 | 92 | PF00498 | 0.505 |
| LIG_GBD_Chelix_1 | 125 | 133 | PF00786 | 0.454 |
| LIG_LIR_Apic_2 | 36 | 42 | PF02991 | 0.644 |
| LIG_LIR_Gen_1 | 162 | 173 | PF02991 | 0.596 |
| LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.317 |
| LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.528 |
| LIG_LIR_Gen_1 | 7 | 13 | PF02991 | 0.357 |
| LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.506 |
| LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.572 |
| LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.542 |
| LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.321 |
| LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.426 |
| LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.339 |
| LIG_SH2_CRK | 165 | 169 | PF00017 | 0.534 |
| LIG_SH2_NCK_1 | 165 | 169 | PF00017 | 0.426 |
| LIG_SH2_NCK_1 | 174 | 178 | PF00017 | 0.512 |
| LIG_SH2_STAT3 | 218 | 221 | PF00017 | 0.286 |
| LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.571 |
| LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.325 |
| LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.292 |
| LIG_SH3_3 | 28 | 34 | PF00018 | 0.630 |
| LIG_SUMO_SIM_par_1 | 231 | 236 | PF11976 | 0.629 |
| LIG_SUMO_SIM_par_1 | 251 | 256 | PF11976 | 0.417 |
| LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.570 |
| LIG_TRAF2_1 | 219 | 222 | PF00917 | 0.523 |
| MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.442 |
| MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.428 |
| MOD_CDK_SPxxK_3 | 30 | 37 | PF00069 | 0.453 |
| MOD_CK1_1 | 128 | 134 | PF00069 | 0.446 |
| MOD_CK1_1 | 26 | 32 | PF00069 | 0.570 |
| MOD_CK1_1 | 266 | 272 | PF00069 | 0.489 |
| MOD_CK1_1 | 274 | 280 | PF00069 | 0.448 |
| MOD_CK1_1 | 298 | 304 | PF00069 | 0.428 |
| MOD_CK2_1 | 114 | 120 | PF00069 | 0.513 |
| MOD_CK2_1 | 206 | 212 | PF00069 | 0.505 |
| MOD_CK2_1 | 216 | 222 | PF00069 | 0.381 |
| MOD_CK2_1 | 30 | 36 | PF00069 | 0.555 |
| MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.286 |
| MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.487 |
| MOD_GSK3_1 | 128 | 135 | PF00069 | 0.330 |
| MOD_GSK3_1 | 14 | 21 | PF00069 | 0.559 |
| MOD_GSK3_1 | 159 | 166 | PF00069 | 0.390 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.417 |
| MOD_GSK3_1 | 262 | 269 | PF00069 | 0.446 |
| MOD_GSK3_1 | 285 | 292 | PF00069 | 0.318 |
| MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.464 |
| MOD_NEK2_1 | 104 | 109 | PF00069 | 0.414 |
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.436 |
| MOD_NEK2_1 | 262 | 267 | PF00069 | 0.320 |
| MOD_NEK2_1 | 296 | 301 | PF00069 | 0.404 |
| MOD_NEK2_1 | 56 | 61 | PF00069 | 0.434 |
| MOD_NEK2_1 | 65 | 70 | PF00069 | 0.431 |
| MOD_OFUCOSY | 295 | 300 | PF10250 | 0.394 |
| MOD_PIKK_1 | 128 | 134 | PF00454 | 0.479 |
| MOD_PKA_2 | 14 | 20 | PF00069 | 0.584 |
| MOD_PKA_2 | 266 | 272 | PF00069 | 0.510 |
| MOD_PKA_2 | 279 | 285 | PF00069 | 0.277 |
| MOD_Plk_1 | 104 | 110 | PF00069 | 0.527 |
| MOD_Plk_1 | 26 | 32 | PF00069 | 0.631 |
| MOD_Plk_2-3 | 236 | 242 | PF00069 | 0.516 |
| MOD_Plk_4 | 104 | 110 | PF00069 | 0.477 |
| MOD_Plk_4 | 229 | 235 | PF00069 | 0.454 |
| MOD_Plk_4 | 236 | 242 | PF00069 | 0.491 |
| MOD_Plk_4 | 271 | 277 | PF00069 | 0.565 |
| MOD_Plk_4 | 85 | 91 | PF00069 | 0.472 |
| MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.428 |
| MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.592 |
| MOD_SUMO_rev_2 | 207 | 216 | PF00179 | 0.568 |
| TRG_DiLeu_BaEn_1 | 96 | 101 | PF01217 | 0.445 |
| TRG_DiLeu_BaEn_2 | 278 | 284 | PF01217 | 0.552 |
| TRG_DiLeu_BaEn_3 | 120 | 126 | PF01217 | 0.555 |
| TRG_DiLeu_BaEn_4 | 81 | 87 | PF01217 | 0.433 |
| TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.545 |
| TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.278 |
| TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.375 |
| TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.388 |
| TRG_NLS_MonoExtN_4 | 264 | 271 | PF00514 | 0.334 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I246 | Leptomonas seymouri | 59% | 100% |
| A0A0N1IMN0 | Leptomonas seymouri | 25% | 100% |
| A0A0S4J7F1 | Bodo saltans | 32% | 100% |
| A0A0S4JKJ1 | Bodo saltans | 27% | 100% |
| A0A1X0P0Y0 | Trypanosomatidae | 37% | 100% |
| A0A1X0P5S4 | Trypanosomatidae | 24% | 100% |
| A0A3Q8IK46 | Leishmania donovani | 77% | 100% |
| A0A3R7MIN3 | Trypanosoma rangeli | 33% | 100% |
| A0A3S7X9G5 | Leishmania donovani | 24% | 100% |
| A0A422P2Q8 | Trypanosoma rangeli | 24% | 100% |
| A4HLJ5 | Leishmania braziliensis | 97% | 100% |
| A4HMT8 | Leishmania braziliensis | 23% | 100% |
| A4I905 | Leishmania infantum | 77% | 100% |
| A4IBD9 | Leishmania infantum | 24% | 100% |
| A8WVD0 | Caenorhabditis briggsae | 25% | 100% |
| C9ZZ78 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
| D0A501 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| E9AF95 | Leishmania major | 24% | 100% |
| E9B3X0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
| E9B6F0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
| O14662 | Homo sapiens | 25% | 97% |
| O16000 | Caenorhabditis elegans | 26% | 100% |
| O65359 | Arabidopsis thaliana | 26% | 98% |
| Q16932 | Aplysia californica | 25% | 100% |
| Q4Q454 | Leishmania major | 75% | 100% |
| Q8BVI5 | Mus musculus | 24% | 96% |
| Q9P6P1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
| Q9SUJ1 | Arabidopsis thaliana | 27% | 95% |
| Q9SWH4 | Arabidopsis thaliana | 25% | 97% |
| V5BLU5 | Trypanosoma cruzi | 33% | 100% |
| V5C306 | Trypanosoma cruzi | 23% | 100% |