| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 1 |
| Forrest at al. (metacyclic) | no | yes: 0 |
| Forrest at al. (procyclic) | no | yes: 2 |
| Silverman et al. | no | yes: 2 |
| 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: 6 |
| 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 | 1 |
| GO:0018444 | translation release factor complex | 2 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6P3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006412 | translation | 4 | 1 |
| GO:0006518 | peptide metabolic process | 4 | 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:0019538 | protein metabolic process | 3 | 1 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
| GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
| GO:0043043 | peptide biosynthetic process | 5 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043603 | amide metabolic process | 3 | 1 |
| GO:0043604 | amide biosynthetic process | 4 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044249 | cellular biosynthetic process | 3 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
| GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
| GO:1901576 | organic substance biosynthetic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 12 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0003924 | GTPase activity | 7 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0005525 | GTP binding | 5 | 12 |
| GO:0016462 | pyrophosphatase activity | 5 | 12 |
| GO:0016787 | hydrolase activity | 2 | 12 |
| GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
| GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
| GO:0017076 | purine nucleotide binding | 4 | 12 |
| GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 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: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 |
| GO:0003676 | nucleic acid binding | 3 | 2 |
| GO:0003747 | translation release factor activity | 5 | 1 |
| GO:0008079 | translation termination factor activity | 4 | 1 |
| GO:0008135 | translation factor activity, RNA binding | 3 | 2 |
| GO:0045182 | translation regulator activity | 1 | 2 |
| GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 2 |
| GO:0003746 | translation elongation factor activity | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 293 | 297 | PF00656 | 0.417 |
| CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.733 |
| CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.603 |
| CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.612 |
| CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.240 |
| CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.217 |
| CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.284 |
| CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.509 |
| CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.609 |
| CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.487 |
| CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.228 |
| CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.218 |
| CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.520 |
| CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.600 |
| CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.520 |
| CLV_PCSK_PC7_1 | 202 | 208 | PF00082 | 0.595 |
| CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.228 |
| CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.122 |
| CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.239 |
| CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.245 |
| CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.217 |
| CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.729 |
| DOC_ANK_TNKS_1 | 625 | 632 | PF00023 | 0.477 |
| DOC_CYCLIN_yCln2_LP_2 | 601 | 607 | PF00134 | 0.519 |
| DOC_MAPK_gen_1 | 206 | 217 | PF00069 | 0.266 |
| DOC_MAPK_gen_1 | 390 | 399 | PF00069 | 0.442 |
| DOC_MAPK_gen_1 | 81 | 89 | PF00069 | 0.629 |
| DOC_PP1_RVXF_1 | 390 | 397 | PF00149 | 0.428 |
| DOC_PP1_RVXF_1 | 528 | 535 | PF00149 | 0.349 |
| DOC_PP2B_LxvP_1 | 295 | 298 | PF13499 | 0.442 |
| DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.399 |
| DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.304 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.692 |
| DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.739 |
| DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.470 |
| DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.417 |
| DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.651 |
| DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.523 |
| DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.682 |
| DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.630 |
| DOC_USP7_UBL2_3 | 452 | 456 | PF12436 | 0.469 |
| DOC_USP7_UBL2_3 | 569 | 573 | PF12436 | 0.417 |
| DOC_USP7_UBL2_3 | 611 | 615 | PF12436 | 0.417 |
| DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.724 |
| DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.704 |
| DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.600 |
| LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.479 |
| LIG_APCC_ABBA_1 | 607 | 612 | PF00400 | 0.484 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
| LIG_BIR_III_4 | 296 | 300 | PF00653 | 0.417 |
| LIG_BRCT_BRCA1_1 | 491 | 495 | PF00533 | 0.449 |
| LIG_BRCT_BRCA1_2 | 491 | 497 | PF00533 | 0.443 |
| LIG_EVH1_1 | 37 | 41 | PF00568 | 0.473 |
| LIG_FHA_1 | 345 | 351 | PF00498 | 0.435 |
| LIG_FHA_1 | 5 | 11 | PF00498 | 0.682 |
| LIG_FHA_1 | 576 | 582 | PF00498 | 0.442 |
| LIG_FHA_1 | 625 | 631 | PF00498 | 0.426 |
| LIG_FHA_1 | 84 | 90 | PF00498 | 0.647 |
| LIG_FHA_2 | 122 | 128 | PF00498 | 0.793 |
| LIG_FHA_2 | 151 | 157 | PF00498 | 0.721 |
| LIG_FHA_2 | 172 | 178 | PF00498 | 0.629 |
| LIG_FHA_2 | 180 | 186 | PF00498 | 0.499 |
| LIG_FHA_2 | 291 | 297 | PF00498 | 0.431 |
| LIG_FHA_2 | 310 | 316 | PF00498 | 0.442 |
| LIG_FHA_2 | 328 | 334 | PF00498 | 0.442 |
| LIG_FHA_2 | 436 | 442 | PF00498 | 0.364 |
| LIG_FHA_2 | 477 | 483 | PF00498 | 0.390 |
| LIG_FHA_2 | 491 | 497 | PF00498 | 0.390 |
| LIG_FHA_2 | 98 | 104 | PF00498 | 0.723 |
| LIG_FXI_DFP_1 | 610 | 614 | PF00024 | 0.242 |
| LIG_IRF3_LxIS_1 | 316 | 322 | PF10401 | 0.417 |
| LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.600 |
| LIG_LIR_Gen_1 | 260 | 267 | PF02991 | 0.417 |
| LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.469 |
| LIG_LIR_Gen_1 | 564 | 574 | PF02991 | 0.432 |
| LIG_LIR_Gen_1 | 612 | 621 | PF02991 | 0.442 |
| LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.417 |
| LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.469 |
| LIG_LIR_Nem_3 | 457 | 463 | PF02991 | 0.461 |
| LIG_LIR_Nem_3 | 564 | 570 | PF02991 | 0.434 |
| LIG_LIR_Nem_3 | 612 | 616 | PF02991 | 0.497 |
| LIG_PCNA_APIM_2 | 616 | 622 | PF02747 | 0.417 |
| LIG_Pex14_1 | 259 | 263 | PF04695 | 0.421 |
| LIG_Pex14_2 | 213 | 217 | PF04695 | 0.428 |
| LIG_Pex14_2 | 328 | 332 | PF04695 | 0.417 |
| LIG_REV1ctd_RIR_1 | 532 | 542 | PF16727 | 0.484 |
| LIG_SH2_CRK | 261 | 265 | PF00017 | 0.417 |
| LIG_SH2_SRC | 261 | 264 | PF00017 | 0.417 |
| LIG_SH2_SRC | 370 | 373 | PF00017 | 0.365 |
| LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.417 |
| LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.386 |
| LIG_SH2_STAT3 | 28 | 31 | PF00017 | 0.639 |
| LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.698 |
| LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.417 |
| LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.442 |
| LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.317 |
| LIG_SH3_1 | 36 | 42 | PF00018 | 0.595 |
| LIG_SH3_3 | 111 | 117 | PF00018 | 0.673 |
| LIG_SH3_3 | 35 | 41 | PF00018 | 0.594 |
| LIG_SH3_3 | 47 | 53 | PF00018 | 0.570 |
| LIG_SH3_3 | 603 | 609 | PF00018 | 0.484 |
| LIG_SH3_3 | 74 | 80 | PF00018 | 0.625 |
| LIG_SH3_3 | 9 | 15 | PF00018 | 0.585 |
| LIG_SUMO_SIM_par_1 | 317 | 323 | PF11976 | 0.417 |
| LIG_SUMO_SIM_par_1 | 538 | 543 | PF11976 | 0.417 |
| LIG_SUMO_SIM_par_1 | 602 | 608 | PF11976 | 0.519 |
| LIG_SxIP_EBH_1 | 518 | 530 | PF03271 | 0.385 |
| LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.532 |
| LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.460 |
| LIG_TRAF2_1 | 560 | 563 | PF00917 | 0.417 |
| LIG_UBA3_1 | 353 | 359 | PF00899 | 0.428 |
| LIG_UBA3_1 | 424 | 432 | PF00899 | 0.434 |
| LIG_UBA3_1 | 570 | 577 | PF00899 | 0.484 |
| MOD_CDK_SPxxK_3 | 179 | 186 | PF00069 | 0.703 |
| MOD_CK1_1 | 102 | 108 | PF00069 | 0.722 |
| MOD_CK1_1 | 116 | 122 | PF00069 | 0.525 |
| MOD_CK1_1 | 135 | 141 | PF00069 | 0.667 |
| MOD_CK1_1 | 226 | 232 | PF00069 | 0.435 |
| MOD_CK1_1 | 322 | 328 | PF00069 | 0.442 |
| MOD_CK1_1 | 489 | 495 | PF00069 | 0.461 |
| MOD_CK1_1 | 524 | 530 | PF00069 | 0.343 |
| MOD_CK1_1 | 549 | 555 | PF00069 | 0.519 |
| MOD_CK2_1 | 121 | 127 | PF00069 | 0.777 |
| MOD_CK2_1 | 135 | 141 | PF00069 | 0.535 |
| MOD_CK2_1 | 150 | 156 | PF00069 | 0.640 |
| MOD_CK2_1 | 179 | 185 | PF00069 | 0.533 |
| MOD_CK2_1 | 198 | 204 | PF00069 | 0.368 |
| MOD_CK2_1 | 265 | 271 | PF00069 | 0.423 |
| MOD_CK2_1 | 327 | 333 | PF00069 | 0.419 |
| MOD_CK2_1 | 476 | 482 | PF00069 | 0.347 |
| MOD_CK2_1 | 490 | 496 | PF00069 | 0.314 |
| MOD_CK2_1 | 557 | 563 | PF00069 | 0.477 |
| MOD_CK2_1 | 636 | 642 | PF00069 | 0.417 |
| MOD_CK2_1 | 97 | 103 | PF00069 | 0.723 |
| MOD_Cter_Amidation | 89 | 92 | PF01082 | 0.654 |
| MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.624 |
| MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.597 |
| MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.580 |
| MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.675 |
| MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.632 |
| MOD_GlcNHglycan | 20 | 24 | PF01048 | 0.469 |
| MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.230 |
| MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.316 |
| MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.319 |
| MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.319 |
| MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.705 |
| MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.667 |
| MOD_GSK3_1 | 102 | 109 | PF00069 | 0.646 |
| MOD_GSK3_1 | 135 | 142 | PF00069 | 0.674 |
| MOD_GSK3_1 | 146 | 153 | PF00069 | 0.697 |
| MOD_GSK3_1 | 270 | 277 | PF00069 | 0.442 |
| MOD_GSK3_1 | 486 | 493 | PF00069 | 0.381 |
| MOD_GSK3_1 | 520 | 527 | PF00069 | 0.373 |
| MOD_GSK3_1 | 636 | 643 | PF00069 | 0.438 |
| MOD_GSK3_1 | 93 | 100 | PF00069 | 0.681 |
| MOD_NEK2_1 | 319 | 324 | PF00069 | 0.433 |
| MOD_NEK2_1 | 344 | 349 | PF00069 | 0.420 |
| MOD_NEK2_1 | 636 | 641 | PF00069 | 0.405 |
| MOD_PIKK_1 | 150 | 156 | PF00454 | 0.685 |
| MOD_PIKK_1 | 309 | 315 | PF00454 | 0.417 |
| MOD_PK_1 | 186 | 192 | PF00069 | 0.384 |
| MOD_PKA_1 | 186 | 192 | PF00069 | 0.595 |
| MOD_PKA_1 | 290 | 296 | PF00069 | 0.417 |
| MOD_PKA_2 | 186 | 192 | PF00069 | 0.484 |
| MOD_PKA_2 | 277 | 283 | PF00069 | 0.427 |
| MOD_PKA_2 | 290 | 296 | PF00069 | 0.382 |
| MOD_PKA_2 | 575 | 581 | PF00069 | 0.484 |
| MOD_PKB_1 | 196 | 204 | PF00069 | 0.577 |
| MOD_Plk_1 | 563 | 569 | PF00069 | 0.428 |
| MOD_Plk_2-3 | 435 | 441 | PF00069 | 0.401 |
| MOD_Plk_2-3 | 486 | 492 | PF00069 | 0.345 |
| MOD_Plk_4 | 290 | 296 | PF00069 | 0.433 |
| MOD_Plk_4 | 303 | 309 | PF00069 | 0.402 |
| MOD_Plk_4 | 420 | 426 | PF00069 | 0.365 |
| MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.724 |
| MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.699 |
| MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.593 |
| MOD_SUMO_for_1 | 190 | 193 | PF00179 | 0.506 |
| MOD_SUMO_rev_2 | 361 | 366 | PF00179 | 0.460 |
| MOD_SUMO_rev_2 | 429 | 438 | PF00179 | 0.409 |
| MOD_SUMO_rev_2 | 453 | 457 | PF00179 | 0.467 |
| TRG_DiLeu_BaEn_1 | 340 | 345 | PF01217 | 0.417 |
| TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.417 |
| TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.426 |
| TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.324 |
| TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.440 |
| TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.418 |
| TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.509 |
| TRG_NES_CRM1_1 | 422 | 435 | PF08389 | 0.291 |
| TRG_NLS_Bipartite_1 | 81 | 95 | PF00514 | 0.661 |
| TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.431 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I5B5 | Leptomonas seymouri | 35% | 100% |
| A0A0N1PAZ5 | Leptomonas seymouri | 78% | 86% |
| A0A0S4IX91 | Bodo saltans | 63% | 96% |
| A0A1X0NV54 | Trypanosomatidae | 71% | 92% |
| A0A3Q8ICH2 | Leishmania donovani | 89% | 86% |
| A0A3R7MLL0 | Trypanosoma rangeli | 69% | 98% |
| A0A3S7WV40 | Leishmania donovani | 24% | 100% |
| A0A3S7X9T0 | Leishmania donovani | 32% | 100% |
| A0A422NK97 | Trypanosoma rangeli | 34% | 98% |
| A0Q6F0 | Francisella tularensis subsp. novicida (strain U112) | 24% | 100% |
| A1JJT0 | Yersinia enterocolitica serotype O:8 / biotype 1B (strain NCTC 13174 / 8081) | 24% | 100% |
| A2BN41 | Hyperthermus butylicus (strain DSM 5456 / JCM 9403 / PLM1-5) | 39% | 100% |
| A2Q0Z0 | Equus caballus | 36% | 100% |
| A4H8V4 | Leishmania braziliensis | 36% | 100% |
| A4HN87 | Leishmania braziliensis | 34% | 100% |
| A4HV24 | Leishmania infantum | 89% | 86% |
| A4HX73 | Leishmania infantum | 36% | 100% |
| A4IBV5 | Leishmania infantum | 32% | 100% |
| A4IXZ5 | Francisella tularensis subsp. tularensis (strain WY96-3418) | 24% | 100% |
| A5DPE3 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 37% | 100% |
| A7FLY2 | Yersinia pseudotuberculosis serotype O:1b (strain IP 31758) | 23% | 100% |
| A7MJ69 | Cronobacter sakazakii (strain ATCC BAA-894) | 24% | 100% |
| A9W4X1 | Methylorubrum extorquens (strain PA1) | 25% | 100% |
| B1Z7C0 | Methylorubrum populi (strain ATCC BAA-705 / NCIMB 13946 / BJ001) | 26% | 100% |
| B2VG01 | Erwinia tasmaniensis (strain DSM 17950 / CFBP 7177 / CIP 109463 / NCPPB 4357 / Et1/99) | 24% | 100% |
| B3PII1 | Cellvibrio japonicus (strain Ueda107) | 25% | 100% |
| B4RTW4 | Alteromonas mediterranea (strain DSM 17117 / CIP 110805 / LMG 28347 / Deep ecotype) | 24% | 100% |
| B7L0X9 | Methylorubrum extorquens (strain CM4 / NCIMB 13688) | 25% | 100% |
| B9JB95 | Agrobacterium radiobacter (strain K84 / ATCC BAA-868) | 27% | 100% |
| C5BSJ5 | Teredinibacter turnerae (strain ATCC 39867 / T7901) | 25% | 100% |
| C9ZYQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| D0A7C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 93% |
| E9AFP2 | Leishmania major | 33% | 100% |
| E9AGP5 | Leishmania infantum | 36% | 100% |
| E9AGP7 | Leishmania infantum | 32% | 100% |
| E9AGQ3 | Leishmania infantum | 24% | 100% |
| E9ANQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 85% |
| E9ARD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
| E9ARL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
| E9B6U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
| O13354 | Candida albicans | 42% | 91% |
| O33581 | Rhizobium tropici | 27% | 100% |
| O42820 | Schizophyllum commune | 37% | 100% |
| O50274 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 25% | 100% |
| O59949 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 37% | 100% |
| O74718 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 98% |
| P02992 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
| P02993 | Artemia salina | 36% | 100% |
| P02994 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 100% |
| P05303 | Drosophila melanogaster | 36% | 100% |
| P06805 | Mucor circinelloides f. lusitanicus | 37% | 100% |
| P08736 | Drosophila melanogaster | 35% | 100% |
| P0CN30 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 38% | 100% |
| P0CN31 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 38% | 100% |
| P0CT53 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 100% |
| P0CT54 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
| P0CT55 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
| P0CY35 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 37% | 100% |
| P10126 | Mus musculus | 36% | 100% |
| P13549 | Xenopus laevis | 36% | 100% |
| P14864 | Mucor circinelloides f. lusitanicus | 37% | 100% |
| P14865 | Mucor circinelloides f. lusitanicus | 38% | 100% |
| P17506 | Xenopus laevis | 36% | 100% |
| P17507 | Xenopus laevis | 36% | 100% |
| P17508 | Xenopus laevis | 35% | 100% |
| P17745 | Arabidopsis thaliana | 28% | 100% |
| P17786 | Solanum lycopersicum | 38% | 100% |
| P19039 | Apis mellifera | 35% | 100% |
| P25166 | Stylonychia lemnae | 34% | 100% |
| P25698 | Glycine max | 37% | 100% |
| P27592 | Onchocerca volvulus | 35% | 100% |
| P28295 | Absidia glauca | 37% | 100% |
| P29520 | Bombyx mori | 35% | 100% |
| P32186 | Puccinia graminis | 37% | 100% |
| P32769 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
| P34825 | Hypocrea jecorina | 36% | 100% |
| P40911 | Ajellomyces capsulatus (strain G186AR / H82 / ATCC MYA-2454 / RMSCC 2432) | 37% | 100% |
| P41745 | Blastobotrys adeninivorans | 37% | 100% |
| P41752 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 38% | 100% |
| P43643 | Nicotiana tabacum | 37% | 100% |
| P46280 | Glycine max | 28% | 100% |
| P49411 | Homo sapiens | 25% | 100% |
| P50257 | Porphyra purpurea | 33% | 100% |
| P51554 | Hydra vulgaris | 36% | 100% |
| P52978 | Rhizobium tropici | 25% | 100% |
| P53013 | Caenorhabditis elegans | 36% | 100% |
| P56893 | Rhizobium meliloti (strain 1021) | 27% | 100% |
| P62629 | Cricetulus griseus | 36% | 100% |
| P62630 | Rattus norvegicus | 36% | 100% |
| P62631 | Mus musculus | 35% | 100% |
| P62632 | Rattus norvegicus | 35% | 100% |
| P68103 | Bos taurus | 36% | 100% |
| P68104 | Homo sapiens | 36% | 100% |
| P68105 | Oryctolagus cuniculus | 36% | 100% |
| P9WNM4 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 23% | 100% |
| P9WNM5 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 23% | 100% |
| Q00251 | Aureobasidium pullulans | 38% | 100% |
| Q01372 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 37% | 100% |
| Q01520 | Podospora anserina | 36% | 100% |
| Q01765 | Podospora curvicolla | 36% | 100% |
| Q04634 | Tetrahymena pyriformis | 36% | 100% |
| Q05639 | Homo sapiens | 35% | 100% |
| Q09069 | Sordaria macrospora | 37% | 100% |
| Q14HG2 | Francisella tularensis subsp. tularensis (strain FSC 198) | 24% | 100% |
| Q21IS6 | Saccharophagus degradans (strain 2-40 / ATCC 43961 / DSM 17024) | 26% | 100% |
| Q27139 | Euplotes crassus | 36% | 100% |
| Q2HJN4 | Oscheius tipulae | 36% | 100% |
| Q2HJN6 | Oscheius tipulae | 37% | 100% |
| Q2HJN8 | Oscheius tipulae | 36% | 100% |
| Q2HJN9 | Oscheius tipulae | 36% | 100% |
| Q2KHZ2 | Bos taurus | 37% | 95% |
| Q2NVM8 | Sodalis glossinidius (strain morsitans) | 23% | 100% |
| Q32PH8 | Bos taurus | 35% | 100% |
| Q482Z9 | Colwellia psychrerythraea (strain 34H / ATCC BAA-681) | 25% | 100% |
| Q4QDW8 | Leishmania major | 24% | 100% |
| Q4QEI8 | Leishmania major | 36% | 100% |
| Q4QEI9 | Leishmania major | 36% | 100% |
| Q4QGW5 | Leishmania major | 88% | 100% |
| Q59QD6 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 37% | 100% |
| Q5NG10 | Francisella tularensis subsp. tularensis (strain SCHU S4 / Schu 4) | 24% | 100% |
| Q5R1X2 | Pan troglodytes | 36% | 100% |
| Q5R4R8 | Pongo abelii | 36% | 100% |
| Q5R6Y0 | Pongo abelii | 37% | 95% |
| Q5VTE0 | Homo sapiens | 36% | 100% |
| Q66EC7 | Yersinia pseudotuberculosis serotype I (strain IP32953) | 23% | 100% |
| Q66RN5 | Felis catus | 36% | 100% |
| Q69ZS7 | Mus musculus | 37% | 95% |
| Q6AXM7 | Rattus norvegicus | 38% | 96% |
| Q71V39 | Oryctolagus cuniculus | 35% | 100% |
| Q7YZN9 | Dictyostelium discoideum | 42% | 100% |
| Q8AAP9 | Bacteroides thetaiotaomicron (strain ATCC 29148 / DSM 2079 / JCM 5827 / CCUG 10774 / NCTC 10582 / VPI-5482 / E50) | 26% | 100% |
| Q8SS29 | Encephalitozoon cuniculi (strain GB-M1) | 30% | 100% |
| Q8ZBP2 | Yersinia pestis | 23% | 100% |
| Q90835 | Gallus gallus | 36% | 100% |
| Q92005 | Danio rerio | 35% | 100% |
| Q95VF2 | Leishmania donovani | 36% | 100% |
| Q96WZ1 | Coccidioides immitis (strain RS) | 37% | 100% |
| Q9HDF6 | Serendipita indica | 36% | 100% |
| Q9HGI6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 40% | 93% |
| Q9HGI8 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 45% | 93% |
| Q9W074 | Drosophila melanogaster | 37% | 97% |
| Q9Y450 | Homo sapiens | 37% | 95% |
| Q9Y713 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 37% | 100% |
| Q9YIC0 | Oryzias latipes | 36% | 100% |
| Q9ZT91 | Arabidopsis thaliana | 26% | 100% |
| V5BT94 | Trypanosoma cruzi | 32% | 98% |
| V5BWI6 | Trypanosoma cruzi | 80% | 100% |