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: 19 |
NetGPI | no | yes: 0, no: 19 |
Related structures:
AlphaFold database: A4HF07
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016787 | hydrolase activity | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.207 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.495 |
DOC_ANK_TNKS_1 | 135 | 142 | PF00023 | 0.432 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.521 |
DOC_CYCLIN_RxL_1 | 66 | 77 | PF00134 | 0.322 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 256 | 265 | PF00134 | 0.189 |
DOC_MAPK_gen_1 | 22 | 29 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 195 | 202 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 22 | 29 | PF00069 | 0.247 |
DOC_PP2B_LxvP_1 | 200 | 203 | PF13499 | 0.386 |
DOC_PP2B_LxvP_1 | 293 | 296 | PF13499 | 0.416 |
DOC_PP4_FxxP_1 | 378 | 381 | PF00568 | 0.309 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.203 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.401 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.266 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.278 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 272 | 278 | PF00244 | 0.438 |
LIG_Actin_WH2_2 | 221 | 239 | PF00022 | 0.398 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.560 |
LIG_Clathr_ClatBox_1 | 197 | 201 | PF01394 | 0.381 |
LIG_EVH1_2 | 25 | 29 | PF00568 | 0.332 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.368 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.375 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.344 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.398 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.376 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.290 |
LIG_GBD_Chelix_1 | 97 | 105 | PF00786 | 0.386 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.189 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.189 |
LIG_MYND_3 | 281 | 285 | PF01753 | 0.309 |
LIG_OCRL_FandH_1 | 28 | 40 | PF00620 | 0.219 |
LIG_PCNA_TLS_4 | 151 | 158 | PF02747 | 0.189 |
LIG_PTB_Apo_2 | 347 | 354 | PF02174 | 0.189 |
LIG_PTB_Phospho_1 | 347 | 353 | PF10480 | 0.189 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.450 |
LIG_SH3_2 | 267 | 272 | PF14604 | 0.411 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.319 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.405 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.415 |
LIG_SUMO_SIM_anti_2 | 383 | 389 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 196 | 201 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 74 | 79 | PF11976 | 0.189 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.344 |
LIG_UBA3_1 | 218 | 226 | PF00899 | 0.432 |
LIG_WRC_WIRS_1 | 158 | 163 | PF05994 | 0.189 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.309 |
MOD_CDC14_SPxK_1 | 179 | 182 | PF00782 | 0.189 |
MOD_CDK_SPxK_1 | 176 | 182 | PF00069 | 0.347 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.512 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.309 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.246 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.379 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.408 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.405 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.356 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.345 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.189 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.329 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.381 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.390 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.499 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.326 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.400 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.402 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.376 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.368 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.313 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.355 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.317 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.320 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.327 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.327 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.373 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.338 |
MOD_PK_1 | 365 | 371 | PF00069 | 0.457 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.309 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.398 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.371 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.412 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.285 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.394 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.378 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.337 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.512 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.278 |
MOD_SUMO_for_1 | 162 | 165 | PF00179 | 0.189 |
MOD_SUMO_rev_2 | 190 | 197 | PF00179 | 0.195 |
TRG_DiLeu_BaEn_1 | 193 | 198 | PF01217 | 0.179 |
TRG_DiLeu_BaEn_1 | 383 | 388 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.259 |
TRG_NES_CRM1_1 | 220 | 231 | PF08389 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.189 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8L5 | Leptomonas seymouri | 25% | 99% |
A0A0N1I6V6 | Leptomonas seymouri | 56% | 100% |
A0A0S4J886 | Bodo saltans | 22% | 96% |
A0A1X0NNK2 | Trypanosomatidae | 25% | 100% |
A0A1X0NS30 | Trypanosomatidae | 34% | 100% |
A0A3Q8I9M0 | Leishmania donovani | 25% | 99% |
A0A3Q8IDU3 | Leishmania donovani | 79% | 99% |
A0A3R7LZE9 | Trypanosoma rangeli | 25% | 100% |
A4H7A0 | Leishmania braziliensis | 25% | 100% |
A4HVP2 | Leishmania infantum | 25% | 99% |
A4I286 | Leishmania infantum | 79% | 99% |
C9ZRQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A6K3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9APD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 99% |
E9AYD1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
Q4Q942 | Leishmania major | 81% | 100% |
Q4QG40 | Leishmania major | 25% | 94% |
V5ARR6 | Trypanosoma cruzi | 25% | 93% |