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:0005737 | cytoplasm | 2 | 2 |
GO:0005886 | plasma membrane | 3 | 3 |
GO:0012505 | endomembrane system | 2 | 3 |
GO:0016020 | membrane | 2 | 13 |
GO:0031201 | SNARE complex | 3 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0098796 | membrane protein complex | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: Q4Q8B8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 13 |
GO:0006886 | intracellular protein transport | 4 | 3 |
GO:0006887 | exocytosis | 4 | 3 |
GO:0006906 | vesicle fusion | 6 | 3 |
GO:0006996 | organelle organization | 4 | 3 |
GO:0008104 | protein localization | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0015031 | protein transport | 4 | 3 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0016050 | vesicle organization | 5 | 3 |
GO:0016192 | vesicle-mediated transport | 4 | 13 |
GO:0022406 | membrane docking | 2 | 3 |
GO:0032940 | secretion by cell | 3 | 3 |
GO:0033036 | macromolecule localization | 2 | 3 |
GO:0045184 | establishment of protein localization | 3 | 3 |
GO:0046903 | secretion | 4 | 3 |
GO:0046907 | intracellular transport | 3 | 3 |
GO:0048278 | vesicle docking | 4 | 3 |
GO:0048284 | organelle fusion | 5 | 3 |
GO:0051179 | localization | 1 | 13 |
GO:0051234 | establishment of localization | 2 | 13 |
GO:0051640 | organelle localization | 2 | 3 |
GO:0051641 | cellular localization | 2 | 3 |
GO:0051649 | establishment of localization in cell | 3 | 3 |
GO:0061024 | membrane organization | 4 | 3 |
GO:0061025 | membrane fusion | 5 | 3 |
GO:0070727 | cellular macromolecule localization | 3 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
GO:0090174 | organelle membrane fusion | 6 | 3 |
GO:0140056 | organelle localization by membrane tethering | 3 | 3 |
GO:0140352 | export from cell | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 3 |
GO:0005484 | SNAP receptor activity | 3 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0005515 | protein binding | 2 | 3 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 3 |
GO:0060090 | molecular adaptor activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.412 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.202 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.355 |
DOC_CYCLIN_yClb1_LxF_4 | 174 | 180 | PF00134 | 0.475 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.500 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 224 | 228 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.520 |
LIG_Actin_WH2_2 | 41 | 58 | PF00022 | 0.490 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.405 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.517 |
LIG_CaM_IQ_9 | 192 | 208 | PF13499 | 0.512 |
LIG_deltaCOP1_diTrp_1 | 259 | 264 | PF00928 | 0.361 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.475 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.477 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.494 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.494 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.566 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.477 |
LIG_GBD_Chelix_1 | 79 | 87 | PF00786 | 0.375 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.483 |
LIG_PCNA_PIPBox_1 | 167 | 176 | PF02747 | 0.517 |
LIG_SH2_GRB2like | 113 | 116 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 113 | 117 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 141 | 144 | PF00017 | 0.557 |
LIG_SH2_STAT3 | 90 | 93 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.556 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.353 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.571 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.564 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.566 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.575 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.517 |
MOD_CMANNOS | 261 | 264 | PF00535 | 0.562 |
MOD_GlcNHglycan | 117 | 121 | PF01048 | 0.317 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.375 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.357 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.575 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.512 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.296 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.485 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.514 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.528 |
MOD_PK_1 | 54 | 60 | PF00069 | 0.494 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.336 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.545 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.510 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.477 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.425 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.435 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.509 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.467 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.410 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.497 |
TRG_DiLeu_BaEn_1 | 183 | 188 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.553 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.549 |
TRG_NLS_Bipartite_1 | 210 | 225 | PF00514 | 0.498 |
TRG_NLS_MonoExtC_3 | 209 | 214 | PF00514 | 0.484 |
TRG_NLS_MonoExtC_3 | 216 | 221 | PF00514 | 0.484 |
TRG_NLS_MonoExtN_4 | 214 | 221 | PF00514 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.294 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JI44 | Bodo saltans | 24% | 100% |
A0A1X0NYQ5 | Trypanosomatidae | 60% | 81% |
A0A3Q8IDT6 | Leishmania donovani | 96% | 100% |
A0A3R7L4L2 | Trypanosoma rangeli | 53% | 84% |
A0A3R7NXH1 | Trypanosoma rangeli | 25% | 100% |
A0A3S7X1I6 | Leishmania donovani | 95% | 100% |
A4HGJ9 | Leishmania braziliensis | 83% | 100% |
A4HGK0 | Leishmania braziliensis | 80% | 100% |
A8WVD0 | Caenorhabditis briggsae | 32% | 91% |
D0A863 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 84% |
E9AHG5 | Leishmania infantum | 95% | 100% |
E9AZW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 77% |
O16000 | Caenorhabditis elegans | 32% | 91% |
O35526 | Mus musculus | 32% | 92% |
O64791 | Arabidopsis thaliana | 30% | 88% |
O75558 | Homo sapiens | 28% | 93% |
P32850 | Bos taurus | 33% | 92% |
P32851 | Rattus norvegicus | 32% | 92% |
P32856 | Homo sapiens | 30% | 92% |
P50279 | Rattus norvegicus | 28% | 92% |
P61264 | Mus musculus | 30% | 92% |
P61265 | Rattus norvegicus | 30% | 92% |
P61266 | Homo sapiens | 30% | 92% |
P61267 | Bos taurus | 30% | 92% |
P61268 | Ovis aries | 30% | 92% |
P70452 | Mus musculus | 27% | 89% |
Q00262 | Mus musculus | 31% | 92% |
Q08849 | Rattus norvegicus | 31% | 92% |
Q08850 | Rattus norvegicus | 27% | 89% |
Q12846 | Homo sapiens | 28% | 90% |
Q13277 | Homo sapiens | 31% | 92% |
Q16623 | Homo sapiens | 32% | 92% |
Q16932 | Aplysia californica | 31% | 92% |
Q20024 | Caenorhabditis elegans | 24% | 87% |
Q3SWZ3 | Bos taurus | 26% | 90% |
Q42374 | Arabidopsis thaliana | 29% | 86% |
Q4Q8B9 | Leishmania major | 98% | 93% |
Q5R4L2 | Pongo abelii | 32% | 92% |
Q64704 | Mus musculus | 31% | 92% |
Q8VZU2 | Arabidopsis thaliana | 28% | 88% |
Q9D3G5 | Mus musculus | 28% | 93% |
Q9SRV7 | Arabidopsis thaliana | 24% | 87% |
Q9SVC2 | Arabidopsis thaliana | 28% | 78% |
Q9SXB0 | Arabidopsis thaliana | 28% | 89% |
Q9ZQZ8 | Arabidopsis thaliana | 27% | 87% |
Q9ZSD4 | Arabidopsis thaliana | 29% | 77% |
V5B7Y5 | Trypanosoma cruzi | 57% | 84% |