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: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 | 12 |
Related structures:
AlphaFold database: Q4QG35
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:0046040 | IMP metabolic process | 7 | 2 |
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 |
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 | 157 | 161 | PF00656 | 0.386 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.442 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 669 | 671 | PF00675 | 0.258 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.213 |
CLV_PCSK_PC1ET2_1 | 667 | 669 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.306 |
CLV_Separin_Metazoa | 85 | 89 | PF03568 | 0.503 |
DEG_SPOP_SBC_1 | 291 | 295 | PF00917 | 0.442 |
DOC_CDC14_PxL_1 | 138 | 146 | PF14671 | 0.405 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.442 |
DOC_CYCLIN_RxL_1 | 279 | 289 | PF00134 | 0.453 |
DOC_CYCLIN_RxL_1 | 506 | 517 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 306 | 314 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 456 | 464 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 456 | 464 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 71 | 79 | PF00069 | 0.751 |
DOC_MAPK_RevD_3 | 223 | 236 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 375 | 381 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 230 | 233 | PF13499 | 0.489 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.237 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.735 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 326 | 330 | PF12436 | 0.489 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 611 | 616 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 119 | 123 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 9 | 15 | PF00244 | 0.732 |
LIG_AP2alpha_1 | 515 | 519 | PF02296 | 0.489 |
LIG_APCC_ABBA_1 | 382 | 387 | PF00400 | 0.453 |
LIG_EH1_1 | 648 | 656 | PF00400 | 0.453 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.493 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.477 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.442 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.661 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.442 |
LIG_FHA_2 | 493 | 499 | PF00498 | 0.453 |
LIG_Integrin_RGD_1 | 597 | 599 | PF01839 | 0.242 |
LIG_IRF3_LxIS_1 | 588 | 593 | PF10401 | 0.442 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 599 | 609 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 599 | 604 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 607 | 613 | PF02991 | 0.442 |
LIG_MAD2 | 692 | 700 | PF02301 | 0.509 |
LIG_NRBOX | 282 | 288 | PF00104 | 0.453 |
LIG_Pex14_2 | 515 | 519 | PF04695 | 0.467 |
LIG_PTB_Apo_2 | 389 | 396 | PF02174 | 0.546 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.468 |
LIG_SH2_CRK | 601 | 605 | PF00017 | 0.467 |
LIG_SH2_GRB2like | 123 | 126 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 123 | 127 | PF00017 | 0.311 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 601 | 605 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 238 | 241 | PF00017 | 0.467 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.489 |
LIG_SH2_STAT3 | 707 | 710 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.245 |
LIG_SH3_1 | 390 | 396 | PF00018 | 0.546 |
LIG_SH3_2 | 393 | 398 | PF14604 | 0.546 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.442 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.603 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.533 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.546 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.442 |
LIG_SUMO_SIM_anti_2 | 78 | 85 | PF11976 | 0.697 |
LIG_TRFH_1 | 223 | 227 | PF08558 | 0.442 |
LIG_WW_3 | 85 | 89 | PF00397 | 0.503 |
MOD_CDK_SPxxK_3 | 275 | 282 | PF00069 | 0.442 |
MOD_CDK_SPxxK_3 | 611 | 618 | PF00069 | 0.477 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.691 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.552 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.568 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.442 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.519 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.504 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.458 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.509 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.251 |
MOD_Cter_Amidation | 233 | 236 | PF01082 | 0.216 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.629 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.242 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.277 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.256 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.242 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.247 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.242 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.281 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.242 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.195 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.713 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.791 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.452 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.462 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.723 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.442 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.442 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.729 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.707 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.242 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.355 |
MOD_N-GLC_2 | 273 | 275 | PF02516 | 0.346 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.438 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.453 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.442 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.442 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.447 |
MOD_NEK2_2 | 127 | 132 | PF00069 | 0.526 |
MOD_NEK2_2 | 134 | 139 | PF00069 | 0.595 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.243 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.442 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.546 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.663 |
MOD_PK_1 | 456 | 462 | PF00069 | 0.493 |
MOD_PK_1 | 692 | 698 | PF00069 | 0.442 |
MOD_PK_1 | 71 | 77 | PF00069 | 0.749 |
MOD_PK_1 | 92 | 98 | PF00069 | 0.815 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.592 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.734 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.402 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.474 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.558 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.457 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.442 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.486 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.347 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.429 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.442 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.489 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.453 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.442 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.502 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.467 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.770 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.442 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.660 |
MOD_ProDKin_1 | 611 | 617 | PF00069 | 0.477 |
MOD_SUMO_for_1 | 56 | 59 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 614 | 620 | PF00179 | 0.455 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.739 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 668 | 670 | PF00400 | 0.546 |
TRG_NLS_MonoCore_2 | 565 | 570 | PF00514 | 0.453 |
TRG_NLS_MonoCore_2 | 666 | 671 | PF00514 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 512 | 517 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAY9 | Leptomonas seymouri | 74% | 100% |
A0A0S4JP31 | Bodo saltans | 67% | 100% |
A0A1X0NMZ2 | Trypanosomatidae | 69% | 100% |
A0A3S5H6P5 | Leishmania donovani | 95% | 100% |
A0A422NLD0 | Trypanosoma rangeli | 69% | 100% |
A4H7A3 | Leishmania braziliensis | 86% | 100% |
A4HVP7 | Leishmania infantum | 95% | 100% |
A7LBL2 | Leishmania donovani | 95% | 100% |
A9TIK2 | Physcomitrium patens | 23% | 100% |
C5WVW2 | Sorghum bicolor | 24% | 100% |
D0A6J7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9APE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O24578 | Zea mays | 23% | 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) | 71% | 100% |
Q4DLT6 | Trypanosoma cruzi (strain CL Brener) | 71% | 100% |
Q4QG35 | Leishmania major | 100% | 100% |
Q851S8 | Oryza sativa subsp. japonica | 22% | 100% |
Q96529 | Arabidopsis thaliana | 24% | 100% |
V5BBP4 | Trypanosoma cruzi | 71% | 100% |