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: A4HC29
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.554 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.277 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.331 |
CLV_Separin_Metazoa | 35 | 39 | PF03568 | 0.448 |
DEG_APCC_DBOX_1 | 361 | 369 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 55 | 63 | PF00400 | 0.265 |
DEG_MDM2_SWIB_1 | 174 | 182 | PF02201 | 0.374 |
DOC_CYCLIN_RxL_1 | 405 | 417 | PF00134 | 0.399 |
DOC_CYCLIN_RxL_1 | 53 | 63 | PF00134 | 0.269 |
DOC_PP2B_LxvP_1 | 93 | 96 | PF13499 | 0.513 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.362 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.579 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 321 | 326 | PF00244 | 0.344 |
LIG_Actin_WH2_2 | 306 | 323 | PF00022 | 0.424 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.263 |
LIG_CtBP_PxDLS_1 | 441 | 447 | PF00389 | 0.425 |
LIG_deltaCOP1_diTrp_1 | 176 | 184 | PF00928 | 0.385 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.236 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.353 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.404 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.526 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.514 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.511 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.510 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.259 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.244 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.417 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.445 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.324 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.413 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.483 |
LIG_LIR_Apic_2 | 79 | 85 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 68 | 78 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.397 |
LIG_NRBOX | 32 | 38 | PF00104 | 0.482 |
LIG_NRBOX | 54 | 60 | PF00104 | 0.266 |
LIG_PCNA_yPIPBox_3 | 168 | 177 | PF02747 | 0.314 |
LIG_PCNA_yPIPBox_3 | 67 | 76 | PF02747 | 0.358 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.438 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.385 |
LIG_Rb_pABgroove_1 | 180 | 188 | PF01858 | 0.232 |
LIG_REV1ctd_RIR_1 | 339 | 348 | PF16727 | 0.469 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.366 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.393 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 212 | 219 | PF11976 | 0.417 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.392 |
LIG_UBA3_1 | 403 | 410 | PF00899 | 0.251 |
LIG_WRC_WIRS_1 | 386 | 391 | PF05994 | 0.253 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.393 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.468 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.447 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.453 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.270 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.319 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.463 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.624 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.530 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.487 |
MOD_Cter_Amidation | 254 | 257 | PF01082 | 0.256 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.438 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.326 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.354 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.478 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.359 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.271 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.597 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.434 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.508 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.239 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.443 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.383 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.466 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.278 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.359 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.591 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.443 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.540 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.374 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.519 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.512 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.440 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.339 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.280 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.265 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.421 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.280 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.385 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.471 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.394 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.241 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.385 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.262 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.475 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.456 |
MOD_PK_1 | 242 | 248 | PF00069 | 0.423 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.330 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.465 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.355 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.363 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.579 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.546 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.239 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.328 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.360 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.362 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.338 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.323 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.343 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.487 |
MOD_SUMO_rev_2 | 161 | 171 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.341 |
TRG_DiLeu_BaEn_2 | 135 | 141 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 399 | 404 | PF01217 | 0.340 |
TRG_DiLeu_LyEn_5 | 194 | 199 | PF01217 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 31 | 35 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 56 | 61 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1III8 | Leptomonas seymouri | 57% | 100% |
A0A1X0NJ75 | Trypanosomatidae | 34% | 100% |
A0A3Q8IC10 | Leishmania donovani | 82% | 100% |
A0A3S5IQQ3 | Trypanosoma rangeli | 32% | 100% |
A4HZH2 | Leishmania infantum | 82% | 100% |
D0A102 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AVG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QC17 | Leishmania major | 82% | 100% |
V5BRG3 | Trypanosoma cruzi | 33% | 100% |