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: 11 |
NetGPI | no | yes: 0, no: 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 147 | 153 | PF00089 | 0.521 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.617 |
CLV_PCSK_PC7_1 | 55 | 61 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.676 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.500 |
DEG_SCF_FBW7_1 | 18 | 24 | PF00400 | 0.507 |
DEG_SPOP_SBC_1 | 42 | 46 | PF00917 | 0.572 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.474 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.697 |
DOC_CYCLIN_RxL_1 | 28 | 37 | PF00134 | 0.668 |
DOC_MAPK_gen_1 | 227 | 235 | PF00069 | 0.582 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.578 |
DOC_USP7_MATH_2 | 257 | 263 | PF00917 | 0.481 |
DOC_USP7_UBL2_3 | 91 | 95 | PF12436 | 0.471 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 13 | 21 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 150 | 158 | PF00244 | 0.234 |
LIG_14-3-3_CanoR_1 | 260 | 267 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 279 | 288 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 60 | 64 | PF00244 | 0.607 |
LIG_14-3-3_CterR_2 | 343 | 347 | PF00244 | 0.754 |
LIG_APCC_ABBA_1 | 303 | 308 | PF00400 | 0.516 |
LIG_APCC_ABBAyCdc20_2 | 302 | 308 | PF00400 | 0.517 |
LIG_Clathr_ClatBox_1 | 33 | 37 | PF01394 | 0.625 |
LIG_deltaCOP1_diTrp_1 | 82 | 90 | PF00928 | 0.484 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.399 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.717 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.414 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.526 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.469 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.474 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.448 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.694 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.523 |
LIG_HP1_1 | 110 | 114 | PF01393 | 0.264 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 178 | 187 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 82 | 90 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.519 |
LIG_LRP6_Inhibitor_1 | 114 | 120 | PF00058 | 0.533 |
LIG_Pex14_2 | 72 | 76 | PF04695 | 0.453 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.458 |
LIG_SH2_PTP2 | 111 | 114 | PF00017 | 0.261 |
LIG_SH2_PTP2 | 245 | 248 | PF00017 | 0.420 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.470 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.394 |
LIG_SH2_STAT3 | 131 | 134 | PF00017 | 0.382 |
LIG_SH2_STAT3 | 291 | 294 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.385 |
LIG_SH3_1 | 192 | 198 | PF00018 | 0.453 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.420 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.434 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.446 |
LIG_SH3_4 | 95 | 102 | PF00018 | 0.431 |
LIG_SUMO_SIM_par_1 | 111 | 116 | PF11976 | 0.359 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.523 |
MOD_CDK_SPxK_1 | 17 | 23 | PF00069 | 0.509 |
MOD_CDK_SPxxK_3 | 135 | 142 | PF00069 | 0.358 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.432 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.556 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.452 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.522 |
MOD_Cter_Amidation | 57 | 60 | PF01082 | 0.618 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.512 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.526 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.475 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.729 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.511 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.353 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.693 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.565 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.580 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.681 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.651 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.629 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.673 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.360 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.541 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.515 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.580 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.487 |
MOD_NEK2_2 | 200 | 205 | PF00069 | 0.600 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.470 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.304 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.265 |
MOD_PIKK_1 | 279 | 285 | PF00454 | 0.607 |
MOD_PKA_1 | 149 | 155 | PF00069 | 0.522 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.666 |
MOD_PKA_1 | 59 | 65 | PF00069 | 0.419 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.744 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.459 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.367 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.489 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.589 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.591 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.385 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.574 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.453 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.696 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.382 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.436 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.534 |
MOD_SUMO_rev_2 | 41 | 51 | PF00179 | 0.713 |
TRG_DiLeu_BaEn_1 | 169 | 174 | PF01217 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.696 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 239 | 244 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PED1 | Leptomonas seymouri | 80% | 100% |
A0A0S4J0P0 | Bodo saltans | 58% | 100% |
A0A1X0NM32 | Trypanosomatidae | 69% | 100% |
A0A3R7MQ73 | Trypanosoma rangeli | 69% | 100% |
A0A3S7XB37 | Leishmania donovani | 92% | 100% |
A4ID79 | Leishmania infantum | 92% | 100% |
D0A3H0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 99% |
E9AT69 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q1C8 | Leishmania major | 91% | 100% |
V5BPU3 | Trypanosoma cruzi | 68% | 100% |