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:0005634 | nucleus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0008023 | transcription elongation factor complex | 3 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032044 | DSIF complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HG07
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0032784 | regulation of DNA-templated transcription elongation | 7 | 12 |
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:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006354 | DNA-templated transcription elongation | 6 | 1 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 23 | 27 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.551 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.679 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.718 |
CLV_PCSK_FUR_1 | 104 | 108 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.718 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 44 | 50 | PF00082 | 0.637 |
CLV_PCSK_PC7_1 | 640 | 646 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.724 |
DEG_APCC_DBOX_1 | 278 | 286 | PF00400 | 0.402 |
DOC_CKS1_1 | 321 | 326 | PF01111 | 0.563 |
DOC_CKS1_1 | 592 | 597 | PF01111 | 0.495 |
DOC_MAPK_gen_1 | 173 | 181 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 200 | 206 | PF00069 | 0.305 |
DOC_MAPK_gen_1 | 264 | 273 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 539 | 547 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 439 | 447 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 478 | 487 | PF00069 | 0.511 |
DOC_PP4_FxxP_1 | 321 | 324 | PF00568 | 0.414 |
DOC_SPAK_OSR1_1 | 241 | 245 | PF12202 | 0.426 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.499 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.446 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 152 | 160 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 259 | 267 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 539 | 548 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 555 | 560 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 640 | 648 | PF00244 | 0.639 |
LIG_Actin_WH2_2 | 399 | 416 | PF00022 | 0.499 |
LIG_APCC_ABBA_1 | 484 | 489 | PF00400 | 0.396 |
LIG_APCC_ABBAyCdc20_2 | 106 | 112 | PF00400 | 0.447 |
LIG_APCC_ABBAyCdc20_2 | 216 | 222 | PF00400 | 0.306 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_CSL_BTD_1 | 592 | 595 | PF09270 | 0.594 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.426 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.619 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.365 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.365 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.473 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.466 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.435 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.401 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.379 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.665 |
LIG_Integrin_RGD_1 | 279 | 281 | PF01839 | 0.513 |
LIG_KLC1_Yacidic_2 | 217 | 222 | PF13176 | 0.306 |
LIG_LIR_Apic_2 | 318 | 324 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 217 | 223 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 269 | 278 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 4 | 14 | PF02991 | 0.707 |
LIG_LIR_Gen_1 | 556 | 565 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 217 | 221 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 479 | 483 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 556 | 562 | PF02991 | 0.534 |
LIG_NRBOX | 9 | 15 | PF00104 | 0.608 |
LIG_PTB_Apo_2 | 183 | 190 | PF02174 | 0.306 |
LIG_PTB_Phospho_1 | 183 | 189 | PF10480 | 0.306 |
LIG_SH2_CRK | 559 | 563 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 126 | 130 | PF00017 | 0.620 |
LIG_SH2_NCK_1 | 559 | 563 | PF00017 | 0.573 |
LIG_SH2_NCK_1 | 661 | 665 | PF00017 | 0.729 |
LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.306 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.496 |
LIG_SH2_SRC | 126 | 129 | PF00017 | 0.615 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.306 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 661 | 665 | PF00017 | 0.729 |
LIG_SH2_STAP1 | 7 | 11 | PF00017 | 0.706 |
LIG_SH2_STAT3 | 377 | 380 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.196 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.620 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.426 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.481 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.480 |
LIG_SH3_4 | 308 | 315 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 482 | 487 | PF11976 | 0.495 |
LIG_SUMO_SIM_anti_2 | 543 | 550 | PF11976 | 0.463 |
LIG_SUMO_SIM_anti_2 | 632 | 638 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 398 | 405 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 524 | 530 | PF11976 | 0.403 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.430 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.530 |
LIG_TRAF2_1 | 648 | 651 | PF00917 | 0.760 |
LIG_TRAF2_2 | 324 | 329 | PF00917 | 0.323 |
LIG_TYR_ITIM | 5 | 10 | PF00017 | 0.697 |
LIG_TYR_ITIM | 557 | 562 | PF00017 | 0.535 |
MOD_CDK_SPK_2 | 320 | 325 | PF00069 | 0.565 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.684 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.517 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.507 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.544 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.708 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.625 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.507 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.429 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.549 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.489 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.530 |
MOD_Cter_Amidation | 638 | 641 | PF01082 | 0.635 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.461 |
MOD_GlcNHglycan | 448 | 452 | PF01048 | 0.546 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.438 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.704 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.704 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.599 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.622 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.679 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.634 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.524 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.458 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.465 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.460 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.553 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.570 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.708 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.693 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.295 |
MOD_N-GLC_1 | 687 | 692 | PF02516 | 0.691 |
MOD_N-GLC_2 | 186 | 188 | PF02516 | 0.306 |
MOD_N-GLC_2 | 502 | 504 | PF02516 | 0.506 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.563 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.344 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.516 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.379 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.433 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.429 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.438 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.398 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.378 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.306 |
MOD_NEK2_2 | 510 | 515 | PF00069 | 0.665 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.640 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.631 |
MOD_PK_1 | 508 | 514 | PF00069 | 0.647 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.571 |
MOD_PKA_1 | 640 | 646 | PF00069 | 0.722 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.426 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.585 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.484 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.403 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.500 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.593 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.667 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.613 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.483 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.566 |
MOD_Plk_1 | 679 | 685 | PF00069 | 0.682 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.692 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.621 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.345 |
MOD_Plk_2-3 | 524 | 530 | PF00069 | 0.516 |
MOD_Plk_2-3 | 680 | 686 | PF00069 | 0.711 |
MOD_Plk_2-3 | 82 | 88 | PF00069 | 0.683 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.515 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.408 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.386 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.711 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.565 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.477 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.503 |
MOD_SUMO_for_1 | 497 | 500 | PF00179 | 0.529 |
MOD_SUMO_for_1 | 629 | 632 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 112 | 119 | PF00179 | 0.661 |
MOD_SUMO_rev_2 | 162 | 168 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 54 | 64 | PF00179 | 0.659 |
TRG_DiLeu_BaEn_1 | 632 | 637 | PF01217 | 0.457 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.608 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 559 | 562 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.704 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 225 | 228 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 271 | 274 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 615 | 618 | PF00400 | 0.373 |
TRG_NES_CRM1_1 | 203 | 213 | PF08389 | 0.321 |
TRG_NLS_MonoExtC_3 | 224 | 230 | PF00514 | 0.426 |
TRG_NLS_MonoExtC_3 | 37 | 42 | PF00514 | 0.635 |
TRG_NLS_MonoExtN_4 | 36 | 42 | PF00514 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 152 | 157 | PF00026 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9I1 | Leptomonas seymouri | 82% | 100% |
A0A0S4IUW1 | Bodo saltans | 41% | 94% |
A0A1X0NRB9 | Trypanosomatidae | 50% | 95% |
A0A3Q8IDN1 | Leishmania donovani | 90% | 99% |
A0A422NAL6 | Trypanosoma rangeli | 51% | 98% |
A4I326 | Leishmania infantum | 90% | 99% |
C9ZJK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 97% |
E9ACU7 | Leishmania major | 91% | 100% |
E9AZD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
O13936 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 70% |
O80770 | Arabidopsis thaliana | 24% | 70% |
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% |
Q5ALX3 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 26% | 72% |
Q5BCN2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 68% |
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% | 67% |
Q6FRZ5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 69% |
Q759T6 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 72% |
Q9STN3 | Arabidopsis thaliana | 24% | 67% |
V5D465 | Trypanosoma cruzi | 51% | 96% |