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: A4HAF6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.619 |
CLV_MEL_PAP_1 | 185 | 191 | PF00089 | 0.572 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.683 |
CLV_PCSK_FUR_1 | 276 | 280 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.683 |
CLV_PCSK_PC7_1 | 64 | 70 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.631 |
CLV_Separin_Metazoa | 357 | 361 | PF03568 | 0.528 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.599 |
DEG_SPOP_SBC_1 | 136 | 140 | PF00917 | 0.455 |
DEG_SPOP_SBC_1 | 77 | 81 | PF00917 | 0.529 |
DOC_MAPK_gen_1 | 115 | 123 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 237 | 245 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 183 | 191 | PF00069 | 0.579 |
DOC_MAPK_MEF2A_6 | 237 | 245 | PF00069 | 0.553 |
DOC_PP1_RVXF_1 | 358 | 364 | PF00149 | 0.533 |
DOC_PP2B_LxvP_1 | 247 | 250 | PF13499 | 0.587 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.603 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.741 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 188 | 192 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 402 | 407 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 85 | 90 | PF00244 | 0.569 |
LIG_Actin_WH2_2 | 178 | 194 | PF00022 | 0.584 |
LIG_APCC_ABBA_1 | 297 | 302 | PF00400 | 0.363 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.606 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.490 |
LIG_Clathr_ClatBox_1 | 148 | 152 | PF01394 | 0.625 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.738 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.528 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.619 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.643 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.731 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.371 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.468 |
LIG_HP1_1 | 187 | 191 | PF01393 | 0.583 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 36 | 45 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 12 | 17 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 5 | 9 | PF02991 | 0.558 |
LIG_RPA_C_Fungi | 232 | 244 | PF08784 | 0.376 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.392 |
LIG_SH2_PTP2 | 14 | 17 | PF00017 | 0.707 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 222 | 225 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.723 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.513 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.716 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.770 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.381 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.453 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.758 |
LIG_SUMO_SIM_anti_2 | 240 | 246 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 147 | 152 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 240 | 246 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 254 | 260 | PF11976 | 0.465 |
MOD_CDK_SPxxK_3 | 137 | 144 | PF00069 | 0.453 |
MOD_CDK_SPxxK_3 | 87 | 94 | PF00069 | 0.681 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.654 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.481 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.618 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.448 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.720 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.399 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.634 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.782 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.573 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.745 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.518 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.485 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.451 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.618 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.670 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.677 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.625 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.368 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.649 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.482 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.745 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.566 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.757 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.683 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.567 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.626 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.410 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.588 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.504 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.491 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.597 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.495 |
MOD_OFUCOSY | 35 | 40 | PF10250 | 0.605 |
MOD_PK_1 | 237 | 243 | PF00069 | 0.489 |
MOD_PK_1 | 402 | 408 | PF00069 | 0.440 |
MOD_PK_1 | 85 | 91 | PF00069 | 0.569 |
MOD_PKA_1 | 68 | 74 | PF00069 | 0.512 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.554 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.558 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.681 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.713 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.508 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.572 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.521 |
MOD_Plk_2-3 | 310 | 316 | PF00069 | 0.621 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.683 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.495 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.617 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.440 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.464 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.686 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.427 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.777 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.618 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.739 |
MOD_SUMO_rev_2 | 265 | 274 | PF00179 | 0.703 |
TRG_DiLeu_BaEn_1 | 357 | 362 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_4 | 62 | 68 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 189 | 194 | PF01217 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 399 | 404 | PF01217 | 0.397 |
TRG_DiLeu_LyEn_5 | 357 | 362 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 279 | 284 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDW8 | Leptomonas seymouri | 36% | 70% |
A0A3S7X7D6 | Leishmania donovani | 70% | 98% |
A4I9L2 | Leishmania infantum | 70% | 98% |
E9B4L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 98% |
Q4Q3G6 | Leishmania major | 71% | 100% |