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: 11, no: 11 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
Related structures:
AlphaFold database: E9ADP5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 23 |
GO:0016787 | hydrolase activity | 2 | 23 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.224 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.609 |
DEG_APCC_KENBOX_2 | 289 | 293 | PF00400 | 0.189 |
DOC_ANK_TNKS_1 | 85 | 92 | PF00023 | 0.300 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.373 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.356 |
DOC_CYCLIN_RxL_1 | 178 | 186 | PF00134 | 0.204 |
DOC_CYCLIN_RxL_1 | 345 | 358 | PF00134 | 0.252 |
DOC_MAPK_gen_1 | 118 | 126 | PF00069 | 0.189 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 345 | 354 | PF00069 | 0.263 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.557 |
DOC_MAPK_HePTP_8 | 287 | 299 | PF00069 | 0.204 |
DOC_MAPK_MEF2A_6 | 119 | 128 | PF00069 | 0.189 |
DOC_MAPK_MEF2A_6 | 290 | 299 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 317 | 325 | PF00069 | 0.339 |
DOC_MAPK_RevD_3 | 336 | 351 | PF00069 | 0.250 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.505 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.448 |
DOC_USP7_UBL2_3 | 346 | 350 | PF12436 | 0.350 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.251 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.378 |
LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.214 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.223 |
LIG_14-3-3_CanoR_1 | 359 | 368 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.222 |
LIG_Actin_WH2_2 | 90 | 107 | PF00022 | 0.258 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.646 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.532 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.532 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.514 |
LIG_Clathr_ClatBox_1 | 318 | 322 | PF01394 | 0.257 |
LIG_eIF4E_1 | 243 | 249 | PF01652 | 0.159 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.277 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.362 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.310 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.436 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.381 |
LIG_LIR_Apic_2 | 176 | 180 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 335 | 344 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.348 |
LIG_PDZ_Class_1 | 375 | 380 | PF00595 | 0.365 |
LIG_Pex14_2 | 34 | 38 | PF04695 | 0.286 |
LIG_PTB_Apo_2 | 328 | 335 | PF02174 | 0.255 |
LIG_PTB_Phospho_1 | 328 | 334 | PF10480 | 0.259 |
LIG_SH2_PTP2 | 177 | 180 | PF00017 | 0.241 |
LIG_SH2_PTP2 | 189 | 192 | PF00017 | 0.241 |
LIG_SH2_SRC | 177 | 180 | PF00017 | 0.247 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.502 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.204 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.289 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.388 |
LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.204 |
LIG_SUMO_SIM_par_1 | 167 | 172 | PF11976 | 0.175 |
LIG_SUMO_SIM_par_1 | 86 | 92 | PF11976 | 0.281 |
LIG_TRFH_1 | 364 | 368 | PF08558 | 0.249 |
LIG_UBA3_1 | 141 | 149 | PF00899 | 0.243 |
LIG_WRC_WIRS_1 | 337 | 342 | PF05994 | 0.227 |
LIG_WW_3 | 2 | 6 | PF00397 | 0.499 |
MOD_CDK_SPxxK_3 | 70 | 77 | PF00069 | 0.306 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.557 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.542 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.491 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.452 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.442 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.372 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.503 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.349 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.431 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.520 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.288 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.336 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.268 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.353 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.333 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.209 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.310 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.349 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.349 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.210 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.310 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.251 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.466 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.364 |
TRG_DiLeu_BaEn_1 | 140 | 145 | PF01217 | 0.189 |
TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.243 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.306 |
TRG_NLS_MonoCore_2 | 347 | 352 | PF00514 | 0.297 |
TRG_NLS_MonoExtC_3 | 344 | 349 | PF00514 | 0.283 |
TRG_NLS_MonoExtN_4 | 342 | 349 | PF00514 | 0.284 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3V2 | Leptomonas seymouri | 29% | 100% |
A0A0N1P9R1 | Leptomonas seymouri | 26% | 100% |
A0A0S4JMN0 | Bodo saltans | 32% | 94% |
A0A0S4KJG1 | Bodo saltans | 27% | 100% |
A0A1X0NU01 | Trypanosomatidae | 27% | 100% |
A0A1X0NZX7 | Trypanosomatidae | 35% | 85% |
A0A1X0P2G6 | Trypanosomatidae | 30% | 100% |
A0A3Q8IBB4 | Leishmania donovani | 28% | 100% |
A0A3Q8IIK0 | Leishmania donovani | 94% | 100% |
A0A3R7NTC0 | Trypanosoma rangeli | 27% | 100% |
A0A3S5IRW3 | Trypanosoma rangeli | 34% | 92% |
A0A3S7X3U9 | Leishmania donovani | 28% | 100% |
A4HCJ2 | Leishmania braziliensis | 30% | 100% |
A4HH45 | Leishmania braziliensis | 74% | 100% |
A4HIR7 | Leishmania braziliensis | 29% | 90% |
A4I008 | Leishmania infantum | 28% | 100% |
A4I498 | Leishmania infantum | 94% | 100% |
A4I612 | Leishmania infantum | 28% | 100% |
C9ZQ86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZRD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 86% |
E9AM35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AVY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1A3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O74480 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
Q4Q6W1 | Leishmania major | 31% | 100% |
Q4QBJ8 | Leishmania major | 29% | 100% |
Q944L7 | Arabidopsis thaliana | 27% | 97% |
V5ARZ9 | Trypanosoma cruzi | 26% | 100% |
V5BPY7 | Trypanosoma cruzi | 33% | 87% |
V5BX32 | Trypanosoma cruzi | 30% | 100% |