A large collection of various protein phosphatases. Very highly expanded in kinetoplastids.
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0005737 | cytoplasm | 2 | 4 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0005955 | calcineurin complex | 3 | 1 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1903293 | phosphatase complex | 3 | 1 |
Related structures:
AlphaFold database: Q4QFZ7
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 3 |
GO:0000725 | recombinational repair | 6 | 3 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006259 | DNA metabolic process | 4 | 3 |
GO:0006281 | DNA repair | 5 | 3 |
GO:0006302 | double-strand break repair | 6 | 3 |
GO:0006310 | DNA recombination | 5 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0006950 | response to stress | 2 | 3 |
GO:0006974 | DNA damage response | 4 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 8 |
GO:0033554 | cellular response to stress | 3 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0050896 | response to stimulus | 1 | 3 |
GO:0051716 | cellular response to stimulus | 2 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:0007165 | signal transduction | 2 | 5 |
GO:0019722 | calcium-mediated signaling | 5 | 5 |
GO:0019932 | second-messenger-mediated signaling | 4 | 5 |
GO:0035556 | intracellular signal transduction | 3 | 5 |
GO:0050789 | regulation of biological process | 2 | 5 |
GO:0050794 | regulation of cellular process | 3 | 5 |
GO:0065007 | biological regulation | 1 | 5 |
GO:0097720 | calcineurin-mediated signaling | 6 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 17 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 17 |
GO:0016791 | phosphatase activity | 5 | 17 |
GO:0017018 | myosin phosphatase activity | 5 | 17 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 17 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 17 |
GO:0004723 | calcium-dependent protein serine/threonine phosphatase activity | 5 | 5 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0033192 | calmodulin-dependent protein phosphatase activity | 6 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.242 |
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.390 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.658 |
DEG_APCC_DBOX_1 | 505 | 513 | PF00400 | 0.242 |
DEG_COP1_1 | 122 | 131 | PF00400 | 0.525 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.543 |
DEG_SPOP_SBC_1 | 215 | 219 | PF00917 | 0.524 |
DOC_ANK_TNKS_1 | 331 | 338 | PF00023 | 0.304 |
DOC_CYCLIN_yClb1_LxF_4 | 506 | 511 | PF00134 | 0.252 |
DOC_CYCLIN_yCln2_LP_2 | 416 | 422 | PF00134 | 0.343 |
DOC_MAPK_HePTP_8 | 288 | 300 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 291 | 300 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 351 | 360 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 413 | 420 | PF00069 | 0.328 |
DOC_MAPK_NFAT4_5 | 413 | 421 | PF00069 | 0.328 |
DOC_PP1_RVXF_1 | 506 | 512 | PF00149 | 0.242 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 180 | 183 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 416 | 419 | PF13499 | 0.343 |
DOC_PP4_FxxP_1 | 535 | 538 | PF00568 | 0.352 |
DOC_SPAK_OSR1_1 | 430 | 434 | PF12202 | 0.328 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.528 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.778 |
LIG_14-3-3_CanoR_1 | 136 | 146 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 195 | 205 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 430 | 440 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 530 | 535 | PF00244 | 0.328 |
LIG_BIR_III_2 | 56 | 60 | PF00653 | 0.535 |
LIG_BIR_III_4 | 154 | 158 | PF00653 | 0.480 |
LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.391 |
LIG_Clathr_ClatBox_1 | 295 | 299 | PF01394 | 0.366 |
LIG_deltaCOP1_diTrp_1 | 569 | 580 | PF00928 | 0.411 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.353 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.495 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.220 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.328 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.250 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.277 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.524 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.521 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.577 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.549 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.422 |
LIG_Integrin_isoDGR_2 | 134 | 136 | PF01839 | 0.545 |
LIG_Integrin_RGD_1 | 251 | 253 | PF01839 | 0.446 |
LIG_IRF3_LxIS_1 | 194 | 199 | PF10401 | 0.540 |
LIG_IRF3_LxIS_1 | 5 | 10 | PF10401 | 0.525 |
LIG_LIR_Apic_2 | 533 | 538 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 318 | 328 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 339 | 349 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 405 | 416 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 426 | 433 | PF02991 | 0.388 |
LIG_LIR_LC3C_4 | 105 | 110 | PF02991 | 0.499 |
LIG_LIR_LC3C_4 | 304 | 308 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 561 | 565 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.454 |
LIG_LYPXL_yS_3 | 369 | 372 | PF13949 | 0.328 |
LIG_MAD2 | 530 | 538 | PF02301 | 0.359 |
LIG_PCNA_PIPBox_1 | 517 | 526 | PF02747 | 0.434 |
LIG_PCNA_yPIPBox_3 | 514 | 524 | PF02747 | 0.340 |
LIG_PDZ_Class_1 | 581 | 586 | PF00595 | 0.443 |
LIG_PTB_Apo_2 | 271 | 278 | PF02174 | 0.364 |
LIG_PTB_Phospho_1 | 271 | 277 | PF10480 | 0.371 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.396 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.318 |
LIG_SH2_NCK_1 | 267 | 271 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 523 | 526 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.554 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.595 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.546 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.534 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.465 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.440 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.516 |
LIG_SPRY_1 | 542 | 547 | PF00622 | 0.294 |
LIG_SUMO_SIM_anti_2 | 297 | 302 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 304 | 311 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 355 | 360 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 2 | 10 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 294 | 299 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 304 | 311 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 529 | 536 | PF11976 | 0.358 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.573 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.523 |
LIG_TYR_ITIM | 367 | 372 | PF00017 | 0.328 |
LIG_UBA3_1 | 360 | 366 | PF00899 | 0.426 |
MOD_CDK_SPK_2 | 229 | 234 | PF00069 | 0.391 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.524 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.537 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.502 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.604 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.525 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.243 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.506 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.524 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.527 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.545 |
MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.634 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.378 |
MOD_GlcNHglycan | 32 | 36 | PF01048 | 0.510 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.517 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.387 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.352 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.410 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.517 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.508 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.500 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.578 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.580 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.335 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.525 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.413 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.310 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.291 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.308 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.263 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.522 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.532 |
MOD_N-GLC_2 | 280 | 282 | PF02516 | 0.269 |
MOD_N-GLC_2 | 539 | 541 | PF02516 | 0.388 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.573 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.565 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.528 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.553 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.490 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.287 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.343 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.262 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.562 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.532 |
MOD_NEK2_2 | 581 | 586 | PF00069 | 0.524 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.656 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.478 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.544 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.551 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.530 |
MOD_Plk_2-3 | 447 | 453 | PF00069 | 0.270 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.433 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.503 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.263 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.427 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.327 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.308 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.480 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.590 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.558 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.494 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.409 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.329 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.331 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.525 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.497 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.780 |
MOD_SUMO_for_1 | 365 | 368 | PF00179 | 0.328 |
MOD_SUMO_rev_2 | 218 | 228 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 381 | 386 | PF00179 | 0.397 |
TRG_DiLeu_BaEn_1 | 357 | 362 | PF01217 | 0.314 |
TRG_DiLeu_BaEn_1 | 368 | 373 | PF01217 | 0.264 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 192 | 197 | PF01217 | 0.560 |
TRG_DiLeu_LyEn_5 | 237 | 242 | PF01217 | 0.368 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.244 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 195 | 200 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I8M6 | Leishmania donovani | 75% | 100% |
A0A3Q8II54 | Leishmania donovani | 91% | 100% |
A0A3S7XAY3 | Leishmania donovani | 32% | 100% |
A0A422N1U7 | Trypanosoma rangeli | 30% | 98% |
A4H7E7 | Leishmania braziliensis | 67% | 100% |
A4HP65 | Leishmania braziliensis | 32% | 100% |
A4HVT0 | Leishmania infantum | 75% | 100% |
A4HVT6 | Leishmania infantum | 90% | 100% |
A4IDH0 | Leishmania infantum | 32% | 100% |
E9APH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
E9API1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9ASX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q1M5 | Leishmania major | 32% | 100% |
Q4QG03 | Leishmania major | 78% | 100% |
V5BBS3 | Trypanosoma cruzi | 31% | 98% |