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: A4HLF8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 23 | 27 | PF00656 | 0.618 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.503 |
CLV_PCSK_FUR_1 | 103 | 107 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 4 | 10 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.428 |
CLV_Separin_Metazoa | 81 | 85 | PF03568 | 0.466 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.662 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.493 |
DEG_SCF_FBW7_1 | 241 | 246 | PF00400 | 0.531 |
DOC_CKS1_1 | 314 | 319 | PF01111 | 0.544 |
DOC_CKS1_1 | 402 | 407 | PF01111 | 0.493 |
DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 199 | 208 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 225 | 233 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 158 | 166 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 267 | 274 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 329 | 336 | PF00069 | 0.603 |
DOC_MAPK_NFAT4_5 | 267 | 275 | PF00069 | 0.445 |
DOC_PP4_FxxP_1 | 311 | 314 | PF00568 | 0.542 |
DOC_PP4_FxxP_1 | 57 | 60 | PF00568 | 0.610 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 159 | 163 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 167 | 171 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 261 | 265 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 71 | 80 | PF00244 | 0.456 |
LIG_Actin_WH2_2 | 83 | 101 | PF00022 | 0.484 |
LIG_BIR_III_4 | 370 | 374 | PF00653 | 0.634 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.456 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.525 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.650 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.584 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.535 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.437 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.453 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.577 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.482 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.465 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.595 |
LIG_FXI_DFP_1 | 54 | 58 | PF00024 | 0.648 |
LIG_LIR_Apic_2 | 310 | 314 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 56 | 60 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 168 | 178 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 260 | 270 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 79 | 88 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 91 | 101 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.307 |
LIG_NRBOX | 269 | 275 | PF00104 | 0.455 |
LIG_PCNA_PIPBox_1 | 251 | 260 | PF02747 | 0.543 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.635 |
LIG_SH2_SRC | 30 | 33 | PF00017 | 0.694 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.694 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.439 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.682 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.615 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 377 | 385 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 242 | 250 | PF11976 | 0.518 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.522 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.800 |
LIG_TRAF2_1 | 37 | 40 | PF00917 | 0.497 |
LIG_UBA3_1 | 219 | 226 | PF00899 | 0.577 |
LIG_UBA3_1 | 97 | 102 | PF00899 | 0.457 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.643 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.676 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.498 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.520 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.468 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.470 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.541 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.683 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.643 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.697 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.714 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.525 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.508 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.483 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.570 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.572 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.591 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.596 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.566 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.528 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.689 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.538 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.570 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.604 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.477 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.570 |
MOD_NEK2_2 | 24 | 29 | PF00069 | 0.486 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.645 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.451 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.539 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.524 |
MOD_PK_1 | 158 | 164 | PF00069 | 0.455 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.560 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.608 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.547 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.585 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.472 |
MOD_Plk_2-3 | 410 | 416 | PF00069 | 0.731 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.503 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.666 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.503 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.420 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.676 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.709 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.547 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.551 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.493 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.598 |
MOD_SUMO_rev_2 | 184 | 190 | PF00179 | 0.578 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.638 |
TRG_DiLeu_LyEn_5 | 240 | 245 | PF01217 | 0.535 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 342 | 345 | PF00400 | 0.400 |
TRG_NES_CRM1_1 | 323 | 338 | PF08389 | 0.585 |
TRG_NLS_MonoExtC_3 | 101 | 106 | PF00514 | 0.511 |
TRG_NLS_MonoExtN_4 | 99 | 106 | PF00514 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCG4 | Leptomonas seymouri | 59% | 100% |
A0A1X0P2F5 | Trypanosomatidae | 29% | 100% |
A0A3R7P2X0 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X6N5 | Leishmania donovani | 80% | 100% |
A4I8W9 | Leishmania infantum | 80% | 100% |
D0A4W4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B3T8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q486 | Leishmania major | 79% | 100% |
V5AZU2 | Trypanosoma cruzi | 33% | 100% |