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. | 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: 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: A4H7D4
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 | 189 | 193 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.604 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 207 | 209 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.451 |
CLV_PCSK_PC7_1 | 203 | 209 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.454 |
DOC_CKS1_1 | 181 | 186 | PF01111 | 0.363 |
DOC_MAPK_DCC_7 | 204 | 214 | PF00069 | 0.287 |
DOC_MAPK_gen_1 | 203 | 214 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 207 | 216 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.339 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.484 |
DOC_USP7_UBL2_3 | 44 | 48 | PF12436 | 0.416 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.521 |
LIG_eIF4E_1 | 235 | 241 | PF01652 | 0.412 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.679 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.478 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.649 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.579 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.366 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.550 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.735 |
LIG_LIR_Apic_2 | 226 | 232 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 237 | 243 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 355 | 364 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.439 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.498 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.470 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.550 |
LIG_SH2_GRB2like | 75 | 78 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.314 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.503 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.518 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.678 |
LIG_SUMO_SIM_anti_2 | 290 | 296 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 210 | 215 | PF11976 | 0.396 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.502 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.420 |
LIG_UBA3_1 | 209 | 218 | PF00899 | 0.282 |
MOD_CDK_SPxxK_3 | 180 | 187 | PF00069 | 0.364 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.631 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.574 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.402 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.560 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.366 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.388 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.701 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.606 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.466 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.694 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.587 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.601 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.564 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.638 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.716 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.810 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.613 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.579 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.395 |
MOD_N-GLC_2 | 354 | 356 | PF02516 | 0.444 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.476 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.539 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.462 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.382 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.515 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.523 |
MOD_PIKK_1 | 251 | 257 | PF00454 | 0.291 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.490 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.458 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.463 |
MOD_PKA_1 | 369 | 375 | PF00069 | 0.529 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.568 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.517 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.399 |
MOD_Plk_2-3 | 410 | 416 | PF00069 | 0.725 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.461 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.477 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.641 |
MOD_SUMO_rev_2 | 45 | 55 | PF00179 | 0.652 |
TRG_DiLeu_BaEn_4 | 151 | 157 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 279 | 283 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I337 | Leptomonas seymouri | 61% | 100% |
A0A0S4J5L6 | Bodo saltans | 28% | 100% |
A0A1X0P9K4 | Trypanosomatidae | 37% | 100% |
A0A3Q8IKP9 | Leishmania donovani | 78% | 100% |
A0A422MZB1 | Trypanosoma rangeli | 38% | 100% |
A4I9M4 | Leishmania infantum | 78% | 100% |
D0A1Z0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B4M3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q3F3 | Leishmania major | 76% | 100% |
V5BRU6 | Trypanosoma cruzi | 35% | 100% |