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: A4HEN2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.597 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.439 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.415 |
CLV_PCSK_PC7_1 | 333 | 339 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.729 |
DEG_APCC_DBOX_1 | 85 | 93 | PF00400 | 0.535 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.568 |
DOC_CYCLIN_RxL_1 | 196 | 205 | PF00134 | 0.689 |
DOC_CYCLIN_RxL_1 | 86 | 98 | PF00134 | 0.405 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.783 |
DOC_MAPK_gen_1 | 2 | 11 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 65 | 75 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 68 | 75 | PF00069 | 0.368 |
DOC_PP1_RVXF_1 | 292 | 299 | PF00149 | 0.440 |
DOC_PP1_RVXF_1 | 88 | 95 | PF00149 | 0.575 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.499 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.545 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.667 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.625 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.423 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 210 | 217 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 345 | 349 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 86 | 90 | PF00244 | 0.526 |
LIG_Actin_WH2_1 | 345 | 363 | PF00022 | 0.654 |
LIG_Actin_WH2_2 | 278 | 296 | PF00022 | 0.436 |
LIG_Clathr_ClatBox_1 | 248 | 252 | PF01394 | 0.587 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.587 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.674 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.478 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.599 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.597 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.386 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.673 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.685 |
LIG_LIR_Gen_1 | 132 | 141 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 185 | 194 | PF02991 | 0.710 |
LIG_LIR_Gen_1 | 353 | 360 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 321 | 325 | PF02991 | 0.779 |
LIG_LIR_Nem_3 | 353 | 357 | PF02991 | 0.679 |
LIG_NRBOX | 149 | 155 | PF00104 | 0.391 |
LIG_PCNA_yPIPBox_3 | 137 | 151 | PF02747 | 0.409 |
LIG_RPA_C_Fungi | 63 | 75 | PF08784 | 0.568 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.717 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.676 |
LIG_SH2_STAT3 | 23 | 26 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.555 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.350 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.536 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.616 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.708 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.615 |
LIG_Sin3_3 | 226 | 233 | PF02671 | 0.345 |
LIG_SUMO_SIM_par_1 | 264 | 271 | PF11976 | 0.538 |
LIG_SUMO_SIM_par_1 | 325 | 331 | PF11976 | 0.520 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.581 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.689 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.640 |
LIG_TYR_ITIM | 352 | 357 | PF00017 | 0.639 |
MOD_CDK_SPK_2 | 328 | 333 | PF00069 | 0.521 |
MOD_CDK_SPxxK_3 | 338 | 345 | PF00069 | 0.740 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.605 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.561 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.598 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.570 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.739 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.556 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.598 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.693 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.521 |
MOD_DYRK1A_RPxSP_1 | 95 | 99 | PF00069 | 0.453 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.668 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.697 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.714 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.611 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.715 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.396 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.683 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.742 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.703 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.581 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.498 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.516 |
MOD_NEK2_2 | 60 | 65 | PF00069 | 0.455 |
MOD_OFUCOSY | 34 | 40 | PF10250 | 0.598 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.492 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.697 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.482 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.414 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.683 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.540 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.539 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.563 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.546 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.560 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.589 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.721 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.658 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.706 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.545 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.661 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.613 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.592 |
MOD_SUMO_rev_2 | 355 | 363 | PF00179 | 0.676 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.532 |
TRG_DiLeu_BaEn_1 | 276 | 281 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_4 | 355 | 361 | PF01217 | 0.674 |
TRG_DiLeu_BaEn_4 | 84 | 90 | PF01217 | 0.628 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.718 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.678 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 68 | 70 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.429 |
TRG_NLS_Bipartite_1 | 68 | 82 | PF00514 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 57 | 62 | PF00026 | 0.633 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P503 | Leptomonas seymouri | 38% | 94% |
A0A3Q8IDK6 | Leishmania donovani | 71% | 100% |
A4I1W0 | Leishmania infantum | 71% | 100% |
E9AY05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4Q9G8 | Leishmania major | 71% | 100% |