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: A4HNU1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.315 |
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.328 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.588 |
CLV_PCSK_FUR_1 | 440 | 444 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 442 | 444 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.515 |
CLV_Separin_Metazoa | 350 | 354 | PF03568 | 0.221 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.408 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.327 |
DOC_CDC14_PxL_1 | 175 | 183 | PF14671 | 0.299 |
DOC_CYCLIN_RxL_1 | 208 | 221 | PF00134 | 0.304 |
DOC_CYCLIN_RxL_1 | 52 | 62 | PF00134 | 0.392 |
DOC_CYCLIN_yCln2_LP_2 | 83 | 89 | PF00134 | 0.392 |
DOC_MAPK_gen_1 | 155 | 163 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 189 | 196 | PF00069 | 0.292 |
DOC_PP1_RVXF_1 | 157 | 164 | PF00149 | 0.337 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.376 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.397 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.307 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.429 |
DOC_USP7_UBL2_3 | 271 | 275 | PF12436 | 0.336 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.253 |
DOC_USP7_UBL2_3 | 433 | 437 | PF12436 | 0.311 |
LIG_14-3-3_CanoR_1 | 213 | 218 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 246 | 252 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 353 | 360 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 446 | 454 | PF00244 | 0.527 |
LIG_BIR_III_4 | 279 | 283 | PF00653 | 0.311 |
LIG_BRCT_BRCA1_1 | 164 | 168 | PF00533 | 0.229 |
LIG_BRCT_BRCA1_1 | 377 | 381 | PF00533 | 0.281 |
LIG_BRCT_BRCA1_2 | 377 | 383 | PF00533 | 0.224 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.415 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.304 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.304 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.414 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.381 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.314 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.396 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.416 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.260 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.396 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.414 |
LIG_GBD_Chelix_1 | 111 | 119 | PF00786 | 0.525 |
LIG_GBD_Chelix_1 | 398 | 406 | PF00786 | 0.575 |
LIG_IBAR_NPY_1 | 204 | 206 | PF08397 | 0.394 |
LIG_LIR_Gen_1 | 165 | 176 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 422 | 429 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 60 | 71 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.363 |
LIG_LYPXL_yS_3 | 178 | 181 | PF13949 | 0.301 |
LIG_MLH1_MIPbox_1 | 377 | 381 | PF16413 | 0.281 |
LIG_PCNA_APIM_2 | 377 | 383 | PF02747 | 0.224 |
LIG_PCNA_PIPBox_1 | 374 | 383 | PF02747 | 0.292 |
LIG_Pex14_2 | 19 | 23 | PF04695 | 0.461 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.316 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.353 |
LIG_SH2_SRC | 416 | 419 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.304 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.504 |
LIG_SUMO_SIM_anti_2 | 190 | 196 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 364 | 370 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 258 | 264 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 364 | 370 | PF11976 | 0.375 |
LIG_UBA3_1 | 402 | 410 | PF00899 | 0.305 |
LIG_UBA3_1 | 425 | 433 | PF00899 | 0.384 |
LIG_UBA3_1 | 83 | 91 | PF00899 | 0.369 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.353 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.276 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.404 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.317 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.256 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.389 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.238 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.427 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.673 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.496 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.787 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.718 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.420 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.365 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.474 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.312 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.424 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.519 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.308 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.286 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.387 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.312 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.676 |
MOD_PKA_1 | 442 | 448 | PF00069 | 0.497 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.348 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.280 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.458 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.368 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.376 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.319 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.380 |
MOD_Plk_2-3 | 72 | 78 | PF00069 | 0.467 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.365 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.391 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.393 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.260 |
MOD_SUMO_for_1 | 436 | 439 | PF00179 | 0.313 |
TRG_DiLeu_BaEn_1 | 350 | 355 | PF01217 | 0.349 |
TRG_DiLeu_BaEn_2 | 325 | 331 | PF01217 | 0.304 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.414 |
TRG_ER_FFAT_1 | 339 | 350 | PF00635 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 113 | 117 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 303 | 307 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM88 | Leptomonas seymouri | 84% | 100% |
A0A0S4JVF0 | Bodo saltans | 58% | 100% |
A0A1X0P8C7 | Trypanosomatidae | 68% | 100% |
A0A3Q8IQJ6 | Leishmania donovani | 90% | 100% |
A0A3R7MNS3 | Trypanosoma rangeli | 68% | 100% |
A4ICQ3 | Leishmania infantum | 91% | 100% |
D0A2Q6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
E9ASK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q1Z5 | Leishmania major | 90% | 100% |