This large family encompasses many diverse protein phosphatases. Some appear to have evolved transmembrane segments. Very tentatively they might regulate transmembrane receptor kinases.. The TM and non-TM groups diverged early in Eukaryota and appear to be distinct enough that they probably should not be part of the same cluster. This latter group has not expanded.
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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 16 |
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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7WTA2
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 24 |
GO:0006793 | phosphorus metabolic process | 3 | 24 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 24 |
GO:0006807 | nitrogen compound metabolic process | 2 | 24 |
GO:0008152 | metabolic process | 1 | 24 |
GO:0009987 | cellular process | 1 | 24 |
GO:0016311 | dephosphorylation | 5 | 24 |
GO:0019538 | protein metabolic process | 3 | 24 |
GO:0036211 | protein modification process | 4 | 24 |
GO:0043170 | macromolecule metabolic process | 3 | 24 |
GO:0043412 | macromolecule modification | 4 | 24 |
GO:0044237 | cellular metabolic process | 2 | 24 |
GO:0044238 | primary metabolic process | 2 | 24 |
GO:0071704 | organic substance metabolic process | 2 | 24 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 24 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 24 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 24 |
GO:0016787 | hydrolase activity | 2 | 24 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 24 |
GO:0016791 | phosphatase activity | 5 | 24 |
GO:0017018 | myosin phosphatase activity | 5 | 5 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 24 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 24 |
GO:0005488 | binding | 1 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.363 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.533 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 6 | 8 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.503 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.542 |
DOC_CKS1_1 | 195 | 200 | PF01111 | 0.311 |
DOC_MAPK_DCC_7 | 359 | 369 | PF00069 | 0.169 |
DOC_MAPK_gen_1 | 359 | 369 | PF00069 | 0.203 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.406 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.402 |
DOC_PP2B_PxIxI_1 | 364 | 370 | PF00149 | 0.169 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.642 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.304 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.570 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.244 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.249 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.342 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.505 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.636 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.299 |
LIG_LIR_Apic_2 | 193 | 198 | PF02991 | 0.217 |
LIG_LIR_Apic_2 | 234 | 239 | PF02991 | 0.217 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.454 |
LIG_NRBOX | 99 | 105 | PF00104 | 0.508 |
LIG_PCNA_yPIPBox_3 | 94 | 108 | PF02747 | 0.477 |
LIG_Pex14_2 | 208 | 212 | PF04695 | 0.335 |
LIG_PTB_Apo_2 | 127 | 134 | PF02174 | 0.403 |
LIG_PTB_Apo_2 | 151 | 158 | PF02174 | 0.244 |
LIG_RPA_C_Fungi | 89 | 101 | PF08784 | 0.404 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.337 |
LIG_SH2_PTP2 | 236 | 239 | PF00017 | 0.408 |
LIG_SH2_PTP2 | 335 | 338 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.408 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.354 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.244 |
LIG_SUMO_SIM_anti_2 | 397 | 402 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.355 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.385 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.335 |
LIG_UBA3_1 | 352 | 360 | PF00899 | 0.408 |
LIG_UBA3_1 | 399 | 404 | PF00899 | 0.360 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.339 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.484 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.456 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.304 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.302 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.319 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.397 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.579 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.348 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.138 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.232 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.349 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.395 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.497 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.475 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.471 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.434 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.263 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.420 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.428 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.620 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.344 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.571 |
MOD_N-GLC_2 | 182 | 184 | PF02516 | 0.203 |
MOD_N-GLC_2 | 375 | 377 | PF02516 | 0.439 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.313 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.558 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.395 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.571 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.609 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.342 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.331 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.303 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.340 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.311 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.303 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.442 |
MOD_SUMO_rev_2 | 264 | 269 | PF00179 | 0.309 |
MOD_SUMO_rev_2 | 354 | 361 | PF00179 | 0.217 |
TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.328 |
TRG_DiLeu_BaEn_3 | 350 | 356 | PF01217 | 0.401 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.408 |
TRG_NLS_MonoExtC_3 | 71 | 77 | PF00514 | 0.582 |
TRG_NLS_MonoExtN_4 | 4 | 10 | PF00514 | 0.711 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C7 | Leptomonas seymouri | 71% | 100% |
A0A0N0P8F8 | Leptomonas seymouri | 38% | 100% |
A0A0N1I0H9 | Leptomonas seymouri | 39% | 100% |
A0A0N1I8W9 | Leptomonas seymouri | 30% | 93% |
A0A0N1IHU6 | Leptomonas seymouri | 31% | 99% |
A0A0N1PAL8 | Leptomonas seymouri | 31% | 100% |
A0A0N1PET0 | Leptomonas seymouri | 38% | 69% |
A0A0S4IY95 | Bodo saltans | 37% | 100% |
A0A0S4J0A6 | Bodo saltans | 29% | 99% |
A0A0S4JPC3 | Bodo saltans | 42% | 100% |
A0A0S4JPM8 | Bodo saltans | 47% | 100% |
A0A0S4KIS4 | Bodo saltans | 35% | 89% |
A0A0S4KJV9 | Bodo saltans | 40% | 93% |
A0A1X0NRG3 | Trypanosomatidae | 37% | 100% |
A0A1X0NVC4 | Trypanosomatidae | 53% | 98% |
A0A1X0P568 | Trypanosomatidae | 32% | 99% |
A0A1X0P991 | Trypanosomatidae | 40% | 100% |
A0A1X0PAN4 | Trypanosomatidae | 28% | 100% |
A0A3Q8IEK6 | Leishmania donovani | 41% | 100% |
A0A3Q8IFG7 | Leishmania donovani | 31% | 100% |
A0A3Q8IGS1 | Leishmania donovani | 36% | 72% |
A0A3Q8IK65 | Leishmania donovani | 41% | 100% |
A0A3S7WZ14 | Leishmania donovani | 30% | 100% |
A0A3S7X808 | Leishmania donovani | 29% | 90% |
A0A422N8D7 | Trypanosoma rangeli | 28% | 100% |
A0A422NAJ1 | Trypanosoma rangeli | 37% | 100% |
A0A422NL94 | Trypanosoma rangeli | 38% | 92% |
A0A422NML6 | Trypanosoma rangeli | 32% | 100% |
A0A422NS77 | Trypanosoma rangeli | 50% | 98% |
A0A422P293 | Trypanosoma rangeli | 40% | 100% |
A0BLX0 | Paramecium tetraurelia | 34% | 100% |
A0BQL0 | Paramecium tetraurelia | 36% | 100% |
A0CUB5 | Paramecium tetraurelia | 32% | 100% |
A0DSB3 | Paramecium tetraurelia | 33% | 100% |
A0DTY1 | Paramecium tetraurelia | 35% | 100% |
A3A8W2 | Oryza sativa subsp. japonica | 30% | 100% |
A3A8W6 | Oryza sativa subsp. japonica | 26% | 70% |
A4H7Y6 | Leishmania braziliensis | 80% | 100% |
A4HAW6 | Leishmania braziliensis | 28% | 90% |
A4HE10 | Leishmania braziliensis | 29% | 100% |
A4HG10 | Leishmania braziliensis | 41% | 100% |
A4HHY5 | Leishmania braziliensis | 31% | 100% |
A4HKF6 | Leishmania braziliensis | 35% | 71% |
A4HNR1 | Leishmania braziliensis | 40% | 100% |
A4HWB4 | Leishmania infantum | 100% | 100% |
A4I1B7 | Leishmania infantum | 30% | 100% |
A4I329 | Leishmania infantum | 41% | 100% |
A4I565 | Leishmania infantum | 31% | 100% |
A4I7Y4 | Leishmania infantum | 36% | 72% |
A4IA26 | Leishmania infantum | 29% | 90% |
A4ICT4 | Leishmania infantum | 41% | 100% |
A5PJZ2 | Bos taurus | 32% | 100% |
C9ZJK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZMJ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZNW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 95% |
D0A2L9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9ACV0 | Leishmania major | 41% | 100% |
E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9ASH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AZD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 72% |
E9B541 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
O62829 | Bos taurus | 35% | 100% |
O62830 | Bos taurus | 37% | 83% |
O75688 | Homo sapiens | 37% | 84% |
O81716 | Arabidopsis thaliana | 32% | 100% |
P20650 | Rattus norvegicus | 35% | 100% |
P34221 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 86% |
P35182 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P35813 | Homo sapiens | 35% | 100% |
P35814 | Oryctolagus cuniculus | 35% | 100% |
P35815 | Rattus norvegicus | 37% | 100% |
P36982 | Leishmania chagasi | 30% | 100% |
P36993 | Mus musculus | 37% | 100% |
P38089 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P39966 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 87% |
P49443 | Mus musculus | 35% | 100% |
P49444 | Paramecium tetraurelia | 34% | 100% |
P49593 | Homo sapiens | 30% | 89% |
P49594 | Caenorhabditis elegans | 25% | 90% |
P49596 | Caenorhabditis elegans | 39% | 100% |
P49599 | Arabidopsis thaliana | 28% | 100% |
Q09172 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 100% |
Q09173 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 98% |
Q0IIF0 | Bos taurus | 31% | 100% |
Q0J2L7 | Oryza sativa subsp. japonica | 33% | 100% |
Q0JL75 | Oryza sativa subsp. japonica | 32% | 100% |
Q0JLP9 | Oryza sativa subsp. japonica | 33% | 87% |
Q10MN6 | Oryza sativa subsp. japonica | 29% | 94% |
Q10MX1 | Oryza sativa subsp. japonica | 30% | 100% |
Q19775 | Caenorhabditis elegans | 35% | 86% |
Q2QWE3 | Oryza sativa subsp. japonica | 27% | 96% |
Q2R637 | Oryza sativa subsp. japonica | 29% | 94% |
Q4Q225 | Leishmania major | 38% | 100% |
Q4Q2U5 | Leishmania major | 29% | 90% |
Q4Q5B1 | Leishmania major | 36% | 72% |
Q4Q7S1 | Leishmania major | 31% | 100% |
Q4QA19 | Leishmania major | 31% | 100% |
Q4QFG7 | Leishmania major | 95% | 100% |
Q53Q11 | Oryza sativa subsp. japonica | 30% | 100% |
Q5SGD2 | Homo sapiens | 32% | 100% |
Q5SMK6 | Oryza sativa subsp. japonica | 28% | 100% |
Q5SN75 | Oryza sativa subsp. japonica | 30% | 100% |
Q5Z6F5 | Oryza sativa subsp. japonica | 31% | 100% |
Q653S3 | Oryza sativa subsp. japonica | 32% | 100% |
Q65XG6 | Oryza sativa subsp. japonica | 33% | 97% |
Q67UP9 | Oryza sativa subsp. japonica | 33% | 100% |
Q67UX7 | Oryza sativa subsp. japonica | 32% | 100% |
Q69QZ0 | Oryza sativa subsp. japonica | 28% | 100% |
Q6AUQ4 | Oryza sativa subsp. japonica | 30% | 100% |
Q6ETK3 | Oryza sativa subsp. japonica | 33% | 100% |
Q6K1U4 | Oryza sativa subsp. japonica | 26% | 78% |
Q6K5I0 | Oryza sativa subsp. japonica | 26% | 78% |
Q6L4R7 | Oryza sativa subsp. japonica | 31% | 91% |
Q6L5H6 | Oryza sativa subsp. japonica | 33% | 100% |
Q6NKS1 | Arabidopsis thaliana | 29% | 100% |
Q7XJ53 | Arabidopsis thaliana | 27% | 100% |
Q7XU84 | Oryza sativa subsp. japonica | 31% | 100% |
Q8BHN0 | Mus musculus | 32% | 100% |
Q8CGA0 | Mus musculus | 30% | 89% |
Q8LAY8 | Arabidopsis thaliana | 31% | 100% |
Q8N819 | Homo sapiens | 34% | 94% |
Q8R0F6 | Mus musculus | 31% | 100% |
Q93YS2 | Arabidopsis thaliana | 24% | 77% |
Q9CAJ0 | Arabidopsis thaliana | 32% | 79% |
Q9FYN7 | Oryza sativa subsp. japonica | 31% | 100% |
Q9H0C8 | Homo sapiens | 31% | 100% |
Q9LNF4 | Arabidopsis thaliana | 29% | 100% |
Q9LNP9 | Arabidopsis thaliana | 31% | 79% |
Q9M1V8 | Arabidopsis thaliana | 24% | 96% |
Q9SZ53 | Arabidopsis thaliana | 33% | 100% |
Q9WVR7 | Rattus norvegicus | 31% | 90% |
Q9Z1Z6 | Rattus norvegicus | 31% | 100% |
V5BA03 | Trypanosoma cruzi | 41% | 100% |
V5BCX6 | Trypanosoma cruzi | 35% | 100% |
V5BH00 | Trypanosoma cruzi | 32% | 100% |
V5DCR6 | Trypanosoma cruzi | 51% | 98% |