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: A4I8W9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.710 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.436 |
CLV_Separin_Metazoa | 60 | 64 | PF03568 | 0.478 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.707 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.706 |
DEG_SCF_FBW7_1 | 235 | 240 | PF00400 | 0.533 |
DEG_SPOP_SBC_1 | 104 | 108 | PF00917 | 0.553 |
DOC_CKS1_1 | 309 | 314 | PF01111 | 0.578 |
DOC_MAPK_gen_1 | 152 | 160 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 193 | 202 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.484 |
DOC_MAPK_JIP1_4 | 154 | 160 | PF00069 | 0.660 |
DOC_MAPK_MEF2A_6 | 324 | 331 | PF00069 | 0.612 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.484 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.585 |
DOC_PP4_FxxP_1 | 36 | 39 | PF00568 | 0.630 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.698 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 114 | 120 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 161 | 165 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 255 | 259 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 50 | 59 | PF00244 | 0.473 |
LIG_Actin_WH2_2 | 62 | 80 | PF00022 | 0.491 |
LIG_BIR_III_4 | 365 | 369 | PF00653 | 0.642 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.481 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.718 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.587 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.537 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.609 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.462 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.640 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.539 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.728 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.481 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.654 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.623 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.585 |
LIG_FXI_DFP_1 | 33 | 37 | PF00024 | 0.674 |
LIG_LIR_Apic_2 | 35 | 39 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.312 |
LIG_MYND_1 | 305 | 309 | PF01753 | 0.612 |
LIG_PCNA_PIPBox_1 | 245 | 254 | PF02747 | 0.549 |
LIG_PDZ_Class_3 | 445 | 450 | PF00595 | 0.622 |
LIG_Pex14_2 | 306 | 310 | PF04695 | 0.682 |
LIG_SH2_SRC | 273 | 276 | PF00017 | 0.654 |
LIG_SH2_SRC | 9 | 12 | PF00017 | 0.713 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.445 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.732 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.663 |
LIG_SUMO_SIM_par_1 | 236 | 244 | PF11976 | 0.518 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.522 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.747 |
LIG_UBA3_1 | 213 | 220 | PF00899 | 0.575 |
LIG_UBA3_1 | 76 | 81 | PF00899 | 0.465 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.669 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.513 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.581 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.641 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.699 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.470 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.714 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.690 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.622 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.482 |
MOD_GlcNHglycan | 137 | 141 | PF01048 | 0.693 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.432 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.631 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.727 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.627 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.710 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.590 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.530 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.671 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.687 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.663 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.502 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.564 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.617 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.673 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.649 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.456 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.535 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.542 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.688 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.571 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.595 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.533 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.530 |
MOD_Plk_2-3 | 405 | 411 | PF00069 | 0.710 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.526 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.503 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.685 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.548 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.587 |
MOD_SUMO_for_1 | 175 | 178 | PF00179 | 0.424 |
MOD_SUMO_rev_2 | 178 | 184 | PF00179 | 0.579 |
TRG_DiLeu_BaEn_1 | 282 | 287 | PF01217 | 0.598 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.635 |
TRG_DiLeu_LyEn_5 | 234 | 239 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.299 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.501 |
TRG_NES_CRM1_1 | 318 | 333 | PF08389 | 0.590 |
TRG_NLS_MonoExtC_3 | 80 | 85 | PF00514 | 0.521 |
TRG_NLS_MonoExtN_4 | 151 | 156 | PF00514 | 0.628 |
TRG_NLS_MonoExtN_4 | 78 | 85 | PF00514 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCG4 | Leptomonas seymouri | 59% | 100% |
A0A1X0P2F5 | Trypanosomatidae | 29% | 100% |
A0A3R7P2X0 | Trypanosoma rangeli | 32% | 100% |
A0A3S7X6N5 | Leishmania donovani | 99% | 100% |
A4HLF8 | Leishmania braziliensis | 80% | 100% |
D0A4W4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 99% |
E9B3T8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q486 | Leishmania major | 93% | 100% |
V5AZU2 | Trypanosoma cruzi | 32% | 100% |