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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 16 |
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: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005634 | nucleus | 5 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0005829 | cytosol | 2 | 1 |
Related structures:
AlphaFold database: A4H7D2
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 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016311 | dephosphorylation | 5 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0036211 | protein modification process | 4 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0043412 | macromolecule modification | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0019722 | calcium-mediated signaling | 5 | 1 |
GO:0019932 | second-messenger-mediated signaling | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0097720 | calcineurin-mediated signaling | 6 | 1 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 26 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 24 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 24 |
GO:0016787 | hydrolase activity | 2 | 26 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 24 |
GO:0016791 | phosphatase activity | 5 | 24 |
GO:0017018 | myosin phosphatase activity | 5 | 24 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 24 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 24 |
GO:0005488 | binding | 1 | 5 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
GO:0004723 | calcium-dependent protein serine/threonine phosphatase activity | 5 | 1 |
GO:0033192 | calmodulin-dependent protein phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.489 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.674 |
CLV_PCSK_FUR_1 | 296 | 300 | PF00082 | 0.189 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.272 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.415 |
DEG_SCF_FBW7_1 | 118 | 124 | PF00400 | 0.475 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.466 |
DEG_SPOP_SBC_1 | 136 | 140 | PF00917 | 0.472 |
DOC_CKS1_1 | 118 | 123 | PF01111 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 374 | 380 | PF00134 | 0.265 |
DOC_MAPK_gen_1 | 503 | 511 | PF00069 | 0.428 |
DOC_MAPK_HePTP_8 | 246 | 258 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 309 | 318 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 371 | 378 | PF00069 | 0.322 |
DOC_MAPK_NFAT4_5 | 371 | 379 | PF00069 | 0.322 |
DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.265 |
DOC_PP4_FxxP_1 | 493 | 496 | PF00568 | 0.342 |
DOC_SPAK_OSR1_1 | 388 | 392 | PF12202 | 0.322 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.553 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.730 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 309 | 315 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 388 | 398 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 411 | 419 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 79 | 88 | PF00244 | 0.466 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.453 |
LIG_BRCT_BRCA1_1 | 192 | 196 | PF00533 | 0.283 |
LIG_BRCT_BRCA1_1 | 457 | 461 | PF00533 | 0.339 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.777 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.324 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.348 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.265 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.237 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.237 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.301 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.349 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.718 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.529 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.498 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.412 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.238 |
LIG_Integrin_RGD_1 | 209 | 211 | PF01839 | 0.352 |
LIG_LIR_Apic_2 | 130 | 136 | PF02991 | 0.471 |
LIG_LIR_Apic_2 | 491 | 496 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 276 | 286 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 384 | 391 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 464 | 473 | PF02991 | 0.208 |
LIG_LIR_Gen_1 | 479 | 489 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 538 | 546 | PF02991 | 0.409 |
LIG_LIR_LC3C_4 | 262 | 266 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 326 | 330 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.208 |
LIG_LYPXL_yS_3 | 327 | 330 | PF13949 | 0.265 |
LIG_PCNA_yPIPBox_3 | 472 | 482 | PF02747 | 0.324 |
LIG_Pex14_1 | 516 | 520 | PF04695 | 0.249 |
LIG_Pex14_1 | 97 | 101 | PF04695 | 0.459 |
LIG_Pex14_2 | 541 | 545 | PF04695 | 0.475 |
LIG_REV1ctd_RIR_1 | 184 | 190 | PF16727 | 0.285 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.482 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.426 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.249 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.344 |
LIG_SH2_NCK_1 | 523 | 527 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 278 | 282 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 459 | 463 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.437 |
LIG_SH3_1 | 90 | 96 | PF00018 | 0.426 |
LIG_SH3_2 | 74 | 79 | PF14604 | 0.498 |
LIG_SH3_2 | 93 | 98 | PF14604 | 0.425 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.380 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.574 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.289 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.564 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 255 | 260 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 262 | 269 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 252 | 257 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 262 | 269 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 488 | 494 | PF11976 | 0.342 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.737 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.265 |
LIG_UBA3_1 | 318 | 324 | PF00899 | 0.305 |
LIG_WW_3 | 76 | 80 | PF00397 | 0.498 |
MOD_CDC14_SPxK_1 | 76 | 79 | PF00782 | 0.496 |
MOD_CDK_SPK_2 | 187 | 192 | PF00069 | 0.286 |
MOD_CDK_SPxK_1 | 73 | 79 | PF00069 | 0.497 |
MOD_CDK_SPxxK_3 | 73 | 80 | PF00069 | 0.498 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.504 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.713 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.776 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.439 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.463 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.605 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.322 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.577 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.435 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.575 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.660 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.393 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.489 |
MOD_DYRK1A_RPxSP_1 | 127 | 131 | PF00069 | 0.464 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.598 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.495 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.328 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.498 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.436 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.382 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.486 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.553 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.492 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.619 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.579 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.703 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.785 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.594 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.473 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.594 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.331 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.194 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.307 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.667 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.208 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.432 |
MOD_N-GLC_2 | 497 | 499 | PF02516 | 0.408 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.596 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.459 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.248 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.238 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.170 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.522 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.438 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.470 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.472 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.559 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.478 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.611 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.211 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.667 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.478 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.601 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.363 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.198 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.435 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.354 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.233 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.403 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.481 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.337 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.314 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.711 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.526 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.480 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.512 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.382 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.292 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.732 |
MOD_SUMO_for_1 | 323 | 326 | PF00179 | 0.220 |
MOD_SUMO_rev_2 | 174 | 183 | PF00179 | 0.425 |
MOD_SUMO_rev_2 | 458 | 467 | PF00179 | 0.170 |
MOD_SUMO_rev_2 | 524 | 533 | PF00179 | 0.423 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.269 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.309 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.487 |
TRG_DiLeu_LyEn_5 | 195 | 200 | PF01217 | 0.255 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.199 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.342 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.683 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDS9 | Leptomonas seymouri | 59% | 76% |
A0A1X0NJI7 | Trypanosomatidae | 46% | 98% |
A0A1X0P9R6 | Trypanosomatidae | 39% | 100% |
A0A3Q8I8M6 | Leishmania donovani | 74% | 100% |
A0A3S5H6T9 | Leishmania donovani | 33% | 100% |
A0A3S5H7Q6 | Leishmania donovani | 34% | 100% |
A0A3S7WUR2 | Leishmania donovani | 34% | 100% |
A0A3S7XAY3 | Leishmania donovani | 31% | 100% |
A0A422N1U7 | Trypanosoma rangeli | 32% | 91% |
A4H7Z3 | Leishmania braziliensis | 33% | 100% |
A4HJQ1 | Leishmania braziliensis | 35% | 100% |
A4HP65 | Leishmania braziliensis | 32% | 100% |
A4HVT0 | Leishmania infantum | 74% | 100% |
A4HWC1 | Leishmania infantum | 33% | 100% |
A4HXP1 | Leishmania infantum | 34% | 100% |
A4I768 | Leishmania infantum | 34% | 100% |
A4IDH0 | Leishmania infantum | 31% | 100% |
C9ZM48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A019 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0A366 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 86% |
E9APH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AQ21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9ARF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9ASX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B262 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
O14829 | Homo sapiens | 24% | 84% |
O42773 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 31% | 85% |
Q4Q1M5 | Leishmania major | 31% | 100% |
Q4Q5Z8 | Leishmania major | 34% | 100% |
Q4QE27 | Leishmania major | 34% | 100% |
Q4QFG0 | Leishmania major | 32% | 100% |
Q4QG03 | Leishmania major | 73% | 100% |
V5BBS3 | Trypanosoma cruzi | 30% | 91% |