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 |
Related structures:
AlphaFold database: A4HGE9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.394 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.330 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.460 |
DEG_SCF_SKP2-CKS1_1 | 123 | 130 | PF00560 | 0.530 |
DOC_CKS1_1 | 141 | 146 | PF01111 | 0.457 |
DOC_CYCLIN_RxL_1 | 283 | 294 | PF00134 | 0.353 |
DOC_MAPK_MEF2A_6 | 21 | 29 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.512 |
DOC_PP1_RVXF_1 | 284 | 291 | PF00149 | 0.390 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.369 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 331 | 336 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 386 | 392 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.367 |
LIG_Actin_WH2_2 | 180 | 197 | PF00022 | 0.305 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.746 |
LIG_BIR_III_4 | 65 | 69 | PF00653 | 0.421 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.367 |
LIG_DLG_GKlike_1 | 331 | 338 | PF00625 | 0.541 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.530 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.340 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.537 |
LIG_LIR_Apic_2 | 265 | 271 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.510 |
LIG_PDZ_Class_2 | 403 | 408 | PF00595 | 0.347 |
LIG_RPA_C_Fungi | 326 | 338 | PF08784 | 0.490 |
LIG_SH2_NCK_1 | 70 | 74 | PF00017 | 0.367 |
LIG_SH2_PTP2 | 268 | 271 | PF00017 | 0.535 |
LIG_SH2_SRC | 205 | 208 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.400 |
LIG_SH3_2 | 101 | 106 | PF14604 | 0.547 |
LIG_SH3_2 | 156 | 161 | PF14604 | 0.364 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.536 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.419 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.688 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 222 | 228 | PF11976 | 0.509 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.301 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.531 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.663 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.511 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.630 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.479 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.588 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.397 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.254 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.524 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.556 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.531 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.769 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.613 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.395 |
MOD_GlcNHglycan | 64 | 69 | PF01048 | 0.456 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.578 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.565 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.670 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.712 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.368 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.653 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.292 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.317 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.641 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.686 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.516 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.542 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.661 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.507 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.363 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.339 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.594 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.406 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.530 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.394 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.481 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.758 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.546 |
MOD_Plk_2-3 | 45 | 51 | PF00069 | 0.590 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.519 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.543 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.624 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.434 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.359 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.717 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.532 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.555 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 286 | 291 | PF00026 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NYD6 | Trypanosomatidae | 32% | 83% |
A0A3S7X1C6 | Leishmania donovani | 70% | 100% |
A4I3I0 | Leishmania infantum | 70% | 100% |
E9AZS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4Q8G2 | Leishmania major | 70% | 100% |