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: 10 |
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 | yes | yes: 5, no: 1 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H829
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.473 |
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.673 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.654 |
DEG_SPOP_SBC_1 | 136 | 140 | PF00917 | 0.559 |
DOC_MAPK_MEF2A_6 | 14 | 22 | PF00069 | 0.411 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.436 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.452 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.534 |
LIG_14-3-3_CanoR_1 | 112 | 122 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 316 | 320 | PF00244 | 0.325 |
LIG_APCC_ABBA_1 | 196 | 201 | PF00400 | 0.501 |
LIG_BRCT_BRCA1_1 | 284 | 288 | PF00533 | 0.381 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.507 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.253 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.481 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.487 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.364 |
LIG_Integrin_isoDGR_2 | 263 | 265 | PF01839 | 0.641 |
LIG_LIR_Gen_1 | 245 | 254 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.392 |
LIG_SH2_GRB2like | 203 | 206 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.485 |
LIG_SH2_NCK_1 | 215 | 219 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.417 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.512 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.489 |
LIG_SUMO_SIM_anti_2 | 318 | 323 | PF11976 | 0.240 |
LIG_SUMO_SIM_par_1 | 317 | 323 | PF11976 | 0.273 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.506 |
LIG_UBA3_1 | 251 | 259 | PF00899 | 0.356 |
LIG_WRC_WIRS_1 | 92 | 97 | PF05994 | 0.417 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.423 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.372 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.492 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.385 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.460 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.434 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.425 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.389 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.515 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.491 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.387 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.498 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.495 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.478 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.645 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.649 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.716 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.511 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.483 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.460 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.607 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.413 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.307 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.640 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.589 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.684 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.671 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.646 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.432 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.231 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.396 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.433 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.504 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.389 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.477 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.436 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.231 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.390 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.233 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.435 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.388 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.408 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.447 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.432 |
MOD_Plk_2-3 | 150 | 156 | PF00069 | 0.478 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.580 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.426 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.468 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.510 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.307 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.354 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P748 | Leptomonas seymouri | 39% | 100% |
A0A3S7WTK4 | Leishmania donovani | 64% | 100% |
A4HWF5 | Leishmania infantum | 64% | 100% |
E9AQ54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4QFC8 | Leishmania major | 62% | 100% |