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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0008023 | transcription elongation factor complex | 3 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032044 | DSIF complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
Related structures:
AlphaFold database: E9ACU7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006354 | DNA-templated transcription elongation | 6 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 12 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 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 | 12 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0032774 | RNA biosynthetic process | 5 | 2 |
GO:0032784 | regulation of DNA-templated transcription elongation | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051252 | regulation of RNA metabolic process | 5 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003729 | mRNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.692 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.726 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.710 |
CLV_PCSK_PC7_1 | 647 | 653 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.731 |
DEG_APCC_DBOX_1 | 285 | 293 | PF00400 | 0.404 |
DOC_CKS1_1 | 328 | 333 | PF01111 | 0.563 |
DOC_CKS1_1 | 599 | 604 | PF01111 | 0.498 |
DOC_CYCLIN_RxL_1 | 111 | 121 | PF00134 | 0.608 |
DOC_MAPK_gen_1 | 180 | 188 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 206 | 213 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 271 | 280 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 546 | 554 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 206 | 213 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 446 | 454 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 485 | 494 | PF00069 | 0.510 |
DOC_PP2B_PxIxI_1 | 404 | 410 | PF00149 | 0.517 |
DOC_PP4_FxxP_1 | 328 | 331 | PF00568 | 0.415 |
DOC_SPAK_OSR1_1 | 248 | 252 | PF12202 | 0.426 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.508 |
DOC_USP7_UBL2_3 | 315 | 319 | PF12436 | 0.448 |
DOC_USP7_UBL2_3 | 41 | 45 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.575 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 159 | 167 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 266 | 274 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 562 | 567 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 647 | 655 | PF00244 | 0.647 |
LIG_Actin_WH2_2 | 406 | 423 | PF00022 | 0.499 |
LIG_APCC_ABBA_1 | 491 | 496 | PF00400 | 0.395 |
LIG_APCC_ABBAyCdc20_2 | 223 | 229 | PF00400 | 0.306 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_CSL_BTD_1 | 599 | 602 | PF09270 | 0.598 |
LIG_eIF4E_1 | 111 | 117 | PF01652 | 0.465 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.426 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.618 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.367 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.371 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.476 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.522 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.464 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.434 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.402 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.380 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.647 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.511 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.665 |
LIG_Integrin_RGD_1 | 286 | 288 | PF01839 | 0.514 |
LIG_KLC1_Yacidic_2 | 224 | 229 | PF13176 | 0.306 |
LIG_LIR_Apic_2 | 325 | 331 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 224 | 230 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 4 | 15 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 563 | 572 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 276 | 280 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.535 |
LIG_NRBOX | 9 | 15 | PF00104 | 0.596 |
LIG_PTB_Apo_2 | 190 | 197 | PF02174 | 0.306 |
LIG_PTB_Phospho_1 | 190 | 196 | PF10480 | 0.306 |
LIG_SH2_CRK | 566 | 570 | PF00017 | 0.547 |
LIG_SH2_NCK_1 | 133 | 137 | PF00017 | 0.611 |
LIG_SH2_NCK_1 | 566 | 570 | PF00017 | 0.573 |
LIG_SH2_NCK_1 | 668 | 672 | PF00017 | 0.737 |
LIG_SH2_PTP2 | 225 | 228 | PF00017 | 0.306 |
LIG_SH2_PTP2 | 277 | 280 | PF00017 | 0.494 |
LIG_SH2_SRC | 133 | 136 | PF00017 | 0.609 |
LIG_SH2_SRC | 225 | 228 | PF00017 | 0.306 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 668 | 672 | PF00017 | 0.737 |
LIG_SH2_STAP1 | 7 | 11 | PF00017 | 0.693 |
LIG_SH2_STAT3 | 384 | 387 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.194 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.626 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.426 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.482 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.482 |
LIG_SH3_4 | 315 | 322 | PF00018 | 0.507 |
LIG_SUMO_SIM_anti_2 | 489 | 494 | PF11976 | 0.495 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 639 | 645 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 531 | 537 | PF11976 | 0.404 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.495 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.439 |
LIG_TRAF2_1 | 655 | 658 | PF00917 | 0.768 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.684 |
LIG_TYR_ITIM | 564 | 569 | PF00017 | 0.536 |
MOD_CDK_SPK_2 | 327 | 332 | PF00069 | 0.565 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.686 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.517 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.505 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.548 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.727 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.628 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.509 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.437 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.489 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.783 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.533 |
MOD_Cter_Amidation | 645 | 648 | PF01082 | 0.647 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.472 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.546 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.441 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.716 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.721 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.591 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.628 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.680 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.633 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.525 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.455 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.465 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.462 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.552 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.568 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.708 |
MOD_N-GLC_1 | 694 | 699 | PF02516 | 0.689 |
MOD_N-GLC_2 | 193 | 195 | PF02516 | 0.306 |
MOD_N-GLC_2 | 509 | 511 | PF02516 | 0.498 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.514 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.376 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.442 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.429 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.434 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.399 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.378 |
MOD_NEK2_2 | 212 | 217 | PF00069 | 0.306 |
MOD_NEK2_2 | 517 | 522 | PF00069 | 0.665 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.638 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.629 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.686 |
MOD_PK_1 | 515 | 521 | PF00069 | 0.646 |
MOD_PKA_1 | 647 | 653 | PF00069 | 0.730 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.426 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.582 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.482 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.404 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.498 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.601 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.680 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.632 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.482 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.569 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.690 |
MOD_Plk_1 | 694 | 700 | PF00069 | 0.688 |
MOD_Plk_2-3 | 122 | 128 | PF00069 | 0.623 |
MOD_Plk_2-3 | 531 | 537 | PF00069 | 0.516 |
MOD_Plk_2-3 | 687 | 693 | PF00069 | 0.718 |
MOD_Plk_2-3 | 84 | 90 | PF00069 | 0.668 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.514 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.411 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.385 |
MOD_Plk_4 | 687 | 693 | PF00069 | 0.718 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.566 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.480 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.505 |
MOD_SUMO_for_1 | 504 | 507 | PF00179 | 0.526 |
MOD_SUMO_for_1 | 636 | 639 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 119 | 126 | PF00179 | 0.659 |
MOD_SUMO_rev_2 | 169 | 175 | PF00179 | 0.453 |
TRG_DiLeu_BaEn_1 | 639 | 644 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.690 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 622 | 625 | PF00400 | 0.376 |
TRG_NES_CRM1_1 | 210 | 220 | PF08389 | 0.321 |
TRG_NLS_Bipartite_1 | 38 | 58 | PF00514 | 0.713 |
TRG_NLS_MonoCore_2 | 53 | 58 | PF00514 | 0.723 |
TRG_NLS_MonoExtC_3 | 231 | 237 | PF00514 | 0.426 |
TRG_NLS_MonoExtC_3 | 37 | 42 | PF00514 | 0.659 |
TRG_NLS_MonoExtC_3 | 43 | 48 | PF00514 | 0.627 |
TRG_NLS_MonoExtC_3 | 53 | 59 | PF00514 | 0.507 |
TRG_NLS_MonoExtN_4 | 36 | 42 | PF00514 | 0.660 |
TRG_NLS_MonoExtN_4 | 44 | 51 | PF00514 | 0.610 |
TRG_NLS_MonoExtN_4 | 53 | 58 | PF00514 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 114 | 119 | PF00026 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 159 | 164 | PF00026 | 0.631 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9I1 | Leptomonas seymouri | 81% | 100% |
A0A0S4IUW1 | Bodo saltans | 42% | 95% |
A0A1X0NRB9 | Trypanosomatidae | 51% | 96% |
A0A3Q8IDN1 | Leishmania donovani | 97% | 100% |
A0A422NAL6 | Trypanosoma rangeli | 52% | 99% |
A4HG07 | Leishmania braziliensis | 91% | 100% |
A4I326 | Leishmania infantum | 97% | 100% |
C9ZJK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 98% |
E9AZD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O13936 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 71% |
O80770 | Arabidopsis thaliana | 25% | 71% |
Q4I5I4 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 26% | 67% |
Q4PIC4 | Ustilago maydis (strain 521 / FGSC 9021) | 23% | 73% |
Q4WP96 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 66% |
Q5ALX3 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 27% | 73% |
Q5BCN2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 69% |
Q6BZG0 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 27% | 72% |
Q6CC84 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 71% |
Q6CWW9 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 68% |
Q6FRZ5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 69% |
Q7S3C4 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 66% |
Q9STN3 | Arabidopsis thaliana | 25% | 67% |
V5D465 | Trypanosoma cruzi | 49% | 97% |