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 Uncharacterized
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: 2 |
Silverman et al. | no | yes: 1 |
Pissara et al. | no | yes: 10 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0005654 | nucleoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4I7Y4
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 16 |
GO:0006793 | phosphorus metabolic process | 3 | 16 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016311 | dephosphorylation | 5 | 16 |
GO:0019538 | protein metabolic process | 3 | 16 |
GO:0036211 | protein modification process | 4 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043412 | macromolecule modification | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
GO:0035970 | peptidyl-threonine dephosphorylation | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 23 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 23 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 23 |
GO:0016787 | hydrolase activity | 2 | 23 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 23 |
GO:0016791 | phosphatase activity | 5 | 23 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 23 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 23 |
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0017018 | myosin phosphatase activity | 5 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.275 |
CLV_C14_Caspase3-7 | 519 | 523 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.414 |
CLV_PCSK_FUR_1 | 43 | 47 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.298 |
CLV_Separin_Metazoa | 109 | 113 | PF03568 | 0.374 |
DEG_APCC_DBOX_1 | 356 | 364 | PF00400 | 0.251 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.301 |
DOC_CKS1_1 | 451 | 456 | PF01111 | 0.499 |
DOC_MAPK_gen_1 | 281 | 289 | PF00069 | 0.213 |
DOC_MAPK_gen_1 | 351 | 360 | PF00069 | 0.238 |
DOC_MAPK_MEF2A_6 | 51 | 59 | PF00069 | 0.537 |
DOC_PP2B_LxvP_1 | 6 | 9 | PF13499 | 0.399 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.251 |
DOC_PP4_MxPP_1 | 412 | 415 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.213 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.222 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.246 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.547 |
LIG_14-3-3_CanoR_1 | 145 | 149 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.372 |
LIG_APCC_ABBA_1 | 226 | 231 | PF00400 | 0.251 |
LIG_Clathr_ClatBox_1 | 154 | 158 | PF01394 | 0.251 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.451 |
LIG_EH1_1 | 47 | 55 | PF00400 | 0.289 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.254 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.529 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.653 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.393 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.317 |
LIG_LIR_Apic_2 | 348 | 352 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.328 |
LIG_PCNA_yPIPBox_3 | 273 | 287 | PF02747 | 0.251 |
LIG_PCNA_yPIPBox_3 | 31 | 45 | PF02747 | 0.389 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.333 |
LIG_SH2_SRC | 211 | 214 | PF00017 | 0.245 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.175 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.251 |
LIG_SH2_STAT3 | 26 | 29 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.215 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.345 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.256 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.752 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.516 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 153 | 158 | PF11976 | 0.244 |
LIG_SUMO_SIM_anti_2 | 385 | 390 | PF11976 | 0.299 |
LIG_SUMO_SIM_anti_2 | 58 | 63 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 152 | 158 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 285 | 290 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 57 | 63 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 72 | 77 | PF11976 | 0.257 |
LIG_UBA3_1 | 1 | 5 | PF00899 | 0.452 |
LIG_UBA3_1 | 154 | 159 | PF00899 | 0.251 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.238 |
LIG_WW_3 | 413 | 417 | PF00397 | 0.442 |
LIG_WW_3 | 7 | 11 | PF00397 | 0.438 |
MOD_CDK_SPK_2 | 487 | 492 | PF00069 | 0.515 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.282 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.529 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.473 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.592 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.494 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.495 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.296 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.371 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.259 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.385 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.318 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.529 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.502 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.748 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.586 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.681 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.503 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.520 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.307 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.535 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.535 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.613 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.693 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.531 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.542 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.605 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.747 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.222 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.357 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.552 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.517 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.320 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.776 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.292 |
MOD_NEK2_2 | 538 | 543 | PF00069 | 0.513 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.364 |
MOD_PK_1 | 249 | 255 | PF00069 | 0.222 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.359 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.254 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.424 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.552 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.357 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.643 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.277 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.290 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.295 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.456 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.246 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.568 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.561 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.583 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.545 |
MOD_SUMO_for_1 | 193 | 196 | PF00179 | 0.229 |
MOD_SUMO_rev_2 | 254 | 263 | PF00179 | 0.302 |
MOD_SUMO_rev_2 | 476 | 486 | PF00179 | 0.561 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.216 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.213 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.226 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.213 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.213 |
TRG_Pf-PMV_PEXEL_1 | 36 | 40 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PET0 | Leptomonas seymouri | 73% | 97% |
A0A3Q8IFG7 | Leishmania donovani | 30% | 100% |
A0A3Q8IGS1 | Leishmania donovani | 100% | 100% |
A0A3Q8IL63 | Leishmania donovani | 29% | 100% |
A0A3S7WTA2 | Leishmania donovani | 36% | 100% |
A0A3S7WZ14 | Leishmania donovani | 32% | 100% |
A4H7Y6 | Leishmania braziliensis | 36% | 100% |
A4HAW5 | Leishmania braziliensis | 30% | 100% |
A4HE10 | Leishmania braziliensis | 31% | 100% |
A4HHY5 | Leishmania braziliensis | 28% | 100% |
A4HKF6 | Leishmania braziliensis | 78% | 100% |
A4HWB4 | Leishmania infantum | 36% | 100% |
A4I1B7 | Leishmania infantum | 32% | 100% |
A4I565 | Leishmania infantum | 31% | 100% |
A4IA25 | Leishmania infantum | 29% | 100% |
D0AA51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4Q2U6 | Leishmania major | 29% | 100% |
Q4Q5B1 | Leishmania major | 92% | 100% |
Q4Q7S1 | Leishmania major | 31% | 100% |
Q4QA19 | Leishmania major | 32% | 100% |
Q4QFG7 | Leishmania major | 35% | 100% |
Q6K5I0 | Oryza sativa subsp. japonica | 30% | 100% |
Q9CAJ0 | Arabidopsis thaliana | 29% | 100% |