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: A0A3S7X4N0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.701 |
CLV_PCSK_FUR_1 | 399 | 403 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.530 |
DEG_MDM2_SWIB_1 | 295 | 302 | PF02201 | 0.519 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.733 |
DEG_SCF_FBW7_2 | 71 | 78 | PF00400 | 0.561 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.630 |
DOC_CKS1_1 | 285 | 290 | PF01111 | 0.602 |
DOC_CKS1_1 | 72 | 77 | PF01111 | 0.689 |
DOC_CYCLIN_yCln2_LP_2 | 69 | 72 | PF00134 | 0.674 |
DOC_MAPK_gen_1 | 109 | 119 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 205 | 215 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.520 |
DOC_MAPK_NFAT4_5 | 112 | 120 | PF00069 | 0.453 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.674 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.691 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 109 | 119 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 60 | 70 | PF00244 | 0.680 |
LIG_Actin_RPEL_3 | 102 | 121 | PF02755 | 0.583 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.681 |
LIG_CaM_NSCaTE_8 | 129 | 136 | PF13499 | 0.420 |
LIG_deltaCOP1_diTrp_1 | 297 | 304 | PF00928 | 0.472 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.540 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.715 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.668 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.783 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.532 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.663 |
LIG_GSK3_LRP6_1 | 71 | 76 | PF00069 | 0.602 |
LIG_LIR_Gen_1 | 113 | 124 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.740 |
LIG_LYPXL_yS_3 | 36 | 39 | PF13949 | 0.665 |
LIG_MYND_1 | 100 | 104 | PF01753 | 0.624 |
LIG_MYND_1 | 18 | 22 | PF01753 | 0.671 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.420 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.529 |
LIG_PTAP_UEV_1 | 31 | 36 | PF05743 | 0.655 |
LIG_SH2_CRK | 223 | 227 | PF00017 | 0.574 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.520 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.636 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 223 | 227 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 357 | 361 | PF00017 | 0.636 |
LIG_SH2_SRC | 223 | 226 | PF00017 | 0.571 |
LIG_SH2_STAT3 | 98 | 101 | PF00017 | 0.675 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.438 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.527 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.674 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.720 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.608 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.688 |
LIG_SUMO_SIM_anti_2 | 319 | 326 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 229 | 237 | PF11976 | 0.595 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.766 |
LIG_TYR_ITIM | 355 | 360 | PF00017 | 0.686 |
LIG_UBA3_1 | 264 | 270 | PF00899 | 0.453 |
LIG_WRC_WIRS_1 | 292 | 297 | PF05994 | 0.594 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.549 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.504 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.668 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.688 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.679 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.764 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.651 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.711 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.729 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.482 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.556 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.709 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.739 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.705 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.659 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.624 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.558 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.630 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.633 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.643 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.646 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.557 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.650 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.701 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.732 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.652 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.427 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.720 |
MOD_NEK2_2 | 291 | 296 | PF00069 | 0.627 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.645 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.635 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.599 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.655 |
MOD_PK_1 | 274 | 280 | PF00069 | 0.455 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.767 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.725 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.733 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.598 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.707 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.690 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.699 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.649 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.547 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.715 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.519 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.540 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.693 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.340 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.647 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.712 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.676 |
MOD_SUMO_rev_2 | 105 | 111 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 126 | 132 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 87 | 95 | PF00179 | 0.748 |
TRG_DiLeu_BaLyEn_6 | 51 | 56 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.665 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.769 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.724 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 60 | 65 | PF00026 | 0.700 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3T2 | Leptomonas seymouri | 48% | 100% |
A0A1X0NVH2 | Trypanosomatidae | 28% | 100% |
A0A3R7MTX4 | Trypanosoma rangeli | 28% | 100% |
A4HJF6 | Leishmania braziliensis | 71% | 99% |
A4I6V1 | Leishmania infantum | 98% | 100% |
D0A7B7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B1X4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q688 | Leishmania major | 93% | 100% |
V5C1D3 | Trypanosoma cruzi | 30% | 100% |