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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 16, no: 11 |
NetGPI | no | yes: 0, no: 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
Related structures:
AlphaFold database: E9AVY1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 28 |
GO:0016787 | hydrolase activity | 2 | 28 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.547 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.272 |
DEG_APCC_DBOX_1 | 252 | 260 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 92 | 100 | PF00400 | 0.261 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.608 |
DOC_MAPK_MEF2A_6 | 298 | 306 | PF00069 | 0.415 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.528 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.135 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 93 | 97 | PF00244 | 0.198 |
LIG_Actin_WH2_2 | 204 | 222 | PF00022 | 0.451 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.588 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.468 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.478 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.241 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.503 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.398 |
LIG_LIR_Gen_1 | 18 | 28 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 357 | 362 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 51 | 60 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.257 |
LIG_PDZ_Class_3 | 357 | 362 | PF00595 | 0.494 |
LIG_SH2_CRK | 12 | 16 | PF00017 | 0.597 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.285 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.453 |
LIG_SH2_GRB2like | 150 | 153 | PF00017 | 0.318 |
LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.481 |
LIG_SUMO_SIM_anti_2 | 130 | 137 | PF11976 | 0.243 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 283 | 288 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.244 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.318 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.586 |
LIG_TRAF2_1 | 352 | 355 | PF00917 | 0.521 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.545 |
LIG_WW_3 | 76 | 80 | PF00397 | 0.185 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.586 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.285 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.285 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.557 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.387 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.498 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.517 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.270 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.324 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.360 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.372 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.406 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.545 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.436 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.512 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.412 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.591 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.274 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.291 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.389 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.482 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.509 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.264 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.503 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.490 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.447 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.507 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.317 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.391 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.311 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.196 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.498 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.239 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.372 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.483 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.286 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.495 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.540 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.636 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.205 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.135 |
MOD_SUMO_rev_2 | 25 | 35 | PF00179 | 0.349 |
TRG_DiLeu_BaEn_1 | 131 | 136 | PF01217 | 0.201 |
TRG_DiLeu_BaEn_2 | 189 | 195 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_4 | 339 | 345 | PF01217 | 0.334 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 32 | 36 | PF00026 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3V2 | Leptomonas seymouri | 29% | 97% |
A0A0N1P9R1 | Leptomonas seymouri | 55% | 100% |
A0A0S4JBT9 | Bodo saltans | 41% | 93% |
A0A0S4JMN0 | Bodo saltans | 33% | 89% |
A0A0S4KJG1 | Bodo saltans | 28% | 97% |
A0A1X0NU01 | Trypanosomatidae | 43% | 97% |
A0A1X0NZX7 | Trypanosomatidae | 31% | 81% |
A0A1X0P2G6 | Trypanosomatidae | 29% | 98% |
A0A3Q8IBB4 | Leishmania donovani | 92% | 100% |
A0A3Q8IIK0 | Leishmania donovani | 28% | 96% |
A0A3R7NTC0 | Trypanosoma rangeli | 29% | 98% |
A0A3S5IRW3 | Trypanosoma rangeli | 29% | 88% |
A0A3S7X3U9 | Leishmania donovani | 27% | 98% |
A4HCJ2 | Leishmania braziliensis | 79% | 100% |
A4HH45 | Leishmania braziliensis | 28% | 100% |
A4HIR7 | Leishmania braziliensis | 29% | 100% |
A4I008 | Leishmania infantum | 92% | 100% |
A4I498 | Leishmania infantum | 28% | 96% |
A4I612 | Leishmania infantum | 27% | 98% |
C9ZQ86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 97% |
C9ZRD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 82% |
E9ADP5 | Leishmania major | 29% | 100% |
E9AM35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1A3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 98% |
O74480 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q4Q6W1 | Leishmania major | 27% | 100% |
Q4QBJ8 | Leishmania major | 91% | 100% |
Q8L774 | Arabidopsis thaliana | 25% | 93% |
Q944L7 | Arabidopsis thaliana | 26% | 93% |
V5ARZ9 | Trypanosoma cruzi | 47% | 96% |
V5BPY7 | Trypanosoma cruzi | 32% | 82% |
V5BX32 | Trypanosoma cruzi | 29% | 99% |