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: 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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S7X808
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016311 | dephosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 11 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016791 | phosphatase activity | 5 | 11 |
GO:0017018 | myosin phosphatase activity | 5 | 10 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.602 |
DEG_APCC_DBOX_1 | 204 | 212 | PF00400 | 0.496 |
DEG_COP1_1 | 430 | 438 | PF00400 | 0.601 |
DEG_SPOP_SBC_1 | 439 | 443 | PF00917 | 0.533 |
DOC_MAPK_DCC_7 | 43 | 53 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 154 | 161 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 45 | 53 | PF00069 | 0.650 |
DOC_MAPK_JIP1_4 | 279 | 285 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 45 | 53 | PF00069 | 0.622 |
DOC_PP1_SILK_1 | 39 | 44 | PF00149 | 0.602 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.675 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.814 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.578 |
DOC_USP7_MATH_2 | 2 | 8 | PF00917 | 0.584 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.643 |
LIG_14-3-3_CanoR_1 | 138 | 147 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 149 | 154 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 172 | 176 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 357 | 365 | PF00244 | 0.356 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.601 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.331 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.331 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.558 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.651 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.311 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.356 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.311 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.470 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.553 |
LIG_GBD_Chelix_1 | 254 | 262 | PF00786 | 0.331 |
LIG_LIR_Gen_1 | 156 | 165 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 361 | 372 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 377 | 384 | PF02991 | 0.275 |
LIG_LIR_LC3C_4 | 259 | 264 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.275 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 378 | 382 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.396 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.547 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.669 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.659 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.396 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.708 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.644 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.538 |
LIG_SUMO_SIM_par_1 | 279 | 284 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 345 | 354 | PF11976 | 0.396 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.331 |
MOD_CDC14_SPxK_1 | 79 | 82 | PF00782 | 0.643 |
MOD_CDK_SPK_2 | 17 | 22 | PF00069 | 0.671 |
MOD_CDK_SPxK_1 | 76 | 82 | PF00069 | 0.658 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.667 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.588 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.327 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.540 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.690 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.627 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.729 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.321 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.302 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.331 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.344 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.452 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.576 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.618 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.649 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.634 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.394 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.648 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.570 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.396 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.716 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.659 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.715 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.539 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.690 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.357 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.396 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.345 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.564 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.685 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.741 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.575 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.348 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.448 |
MOD_N-GLC_1 | 445 | 450 | PF02516 | 0.632 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.649 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.599 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.396 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.331 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.277 |
MOD_PK_1 | 298 | 304 | PF00069 | 0.321 |
MOD_PK_1 | 37 | 43 | PF00069 | 0.647 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.647 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.618 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.497 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.498 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.583 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.296 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.449 |
MOD_Plk_2-3 | 374 | 380 | PF00069 | 0.396 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.367 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.706 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.555 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.665 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.786 |
TRG_DiLeu_BaEn_1 | 361 | 366 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.331 |
TRG_NES_CRM1_1 | 202 | 217 | PF08389 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8W9 | Leptomonas seymouri | 74% | 100% |
A0A0S4ILP4 | Bodo saltans | 23% | 86% |
A0A3Q8IEK6 | Leishmania donovani | 32% | 100% |
A0A3Q8IFG7 | Leishmania donovani | 29% | 100% |
A0A3Q8IK65 | Leishmania donovani | 31% | 100% |
A0A3Q8IL63 | Leishmania donovani | 42% | 100% |
A0A3S7WTA2 | Leishmania donovani | 29% | 100% |
A3A8W6 | Oryza sativa subsp. japonica | 25% | 78% |
A4H7Y6 | Leishmania braziliensis | 32% | 100% |
A4HAW5 | Leishmania braziliensis | 49% | 100% |
A4HAW6 | Leishmania braziliensis | 88% | 100% |
A4HG10 | Leishmania braziliensis | 31% | 100% |
A4HHY5 | Leishmania braziliensis | 29% | 100% |
A4HNR1 | Leishmania braziliensis | 32% | 100% |
A4HWB4 | Leishmania infantum | 30% | 100% |
A4I329 | Leishmania infantum | 32% | 100% |
A4I565 | Leishmania infantum | 29% | 100% |
A4IA25 | Leishmania infantum | 42% | 100% |
A4IA26 | Leishmania infantum | 100% | 100% |
A4ICT4 | Leishmania infantum | 31% | 100% |
D0AA51 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ACV0 | Leishmania major | 32% | 100% |
E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ASH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AZD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
O81716 | Arabidopsis thaliana | 31% | 100% |
O81760 | Arabidopsis thaliana | 22% | 100% |
P38089 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
P39966 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 97% |
P49597 | Arabidopsis thaliana | 29% | 100% |
P49599 | Arabidopsis thaliana | 28% | 100% |
Q0IIF0 | Bos taurus | 29% | 100% |
Q0J2L7 | Oryza sativa subsp. japonica | 31% | 100% |
Q3EAF9 | Arabidopsis thaliana | 32% | 100% |
Q4Q225 | Leishmania major | 32% | 100% |
Q4Q2U5 | Leishmania major | 97% | 100% |
Q4Q2U6 | Leishmania major | 49% | 100% |
Q4Q7S1 | Leishmania major | 28% | 100% |
Q4QFG7 | Leishmania major | 28% | 100% |
Q5JKN1 | Oryza sativa subsp. japonica | 28% | 100% |
Q5MFV5 | Oryza sativa subsp. indica | 26% | 100% |
Q5N9N2 | Oryza sativa subsp. japonica | 29% | 100% |
Q5SN75 | Oryza sativa subsp. japonica | 30% | 100% |
Q653S3 | Oryza sativa subsp. japonica | 30% | 100% |
Q65XK7 | Oryza sativa subsp. japonica | 30% | 100% |
Q67UP9 | Oryza sativa subsp. japonica | 28% | 100% |
Q6AUQ4 | Oryza sativa subsp. japonica | 31% | 100% |
Q6ETK3 | Oryza sativa subsp. japonica | 28% | 100% |
Q6K1U4 | Oryza sativa subsp. japonica | 27% | 87% |
Q6K5I0 | Oryza sativa subsp. japonica | 29% | 87% |
Q6NKS1 | Arabidopsis thaliana | 26% | 100% |
Q7XHN8 | Oryza sativa subsp. japonica | 29% | 100% |
Q7XU84 | Oryza sativa subsp. japonica | 34% | 100% |
Q94H98 | Oryza sativa subsp. japonica | 26% | 100% |
Q9CAJ0 | Arabidopsis thaliana | 32% | 88% |
Q9FG61 | Arabidopsis thaliana | 25% | 100% |
Q9FLI3 | Arabidopsis thaliana | 27% | 100% |
Q9H0C8 | Homo sapiens | 28% | 100% |
Q9LNP9 | Arabidopsis thaliana | 30% | 88% |
Q9LUS8 | Arabidopsis thaliana | 25% | 91% |
Q9SLA1 | Arabidopsis thaliana | 36% | 100% |
Q9SZ53 | Arabidopsis thaliana | 31% | 100% |
Q9ZW21 | Arabidopsis thaliana | 31% | 100% |