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 | no | yes: 13, no: 12 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
Related structures:
AlphaFold database: A4HH45
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 26 |
GO:0016787 | hydrolase activity | 2 | 26 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.595 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.297 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.490 |
CLV_PCSK_PC7_1 | 346 | 352 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.161 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.603 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.150 |
DOC_ANK_TNKS_1 | 85 | 92 | PF00023 | 0.514 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.355 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.221 |
DOC_CYCLIN_RxL_1 | 178 | 189 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 288 | 299 | PF00069 | 0.328 |
DOC_MAPK_HePTP_8 | 287 | 299 | PF00069 | 0.198 |
DOC_MAPK_MEF2A_6 | 288 | 297 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 317 | 325 | PF00069 | 0.351 |
DOC_MAPK_NFAT4_5 | 292 | 300 | PF00069 | 0.150 |
DOC_PP1_SILK_1 | 77 | 82 | PF00149 | 0.155 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.389 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.251 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.221 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.536 |
LIG_Actin_WH2_2 | 90 | 107 | PF00022 | 0.443 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
LIG_Clathr_ClatBox_1 | 318 | 322 | PF01394 | 0.248 |
LIG_EH_1 | 253 | 257 | PF12763 | 0.150 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.453 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.368 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.356 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.364 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.358 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.422 |
LIG_LIR_Gen_1 | 331 | 342 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.358 |
LIG_PDZ_Class_1 | 374 | 379 | PF00595 | 0.347 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.538 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.398 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.344 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.221 |
LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.217 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 167 | 172 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 319 | 324 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 86 | 92 | PF11976 | 0.468 |
LIG_UBA3_1 | 141 | 149 | PF00899 | 0.428 |
LIG_WRC_WIRS_1 | 337 | 342 | PF05994 | 0.224 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.155 |
MOD_CDK_SPxK_1 | 300 | 306 | PF00069 | 0.228 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.443 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.316 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.155 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.449 |
MOD_Cter_Amidation | 348 | 351 | PF01082 | 0.471 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.322 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.245 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.234 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.260 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.223 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.554 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.516 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.451 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.269 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.377 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.427 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.334 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.542 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.308 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.556 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.531 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.457 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.414 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.218 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.311 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.327 |
MOD_NEK2_2 | 336 | 341 | PF00069 | 0.171 |
MOD_NEK2_2 | 368 | 373 | PF00069 | 0.229 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.534 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.270 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.562 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.353 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.369 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.350 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.343 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.437 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.251 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.319 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.431 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.221 |
MOD_SUMO_for_1 | 111 | 114 | PF00179 | 0.350 |
MOD_SUMO_rev_2 | 146 | 150 | PF00179 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 178 | 183 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.505 |
TRG_NLS_MonoExtN_4 | 342 | 349 | PF00514 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 351 | 355 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3V2 | Leptomonas seymouri | 27% | 100% |
A0A0N1P9R1 | Leptomonas seymouri | 25% | 100% |
A0A0S4JMN0 | Bodo saltans | 34% | 94% |
A0A0S4KJG1 | Bodo saltans | 28% | 100% |
A0A1X0NU01 | Trypanosomatidae | 25% | 100% |
A0A1X0NZX7 | Trypanosomatidae | 33% | 85% |
A0A1X0P2G6 | Trypanosomatidae | 29% | 100% |
A0A3Q8IBB4 | Leishmania donovani | 29% | 100% |
A0A3Q8IIK0 | Leishmania donovani | 73% | 100% |
A0A3R7NTC0 | Trypanosoma rangeli | 30% | 100% |
A0A3S5IRW3 | Trypanosoma rangeli | 31% | 92% |
A0A3S7X3U9 | Leishmania donovani | 29% | 100% |
A4HCJ2 | Leishmania braziliensis | 28% | 100% |
A4HIR7 | Leishmania braziliensis | 29% | 90% |
A4I008 | Leishmania infantum | 29% | 100% |
A4I498 | Leishmania infantum | 73% | 100% |
A4I612 | Leishmania infantum | 29% | 100% |
C9ZQ86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZRD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 85% |
E9ADP5 | Leishmania major | 74% | 100% |
E9AM35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AVY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B1A3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q6W1 | Leishmania major | 31% | 100% |
Q4QBJ8 | Leishmania major | 28% | 100% |
Q8L774 | Arabidopsis thaliana | 24% | 97% |
Q944L7 | Arabidopsis thaliana | 27% | 97% |
V5ARZ9 | Trypanosoma cruzi | 24% | 100% |
V5BPY7 | Trypanosoma cruzi | 32% | 86% |
V5BX32 | Trypanosoma cruzi | 30% | 100% |