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: A4I6V1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.637 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.492 |
DEG_MDM2_SWIB_1 | 295 | 302 | PF02201 | 0.459 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.785 |
DEG_SCF_FBW7_2 | 71 | 78 | PF00400 | 0.517 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.570 |
DOC_CKS1_1 | 285 | 290 | PF01111 | 0.474 |
DOC_CKS1_1 | 72 | 77 | PF01111 | 0.592 |
DOC_CYCLIN_yCln2_LP_2 | 69 | 72 | PF00134 | 0.581 |
DOC_MAPK_gen_1 | 109 | 119 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 205 | 215 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.481 |
DOC_MAPK_NFAT4_5 | 112 | 120 | PF00069 | 0.339 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.461 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.581 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.599 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 109 | 119 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 60 | 70 | PF00244 | 0.570 |
LIG_Actin_RPEL_3 | 102 | 121 | PF02755 | 0.433 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.603 |
LIG_CaM_NSCaTE_8 | 129 | 136 | PF13499 | 0.345 |
LIG_deltaCOP1_diTrp_1 | 297 | 304 | PF00928 | 0.396 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.505 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.575 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.573 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.655 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.511 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.627 |
LIG_GSK3_LRP6_1 | 71 | 76 | PF00069 | 0.541 |
LIG_LIR_Gen_1 | 113 | 124 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.753 |
LIG_LYPXL_yS_3 | 36 | 39 | PF13949 | 0.565 |
LIG_MYND_1 | 100 | 104 | PF01753 | 0.500 |
LIG_MYND_1 | 18 | 22 | PF01753 | 0.579 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.342 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.467 |
LIG_PTAP_UEV_1 | 31 | 36 | PF05743 | 0.560 |
LIG_SH2_CRK | 223 | 227 | PF00017 | 0.439 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.471 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 223 | 227 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 357 | 361 | PF00017 | 0.576 |
LIG_SH2_SRC | 223 | 226 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 98 | 101 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.366 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.448 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.580 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.671 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.656 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 319 | 327 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 231 | 237 | PF11976 | 0.545 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.748 |
LIG_TYR_ITIM | 355 | 360 | PF00017 | 0.544 |
LIG_UBA3_1 | 264 | 270 | PF00899 | 0.472 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.435 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.565 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.448 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.643 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.668 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.711 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.740 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.607 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.594 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.691 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.479 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.444 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.711 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.690 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.646 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.567 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.527 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.566 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.599 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.708 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.659 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.477 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.652 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.678 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.627 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.574 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.376 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.616 |
MOD_NEK2_2 | 291 | 296 | PF00069 | 0.451 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.540 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.586 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.543 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.500 |
MOD_PK_1 | 274 | 280 | PF00069 | 0.370 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.641 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.684 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.717 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.479 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.593 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.601 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.550 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.600 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.511 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.598 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.343 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.486 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.660 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.287 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.589 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.613 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.629 |
MOD_SUMO_rev_2 | 105 | 111 | PF00179 | 0.349 |
MOD_SUMO_rev_2 | 126 | 132 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 87 | 95 | PF00179 | 0.733 |
TRG_DiLeu_BaLyEn_6 | 51 | 56 | PF01217 | 0.429 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.565 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.687 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 60 | 65 | PF00026 | 0.547 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3T2 | Leptomonas seymouri | 49% | 100% |
A0A1X0NVH2 | Trypanosomatidae | 28% | 100% |
A0A3R7MTX4 | Trypanosoma rangeli | 28% | 100% |
A0A3S7X4N0 | Leishmania donovani | 98% | 100% |
A4HJF6 | Leishmania braziliensis | 71% | 99% |
D0A7B7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B1X4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q688 | Leishmania major | 92% | 100% |
V5C1D3 | Trypanosoma cruzi | 30% | 100% |