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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H4V7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 8 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 8 |
GO:0016192 | vesicle-mediated transport | 4 | 8 |
GO:0048193 | Golgi vesicle transport | 5 | 8 |
GO:0051179 | localization | 1 | 8 |
GO:0051234 | establishment of localization | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.518 |
CLV_Separin_Metazoa | 237 | 241 | PF03568 | 0.564 |
DEG_SCF_FBW7_1 | 275 | 282 | PF00400 | 0.788 |
DOC_CDC14_PxL_1 | 1 | 9 | PF14671 | 0.543 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.796 |
DOC_CYCLIN_RxL_1 | 257 | 266 | PF00134 | 0.694 |
DOC_CYCLIN_yCln2_LP_2 | 262 | 265 | PF00134 | 0.773 |
DOC_MAPK_FxFP_2 | 233 | 236 | PF00069 | 0.678 |
DOC_MAPK_gen_1 | 249 | 259 | PF00069 | 0.555 |
DOC_PP2B_LxvP_1 | 262 | 265 | PF13499 | 0.773 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.678 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.455 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.715 |
LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 101 | 117 | PF00022 | 0.501 |
LIG_Actin_WH2_2 | 227 | 242 | PF00022 | 0.741 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.546 |
LIG_deltaCOP1_diTrp_1 | 196 | 201 | PF00928 | 0.303 |
LIG_eIF4E_1 | 88 | 94 | PF01652 | 0.549 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.411 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.815 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.380 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.220 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.359 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.707 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.308 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.179 |
LIG_GBD_Chelix_1 | 137 | 145 | PF00786 | 0.311 |
LIG_LIR_Apic_2 | 122 | 128 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 231 | 236 | PF02991 | 0.732 |
LIG_LIR_Gen_1 | 85 | 94 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.171 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.556 |
LIG_NRBOX | 249 | 255 | PF00104 | 0.548 |
LIG_RPA_C_Fungi | 308 | 320 | PF08784 | 0.605 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 125 | 129 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.249 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.249 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.380 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.596 |
LIG_SUMO_SIM_anti_2 | 181 | 187 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 99 | 105 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.459 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.578 |
LIG_TRFH_1 | 44 | 48 | PF08558 | 0.468 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.506 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.348 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.752 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.514 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.618 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.352 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.182 |
MOD_CMANNOS | 198 | 201 | PF00535 | 0.343 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.557 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.594 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.515 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.594 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.501 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.394 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.767 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.701 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.590 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.693 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.702 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.320 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.481 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.279 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.617 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.414 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.410 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.474 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.440 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.437 |
MOD_PKB_1 | 147 | 155 | PF00069 | 0.544 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.413 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.584 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.482 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.191 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.503 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.581 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.469 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.472 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.319 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.767 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.656 |
TRG_DiLeu_BaEn_1 | 310 | 315 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_2 | 86 | 92 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.419 |
TRG_DiLeu_LyEn_5 | 310 | 315 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.501 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.612 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEF2 | Leptomonas seymouri | 36% | 93% |
A0A1X0NKP0 | Trypanosomatidae | 27% | 100% |
A0A3S5H5W2 | Leishmania donovani | 70% | 99% |
A4HT54 | Leishmania infantum | 70% | 99% |
E9AL24 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 99% |
Q4QIT0 | Leishmania major | 70% | 100% |