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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.520 |
DEG_APCC_DBOX_1 | 194 | 202 | PF00400 | 0.423 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.614 |
DOC_ANK_TNKS_1 | 56 | 63 | PF00023 | 0.508 |
DOC_PP1_RVXF_1 | 143 | 150 | PF00149 | 0.473 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.429 |
DOC_USP7_UBL2_3 | 10 | 14 | PF12436 | 0.703 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 282 | 288 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 67 | 76 | PF00244 | 0.446 |
LIG_AP_GAE_1 | 106 | 112 | PF02883 | 0.518 |
LIG_CSL_BTD_1 | 82 | 85 | PF09270 | 0.491 |
LIG_deltaCOP1_diTrp_1 | 265 | 268 | PF00928 | 0.431 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.383 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.677 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.422 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.422 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.422 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.582 |
LIG_LIR_Apic_2 | 91 | 95 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 257 | 264 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.519 |
LIG_LYPXL_yS_3 | 81 | 84 | PF13949 | 0.532 |
LIG_PCNA_yPIPBox_3 | 118 | 128 | PF02747 | 0.436 |
LIG_Pex14_1 | 105 | 109 | PF04695 | 0.428 |
LIG_Pex14_1 | 77 | 81 | PF04695 | 0.495 |
LIG_PTB_Apo_2 | 162 | 169 | PF02174 | 0.555 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.582 |
LIG_SH2_SRC | 92 | 95 | PF00017 | 0.605 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.606 |
LIG_SH3_1 | 232 | 238 | PF00018 | 0.613 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.514 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.471 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.468 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.494 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.549 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.373 |
LIG_TRFH_1 | 186 | 190 | PF08558 | 0.394 |
MOD_CDK_SPK_2 | 93 | 98 | PF00069 | 0.604 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.478 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.435 |
MOD_CMANNOS | 74 | 77 | PF00535 | 0.440 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.491 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.451 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.537 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.687 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.441 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.473 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.407 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.589 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.468 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.414 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.450 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.637 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.452 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.417 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.476 |
MOD_Plk_2-3 | 169 | 175 | PF00069 | 0.417 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.514 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.542 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.389 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.567 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.586 |
TRG_NLS_MonoExtC_3 | 17 | 22 | PF00514 | 0.706 |
TRG_Pf-PMV_PEXEL_1 | 145 | 150 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.284 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P900 | Leptomonas seymouri | 82% | 100% |
A0A0S4KF76 | Bodo saltans | 59% | 100% |
A0A1X0P370 | Trypanosomatidae | 63% | 94% |
A0A3R7NW18 | Trypanosoma rangeli | 65% | 98% |
A0A3S7XC20 | Leishmania donovani | 90% | 100% |
A4IE17 | Leishmania infantum | 90% | 100% |
D0A8R6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 99% |
E9AU40 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q0F5 | Leishmania major | 89% | 100% |
V5BRZ1 | Trypanosoma cruzi | 67% | 98% |