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: A4HFR1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.739 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.856 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.576 |
DEG_APCC_DBOX_1 | 190 | 198 | PF00400 | 0.573 |
DEG_SCF_FBW7_1 | 113 | 120 | PF00400 | 0.774 |
DOC_CYCLIN_RxL_1 | 191 | 203 | PF00134 | 0.416 |
DOC_CYCLIN_RxL_1 | 260 | 271 | PF00134 | 0.482 |
DOC_CYCLIN_RxL_1 | 27 | 40 | PF00134 | 0.447 |
DOC_CYCLIN_yClb1_LxF_4 | 150 | 156 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 69 | 75 | PF00134 | 0.684 |
DOC_MAPK_gen_1 | 191 | 199 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 32 | 38 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.664 |
DOC_MAPK_MEF2A_6 | 193 | 201 | PF00069 | 0.672 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.647 |
DOC_PP2B_LxvP_1 | 62 | 65 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.503 |
DOC_SPAK_OSR1_1 | 207 | 211 | PF12202 | 0.563 |
DOC_SPAK_OSR1_1 | 252 | 256 | PF12202 | 0.401 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.413 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.584 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.472 |
DOC_USP7_UBL2_3 | 83 | 87 | PF12436 | 0.787 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 196 | 202 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 242 | 250 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 285 | 293 | PF00244 | 0.430 |
LIG_APCC_ABBA_1 | 371 | 376 | PF00400 | 0.470 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.504 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.374 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.497 |
LIG_deltaCOP1_diTrp_1 | 376 | 384 | PF00928 | 0.464 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.542 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.377 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.450 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.791 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.560 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.707 |
LIG_Integrin_RGD_1 | 343 | 345 | PF01839 | 0.605 |
LIG_LIR_Gen_1 | 206 | 214 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 247 | 258 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 376 | 385 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 376 | 381 | PF02991 | 0.459 |
LIG_NRBOX | 193 | 199 | PF00104 | 0.574 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.586 |
LIG_PTAP_UEV_1 | 333 | 338 | PF05743 | 0.587 |
LIG_RPA_C_Fungi | 338 | 350 | PF08784 | 0.597 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.378 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.609 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.633 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.584 |
LIG_SH3_4 | 83 | 90 | PF00018 | 0.750 |
LIG_SUMO_SIM_par_1 | 197 | 203 | PF11976 | 0.664 |
LIG_UBA3_1 | 381 | 387 | PF00899 | 0.508 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.447 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.658 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.679 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.849 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.576 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.577 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.717 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.483 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.541 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.620 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.741 |
MOD_GlcNHglycan | 107 | 111 | PF01048 | 0.628 |
MOD_GlcNHglycan | 324 | 328 | PF01048 | 0.628 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.801 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.542 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.720 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.586 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.669 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.661 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.783 |
MOD_N-GLC_2 | 122 | 124 | PF02516 | 0.518 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.629 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.439 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.441 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.527 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.597 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.538 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.677 |
MOD_PK_1 | 377 | 383 | PF00069 | 0.465 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.596 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.826 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.613 |
MOD_PKB_1 | 375 | 383 | PF00069 | 0.464 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.419 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.747 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.656 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.518 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.560 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.538 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.501 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.776 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.577 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.577 |
MOD_SUMO_rev_2 | 162 | 167 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 212 | 217 | PF00179 | 0.403 |
TRG_DiLeu_BaEn_2 | 212 | 218 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.646 |
TRG_NLS_Bipartite_1 | 349 | 364 | PF00514 | 0.587 |
TRG_NLS_MonoExtC_3 | 359 | 364 | PF00514 | 0.574 |
TRG_NLS_MonoExtN_4 | 357 | 364 | PF00514 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 233 | 238 | PF00026 | 0.672 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.350 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAE2 | Leptomonas seymouri | 40% | 82% |
A0A3S7X0P6 | Leishmania donovani | 55% | 100% |
A4I2T7 | Leishmania infantum | 55% | 100% |
E9ADB5 | Leishmania major | 57% | 100% |
E9AZ40 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |