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: 18 |
NetGPI | no | yes: 0, no: 18 |
Related structures:
AlphaFold database: E9AYD1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016787 | hydrolase activity | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.408 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.428 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.353 |
DOC_ANK_TNKS_1 | 135 | 142 | PF00023 | 0.425 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.506 |
DOC_MAPK_gen_1 | 22 | 29 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 195 | 202 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 22 | 29 | PF00069 | 0.259 |
DOC_PP2B_LxvP_1 | 200 | 203 | PF13499 | 0.375 |
DOC_PP2B_LxvP_1 | 293 | 296 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 378 | 381 | PF00568 | 0.304 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.382 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.291 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.280 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 272 | 278 | PF00244 | 0.478 |
LIG_Actin_WH2_2 | 221 | 239 | PF00022 | 0.388 |
LIG_APCC_Cbox_2 | 155 | 161 | PF00515 | 0.269 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.542 |
LIG_BIR_III_2 | 343 | 347 | PF00653 | 0.173 |
LIG_Clathr_ClatBox_1 | 197 | 201 | PF01394 | 0.370 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.365 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.357 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.371 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.311 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.326 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.393 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.288 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.384 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.388 |
LIG_GBD_Chelix_1 | 97 | 105 | PF00786 | 0.375 |
LIG_LIR_Apic_2 | 297 | 302 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 375 | 381 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 350 | 361 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.410 |
LIG_LYPXL_yS_3 | 329 | 332 | PF13949 | 0.269 |
LIG_MYND_3 | 281 | 285 | PF01753 | 0.304 |
LIG_PCNA_PIPBox_1 | 151 | 160 | PF02747 | 0.269 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.431 |
LIG_SH2_SRC | 157 | 160 | PF00017 | 0.216 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.460 |
LIG_SH3_2 | 267 | 272 | PF14604 | 0.402 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.304 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.392 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.602 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.462 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.486 |
LIG_SUMO_SIM_anti_2 | 383 | 389 | PF11976 | 0.424 |
LIG_SUMO_SIM_anti_2 | 44 | 50 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 196 | 201 | PF11976 | 0.345 |
LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.269 |
LIG_TYR_ITIM | 351 | 356 | PF00017 | 0.173 |
LIG_UBA3_1 | 218 | 226 | PF00899 | 0.425 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.304 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.501 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.304 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.287 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.345 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.391 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.412 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.308 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.407 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.460 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.349 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.335 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.379 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.315 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.306 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.422 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.379 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.412 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.477 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.375 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.291 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.316 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.410 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.314 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.340 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.304 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.333 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.400 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.269 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.155 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.416 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.407 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.334 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.413 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.345 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.398 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.408 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.408 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.225 |
MOD_PK_1 | 365 | 371 | PF00069 | 0.453 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.304 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.252 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.435 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.287 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.428 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.454 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.360 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.403 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.274 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.408 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.395 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.346 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.338 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.501 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.280 |
MOD_SUMO_rev_2 | 187 | 197 | PF00179 | 0.299 |
TRG_DiLeu_BaEn_1 | 383 | 388 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.384 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.269 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.258 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8L5 | Leptomonas seymouri | 26% | 99% |
A0A0N1I6V6 | Leptomonas seymouri | 58% | 100% |
A0A1X0NNK2 | Trypanosomatidae | 23% | 100% |
A0A1X0NS30 | Trypanosomatidae | 32% | 100% |
A0A3Q8I9M0 | Leishmania donovani | 25% | 100% |
A0A3Q8IDU3 | Leishmania donovani | 91% | 100% |
A0A3R7LZE9 | Trypanosoma rangeli | 26% | 100% |
A4H7A0 | Leishmania braziliensis | 26% | 100% |
A4HF07 | Leishmania braziliensis | 80% | 100% |
A4HVP2 | Leishmania infantum | 25% | 100% |
A4I286 | Leishmania infantum | 91% | 100% |
C9ZRQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A6K3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9APD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q942 | Leishmania major | 91% | 100% |
Q4QG40 | Leishmania major | 25% | 100% |
V5ARR6 | Trypanosoma cruzi | 25% | 94% |