Uncharacterized Protein, Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 4 |
Forrest at al. (procyclic) | yes | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HSY4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.322 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.362 |
DEG_APCC_DBOX_1 | 37 | 45 | PF00400 | 0.341 |
DEG_APCC_DBOX_1 | 403 | 411 | PF00400 | 0.540 |
DEG_COP1_1 | 383 | 393 | PF00400 | 0.592 |
DEG_SCF_TRCP1_1 | 263 | 269 | PF00400 | 0.518 |
DOC_CYCLIN_RxL_1 | 1 | 9 | PF00134 | 0.380 |
DOC_CYCLIN_yCln2_LP_2 | 370 | 376 | PF00134 | 0.598 |
DOC_MAPK_gen_1 | 104 | 111 | PF00069 | 0.352 |
DOC_MAPK_gen_1 | 205 | 213 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.329 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.590 |
DOC_PP2B_PxIxI_1 | 417 | 423 | PF00149 | 0.589 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.577 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 30 | 37 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.331 |
LIG_AP2alpha_2 | 362 | 364 | PF02296 | 0.608 |
LIG_BIR_III_2 | 415 | 419 | PF00653 | 0.562 |
LIG_CaM_IQ_9 | 213 | 228 | PF13499 | 0.445 |
LIG_Clathr_ClatBox_1 | 110 | 114 | PF01394 | 0.349 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.436 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.469 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.457 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.177 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.300 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.377 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.374 |
LIG_LIR_Gen_1 | 361 | 372 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.414 |
LIG_LIR_LC3C_4 | 176 | 181 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.346 |
LIG_MYND_1 | 255 | 259 | PF01753 | 0.713 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.450 |
LIG_PDZ_Class_2 | 444 | 449 | PF00595 | 0.606 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.502 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.633 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.407 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.633 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.361 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.384 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.524 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.572 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.632 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.480 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.575 |
LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 176 | 181 | PF11976 | 0.334 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 209 | 215 | PF11976 | 0.353 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.493 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.610 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.721 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.470 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.591 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.323 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.472 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.533 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.652 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.528 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.434 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.628 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.613 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.620 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.768 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.689 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.703 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.684 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.720 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.445 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.409 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.182 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.708 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.740 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.477 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.675 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.465 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.495 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.712 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.572 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.460 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.469 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.523 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.512 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.389 |
MOD_NEK2_2 | 399 | 404 | PF00069 | 0.519 |
MOD_PK_1 | 105 | 111 | PF00069 | 0.292 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.533 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.390 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.535 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.620 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.370 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.454 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.472 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.426 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.434 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.350 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.292 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.474 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.340 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.336 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.663 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.554 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.360 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.405 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.757 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.570 |
MOD_SUMO_rev_2 | 190 | 199 | PF00179 | 0.474 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.391 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.332 |
TRG_DiLeu_BaEn_2 | 429 | 435 | PF01217 | 0.578 |
TRG_DiLeu_LyEn_5 | 40 | 45 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.460 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKD5 | Leptomonas seymouri | 66% | 100% |
A0A3R7KW02 | Trypanosoma rangeli | 37% | 100% |
A0A3S5H5T3 | Leishmania donovani | 100% | 100% |
A4H4Q5 | Leishmania braziliensis | 73% | 100% |
E9AKX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 97% |
Q4QIY5 | Leishmania major | 92% | 100% |
V5BXU6 | Trypanosoma cruzi | 35% | 100% |