Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 12 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H3U4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.640 |
DEG_APCC_DBOX_1 | 195 | 203 | PF00400 | 0.408 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.658 |
DEG_SCF_FBW7_2 | 221 | 227 | PF00400 | 0.246 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.452 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.242 |
DOC_CYCLIN_yCln2_LP_2 | 249 | 255 | PF00134 | 0.509 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 267 | 275 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 213 | 221 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 306 | 313 | PF00069 | 0.312 |
DOC_PP1_RVXF_1 | 137 | 143 | PF00149 | 0.256 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.704 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.571 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 157 | 165 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 43 | 53 | PF00244 | 0.444 |
LIG_eIF4E_1 | 12 | 18 | PF01652 | 0.447 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.461 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.346 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.484 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.479 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.543 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.649 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.452 |
LIG_LIR_Apic_2 | 19 | 25 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 10 | 20 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 174 | 182 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 295 | 304 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 95 | 104 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 10 | 15 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.524 |
LIG_PDZ_Class_3 | 314 | 319 | PF00595 | 0.394 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.334 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.459 |
LIG_SH2_PTP2 | 14 | 17 | PF00017 | 0.411 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.509 |
LIG_SH2_SRC | 300 | 303 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 129 | 132 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.328 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.521 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.264 |
LIG_SUMO_SIM_par_1 | 107 | 112 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 16 | 21 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 223 | 230 | PF11976 | 0.339 |
LIG_TRFH_1 | 247 | 251 | PF08558 | 0.486 |
LIG_UBA3_1 | 96 | 101 | PF00899 | 0.649 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.541 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.350 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.419 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.500 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.563 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.463 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.547 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.334 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.334 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.599 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.636 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.649 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.549 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.538 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.479 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.474 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.372 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.513 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.428 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.589 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.467 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.407 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.463 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.441 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.441 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.417 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.584 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.422 |
MOD_PK_1 | 87 | 93 | PF00069 | 0.442 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.486 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.675 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.459 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.430 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.337 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.309 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.438 |
MOD_SUMO_rev_2 | 283 | 292 | PF00179 | 0.373 |
TRG_DiLeu_BaEn_1 | 147 | 152 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.327 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAZ3 | Leptomonas seymouri | 50% | 93% |
A0A0S4IUM5 | Bodo saltans | 33% | 100% |
A0A1X0NMU9 | Trypanosomatidae | 43% | 100% |
A0A3R7NSA7 | Trypanosoma rangeli | 42% | 100% |
A0A3S5H589 | Leishmania donovani | 58% | 100% |
A4HS19 | Leishmania infantum | 58% | 100% |
C9ZY11 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AK06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
Q9XZY4 | Leishmania major | 56% | 91% |
V5D9R6 | Trypanosoma cruzi | 40% | 100% |