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: 14 |
NetGPI | no | yes: 0, no: 14 |
Related structures:
AlphaFold database: E9AXT5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 14 |
GO:0016787 | hydrolase activity | 2 | 14 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 14 |
GO:0016791 | phosphatase activity | 5 | 14 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 14 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.375 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.282 |
CLV_Separin_Metazoa | 329 | 333 | PF03568 | 0.333 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.675 |
DEG_SCF_FBW7_1 | 78 | 83 | PF00400 | 0.528 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.547 |
DOC_CDC14_PxL_1 | 331 | 339 | PF14671 | 0.322 |
DOC_CYCLIN_yCln2_LP_2 | 174 | 180 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 182 | 191 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.244 |
DOC_MAPK_MEF2A_6 | 182 | 191 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 205 | 214 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 216 | 224 | PF00069 | 0.249 |
DOC_MAPK_NFAT4_5 | 184 | 192 | PF00069 | 0.302 |
DOC_MAPK_RevD_3 | 171 | 185 | PF00069 | 0.391 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.655 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.594 |
LIG_APCC_ABBA_1 | 270 | 275 | PF00400 | 0.333 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.521 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.448 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.279 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.357 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.622 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.506 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.442 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.326 |
LIG_LIR_Apic_2 | 251 | 256 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 344 | 355 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 351 | 356 | PF02991 | 0.310 |
LIG_MYND_1 | 171 | 175 | PF01753 | 0.469 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.339 |
LIG_SH2_GRB2like | 200 | 203 | PF00017 | 0.249 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.389 |
LIG_SH2_STAT3 | 308 | 311 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.267 |
LIG_SH3_2 | 51 | 56 | PF14604 | 0.575 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.333 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.692 |
LIG_SUMO_SIM_anti_2 | 287 | 292 | PF11976 | 0.251 |
LIG_SUMO_SIM_anti_2 | 296 | 302 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 187 | 194 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 210 | 215 | PF11976 | 0.335 |
LIG_UBA3_1 | 257 | 263 | PF00899 | 0.333 |
MOD_CDC14_SPxK_1 | 53 | 56 | PF00782 | 0.580 |
MOD_CDK_SPxK_1 | 50 | 56 | PF00069 | 0.576 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.723 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.526 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.271 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.835 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.526 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.271 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.624 |
MOD_GlcNHglycan | 112 | 116 | PF01048 | 0.718 |
MOD_GlcNHglycan | 117 | 121 | PF01048 | 0.633 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.523 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.519 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.597 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.489 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.321 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.329 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.333 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.588 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.773 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.699 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.465 |
MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.419 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.717 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.348 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.319 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.612 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.555 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.310 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.586 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.791 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.326 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.304 |
MOD_Plk_2-3 | 342 | 348 | PF00069 | 0.343 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.590 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.441 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.328 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.290 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.237 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.307 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.303 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.549 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.489 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.326 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.740 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.622 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.664 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.626 |
TRG_DiLeu_BaEn_1 | 329 | 334 | PF01217 | 0.322 |
TRG_DiLeu_LyEn_5 | 329 | 334 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG96 | Leptomonas seymouri | 68% | 100% |
A0A0S4IJH3 | Bodo saltans | 46% | 100% |
A0A3Q8IDG4 | Leishmania donovani | 94% | 100% |
A0A3S7WZH2 | Leishmania donovani | 51% | 100% |
A4HEA5 | Leishmania braziliensis | 86% | 99% |
A4HEM1 | Leishmania braziliensis | 50% | 100% |
A4I1Q1 | Leishmania infantum | 94% | 100% |
A4I1V3 | Leishmania infantum | 50% | 100% |
A4ICB8 | Leishmania infantum | 27% | 100% |
C9ZKA3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 87% |
E9AXZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
Q4Q9H6 | Leishmania major | 51% | 100% |
Q4Q9N6 | Leishmania major | 93% | 99% |