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. | yes | 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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: E9APE3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006163 | purine nucleotide metabolic process | 5 | 12 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 12 |
GO:0006167 | AMP biosynthetic process | 8 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009117 | nucleotide metabolic process | 5 | 12 |
GO:0009123 | nucleoside monophosphate metabolic process | 5 | 12 |
GO:0009124 | nucleoside monophosphate biosynthetic process | 6 | 12 |
GO:0009126 | purine nucleoside monophosphate metabolic process | 6 | 12 |
GO:0009127 | purine nucleoside monophosphate biosynthetic process | 7 | 12 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 12 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 12 |
GO:0009156 | ribonucleoside monophosphate biosynthetic process | 7 | 12 |
GO:0009161 | ribonucleoside monophosphate metabolic process | 6 | 12 |
GO:0009165 | nucleotide biosynthetic process | 6 | 12 |
GO:0009167 | purine ribonucleoside monophosphate metabolic process | 7 | 12 |
GO:0009168 | purine ribonucleoside monophosphate biosynthetic process | 8 | 12 |
GO:0009259 | ribonucleotide metabolic process | 5 | 12 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0018130 | heterocycle biosynthetic process | 4 | 12 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0019693 | ribose phosphate metabolic process | 4 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 12 |
GO:0044208 | 'de novo' AMP biosynthetic process | 9 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0046033 | AMP metabolic process | 7 | 12 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0072521 | purine-containing compound metabolic process | 4 | 12 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 12 |
GO:0090407 | organophosphate biosynthetic process | 4 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 12 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:0046040 | IMP metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0000287 | magnesium ion binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004019 | adenylosuccinate synthase activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.504 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.736 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.320 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 669 | 671 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.268 |
CLV_PCSK_PC1ET2_1 | 669 | 671 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.362 |
CLV_Separin_Metazoa | 324 | 328 | PF03568 | 0.482 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.552 |
DEG_SPOP_SBC_1 | 293 | 297 | PF00917 | 0.504 |
DOC_CDC14_PxL_1 | 140 | 148 | PF14671 | 0.492 |
DOC_CKS1_1 | 278 | 283 | PF01111 | 0.504 |
DOC_CYCLIN_RxL_1 | 281 | 291 | PF00134 | 0.515 |
DOC_CYCLIN_RxL_1 | 511 | 519 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 92 | 98 | PF00134 | 0.524 |
DOC_MAPK_gen_1 | 308 | 316 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 377 | 386 | PF00069 | 0.578 |
DOC_MAPK_gen_1 | 458 | 466 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 458 | 466 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 545 | 552 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 71 | 79 | PF00069 | 0.789 |
DOC_MAPK_RevD_3 | 225 | 238 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 377 | 383 | PF00149 | 0.564 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.609 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.718 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 218 | 222 | PF12436 | 0.590 |
DOC_USP7_UBL2_3 | 328 | 332 | PF12436 | 0.609 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 129 | 134 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 9 | 15 | PF00244 | 0.784 |
LIG_AP2alpha_1 | 517 | 521 | PF02296 | 0.609 |
LIG_APCC_ABBA_1 | 384 | 389 | PF00400 | 0.515 |
LIG_EH1_1 | 650 | 658 | PF00400 | 0.515 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.604 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.504 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.783 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.497 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.515 |
LIG_Integrin_RGD_1 | 599 | 601 | PF01839 | 0.304 |
LIG_IRF3_LxIS_1 | 590 | 595 | PF10401 | 0.504 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 601 | 611 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 601 | 606 | PF02991 | 0.504 |
LIG_MAD2 | 694 | 702 | PF02301 | 0.564 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.515 |
LIG_Pex14_2 | 517 | 521 | PF04695 | 0.528 |
LIG_PTB_Apo_2 | 391 | 398 | PF02174 | 0.590 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.504 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.485 |
LIG_SH2_CRK | 603 | 607 | PF00017 | 0.528 |
LIG_SH2_GRB2like | 125 | 128 | PF00017 | 0.598 |
LIG_SH2_GRB2like | 55 | 58 | PF00017 | 0.651 |
LIG_SH2_NCK_1 | 155 | 159 | PF00017 | 0.369 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.564 |
LIG_SH2_NCK_1 | 603 | 607 | PF00017 | 0.528 |
LIG_SH2_PTP2 | 240 | 243 | PF00017 | 0.528 |
LIG_SH2_SRC | 369 | 372 | PF00017 | 0.609 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.615 |
LIG_SH2_STAT3 | 709 | 712 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 689 | 692 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 709 | 712 | PF00017 | 0.271 |
LIG_SH3_1 | 392 | 398 | PF00018 | 0.590 |
LIG_SH3_2 | 395 | 400 | PF14604 | 0.590 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.504 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.789 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.581 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.590 |
LIG_TRFH_1 | 225 | 229 | PF08558 | 0.504 |
MOD_CDK_SPxxK_3 | 277 | 284 | PF00069 | 0.504 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.713 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.487 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.762 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.504 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.571 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.572 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.497 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.564 |
MOD_Cter_Amidation | 219 | 222 | PF01082 | 0.315 |
MOD_Cter_Amidation | 235 | 238 | PF01082 | 0.344 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.710 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.533 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.294 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.315 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.301 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.294 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.308 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.304 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.342 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.304 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.353 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.746 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.825 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.604 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.531 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.772 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.504 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.705 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.498 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.474 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.783 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.769 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.304 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.390 |
MOD_N-GLC_2 | 275 | 277 | PF02516 | 0.390 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.516 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.511 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.686 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.504 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.504 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.509 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.632 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.500 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.588 |
MOD_PK_1 | 129 | 135 | PF00069 | 0.311 |
MOD_PK_1 | 458 | 464 | PF00069 | 0.552 |
MOD_PK_1 | 694 | 700 | PF00069 | 0.504 |
MOD_PK_1 | 71 | 77 | PF00069 | 0.788 |
MOD_PK_1 | 94 | 100 | PF00069 | 0.829 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.490 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.504 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.553 |
MOD_Plk_2-3 | 248 | 254 | PF00069 | 0.504 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.612 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.454 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.495 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.500 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.615 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.504 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.528 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.816 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.762 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.504 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.740 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.435 |
MOD_SUMO_rev_2 | 616 | 622 | PF00179 | 0.517 |
TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 591 | 594 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.504 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.785 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.590 |
TRG_NLS_MonoCore_2 | 567 | 572 | PF00514 | 0.515 |
TRG_NLS_MonoCore_2 | 668 | 673 | PF00514 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 141 | 145 | PF00026 | 0.620 |
TRG_Pf-PMV_PEXEL_1 | 416 | 420 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 514 | 519 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAY9 | Leptomonas seymouri | 74% | 100% |
A0A0S4JP31 | Bodo saltans | 65% | 100% |
A0A1X0NMZ2 | Trypanosomatidae | 71% | 100% |
A0A3S5H6P5 | Leishmania donovani | 95% | 100% |
A0A422NLD0 | Trypanosoma rangeli | 66% | 100% |
A2XD35 | Oryza sativa subsp. indica | 24% | 100% |
A4H7A3 | Leishmania braziliensis | 87% | 100% |
A4HVP7 | Leishmania infantum | 95% | 100% |
A7LBL2 | Leishmania donovani | 95% | 100% |
A9TIK2 | Physcomitrium patens | 24% | 100% |
C5WVW2 | Sorghum bicolor | 24% | 100% |
D0A6J7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
O24396 | Triticum aestivum | 23% | 100% |
O24578 | Zea mays | 24% | 100% |
Q017T9 | Ostreococcus tauri | 23% | 100% |
Q10R17 | Oryza sativa subsp. japonica | 24% | 100% |
Q386E7 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 68% | 100% |
Q4CWX1 | Trypanosoma cruzi (strain CL Brener) | 70% | 100% |
Q4DLT6 | Trypanosoma cruzi (strain CL Brener) | 71% | 100% |
Q4QG35 | Leishmania major | 93% | 100% |
Q851S8 | Oryza sativa subsp. japonica | 22% | 100% |
Q96529 | Arabidopsis thaliana | 23% | 100% |
V5BBP4 | Trypanosoma cruzi | 71% | 100% |