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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4QIT0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 7 |
GO:0016192 | vesicle-mediated transport | 4 | 7 |
GO:0048193 | Golgi vesicle transport | 5 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.487 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.564 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.547 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.726 |
DEG_SCF_FBW7_1 | 276 | 282 | PF00400 | 0.806 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.779 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.810 |
DOC_CYCLIN_yCln2_LP_2 | 262 | 265 | PF00134 | 0.773 |
DOC_MAPK_FxFP_2 | 233 | 236 | PF00069 | 0.671 |
DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.713 |
DOC_MAPK_RevD_3 | 203 | 219 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 262 | 265 | PF13499 | 0.773 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.671 |
DOC_PP4_FxxP_1 | 261 | 264 | PF00568 | 0.716 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.781 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.424 |
LIG_Actin_WH2_2 | 101 | 117 | PF00022 | 0.513 |
LIG_Actin_WH2_2 | 144 | 162 | PF00022 | 0.615 |
LIG_Actin_WH2_2 | 227 | 242 | PF00022 | 0.747 |
LIG_Clathr_ClatBox_1 | 108 | 112 | PF01394 | 0.397 |
LIG_EH_1 | 287 | 291 | PF12763 | 0.658 |
LIG_eIF4E_1 | 88 | 94 | PF01652 | 0.356 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.380 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.416 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.821 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.385 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.480 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.425 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.395 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.774 |
LIG_LIR_Apic_2 | 231 | 236 | PF02991 | 0.742 |
LIG_LIR_Gen_1 | 41 | 52 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 85 | 94 | PF02991 | 0.580 |
LIG_LIR_LC3C_4 | 184 | 187 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.552 |
LIG_NRBOX | 25 | 31 | PF00104 | 0.398 |
LIG_Pex14_2 | 47 | 51 | PF04695 | 0.427 |
LIG_RPA_C_Fungi | 312 | 324 | PF08784 | 0.709 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.631 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.362 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.682 |
LIG_SUMO_SIM_anti_2 | 181 | 187 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 207 | 213 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 99 | 107 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 25 | 33 | PF11976 | 0.507 |
LIG_SUMO_SIM_par_1 | 99 | 107 | PF11976 | 0.431 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.633 |
LIG_TRFH_1 | 261 | 265 | PF08558 | 0.653 |
LIG_TRFH_1 | 44 | 48 | PF08558 | 0.642 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.436 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.706 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.729 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.669 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.678 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.710 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.561 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.608 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.687 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.657 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.503 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.595 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.700 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.644 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.593 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.637 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.655 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.520 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.313 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.702 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.486 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.346 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.458 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.557 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.594 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.513 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.468 |
MOD_PKA_1 | 218 | 224 | PF00069 | 0.583 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.583 |
MOD_PKB_1 | 147 | 155 | PF00069 | 0.592 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.612 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.513 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.513 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.473 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.633 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.740 |
TRG_DiLeu_BaEn_2 | 86 | 92 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 326 | 330 | PF00026 | 0.611 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEF2 | Leptomonas seymouri | 37% | 94% |
A0A3S5H5W2 | Leishmania donovani | 90% | 100% |
A4H4V7 | Leishmania braziliensis | 70% | 100% |
A4HT54 | Leishmania infantum | 90% | 100% |
E9AL24 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |