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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q5W5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.489 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.452 |
CLV_Separin_Metazoa | 122 | 126 | PF03568 | 0.395 |
DOC_CDC14_PxL_1 | 240 | 248 | PF14671 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.360 |
DOC_MAPK_gen_1 | 25 | 34 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 52 | 60 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 52 | 60 | PF00069 | 0.412 |
DOC_PP1_RVXF_1 | 278 | 285 | PF00149 | 0.359 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.452 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.522 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 25 | 34 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.353 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.375 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.441 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.502 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.446 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.447 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.415 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.365 |
LIG_GBD_Chelix_1 | 3 | 11 | PF00786 | 0.455 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.635 |
LIG_LIR_Apic_2 | 62 | 68 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 176 | 187 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 216 | 225 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 107 | 111 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.538 |
LIG_LYPXL_yS_3 | 243 | 246 | PF13949 | 0.482 |
LIG_NRBOX | 274 | 280 | PF00104 | 0.372 |
LIG_PDZ_Class_2 | 289 | 294 | PF00595 | 0.461 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.455 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.374 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.474 |
LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.478 |
LIG_SH3_1 | 189 | 195 | PF00018 | 0.473 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.458 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.456 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.474 |
LIG_SUMO_SIM_anti_2 | 135 | 142 | PF11976 | 0.379 |
LIG_SUMO_SIM_anti_2 | 180 | 186 | PF11976 | 0.366 |
LIG_SUMO_SIM_anti_2 | 55 | 62 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 109 | 115 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 135 | 142 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 180 | 186 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 55 | 62 | PF11976 | 0.356 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.412 |
LIG_TYR_ITIM | 106 | 111 | PF00017 | 0.444 |
LIG_UBA3_1 | 278 | 285 | PF00899 | 0.359 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.438 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.586 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.452 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.485 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.427 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.327 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.590 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.423 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.510 |
MOD_GlcNHglycan | 171 | 175 | PF01048 | 0.493 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.622 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.492 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.412 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.468 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.488 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.537 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.567 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.505 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.411 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.458 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.411 |
MOD_N-GLC_2 | 271 | 273 | PF02516 | 0.464 |
MOD_N-GLC_2 | 51 | 53 | PF02516 | 0.402 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.582 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.558 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.382 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.486 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.394 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.488 |
MOD_PK_1 | 27 | 33 | PF00069 | 0.497 |
MOD_PK_1 | 52 | 58 | PF00069 | 0.350 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.366 |
MOD_PKB_1 | 33 | 41 | PF00069 | 0.461 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.411 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.298 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.545 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.376 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.429 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.370 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.402 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.474 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.477 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.412 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.482 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 65 | 70 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 32 | 35 | PF00400 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJH1 | Leptomonas seymouri | 47% | 100% |
A0A3Q8IF52 | Leishmania donovani | 94% | 100% |
A4HJT2 | Leishmania braziliensis | 72% | 100% |
A4I798 | Leishmania infantum | 94% | 100% |
E9B293 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |