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.
Phosphatase, phosphatase 2C
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. | yes | 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: A4HWB4
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:0042578 | phosphoric ester hydrolase activity | 4 | 24 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 24 |
GO:0017018 | myosin phosphatase activity | 5 | 4 |
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 | 330 | 334 | PF00656 | 0.405 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.362 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 6 | 8 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.313 |
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 | 0.299 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.515 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.559 |
DOC_CKS1_1 | 195 | 200 | PF01111 | 0.311 |
DOC_MAPK_DCC_7 | 359 | 369 | PF00069 | 0.186 |
DOC_MAPK_gen_1 | 359 | 369 | PF00069 | 0.215 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.413 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.226 |
DOC_PP2B_PxIxI_1 | 364 | 370 | PF00149 | 0.186 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.437 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.305 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.577 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.249 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.253 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.352 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.534 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.655 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.308 |
LIG_LIR_Apic_2 | 193 | 198 | PF02991 | 0.226 |
LIG_LIR_Apic_2 | 234 | 239 | PF02991 | 0.226 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.482 |
LIG_NRBOX | 99 | 105 | PF00104 | 0.489 |
LIG_PCNA_yPIPBox_3 | 94 | 108 | PF02747 | 0.463 |
LIG_Pex14_2 | 208 | 212 | PF04695 | 0.336 |
LIG_PTB_Apo_2 | 127 | 134 | PF02174 | 0.400 |
LIG_PTB_Apo_2 | 151 | 158 | PF02174 | 0.249 |
LIG_RPA_C_Fungi | 89 | 101 | PF08784 | 0.402 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.338 |
LIG_SH2_PTP2 | 236 | 239 | PF00017 | 0.416 |
LIG_SH2_PTP2 | 335 | 338 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.416 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.364 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.249 |
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 | 0.390 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.336 |
LIG_UBA3_1 | 352 | 360 | PF00899 | 0.416 |
LIG_UBA3_1 | 399 | 404 | PF00899 | 0.364 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.347 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.515 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.469 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.340 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.302 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.299 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.403 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.597 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.349 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.277 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.266 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.350 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.404 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.507 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.477 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.487 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.432 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.274 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.448 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.428 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.469 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.608 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.343 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.579 |
MOD_N-GLC_2 | 182 | 184 | PF02516 | 0.215 |
MOD_N-GLC_2 | 375 | 377 | PF02516 | 0.453 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.313 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.565 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.393 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.577 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.627 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.342 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.332 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.303 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.342 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.311 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.328 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.457 |
MOD_SUMO_rev_2 | 264 | 269 | PF00179 | 0.309 |
MOD_SUMO_rev_2 | 354 | 361 | PF00179 | 0.226 |
TRG_DiLeu_BaEn_1 | 148 | 153 | PF01217 | 0.328 |
TRG_DiLeu_BaEn_3 | 350 | 356 | PF01217 | 0.407 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.416 |
TRG_NLS_MonoExtC_3 | 71 | 77 | PF00514 | 0.587 |
TRG_NLS_MonoExtN_4 | 4 | 10 | PF00514 | 0.722 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C7 | Leptomonas seymouri | 71% | 100% |
A0A0N0P8F8 | Leptomonas seymouri | 39% | 100% |
A0A0N1I0H9 | Leptomonas seymouri | 40% | 100% |
A0A0N1I8W9 | Leptomonas seymouri | 30% | 93% |
A0A0N1IHU6 | Leptomonas seymouri | 30% | 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 | 41% | 100% |
A0A1X0PAN4 | Trypanosomatidae | 28% | 100% |
A0A3Q8IEK6 | Leishmania donovani | 42% | 100% |
A0A3Q8IFG7 | Leishmania donovani | 31% | 100% |
A0A3Q8IGS1 | Leishmania donovani | 36% | 72% |
A0A3Q8IK65 | Leishmania donovani | 41% | 100% |
A0A3S7WTA2 | Leishmania donovani | 100% | 100% |
A0A3S7WZ14 | Leishmania donovani | 30% | 100% |
A0A3S7X808 | Leishmania donovani | 30% | 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 | 33% | 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 | 42% | 100% |
A4HHY5 | Leishmania braziliensis | 31% | 100% |
A4HKF6 | Leishmania braziliensis | 36% | 71% |
A4HNR1 | Leishmania braziliensis | 40% | 100% |
A4I1B7 | Leishmania infantum | 30% | 100% |
A4I329 | Leishmania infantum | 42% | 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 | 42% | 100% |
E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9ASH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AZD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 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 | 33% | 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 | 38% | 100% |
P36982 | Leishmania chagasi | 30% | 100% |
P36993 | Mus musculus | 38% | 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 | 35% | 100% |
P49593 | Homo sapiens | 30% | 89% |
P49594 | Caenorhabditis elegans | 26% | 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 | 28% | 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 | 30% | 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 | 34% | 100% |
Q67UX7 | Oryza sativa subsp. japonica | 32% | 100% |
Q69QZ0 | Oryza sativa subsp. japonica | 29% | 100% |
Q6AUQ4 | Oryza sativa subsp. japonica | 31% | 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 | 30% | 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 | 30% | 100% |
Q9LNP9 | Arabidopsis thaliana | 31% | 79% |
Q9M1V8 | Arabidopsis thaliana | 25% | 96% |
Q9SZ53 | Arabidopsis thaliana | 33% | 100% |
Q9WVR7 | Rattus norvegicus | 31% | 90% |
Q9Z1Z6 | Rattus norvegicus | 31% | 100% |
V5BA03 | Trypanosoma cruzi | 42% | 100% |
V5BCX6 | Trypanosoma cruzi | 35% | 100% |
V5BH00 | Trypanosoma cruzi | 32% | 100% |
V5DCR6 | Trypanosoma cruzi | 51% | 98% |