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: 1 |
Forrest at al. (metacyclic) | no | yes: 1 |
Forrest at al. (procyclic) | no | yes: 3 |
Silverman et al. | no | yes: 1 |
Pissara et al. | no | yes: 7 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 3 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 3 |
GO:0099568 | cytoplasmic region | 3 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005654 | nucleoplasm | 2 | 1 |
Related structures:
AlphaFold database: Q4Q7S1
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0035970 | peptidyl-threonine dephosphorylation | 6 | 3 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 27 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 27 |
GO:0016787 | hydrolase activity | 2 | 27 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 27 |
GO:0016791 | phosphatase activity | 5 | 27 |
GO:0017018 | myosin phosphatase activity | 5 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 27 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 27 |
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.394 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.302 |
DOC_MAPK_DCC_7 | 196 | 205 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 116 | 123 | PF00069 | 0.266 |
DOC_MAPK_gen_1 | 190 | 200 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 116 | 123 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.270 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.498 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.395 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.271 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.250 |
LIG_deltaCOP1_diTrp_1 | 355 | 361 | PF00928 | 0.358 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.270 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.253 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.372 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.514 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.158 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.421 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.405 |
LIG_LIR_LC3C_4 | 267 | 271 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.387 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.250 |
LIG_REV1ctd_RIR_1 | 358 | 364 | PF16727 | 0.427 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.316 |
LIG_SH2_SRC | 149 | 152 | PF00017 | 0.191 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.352 |
LIG_SH2_STAT3 | 192 | 195 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.294 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.348 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.349 |
LIG_SUMO_SIM_anti_2 | 202 | 207 | PF11976 | 0.341 |
LIG_SUMO_SIM_anti_2 | 244 | 250 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 196 | 202 | PF11976 | 0.257 |
LIG_TYR_ITIM | 50 | 55 | PF00017 | 0.394 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.394 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.424 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.456 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.408 |
MOD_GlcNHglycan | 63 | 67 | PF01048 | 0.335 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.427 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.583 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.306 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.300 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.394 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.283 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.557 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.438 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.469 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.263 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.384 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.317 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.283 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.235 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.275 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.309 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.300 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.514 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.375 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.394 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.369 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.413 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.403 |
MOD_SUMO_rev_2 | 144 | 148 | PF00179 | 0.289 |
TRG_DiLeu_BaEn_2 | 208 | 214 | PF01217 | 0.203 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.394 |
TRG_NES_CRM1_1 | 81 | 97 | PF08389 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C7 | Leptomonas seymouri | 31% | 97% |
A0A0N1I8W9 | Leptomonas seymouri | 29% | 88% |
A0A0N1IHU6 | Leptomonas seymouri | 44% | 94% |
A0A0N1PAL8 | Leptomonas seymouri | 86% | 100% |
A0A0N1PEL9 | Leptomonas seymouri | 30% | 100% |
A0A0S4IY95 | Bodo saltans | 32% | 100% |
A0A0S4J0A6 | Bodo saltans | 41% | 94% |
A0A0S4J8Y7 | Bodo saltans | 34% | 74% |
A0A0S4JHB4 | Bodo saltans | 54% | 100% |
A0A0S4JPC3 | Bodo saltans | 34% | 100% |
A0A0S4JPM8 | Bodo saltans | 33% | 100% |
A0A1X0NRG3 | Trypanosomatidae | 31% | 100% |
A0A1X0NUB7 | Trypanosomatidae | 32% | 80% |
A0A1X0NVC4 | Trypanosomatidae | 33% | 93% |
A0A1X0P2A0 | Trypanosomatidae | 56% | 100% |
A0A1X0P568 | Trypanosomatidae | 40% | 94% |
A0A1X0P991 | Trypanosomatidae | 33% | 100% |
A0A1X0PAN4 | Trypanosomatidae | 31% | 100% |
A0A3Q8IEK6 | Leishmania donovani | 33% | 100% |
A0A3Q8IFG7 | Leishmania donovani | 98% | 100% |
A0A3Q8IGS1 | Leishmania donovani | 31% | 68% |
A0A3Q8IK65 | Leishmania donovani | 38% | 100% |
A0A3Q8IL63 | Leishmania donovani | 30% | 98% |
A0A3S7WTA2 | Leishmania donovani | 31% | 95% |
A0A3S7WZ14 | Leishmania donovani | 45% | 95% |
A0A3S7X808 | Leishmania donovani | 28% | 85% |
A0A422N8D7 | Trypanosoma rangeli | 28% | 100% |
A0A422NAJ1 | Trypanosoma rangeli | 30% | 100% |
A0A422NBV9 | Trypanosoma rangeli | 41% | 94% |
A0A422NL94 | Trypanosoma rangeli | 31% | 88% |
A0A422NML6 | Trypanosoma rangeli | 56% | 100% |
A0A422NS77 | Trypanosoma rangeli | 35% | 93% |
A0A422P293 | Trypanosoma rangeli | 33% | 100% |
A0CUB5 | Paramecium tetraurelia | 30% | 100% |
A0DSB3 | Paramecium tetraurelia | 30% | 100% |
A0DTY1 | Paramecium tetraurelia | 30% | 100% |
A3A8W2 | Oryza sativa subsp. japonica | 29% | 100% |
A3A8W6 | Oryza sativa subsp. japonica | 25% | 66% |
A3CCP9 | Oryza sativa subsp. japonica | 26% | 77% |
A4H7Y6 | Leishmania braziliensis | 32% | 95% |
A4HAW5 | Leishmania braziliensis | 32% | 97% |
A4HAW6 | Leishmania braziliensis | 29% | 85% |
A4HE10 | Leishmania braziliensis | 44% | 95% |
A4HG10 | Leishmania braziliensis | 32% | 100% |
A4HHY5 | Leishmania braziliensis | 92% | 100% |
A4HKF6 | Leishmania braziliensis | 31% | 68% |
A4HNR1 | Leishmania braziliensis | 36% | 100% |
A4HWB4 | Leishmania infantum | 31% | 95% |
A4I1B7 | Leishmania infantum | 45% | 95% |
A4I329 | Leishmania infantum | 33% | 100% |
A4I565 | Leishmania infantum | 98% | 100% |
A4I7Y4 | Leishmania infantum | 31% | 68% |
A4IA25 | Leishmania infantum | 30% | 98% |
A4IA26 | Leishmania infantum | 28% | 85% |
A4ICT4 | Leishmania infantum | 37% | 100% |
A5PJZ2 | Bos taurus | 32% | 100% |
C9ZJK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZMJ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZNW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 90% |
C9ZQJ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
D0A2L9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
D0A5L0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 94% |
D0AA51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 90% |
E9ACV0 | Leishmania major | 31% | 100% |
E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 95% |
E9ASH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 95% |
E9AZD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 68% |
E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 98% |
E9B541 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
O04719 | Arabidopsis thaliana | 30% | 91% |
O62829 | Bos taurus | 34% | 100% |
O62830 | Bos taurus | 33% | 79% |
O75688 | Homo sapiens | 32% | 80% |
O80492 | Arabidopsis thaliana | 28% | 90% |
O80871 | Arabidopsis thaliana | 27% | 97% |
P20650 | Rattus norvegicus | 34% | 100% |
P34221 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 82% |
P35182 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P35813 | Homo sapiens | 34% | 100% |
P35814 | Oryctolagus cuniculus | 34% | 100% |
P35815 | Rattus norvegicus | 33% | 98% |
P36982 | Leishmania chagasi | 45% | 95% |
P36993 | Mus musculus | 32% | 98% |
P38089 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 98% |
P40371 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
P49443 | Mus musculus | 34% | 100% |
P49593 | Homo sapiens | 29% | 85% |
P49596 | Caenorhabditis elegans | 34% | 100% |
P49597 | Arabidopsis thaliana | 29% | 88% |
P49599 | Arabidopsis thaliana | 28% | 99% |
P93006 | Arabidopsis thaliana | 27% | 100% |
Q0DBU3 | Oryza sativa subsp. japonica | 31% | 100% |
Q0IIF0 | Bos taurus | 32% | 100% |
Q0J2L7 | Oryza sativa subsp. japonica | 33% | 100% |
Q0J2R1 | Oryza sativa subsp. japonica | 34% | 100% |
Q0JL75 | Oryza sativa subsp. japonica | 32% | 100% |
Q0JLP9 | Oryza sativa subsp. japonica | 29% | 82% |
Q10MN6 | Oryza sativa subsp. japonica | 27% | 89% |
Q10MX1 | Oryza sativa subsp. japonica | 30% | 98% |
Q19775 | Caenorhabditis elegans | 33% | 82% |
Q2PC20 | Bos taurus | 31% | 100% |
Q2QWE3 | Oryza sativa subsp. japonica | 28% | 91% |
Q2R637 | Oryza sativa subsp. japonica | 27% | 89% |
Q3EAF9 | Arabidopsis thaliana | 28% | 100% |
Q4PSE8 | Arabidopsis thaliana | 36% | 86% |
Q4Q225 | Leishmania major | 38% | 100% |
Q4Q2U5 | Leishmania major | 28% | 85% |
Q4Q2U6 | Leishmania major | 30% | 100% |
Q4Q5B1 | Leishmania major | 31% | 68% |
Q4QA19 | Leishmania major | 45% | 100% |
Q4QFG7 | Leishmania major | 31% | 95% |
Q53Q11 | Oryza sativa subsp. japonica | 31% | 97% |
Q5JKN1 | Oryza sativa subsp. japonica | 28% | 99% |
Q5N9N2 | Oryza sativa subsp. japonica | 31% | 93% |
Q5SGD2 | Homo sapiens | 34% | 100% |
Q5SMK6 | Oryza sativa subsp. japonica | 27% | 100% |
Q5Z6F5 | Oryza sativa subsp. japonica | 35% | 100% |
Q652Z7 | Oryza sativa subsp. japonica | 30% | 100% |
Q653S3 | Oryza sativa subsp. japonica | 28% | 100% |
Q65XK7 | Oryza sativa subsp. japonica | 27% | 100% |
Q67J17 | Oryza sativa subsp. japonica | 25% | 91% |
Q67UX7 | Oryza sativa subsp. japonica | 35% | 100% |
Q69QZ0 | Oryza sativa subsp. japonica | 28% | 100% |
Q69VD9 | Oryza sativa subsp. japonica | 28% | 100% |
Q6AUQ4 | Oryza sativa subsp. japonica | 27% | 99% |
Q6EN45 | Oryza sativa subsp. japonica | 33% | 100% |
Q6ING9 | Xenopus laevis | 30% | 100% |
Q6K1U4 | Oryza sativa subsp. japonica | 24% | 74% |
Q6K5I0 | Oryza sativa subsp. japonica | 24% | 74% |
Q6L4R7 | Oryza sativa subsp. japonica | 28% | 86% |
Q6L5C4 | Oryza sativa subsp. japonica | 33% | 78% |
Q6L5H6 | Oryza sativa subsp. japonica | 29% | 99% |
Q6YTI2 | Oryza sativa subsp. japonica | 24% | 87% |
Q6ZKL8 | Oryza sativa subsp. japonica | 28% | 72% |
Q7XJ53 | Arabidopsis thaliana | 25% | 100% |
Q7XR06 | Oryza sativa subsp. japonica | 33% | 100% |
Q7XU84 | Oryza sativa subsp. japonica | 30% | 100% |
Q8BGL1 | Mus musculus | 32% | 95% |
Q8BHN0 | Mus musculus | 34% | 100% |
Q8BXN7 | Mus musculus | 32% | 100% |
Q8CGA0 | Mus musculus | 29% | 85% |
Q8LAY8 | Arabidopsis thaliana | 37% | 100% |
Q8N3J5 | Homo sapiens | 32% | 100% |
Q8N819 | Homo sapiens | 33% | 89% |
Q8R0F6 | Mus musculus | 32% | 98% |
Q8RX37 | Arabidopsis thaliana | 27% | 100% |
Q8RXV3 | Arabidopsis thaliana | 34% | 100% |
Q8VZN9 | Arabidopsis thaliana | 34% | 100% |
Q93YS2 | Arabidopsis thaliana | 27% | 73% |
Q9FX08 | Arabidopsis thaliana | 25% | 90% |
Q9FYN7 | Oryza sativa subsp. japonica | 28% | 100% |
Q9H0C8 | Homo sapiens | 32% | 98% |
Q9LME4 | Arabidopsis thaliana | 31% | 100% |
Q9LMT1 | Arabidopsis thaliana | 30% | 100% |
Q9LNF4 | Arabidopsis thaliana | 28% | 100% |
Q9LNP9 | Arabidopsis thaliana | 27% | 75% |
Q9LR65 | Arabidopsis thaliana | 27% | 83% |
Q9LUU7 | Arabidopsis thaliana | 29% | 91% |
Q9M9C6 | Arabidopsis thaliana | 30% | 88% |
Q9M9W9 | Arabidopsis thaliana | 31% | 100% |
Q9S9Z7 | Arabidopsis thaliana | 32% | 100% |
Q9SD02 | Arabidopsis thaliana | 28% | 100% |
Q9SLA1 | Arabidopsis thaliana | 28% | 98% |
Q9WVR7 | Rattus norvegicus | 29% | 85% |
Q9XEE8 | Arabidopsis thaliana | 28% | 98% |
Q9Z1Z6 | Rattus norvegicus | 32% | 98% |
V5AZJ4 | Trypanosoma cruzi | 30% | 97% |
V5BA03 | Trypanosoma cruzi | 33% | 100% |
V5BCX6 | Trypanosoma cruzi | 32% | 100% |
V5BH00 | Trypanosoma cruzi | 57% | 100% |
V5BSS7 | Trypanosoma cruzi | 41% | 94% |
V5DCR6 | Trypanosoma cruzi | 34% | 93% |