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: 16 |
NetGPI | no | yes: 0, no: 16 |
Related structures:
AlphaFold database: Q4Q9N6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 3 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 16 |
GO:0016791 | phosphatase activity | 5 | 16 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.397 |
CLV_Separin_Metazoa | 325 | 329 | PF03568 | 0.342 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.693 |
DEG_SCF_FBW7_1 | 75 | 80 | PF00400 | 0.496 |
DEG_SPOP_SBC_1 | 38 | 42 | PF00917 | 0.656 |
DOC_CDC14_PxL_1 | 327 | 335 | PF14671 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 170 | 176 | PF00134 | 0.486 |
DOC_MAPK_gen_1 | 178 | 187 | PF00069 | 0.278 |
DOC_MAPK_MEF2A_6 | 178 | 187 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 201 | 210 | PF00069 | 0.217 |
DOC_MAPK_MEF2A_6 | 212 | 220 | PF00069 | 0.212 |
DOC_MAPK_NFAT4_5 | 180 | 188 | PF00069 | 0.265 |
DOC_MAPK_RevD_3 | 167 | 181 | PF00069 | 0.357 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.229 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.467 |
LIG_APCC_ABBA_1 | 266 | 271 | PF00400 | 0.282 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.471 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.486 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.359 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.263 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.356 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.558 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.235 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.328 |
LIG_LIR_Apic_2 | 247 | 252 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 340 | 351 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.260 |
LIG_MYND_1 | 167 | 171 | PF01753 | 0.436 |
LIG_REV1ctd_RIR_1 | 12 | 20 | PF16727 | 0.463 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.281 |
LIG_SH2_GRB2like | 196 | 199 | PF00017 | 0.213 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.342 |
LIG_SH2_STAT3 | 304 | 307 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.251 |
LIG_SH3_2 | 48 | 53 | PF14604 | 0.544 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.342 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.595 |
LIG_SUMO_SIM_anti_2 | 283 | 288 | PF11976 | 0.215 |
LIG_SUMO_SIM_anti_2 | 292 | 298 | PF11976 | 0.215 |
LIG_SUMO_SIM_par_1 | 183 | 190 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 206 | 211 | PF11976 | 0.295 |
LIG_UBA3_1 | 253 | 259 | PF00899 | 0.342 |
MOD_CDC14_SPxK_1 | 50 | 53 | PF00782 | 0.546 |
MOD_CDK_SPxK_1 | 47 | 53 | PF00069 | 0.543 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.705 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.235 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.601 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.699 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.483 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.366 |
MOD_GlcNHglycan | 108 | 112 | PF01048 | 0.680 |
MOD_GlcNHglycan | 113 | 117 | PF01048 | 0.666 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.532 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.775 |
MOD_GlcNHglycan | 360 | 364 | PF01048 | 0.517 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.662 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.686 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.637 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.514 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.275 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.247 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.353 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.608 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.684 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.439 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.375 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.665 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.296 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.263 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.481 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.318 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.726 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.290 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.268 |
MOD_Plk_2-3 | 338 | 344 | PF00069 | 0.328 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.456 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.410 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.288 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.248 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.247 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.283 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.321 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.514 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.438 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.290 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.632 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.658 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.717 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.615 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.271 |
TRG_DiLeu_LyEn_5 | 325 | 330 | PF01217 | 0.249 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.278 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 147 | 150 | PF00400 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 289 | 293 | PF00026 | 0.288 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG96 | Leptomonas seymouri | 68% | 100% |
A0A0S4IJH3 | Bodo saltans | 46% | 100% |
A0A1X0NYI7 | Trypanosomatidae | 44% | 91% |
A0A3Q8IDG4 | Leishmania donovani | 96% | 99% |
A0A3S7WZH2 | Leishmania donovani | 51% | 100% |
A0A422P4K3 | Trypanosoma rangeli | 41% | 89% |
A4HEA5 | Leishmania braziliensis | 86% | 99% |
A4HEM1 | Leishmania braziliensis | 50% | 100% |
A4I1Q1 | Leishmania infantum | 96% | 99% |
A4I1V3 | Leishmania infantum | 51% | 100% |
A4ICB8 | Leishmania infantum | 27% | 100% |
C9ZKA3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 86% |
E9AXT5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
E9AXZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
Q4Q9H6 | Leishmania major | 51% | 100% |
Q6NWD4 | Danio rerio | 26% | 94% |
V5BAV0 | Trypanosoma cruzi | 24% | 100% |