A metalloenzyme with the catalytic domain facing outwards. Related to plant Shewanella-like protein phosphatases. Kinetoplastids have multiple copies of these genes but probably from a very ancient gene duplication.. The cluster might merge two separate, very distantly related groups.
| 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 | yes | yes: 12, no: 1 | 
| NetGPI | no | yes: 0, no: 13 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 2 | 
| GO:0110165 | cellular anatomical entity | 1 | 2 | 
Related structures:
AlphaFold database: Q4QBJ8
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 14 | 
| GO:0016787 | hydrolase activity | 2 | 14 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.372 | 
| CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.519 | 
| CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.364 | 
| CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.399 | 
| DEG_APCC_DBOX_1 | 252 | 260 | PF00400 | 0.366 | 
| DEG_APCC_DBOX_1 | 92 | 100 | PF00400 | 0.372 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.603 | 
| DEG_SCF_FBW7_1 | 266 | 273 | PF00400 | 0.323 | 
| DOC_MAPK_gen_1 | 29 | 37 | PF00069 | 0.527 | 
| DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.566 | 
| DOC_MAPK_MEF2A_6 | 298 | 306 | PF00069 | 0.475 | 
| DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.441 | 
| DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.294 | 
| DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.323 | 
| LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.443 | 
| LIG_14-3-3_CanoR_1 | 93 | 97 | PF00244 | 0.267 | 
| LIG_Actin_WH2_2 | 204 | 222 | PF00022 | 0.366 | 
| LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.503 | 
| LIG_eIF4E_1 | 12 | 18 | PF01652 | 0.568 | 
| LIG_FHA_1 | 260 | 266 | PF00498 | 0.416 | 
| LIG_FHA_1 | 92 | 98 | PF00498 | 0.337 | 
| LIG_FHA_2 | 267 | 273 | PF00498 | 0.381 | 
| LIG_FHA_2 | 334 | 340 | PF00498 | 0.642 | 
| LIG_IRF3_LxIS_1 | 18 | 25 | PF10401 | 0.592 | 
| LIG_LIR_Gen_1 | 356 | 361 | PF02991 | 0.710 | 
| LIG_LIR_Gen_1 | 51 | 60 | PF02991 | 0.426 | 
| LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.321 | 
| LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.450 | 
| LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.689 | 
| LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.373 | 
| LIG_PDZ_Class_3 | 356 | 361 | PF00595 | 0.678 | 
| LIG_Pex14_2 | 224 | 228 | PF04695 | 0.439 | 
| LIG_SH2_CRK | 12 | 16 | PF00017 | 0.613 | 
| LIG_SH2_CRK | 148 | 152 | PF00017 | 0.396 | 
| LIG_SH2_CRK | 296 | 300 | PF00017 | 0.351 | 
| LIG_SH2_GRB2like | 150 | 153 | PF00017 | 0.396 | 
| LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.472 | 
| LIG_SH2_PTP2 | 20 | 23 | PF00017 | 0.368 | 
| LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.499 | 
| LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.295 | 
| LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.341 | 
| LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.506 | 
| LIG_SUMO_SIM_anti_2 | 130 | 137 | PF11976 | 0.357 | 
| LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.605 | 
| LIG_SUMO_SIM_par_1 | 283 | 288 | PF11976 | 0.328 | 
| LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.318 | 
| LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.426 | 
| LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.426 | 
| LIG_TYR_ITIM | 18 | 23 | PF00017 | 0.586 | 
| LIG_WW_3 | 76 | 80 | PF00397 | 0.443 | 
| MOD_CK1_1 | 84 | 90 | PF00069 | 0.231 | 
| MOD_CK1_1 | 91 | 97 | PF00069 | 0.231 | 
| MOD_CK2_1 | 115 | 121 | PF00069 | 0.396 | 
| MOD_CK2_1 | 125 | 131 | PF00069 | 0.396 | 
| MOD_CK2_1 | 266 | 272 | PF00069 | 0.426 | 
| MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.429 | 
| MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.377 | 
| MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.476 | 
| MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.509 | 
| MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.627 | 
| MOD_GlcNHglycan | 339 | 344 | PF01048 | 0.661 | 
| MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.446 | 
| MOD_GSK3_1 | 224 | 231 | PF00069 | 0.420 | 
| MOD_GSK3_1 | 243 | 250 | PF00069 | 0.438 | 
| MOD_GSK3_1 | 266 | 273 | PF00069 | 0.333 | 
| MOD_GSK3_1 | 311 | 318 | PF00069 | 0.518 | 
| MOD_GSK3_1 | 339 | 346 | PF00069 | 0.652 | 
| MOD_GSK3_1 | 80 | 87 | PF00069 | 0.386 | 
| MOD_GSK3_1 | 88 | 95 | PF00069 | 0.317 | 
| MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.402 | 
| MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.394 | 
| MOD_NEK2_1 | 169 | 174 | PF00069 | 0.398 | 
| MOD_NEK2_1 | 22 | 27 | PF00069 | 0.567 | 
| MOD_NEK2_1 | 224 | 229 | PF00069 | 0.416 | 
| MOD_NEK2_1 | 259 | 264 | PF00069 | 0.351 | 
| MOD_NEK2_1 | 304 | 309 | PF00069 | 0.372 | 
| MOD_NEK2_1 | 333 | 338 | PF00069 | 0.640 | 
| MOD_NEK2_1 | 344 | 349 | PF00069 | 0.633 | 
| MOD_PIKK_1 | 125 | 131 | PF00454 | 0.413 | 
| MOD_PKA_2 | 224 | 230 | PF00069 | 0.426 | 
| MOD_PKA_2 | 92 | 98 | PF00069 | 0.345 | 
| MOD_Plk_1 | 199 | 205 | PF00069 | 0.410 | 
| MOD_Plk_1 | 259 | 265 | PF00069 | 0.376 | 
| MOD_Plk_1 | 344 | 350 | PF00069 | 0.655 | 
| MOD_Plk_1 | 63 | 69 | PF00069 | 0.249 | 
| MOD_Plk_2-3 | 243 | 249 | PF00069 | 0.288 | 
| MOD_Plk_4 | 224 | 230 | PF00069 | 0.451 | 
| MOD_Plk_4 | 317 | 323 | PF00069 | 0.531 | 
| MOD_Plk_4 | 92 | 98 | PF00069 | 0.324 | 
| MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.323 | 
| MOD_SUMO_rev_2 | 25 | 35 | PF00179 | 0.578 | 
| TRG_DiLeu_BaEn_1 | 131 | 136 | PF01217 | 0.352 | 
| TRG_DiLeu_BaEn_2 | 189 | 195 | PF01217 | 0.420 | 
| TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.553 | 
| TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.396 | 
| TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.396 | 
| TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.554 | 
| TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.353 | 
| TRG_Pf-PMV_PEXEL_1 | 32 | 36 | PF00026 | 0.495 | 
| TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.494 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1I3V2 | Leptomonas seymouri | 29% | 97% | 
| A0A0N1P9R1 | Leptomonas seymouri | 57% | 100% | 
| A0A0S4JBT9 | Bodo saltans | 39% | 93% | 
| A0A0S4JMN0 | Bodo saltans | 33% | 89% | 
| A0A0S4KJG1 | Bodo saltans | 27% | 97% | 
| A0A1X0NU01 | Trypanosomatidae | 45% | 97% | 
| A0A1X0NZX7 | Trypanosomatidae | 31% | 81% | 
| A0A1X0P2G6 | Trypanosomatidae | 28% | 97% | 
| A0A3Q8IBB4 | Leishmania donovani | 94% | 100% | 
| A0A3Q8IIK0 | Leishmania donovani | 28% | 95% | 
| A0A3R7NTC0 | Trypanosoma rangeli | 29% | 98% | 
| A0A3S5IRW3 | Trypanosoma rangeli | 29% | 87% | 
| A0A3S7X3U9 | Leishmania donovani | 27% | 97% | 
| A4HCJ2 | Leishmania braziliensis | 79% | 100% | 
| A4HH45 | Leishmania braziliensis | 28% | 95% | 
| A4HIR7 | Leishmania braziliensis | 28% | 86% | 
| A4I008 | Leishmania infantum | 94% | 100% | 
| A4I498 | Leishmania infantum | 28% | 95% | 
| A4I612 | Leishmania infantum | 27% | 97% | 
| C9ZQ86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 97% | 
| C9ZRD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 81% | 
| E9ADP5 | Leishmania major | 29% | 100% | 
| E9AM35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 95% | 
| E9AVY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% | 
| E9B1A3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 97% | 
| O74480 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% | 
| Q4Q6W1 | Leishmania major | 27% | 100% | 
| Q8L774 | Arabidopsis thaliana | 25% | 93% | 
| Q944L7 | Arabidopsis thaliana | 26% | 92% | 
| V5ARZ9 | Trypanosoma cruzi | 46% | 96% | 
| V5BPY7 | Trypanosoma cruzi | 32% | 82% | 
| V5BX32 | Trypanosoma cruzi | 29% | 98% |