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: 1 |
Forrest at al. (metacyclic) | no | yes: 1 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 1 |
Pissara et al. | yes | 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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I565
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 4 |
GO:0006793 | phosphorus metabolic process | 3 | 4 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016311 | dephosphorylation | 5 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0035970 | peptidyl-threonine dephosphorylation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0043412 | macromolecule modification | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 25 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 25 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 25 |
GO:0016787 | hydrolase activity | 2 | 25 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 25 |
GO:0016791 | phosphatase activity | 5 | 25 |
GO:0017018 | myosin phosphatase activity | 5 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 25 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 25 |
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 | 0.371 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.280 |
DOC_MAPK_DCC_7 | 196 | 205 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 116 | 123 | PF00069 | 0.244 |
DOC_MAPK_gen_1 | 190 | 200 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 116 | 123 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.371 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.248 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.482 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.372 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.233 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.238 |
LIG_deltaCOP1_diTrp_1 | 355 | 361 | PF00928 | 0.365 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.247 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.231 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.331 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.457 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.414 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 372 | 378 | PF02991 | 0.366 |
LIG_LIR_LC3C_4 | 267 | 271 | PF02991 | 0.214 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.349 |
LIG_Pex14_2 | 222 | 226 | PF04695 | 0.229 |
LIG_REV1ctd_RIR_1 | 358 | 364 | PF16727 | 0.401 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.293 |
LIG_SH2_SRC | 149 | 152 | PF00017 | 0.169 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.330 |
LIG_SH2_STAT3 | 192 | 195 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.197 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.246 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.323 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.303 |
LIG_SUMO_SIM_anti_2 | 202 | 207 | PF11976 | 0.197 |
LIG_SUMO_SIM_anti_2 | 244 | 250 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 196 | 202 | PF11976 | 0.236 |
LIG_TYR_ITIM | 50 | 55 | PF00017 | 0.371 |
LIG_WRC_WIRS_1 | 280 | 285 | PF05994 | 0.246 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.371 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.415 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.413 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.432 |
MOD_GlcNHglycan | 63 | 67 | PF01048 | 0.313 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.400 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.329 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.589 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.285 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.275 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.371 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.258 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.472 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.382 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.485 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.241 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.361 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.286 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.258 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.213 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.250 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.275 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.275 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.502 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.376 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.349 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.373 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.330 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.387 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.351 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.429 |
MOD_SUMO_rev_2 | 144 | 148 | PF00179 | 0.264 |
TRG_DiLeu_BaEn_2 | 208 | 214 | PF01217 | 0.180 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.371 |
TRG_NES_CRM1_1 | 81 | 97 | PF08389 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.345 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C7 | Leptomonas seymouri | 32% | 97% |
A0A0N1I8W9 | Leptomonas seymouri | 28% | 88% |
A0A0N1IHU6 | Leptomonas seymouri | 44% | 94% |
A0A0N1PAL8 | Leptomonas seymouri | 87% | 100% |
A0A0N1PEL9 | Leptomonas seymouri | 30% | 100% |
A0A0S4IY95 | Bodo saltans | 32% | 100% |
A0A0S4J0A6 | Bodo saltans | 41% | 94% |
A0A0S4J8Y7 | Bodo saltans | 33% | 74% |
A0A0S4JHB4 | Bodo saltans | 54% | 100% |
A0A0S4JPC3 | Bodo saltans | 33% | 100% |
A0A0S4JPM8 | Bodo saltans | 33% | 100% |
A0A1X0NRG3 | Trypanosomatidae | 31% | 100% |
A0A1X0NUB7 | Trypanosomatidae | 32% | 80% |
A0A1X0NVC4 | Trypanosomatidae | 33% | 93% |
A0A1X0P2A0 | Trypanosomatidae | 57% | 100% |
A0A1X0P568 | Trypanosomatidae | 40% | 94% |
A0A1X0P991 | Trypanosomatidae | 33% | 100% |
A0A1X0PAN4 | Trypanosomatidae | 31% | 100% |
A0A3Q8IEK6 | Leishmania donovani | 35% | 100% |
A0A3Q8IFG7 | Leishmania donovani | 100% | 100% |
A0A3Q8IGS1 | Leishmania donovani | 31% | 68% |
A0A3Q8IK65 | Leishmania donovani | 37% | 100% |
A0A3Q8IL63 | Leishmania donovani | 30% | 98% |
A0A3S7WTA2 | Leishmania donovani | 31% | 95% |
A0A3S7WZ14 | Leishmania donovani | 45% | 95% |
A0A3S7X808 | Leishmania donovani | 29% | 85% |
A0A422N8D7 | Trypanosoma rangeli | 28% | 100% |
A0A422NAJ1 | Trypanosoma rangeli | 31% | 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 | 29% | 100% |
A0DSB3 | Paramecium tetraurelia | 30% | 100% |
A0DTY1 | Paramecium tetraurelia | 30% | 100% |
A3A8W2 | Oryza sativa subsp. japonica | 29% | 100% |
A3A8W6 | Oryza sativa subsp. japonica | 24% | 66% |
A3CCP9 | Oryza sativa subsp. japonica | 26% | 77% |
A4H7Y6 | Leishmania braziliensis | 33% | 100% |
A4HAW5 | Leishmania braziliensis | 32% | 100% |
A4HAW6 | Leishmania braziliensis | 29% | 85% |
A4HE10 | Leishmania braziliensis | 44% | 100% |
A4HG10 | Leishmania braziliensis | 34% | 100% |
A4HHY5 | Leishmania braziliensis | 92% | 100% |
A4HKF6 | Leishmania braziliensis | 30% | 68% |
A4HNR1 | Leishmania braziliensis | 36% | 100% |
A4HWB4 | Leishmania infantum | 31% | 100% |
A4I1B7 | Leishmania infantum | 45% | 100% |
A4I329 | Leishmania infantum | 35% | 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) | 33% | 90% |
C9ZQJ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 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 | 34% | 100% |
E9AQ14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9ASH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AXF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AZD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B0G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B2U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 68% |
E9B540 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B541 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
O04719 | Arabidopsis thaliana | 31% | 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 | 32% | 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) | 29% | 100% |
P49443 | Mus musculus | 34% | 100% |
P49593 | Homo sapiens | 28% | 85% |
P49596 | Caenorhabditis elegans | 33% | 100% |
P49597 | Arabidopsis thaliana | 29% | 88% |
P49599 | Arabidopsis thaliana | 29% | 99% |
P93006 | Arabidopsis thaliana | 28% | 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 | 33% | 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 | 32% | 82% |
Q2PC20 | Bos taurus | 32% | 100% |
Q2QWE3 | Oryza sativa subsp. japonica | 27% | 91% |
Q2R637 | Oryza sativa subsp. japonica | 27% | 89% |
Q3EAF9 | Arabidopsis thaliana | 28% | 100% |
Q4PSE8 | Arabidopsis thaliana | 36% | 86% |
Q4Q225 | Leishmania major | 37% | 100% |
Q4Q2U5 | Leishmania major | 28% | 85% |
Q4Q2U6 | Leishmania major | 30% | 100% |
Q4Q5B1 | Leishmania major | 31% | 68% |
Q4Q7S1 | Leishmania major | 98% | 100% |
Q4QA19 | Leishmania major | 45% | 100% |
Q4QFG7 | Leishmania major | 32% | 100% |
Q53Q11 | Oryza sativa subsp. japonica | 30% | 97% |
Q5JKN1 | Oryza sativa subsp. japonica | 29% | 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 | 31% | 100% |
Q653S3 | Oryza sativa subsp. japonica | 28% | 100% |
Q65XK7 | Oryza sativa subsp. japonica | 27% | 100% |
Q67J17 | Oryza sativa subsp. japonica | 24% | 91% |
Q67UX7 | Oryza sativa subsp. japonica | 34% | 100% |
Q69QZ0 | Oryza sativa subsp. japonica | 29% | 100% |
Q69VD9 | Oryza sativa subsp. japonica | 28% | 100% |
Q6AUQ4 | Oryza sativa subsp. japonica | 28% | 99% |
Q6EN45 | Oryza sativa subsp. japonica | 33% | 100% |
Q6ING9 | Xenopus laevis | 29% | 100% |
Q6K1U4 | Oryza sativa subsp. japonica | 25% | 74% |
Q6K5I0 | Oryza sativa subsp. japonica | 24% | 74% |
Q6L4R7 | Oryza sativa subsp. japonica | 28% | 86% |
Q6L5C4 | Oryza sativa subsp. japonica | 32% | 78% |
Q6L5H6 | Oryza sativa subsp. japonica | 29% | 99% |
Q6YTI2 | Oryza sativa subsp. japonica | 24% | 87% |
Q6ZKL8 | Oryza sativa subsp. japonica | 25% | 72% |
Q7XJ53 | Arabidopsis thaliana | 25% | 100% |
Q7XR06 | Oryza sativa subsp. japonica | 32% | 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 | 31% | 98% |
Q8RX37 | Arabidopsis thaliana | 28% | 100% |
Q8RXV3 | Arabidopsis thaliana | 35% | 100% |
Q8VZN9 | Arabidopsis thaliana | 34% | 100% |
Q93YS2 | Arabidopsis thaliana | 27% | 73% |
Q94AT1 | Arabidopsis thaliana | 32% | 91% |
Q9CAJ0 | Arabidopsis thaliana | 26% | 75% |
Q9FX08 | Arabidopsis thaliana | 25% | 90% |
Q9FYN7 | Oryza sativa subsp. japonica | 28% | 100% |
Q9H0C8 | Homo sapiens | 32% | 98% |
Q9LME4 | Arabidopsis thaliana | 30% | 100% |
Q9LMT1 | Arabidopsis thaliana | 30% | 100% |
Q9LNF4 | Arabidopsis thaliana | 27% | 100% |
Q9LNP9 | Arabidopsis thaliana | 28% | 75% |
Q9LUU7 | Arabidopsis thaliana | 29% | 91% |
Q9M1V8 | Arabidopsis thaliana | 27% | 91% |
Q9M9C6 | Arabidopsis thaliana | 29% | 88% |
Q9M9W9 | Arabidopsis thaliana | 31% | 100% |
Q9S9Z7 | Arabidopsis thaliana | 32% | 100% |
Q9SD02 | Arabidopsis thaliana | 28% | 100% |
Q9SLA1 | Arabidopsis thaliana | 29% | 98% |
Q9WVR7 | Rattus norvegicus | 29% | 85% |
Q9XEE8 | Arabidopsis thaliana | 29% | 98% |
Q9Z1Z6 | Rattus norvegicus | 31% | 98% |
V5AZJ4 | Trypanosoma cruzi | 29% | 97% |
V5BA03 | Trypanosoma cruzi | 33% | 100% |
V5BCX6 | Trypanosoma cruzi | 32% | 100% |
V5BH00 | Trypanosoma cruzi | 57% | 100% |
V5BSS7 | Trypanosoma cruzi | 41% | 94% |
V5DCR6 | Trypanosoma cruzi | 35% | 93% |