Homologous to animal syntaxin proteins, involved in vesulcular fusion to membranes. Although most proteins appear to be membrane-embedded, some Lesihmaniid members are likely not.. For some reason, multiple copies are seen in Leptomonas
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 11 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0012505 | endomembrane system | 2 | 2 |
GO:0031201 | SNARE complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
Related structures:
AlphaFold database: E9AZW7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 13 |
GO:0016192 | vesicle-mediated transport | 4 | 13 |
GO:0051179 | localization | 1 | 13 |
GO:0051234 | establishment of localization | 2 | 13 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006887 | exocytosis | 4 | 2 |
GO:0006906 | vesicle fusion | 6 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016050 | vesicle organization | 5 | 2 |
GO:0022406 | membrane docking | 2 | 2 |
GO:0032940 | secretion by cell | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046903 | secretion | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0048278 | vesicle docking | 4 | 2 |
GO:0048284 | organelle fusion | 5 | 2 |
GO:0051640 | organelle localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0061024 | membrane organization | 4 | 2 |
GO:0061025 | membrane fusion | 5 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090174 | organelle membrane fusion | 6 | 2 |
GO:0140056 | organelle localization by membrane tethering | 3 | 2 |
GO:0140352 | export from cell | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 2 |
GO:0005484 | SNAP receptor activity | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 124 | 128 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.331 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.283 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.590 |
DEG_SPOP_SBC_1 | 128 | 132 | PF00917 | 0.444 |
DOC_CDC14_PxL_1 | 1 | 9 | PF14671 | 0.551 |
DOC_CYCLIN_yClb1_LxF_4 | 255 | 261 | PF00134 | 0.479 |
DOC_PP4_FxxP_1 | 46 | 49 | PF00568 | 0.571 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 298 | 302 | PF12436 | 0.536 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 173 | 182 | PF00244 | 0.505 |
LIG_Actin_WH2_2 | 122 | 139 | PF00022 | 0.493 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.521 |
LIG_CaM_IQ_9 | 273 | 289 | PF13499 | 0.516 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.480 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.764 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.476 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.511 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.480 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.420 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.533 |
LIG_GBD_Chelix_1 | 160 | 168 | PF00786 | 0.378 |
LIG_IBAR_NPY_1 | 311 | 313 | PF08397 | 0.171 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.384 |
LIG_PCNA_PIPBox_1 | 248 | 257 | PF02747 | 0.521 |
LIG_PCNA_yPIPBox_3 | 263 | 272 | PF02747 | 0.419 |
LIG_SH2_GRB2like | 194 | 197 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 194 | 198 | PF00017 | 0.461 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 182 | 185 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.364 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.254 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.383 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.594 |
LIG_UBA3_1 | 254 | 263 | PF00899 | 0.364 |
MOD_CDK_SPK_2 | 31 | 36 | PF00069 | 0.578 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.568 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.522 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.611 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.580 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.523 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.578 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.595 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.552 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.376 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.321 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.516 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.672 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.578 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.556 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.283 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.507 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.400 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.444 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.532 |
MOD_PK_1 | 135 | 141 | PF00069 | 0.498 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.559 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.480 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.234 |
MOD_Plk_2-3 | 54 | 60 | PF00069 | 0.490 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.517 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.494 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.604 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.624 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.664 |
MOD_SUMO_rev_2 | 338 | 343 | PF00179 | 0.326 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.384 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.406 |
TRG_NES_CRM1_1 | 156 | 170 | PF08389 | 0.364 |
TRG_NLS_Bipartite_1 | 291 | 306 | PF00514 | 0.505 |
TRG_NLS_MonoExtC_3 | 290 | 295 | PF00514 | 0.488 |
TRG_NLS_MonoExtC_3 | 297 | 302 | PF00514 | 0.488 |
TRG_NLS_MonoExtN_4 | 295 | 302 | PF00514 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.280 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JI44 | Bodo saltans | 24% | 100% |
A0A1X0NYQ5 | Trypanosomatidae | 51% | 100% |
A0A3Q8IDT6 | Leishmania donovani | 94% | 100% |
A0A3R7L4L2 | Trypanosoma rangeli | 46% | 100% |
A0A3S7X1I6 | Leishmania donovani | 91% | 100% |
A0A422NLX7 | Trypanosoma rangeli | 23% | 100% |
A4HGJ9 | Leishmania braziliensis | 82% | 100% |
A4HGK0 | Leishmania braziliensis | 78% | 100% |
A8WVD0 | Caenorhabditis briggsae | 29% | 100% |
D0A863 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AHG5 | Leishmania infantum | 91% | 100% |
O16000 | Caenorhabditis elegans | 29% | 100% |
O35526 | Mus musculus | 29% | 100% |
O64791 | Arabidopsis thaliana | 28% | 100% |
O75558 | Homo sapiens | 24% | 100% |
P32850 | Bos taurus | 30% | 100% |
P32851 | Rattus norvegicus | 29% | 100% |
P32856 | Homo sapiens | 29% | 100% |
P50279 | Rattus norvegicus | 28% | 100% |
P61264 | Mus musculus | 27% | 100% |
P61265 | Rattus norvegicus | 27% | 100% |
P61266 | Homo sapiens | 27% | 100% |
P61267 | Bos taurus | 27% | 100% |
P61268 | Ovis aries | 27% | 100% |
P70452 | Mus musculus | 26% | 100% |
Q00262 | Mus musculus | 27% | 100% |
Q08850 | Rattus norvegicus | 26% | 100% |
Q16623 | Homo sapiens | 29% | 100% |
Q16932 | Aplysia californica | 28% | 100% |
Q20024 | Caenorhabditis elegans | 22% | 100% |
Q24547 | Drosophila melanogaster | 28% | 100% |
Q3SWZ3 | Bos taurus | 25% | 100% |
Q42374 | Arabidopsis thaliana | 27% | 100% |
Q4Q8B8 | Leishmania major | 90% | 100% |
Q4Q8B9 | Leishmania major | 94% | 100% |
Q5R4L2 | Pongo abelii | 29% | 100% |
Q8VZU2 | Arabidopsis thaliana | 27% | 100% |
Q9SRV7 | Arabidopsis thaliana | 23% | 100% |
Q9SVC2 | Arabidopsis thaliana | 28% | 100% |
Q9SWH4 | Arabidopsis thaliana | 25% | 100% |
Q9SXB0 | Arabidopsis thaliana | 29% | 100% |
Q9USH7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 20% | 100% |
Q9ZQZ8 | Arabidopsis thaliana | 28% | 100% |
Q9ZSD4 | Arabidopsis thaliana | 29% | 99% |
V5B7Y5 | Trypanosoma cruzi | 50% | 100% |
V5BNX1 | Trypanosoma cruzi | 21% | 100% |