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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AP73
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.660 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.447 |
CLV_PCSK_FUR_1 | 336 | 340 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.486 |
CLV_PCSK_PC7_1 | 17 | 23 | PF00082 | 0.568 |
CLV_PCSK_PC7_1 | 179 | 185 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.585 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.310 |
DEG_SCF_FBW7_1 | 370 | 376 | PF00400 | 0.708 |
DOC_ANK_TNKS_1 | 85 | 92 | PF00023 | 0.498 |
DOC_CDC14_PxL_1 | 71 | 79 | PF14671 | 0.575 |
DOC_CKS1_1 | 370 | 375 | PF01111 | 0.790 |
DOC_CYCLIN_yCln2_LP_2 | 278 | 281 | PF00134 | 0.444 |
DOC_MAPK_DCC_7 | 375 | 384 | PF00069 | 0.668 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 94 | 100 | PF00149 | 0.584 |
DOC_PP2B_LxvP_1 | 278 | 281 | PF13499 | 0.444 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.666 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.608 |
DOC_USP7_UBL2_3 | 354 | 358 | PF12436 | 0.735 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.725 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 184 | 193 | PF00244 | 0.798 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 9 | 14 | PF00244 | 0.559 |
LIG_APCC_ABBA_1 | 54 | 59 | PF00400 | 0.385 |
LIG_APCC_ABBAyCdc20_2 | 53 | 59 | PF00400 | 0.396 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.466 |
LIG_deltaCOP1_diTrp_1 | 64 | 71 | PF00928 | 0.526 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.572 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.468 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.665 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.493 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.483 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.755 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.282 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.525 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.615 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.541 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.420 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.518 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.608 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.423 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 312 | 321 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.483 |
LIG_MYND_1 | 276 | 280 | PF01753 | 0.560 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.518 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 311 | 315 | PF00017 | 0.592 |
LIG_SH2_PTP2 | 57 | 60 | PF00017 | 0.503 |
LIG_SH2_SRC | 57 | 60 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.479 |
LIG_SH3_1 | 375 | 381 | PF00018 | 0.666 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.551 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.496 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.743 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.657 |
LIG_SUMO_SIM_par_1 | 239 | 245 | PF11976 | 0.601 |
LIG_SxIP_EBH_1 | 107 | 117 | PF03271 | 0.564 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.558 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.571 |
LIG_TYR_ITIM | 313 | 318 | PF00017 | 0.474 |
LIG_TYR_ITIM | 8 | 13 | PF00017 | 0.540 |
LIG_UBA3_1 | 110 | 115 | PF00899 | 0.568 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.504 |
MOD_CDK_SPK_2 | 189 | 194 | PF00069 | 0.714 |
MOD_CDK_SPxK_1 | 369 | 375 | PF00069 | 0.714 |
MOD_CDK_SPxxK_3 | 30 | 37 | PF00069 | 0.437 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.619 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.797 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.494 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.479 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.723 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.640 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.461 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.500 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.450 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.572 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.554 |
MOD_DYRK1A_RPxSP_1 | 377 | 381 | PF00069 | 0.732 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.528 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.456 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.671 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.517 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.561 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.764 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.724 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.599 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.422 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.368 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.408 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.689 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.566 |
MOD_NEK2_2 | 25 | 30 | PF00069 | 0.551 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.804 |
MOD_PK_1 | 339 | 345 | PF00069 | 0.521 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.525 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.743 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.577 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.641 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.678 |
MOD_PKB_1 | 337 | 345 | PF00069 | 0.650 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.521 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.410 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.532 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.516 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.790 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.432 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.696 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.721 |
MOD_SUMO_rev_2 | 162 | 169 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_1 | 120 | 125 | PF01217 | 0.583 |
TRG_DiLeu_BaEn_4 | 120 | 126 | PF01217 | 0.585 |
TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.574 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.740 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.711 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P925 | Leptomonas seymouri | 63% | 79% |
A0A1X0NN77 | Trypanosomatidae | 32% | 88% |
A0A3Q8I8G2 | Leishmania donovani | 92% | 79% |
A0A3R7KJL2 | Trypanosoma rangeli | 31% | 100% |
A4H738 | Leishmania braziliensis | 81% | 100% |
A4HVH8 | Leishmania infantum | 92% | 79% |
D0A6T3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 95% |
Q4QGA5 | Leishmania major | 91% | 100% |
V5BFH7 | Trypanosoma cruzi | 37% | 100% |