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: 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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031201 | SNARE complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
Related structures:
AlphaFold database: E9B4M3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 1 |
GO:0005483 | soluble NSF attachment protein activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019905 | syntaxin binding | 4 | 1 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.707 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 179 | 181 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 228 | 230 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.381 |
CLV_Separin_Fungi | 283 | 289 | PF03568 | 0.232 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.522 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.561 |
DOC_CYCLIN_RxL_1 | 338 | 346 | PF00134 | 0.464 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 247 | 253 | PF00134 | 0.488 |
DOC_MAPK_MEF2A_6 | 261 | 268 | PF00069 | 0.309 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.375 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.424 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 151 | 161 | PF00244 | 0.601 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.532 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.382 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.444 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.494 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.611 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.484 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.716 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.411 |
LIG_LIR_Apic_2 | 155 | 161 | PF02991 | 0.533 |
LIG_LIR_Apic_2 | 198 | 204 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 209 | 215 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 177 | 181 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.446 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.564 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.451 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.426 |
LIG_SH2_GRB2like | 47 | 50 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.426 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.426 |
LIG_SH2_SRC | 243 | 246 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.392 |
LIG_SUMO_SIM_anti_2 | 184 | 190 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 265 | 270 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.437 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.432 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.406 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.446 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.578 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.425 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.376 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.370 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.670 |
MOD_Cter_Amidation | 17 | 20 | PF01082 | 0.519 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.491 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.658 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.438 |
MOD_GlcNHglycan | 365 | 369 | PF01048 | 0.725 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.434 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.392 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.324 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.600 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.526 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.790 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.218 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.429 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.383 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.376 |
MOD_N-GLC_2 | 326 | 328 | PF02516 | 0.449 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.487 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.348 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.153 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.646 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.383 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.426 |
MOD_PKA_1 | 341 | 347 | PF00069 | 0.513 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.389 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.477 |
MOD_Plk_2-3 | 382 | 388 | PF00069 | 0.715 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.610 |
MOD_SUMO_rev_2 | 194 | 201 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 240 | 249 | PF00179 | 0.524 |
TRG_DiLeu_BaEn_1 | 184 | 189 | PF01217 | 0.395 |
TRG_DiLeu_BaEn_4 | 123 | 129 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I337 | Leptomonas seymouri | 67% | 99% |
A0A0S4J5L6 | Bodo saltans | 31% | 100% |
A0A1X0P9K4 | Trypanosomatidae | 38% | 100% |
A0A3Q8IKP9 | Leishmania donovani | 91% | 100% |
A0A422MZB1 | Trypanosoma rangeli | 37% | 100% |
A4H7D4 | Leishmania braziliensis | 76% | 100% |
A4I9M4 | Leishmania infantum | 91% | 100% |
D0A1Z0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4Q3F3 | Leishmania major | 89% | 100% |
V5BRU6 | Trypanosoma cruzi | 37% | 100% |