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: 15 |
NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: A0A3Q8IL63
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 16 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 16 |
GO:0016791 | phosphatase activity | 5 | 16 |
GO:0017018 | myosin phosphatase activity | 5 | 13 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043169 | cation binding | 3 | 16 |
GO:0046872 | metal ion binding | 4 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.350 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.303 |
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.473 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.440 |
DEG_SPOP_SBC_1 | 91 | 95 | PF00917 | 0.465 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.693 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.712 |
DOC_CYCLIN_yCln2_LP_2 | 378 | 384 | PF00134 | 0.357 |
DOC_MAPK_gen_1 | 161 | 169 | PF00069 | 0.303 |
DOC_MAPK_HePTP_8 | 229 | 241 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.346 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.756 |
DOC_PP4_FxxP_1 | 85 | 88 | PF00568 | 0.578 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.661 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.611 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 179 | 189 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.545 |
LIG_Actin_WH2_2 | 160 | 177 | PF00022 | 0.253 |
LIG_Actin_WH2_2 | 351 | 366 | PF00022 | 0.346 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.617 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.399 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.589 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.390 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.364 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.749 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.654 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.349 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.576 |
LIG_GBD_Chelix_1 | 10 | 18 | PF00786 | 0.558 |
LIG_LIR_Apic_2 | 84 | 88 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 101 | 110 | PF02991 | 0.693 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 317 | 328 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 372 | 382 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 68 | 78 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 68 | 73 | PF02991 | 0.567 |
LIG_MLH1_MIPbox_1 | 100 | 104 | PF16413 | 0.511 |
LIG_MYND_1 | 270 | 274 | PF01753 | 0.372 |
LIG_PTB_Apo_2 | 42 | 49 | PF02174 | 0.546 |
LIG_SH2_CRK | 70 | 74 | PF00017 | 0.534 |
LIG_SH2_GRB2like | 295 | 298 | PF00017 | 0.303 |
LIG_SH2_GRB2like | 42 | 45 | PF00017 | 0.583 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.679 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.303 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.348 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.460 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.661 |
LIG_SUMO_SIM_anti_2 | 131 | 139 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 235 | 240 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 301 | 311 | PF11976 | 0.440 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.622 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.363 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.755 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.682 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.579 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.524 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.377 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.183 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.425 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.363 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.654 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.576 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.634 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.330 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.329 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.724 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.444 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.405 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.329 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.697 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.727 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.602 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.599 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.362 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.547 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.460 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.637 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.608 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.329 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.367 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.720 |
MOD_PKA_1 | 364 | 370 | PF00069 | 0.303 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.349 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.602 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.399 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.303 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.362 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.549 |
MOD_Plk_2-3 | 133 | 139 | PF00069 | 0.263 |
MOD_Plk_2-3 | 330 | 336 | PF00069 | 0.329 |
MOD_Plk_2-3 | 350 | 356 | PF00069 | 0.143 |
MOD_Plk_2-3 | 49 | 55 | PF00069 | 0.697 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.420 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.433 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.325 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.650 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.674 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.617 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.612 |
MOD_SUMO_for_1 | 290 | 293 | PF00179 | 0.303 |
TRG_DiLeu_BaEn_1 | 317 | 322 | PF01217 | 0.372 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F8 | Leptomonas seymouri | 29% | 100% |
A0A0N1I0H9 | Leptomonas seymouri | 30% | 100% |
A0A0N1I8W9 | Leptomonas seymouri | 48% | 90% |
A0A0N1IHU6 | Leptomonas seymouri | 30% | 96% |
A0A0N1PAL8 | Leptomonas seymouri | 31% | 100% |
A0A0N1PEL9 | Leptomonas seymouri | 63% | 100% |
A0A0N1PET0 | Leptomonas seymouri | 28% | 67% |
A0A0S4ILP4 | Bodo saltans | 25% | 75% |
A0A0S4IY95 | Bodo saltans | 28% | 100% |
A0A0S4J0A6 | Bodo saltans | 31% | 96% |
A0A0S4J8Y7 | Bodo saltans | 30% | 76% |
A0A0S4JHB4 | Bodo saltans | 30% | 100% |
A0A0S4JPC3 | Bodo saltans | 30% | 100% |
A0A0S4KIS4 | Bodo saltans | 29% | 86% |
A0A0S4KJV9 | Bodo saltans | 31% | 90% |
A0A1X0NRG3 | Trypanosomatidae | 30% | 100% |
A0A1X0NUB7 | Trypanosomatidae | 31% | 82% |
A0A1X0NVC4 | Trypanosomatidae | 28% | 95% |
A0A1X0P2A0 | Trypanosomatidae | 33% | 100% |
A0A1X0P568 | Trypanosomatidae | 29% | 96% |
A0A1X0PAN4 | Trypanosomatidae | 49% | 100% |
A0A3Q8IEK6 | Leishmania donovani | 29% | 100% |
A0A3Q8IFG7 | Leishmania donovani | 30% | 100% |
A0A3Q8IGS1 | Leishmania donovani | 29% | 69% |
A0A3Q8IK65 | Leishmania donovani | 31% | 100% |
A0A3S7WZ14 | Leishmania donovani | 28% | 96% |
A0A3S7X808 | Leishmania donovani | 42% | 87% |
A0A422N8D7 | Trypanosoma rangeli | 46% | 100% |
A0A422NAJ1 | Trypanosoma rangeli | 27% | 100% |
A0A422NBV9 | Trypanosoma rangeli | 30% | 96% |
A0A422NS77 | Trypanosoma rangeli | 29% | 95% |
A0A422P293 | Trypanosoma rangeli | 28% | 100% |
A0BLX0 | Paramecium tetraurelia | 30% | 100% |
A0BQL0 | Paramecium tetraurelia | 28% | 100% |
A0CUB5 | Paramecium tetraurelia | 27% | 100% |
A0DSB3 | Paramecium tetraurelia | 26% | 100% |
A0DTY1 | Paramecium tetraurelia | 28% | 100% |
A3A8W2 | Oryza sativa subsp. japonica | 29% | 100% |
A4H7Y6 | Leishmania braziliensis | 26% | 100% |
A4HAW5 | Leishmania braziliensis | 85% | 100% |
A4HAW6 | Leishmania braziliensis | 48% | 87% |
A4HE10 | Leishmania braziliensis | 29% | 100% |
A4HG10 | Leishmania braziliensis | 27% | 100% |
A4HHY5 | Leishmania braziliensis | 29% | 100% |
A4HKF6 | Leishmania braziliensis | 28% | 69% |
A4HNR1 | Leishmania braziliensis | 31% | 98% |
A4I1B7 | Leishmania infantum | 28% | 100% |
A4I329 | Leishmania infantum | 29% | 100% |
A4I565 | Leishmania infantum | 30% | 100% |
A4I7Y4 | Leishmania infantum | 29% | 69% |
A4IA25 | Leishmania infantum | 100% | 100% |
A4IA26 | Leishmania infantum | 41% | 100% |
A4ICT4 | Leishmania infantum | 31% | 100% |
A5PJZ2 | Bos taurus | 32% | 100% |
C9ZJK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZMJ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
C9ZNW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 92% |
C9ZQJ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A2L9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A5L0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 96% |
E9ACV0 | Leishmania major | 29% | 100% |
E9ASH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AZD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 69% |
E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B541 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
O04719 | Arabidopsis thaliana | 29% | 92% |
O14189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 88% |
O62829 | Bos taurus | 29% | 100% |
O62830 | Bos taurus | 31% | 81% |
O75688 | Homo sapiens | 31% | 82% |
O80871 | Arabidopsis thaliana | 31% | 99% |
O81716 | Arabidopsis thaliana | 28% | 100% |
O81760 | Arabidopsis thaliana | 26% | 100% |
P20650 | Rattus norvegicus | 29% | 100% |
P35182 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
P35813 | Homo sapiens | 29% | 100% |
P35814 | Oryctolagus cuniculus | 29% | 100% |
P35815 | Rattus norvegicus | 30% | 100% |
P36982 | Leishmania chagasi | 28% | 96% |
P36993 | Mus musculus | 30% | 100% |
P38089 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 99% |
P40371 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P46014 | Arabidopsis thaliana | 25% | 67% |
P49443 | Mus musculus | 29% | 100% |
P49444 | Paramecium tetraurelia | 29% | 100% |
P49593 | Homo sapiens | 29% | 86% |
P49596 | Caenorhabditis elegans | 31% | 100% |
P49597 | Arabidopsis thaliana | 31% | 90% |
P49598 | Arabidopsis thaliana | 29% | 98% |
P49599 | Arabidopsis thaliana | 28% | 100% |
P93006 | Arabidopsis thaliana | 34% | 100% |
Q09173 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 94% |
Q0DBU3 | Oryza sativa subsp. japonica | 35% | 100% |
Q0IIF0 | Bos taurus | 27% | 100% |
Q0J2L7 | Oryza sativa subsp. japonica | 31% | 100% |
Q0J2R1 | Oryza sativa subsp. japonica | 31% | 100% |
Q0JL75 | Oryza sativa subsp. japonica | 32% | 100% |
Q0JLP9 | Oryza sativa subsp. japonica | 32% | 84% |
Q0V7V2 | Arabidopsis thaliana | 27% | 100% |
Q0WRB2 | Arabidopsis thaliana | 31% | 100% |
Q10MX1 | Oryza sativa subsp. japonica | 35% | 100% |
Q10S32 | Oryza sativa subsp. japonica | 26% | 98% |
Q19775 | Caenorhabditis elegans | 27% | 84% |
Q2PC20 | Bos taurus | 31% | 100% |
Q2QN36 | Oryza sativa subsp. japonica | 28% | 100% |
Q2QWE3 | Oryza sativa subsp. japonica | 32% | 93% |
Q2RBJ6 | Oryza sativa subsp. japonica | 27% | 93% |
Q3EAF9 | Arabidopsis thaliana | 30% | 100% |
Q4PSE8 | Arabidopsis thaliana | 36% | 87% |
Q4Q225 | Leishmania major | 30% | 100% |
Q4Q2U5 | Leishmania major | 45% | 100% |
Q4Q2U6 | Leishmania major | 94% | 100% |
Q4Q5B1 | Leishmania major | 29% | 69% |
Q4Q7S1 | Leishmania major | 30% | 100% |
Q4QA19 | Leishmania major | 29% | 100% |
Q4QFG7 | Leishmania major | 27% | 100% |
Q501F9 | Arabidopsis thaliana | 30% | 100% |
Q53Q11 | Oryza sativa subsp. japonica | 33% | 98% |
Q5JKN1 | Oryza sativa subsp. japonica | 30% | 100% |
Q5MFV5 | Oryza sativa subsp. indica | 30% | 100% |
Q5N9N2 | Oryza sativa subsp. japonica | 30% | 94% |
Q5PNS9 | Arabidopsis thaliana | 26% | 98% |
Q5SGD2 | Homo sapiens | 32% | 100% |
Q5SMK6 | Oryza sativa subsp. japonica | 31% | 100% |
Q5SN75 | Oryza sativa subsp. japonica | 32% | 97% |
Q5Z6F5 | Oryza sativa subsp. japonica | 36% | 100% |
Q5Z8P0 | Oryza sativa subsp. japonica | 25% | 100% |
Q652Z7 | Oryza sativa subsp. japonica | 33% | 100% |
Q653S3 | Oryza sativa subsp. japonica | 28% | 100% |
Q65XG6 | Oryza sativa subsp. japonica | 29% | 94% |
Q67J17 | Oryza sativa subsp. japonica | 28% | 93% |
Q67UP9 | Oryza sativa subsp. japonica | 30% | 100% |
Q67UX7 | Oryza sativa subsp. japonica | 33% | 100% |
Q69QZ0 | Oryza sativa subsp. japonica | 32% | 100% |
Q69VD9 | Oryza sativa subsp. japonica | 30% | 100% |
Q6AUQ4 | Oryza sativa subsp. japonica | 31% | 100% |
Q6EN45 | Oryza sativa subsp. japonica | 34% | 100% |
Q6ETK3 | Oryza sativa subsp. japonica | 29% | 100% |
Q6ING9 | Xenopus laevis | 29% | 100% |
Q6K1U4 | Oryza sativa subsp. japonica | 25% | 75% |
Q6K5I0 | Oryza sativa subsp. japonica | 26% | 76% |
Q6L482 | Oryza sativa subsp. japonica | 31% | 100% |
Q6L4R7 | Oryza sativa subsp. japonica | 32% | 88% |
Q6L5C4 | Oryza sativa subsp. japonica | 33% | 80% |
Q6L5H6 | Oryza sativa subsp. japonica | 29% | 100% |
Q6ZHC8 | Oryza sativa subsp. japonica | 27% | 100% |
Q7XCJ7 | Oryza sativa subsp. japonica | 23% | 99% |
Q7XHN8 | Oryza sativa subsp. japonica | 27% | 100% |
Q7XJ53 | Arabidopsis thaliana | 27% | 100% |
Q7XR06 | Oryza sativa subsp. japonica | 33% | 100% |
Q7XU84 | Oryza sativa subsp. japonica | 26% | 100% |
Q7XUC5 | Oryza sativa subsp. japonica | 27% | 100% |
Q8BGL1 | Mus musculus | 31% | 97% |
Q8BHN0 | Mus musculus | 32% | 100% |
Q8BXN7 | Mus musculus | 30% | 100% |
Q8CGA0 | Mus musculus | 29% | 87% |
Q8GY60 | Arabidopsis thaliana | 26% | 84% |
Q8H063 | Oryza sativa subsp. japonica | 27% | 100% |
Q8LAY8 | Arabidopsis thaliana | 35% | 100% |
Q8N3J5 | Homo sapiens | 30% | 100% |
Q8N819 | Homo sapiens | 32% | 91% |
Q8R0F6 | Mus musculus | 28% | 100% |
Q8RX37 | Arabidopsis thaliana | 30% | 100% |
Q8RXV3 | Arabidopsis thaliana | 35% | 100% |
Q8VZN9 | Arabidopsis thaliana | 36% | 100% |
Q94AT1 | Arabidopsis thaliana | 33% | 93% |
Q94CL8 | Arabidopsis thaliana | 29% | 100% |
Q94H98 | Oryza sativa subsp. japonica | 30% | 100% |
Q9CAJ0 | Arabidopsis thaliana | 29% | 77% |
Q9FIF5 | Arabidopsis thaliana | 30% | 95% |
Q9FLI3 | Arabidopsis thaliana | 27% | 94% |
Q9FXE4 | Arabidopsis thaliana | 35% | 88% |
Q9FYN7 | Oryza sativa subsp. japonica | 30% | 100% |
Q9H0C8 | Homo sapiens | 28% | 100% |
Q9LHJ9 | Arabidopsis thaliana | 28% | 100% |
Q9LMT1 | Arabidopsis thaliana | 31% | 100% |
Q9LNF4 | Arabidopsis thaliana | 30% | 100% |
Q9LNP9 | Arabidopsis thaliana | 29% | 77% |
Q9LR65 | Arabidopsis thaliana | 26% | 85% |
Q9LRZ4 | Arabidopsis thaliana | 28% | 100% |
Q9LUS8 | Arabidopsis thaliana | 25% | 79% |
Q9LUU7 | Arabidopsis thaliana | 29% | 93% |
Q9M9W9 | Arabidopsis thaliana | 29% | 100% |
Q9SD02 | Arabidopsis thaliana | 32% | 100% |
Q9SLA1 | Arabidopsis thaliana | 33% | 100% |
Q9SZ53 | Arabidopsis thaliana | 29% | 100% |
Q9WVR7 | Rattus norvegicus | 30% | 87% |
Q9XEE8 | Arabidopsis thaliana | 28% | 100% |
Q9Z1Z6 | Rattus norvegicus | 27% | 100% |
Q9ZW21 | Arabidopsis thaliana | 29% | 100% |
V5BCX6 | Trypanosoma cruzi | 30% | 100% |
V5BH00 | Trypanosoma cruzi | 30% | 100% |
V5BSS7 | Trypanosoma cruzi | 29% | 96% |
V5DCR6 | Trypanosoma cruzi | 29% | 95% |