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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q2R0
Term | Name | Level | Count |
---|---|---|---|
GO:0001514 | selenocysteine incorporation | 7 | 2 |
GO:0006414 | translational elongation | 5 | 2 |
GO:0006417 | regulation of translation | 6 | 2 |
GO:0006451 | translational readthrough | 6 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0034248 | regulation of amide metabolic process | 5 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003746 | translation elongation factor activity | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003924 | GTPase activity | 7 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005525 | GTP binding | 5 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019001 | guanyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0045182 | translation regulator activity | 1 | 10 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 573 | 577 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 644 | 648 | PF00656 | 0.559 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 633 | 637 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 635 | 637 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.489 |
DEG_COP1_1 | 253 | 260 | PF00400 | 0.500 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.480 |
DEG_SCF_FBW7_1 | 579 | 585 | PF00400 | 0.650 |
DEG_SPOP_SBC_1 | 22 | 26 | PF00917 | 0.462 |
DOC_CKS1_1 | 579 | 584 | PF01111 | 0.653 |
DOC_CYCLIN_yCln2_LP_2 | 126 | 132 | PF00134 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 422 | 428 | PF00134 | 0.372 |
DOC_MAPK_gen_1 | 164 | 173 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 495 | 503 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 540 | 548 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 562 | 570 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 600 | 608 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 656 | 665 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 164 | 173 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 41 | 49 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 562 | 570 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 600 | 608 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 656 | 665 | PF00069 | 0.514 |
DOC_PP1_RVXF_1 | 603 | 609 | PF00149 | 0.372 |
DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.584 |
DOC_PP2B_LxvP_1 | 427 | 430 | PF13499 | 0.449 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.438 |
DOC_PP4_FxxP_1 | 608 | 611 | PF00568 | 0.414 |
DOC_PP4_FxxP_1 | 613 | 616 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 655 | 658 | PF00568 | 0.561 |
DOC_SPAK_OSR1_1 | 337 | 341 | PF12202 | 0.279 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.522 |
DOC_USP7_UBL2_3 | 634 | 638 | PF12436 | 0.700 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 310 | 319 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 392 | 402 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 636 | 643 | PF00244 | 0.763 |
LIG_Actin_WH2_2 | 119 | 137 | PF00022 | 0.511 |
LIG_Actin_WH2_2 | 194 | 212 | PF00022 | 0.535 |
LIG_APCC_ABBAyCdc20_2 | 553 | 559 | PF00400 | 0.447 |
LIG_CtBP_PxDLS_1 | 275 | 279 | PF00389 | 0.436 |
LIG_eIF4E_1 | 416 | 422 | PF01652 | 0.344 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.471 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.522 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.532 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.352 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.379 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.549 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.619 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.447 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.398 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.314 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.702 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.522 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.507 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.447 |
LIG_LIR_Apic_2 | 653 | 658 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 415 | 425 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 444 | 452 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 555 | 564 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 555 | 560 | PF02991 | 0.541 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.466 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.519 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.358 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.475 |
LIG_SH3_1 | 405 | 411 | PF00018 | 0.541 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.452 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.491 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.530 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.563 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.447 |
LIG_SUMO_SIM_anti_2 | 170 | 175 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 100 | 107 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 169 | 175 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 253 | 259 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 418 | 423 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 515 | 522 | PF11976 | 0.588 |
LIG_SUMO_SIM_par_1 | 565 | 571 | PF11976 | 0.497 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.512 |
LIG_UBA3_1 | 661 | 667 | PF00899 | 0.495 |
LIG_ULM_U2AF65_1 | 164 | 169 | PF00076 | 0.527 |
LIG_WRC_WIRS_1 | 625 | 630 | PF05994 | 0.664 |
MOD_CDK_SPxxK_3 | 141 | 148 | PF00069 | 0.478 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.447 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.447 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.586 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.439 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.554 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.573 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.680 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.609 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.669 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.557 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.478 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.513 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.527 |
MOD_CK2_1 | 671 | 677 | PF00069 | 0.641 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.247 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.499 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.425 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.497 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.534 |
MOD_GlcNHglycan | 477 | 481 | PF01048 | 0.726 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.247 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.664 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.652 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.712 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.672 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.621 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.629 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.458 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.482 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.478 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.495 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.370 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.447 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.571 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.695 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.732 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.530 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.423 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.590 |
MOD_N-GLC_2 | 445 | 447 | PF02516 | 0.408 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.447 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.461 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.348 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.231 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.418 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.400 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.449 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.447 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.426 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.447 |
MOD_NEK2_2 | 235 | 240 | PF00069 | 0.366 |
MOD_NEK2_2 | 650 | 655 | PF00069 | 0.434 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.491 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.461 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.411 |
MOD_PKA_1 | 634 | 640 | PF00069 | 0.593 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.512 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.394 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.461 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.661 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.550 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.539 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.444 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.364 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.380 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.520 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.366 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.456 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.661 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.494 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.447 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.447 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.478 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.447 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.656 |
TRG_DiLeu_BaEn_2 | 558 | 564 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.543 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 655 | 657 | PF00400 | 0.360 |
TRG_NLS_MonoCore_2 | 632 | 637 | PF00514 | 0.750 |
TRG_NLS_MonoExtC_3 | 633 | 638 | PF00514 | 0.743 |
TRG_NLS_MonoExtN_4 | 633 | 639 | PF00514 | 0.712 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 499 | 504 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZH5 | Leptomonas seymouri | 66% | 96% |
A0A1X0PAN1 | Trypanosomatidae | 49% | 100% |
A0A3Q8IIB7 | Leishmania donovani | 93% | 100% |
A0A3S5IRQ8 | Trypanosoma rangeli | 50% | 100% |
A0A3S7WV40 | Leishmania donovani | 27% | 100% |
A4H9I5 | Leishmania braziliensis | 25% | 100% |
A4HB07 | Leishmania braziliensis | 79% | 100% |
A4IA63 | Leishmania infantum | 93% | 100% |
C9ZM43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AGQ3 | Leishmania infantum | 27% | 100% |
E9ARL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B575 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P57772 | Homo sapiens | 35% | 100% |
Q4QDW8 | Leishmania major | 25% | 100% |
Q9JHW4 | Mus musculus | 36% | 100% |
V5BQE1 | Trypanosoma cruzi | 48% | 100% |