Appears to be a secreted chaperone, related to mammalian HYOU1 proteins. Probably ER-localized as in other eukaryotes
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. | yes | yes: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 11, no: 2 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0034663 | endoplasmic reticulum chaperone complex | 3 | 2 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 2 |
GO:0043226 | organelle | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9AFU8
Term | Name | Level | Count |
---|---|---|---|
GO:0001666 | response to hypoxia | 3 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0009966 | regulation of signal transduction | 4 | 2 |
GO:0009968 | negative regulation of signal transduction | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010646 | regulation of cell communication | 4 | 2 |
GO:0010648 | negative regulation of cell communication | 5 | 2 |
GO:0010941 | regulation of cell death | 4 | 2 |
GO:0023051 | regulation of signaling | 3 | 2 |
GO:0023057 | negative regulation of signaling | 4 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0036293 | response to decreased oxygen levels | 4 | 2 |
GO:0036294 | cellular response to decreased oxygen levels | 5 | 2 |
GO:0042221 | response to chemical | 2 | 2 |
GO:0042981 | regulation of apoptotic process | 6 | 2 |
GO:0043066 | negative regulation of apoptotic process | 7 | 2 |
GO:0043067 | regulation of programmed cell death | 5 | 2 |
GO:0043069 | negative regulation of programmed cell death | 6 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0048583 | regulation of response to stimulus | 3 | 2 |
GO:0048585 | negative regulation of response to stimulus | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0060548 | negative regulation of cell death | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0070482 | response to oxygen levels | 3 | 2 |
GO:0070887 | cellular response to chemical stimulus | 3 | 2 |
GO:0071453 | cellular response to oxygen levels | 4 | 2 |
GO:0071456 | cellular response to hypoxia | 4 | 2 |
GO:0080134 | regulation of response to stress | 4 | 2 |
GO:0080135 | regulation of cellular response to stress | 4 | 2 |
GO:1900037 | regulation of cellular response to hypoxia | 5 | 2 |
GO:1900038 | negative regulation of cellular response to hypoxia | 5 | 2 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 2 |
GO:1902532 | negative regulation of intracellular signal transduction | 6 | 2 |
GO:1903297 | regulation of hypoxia-induced intrinsic apoptotic signaling pathway | 7 | 2 |
GO:1903298 | negative regulation of hypoxia-induced intrinsic apoptotic signaling pathway | 6 | 2 |
GO:2001233 | regulation of apoptotic signaling pathway | 5 | 2 |
GO:2001234 | negative regulation of apoptotic signaling pathway | 6 | 2 |
GO:2001242 | regulation of intrinsic apoptotic signaling pathway | 6 | 2 |
GO:2001243 | negative regulation of intrinsic apoptotic signaling pathway | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0044183 | protein folding chaperone | 1 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.462 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.463 |
DOC_CYCLIN_RxL_1 | 424 | 434 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.608 |
DOC_MAPK_gen_1 | 353 | 361 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 67 | 73 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 97 | 107 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 162 | 170 | PF00069 | 0.388 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.462 |
DOC_PP1_RVXF_1 | 436 | 442 | PF00149 | 0.446 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.492 |
DOC_USP7_MATH_2 | 704 | 710 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 568 | 572 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.296 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 425 | 430 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 456 | 466 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 567 | 571 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 57 | 66 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 623 | 630 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.345 |
LIG_AP2alpha_2 | 134 | 136 | PF02296 | 0.479 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 470 | 474 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.377 |
LIG_Clathr_ClatBox_1 | 535 | 539 | PF01394 | 0.369 |
LIG_EVH1_1 | 237 | 241 | PF00568 | 0.246 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.407 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.479 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.318 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.339 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.462 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.444 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.366 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.348 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.449 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.363 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.764 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.344 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.341 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.440 |
LIG_GBD_Chelix_1 | 24 | 32 | PF00786 | 0.479 |
LIG_LIR_Apic_2 | 235 | 239 | PF02991 | 0.246 |
LIG_LIR_Apic_2 | 589 | 595 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 300 | 308 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 34 | 42 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 374 | 381 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 491 | 501 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.341 |
LIG_PCNA_TLS_4 | 627 | 634 | PF02747 | 0.387 |
LIG_PDZ_Class_3 | 718 | 723 | PF00595 | 0.792 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.479 |
LIG_PTB_Apo_2 | 363 | 370 | PF02174 | 0.479 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.446 |
LIG_SH2_PTP2 | 36 | 39 | PF00017 | 0.369 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.479 |
LIG_SH2_SRC | 236 | 239 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 485 | 489 | PF00017 | 0.246 |
LIG_SH2_STAP1 | 547 | 551 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 686 | 690 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.462 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.375 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.387 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.246 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.354 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.463 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.263 |
LIG_SH3_5 | 330 | 334 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 187 | 193 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 124 | 132 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 532 | 539 | PF11976 | 0.325 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.354 |
LIG_TRAF2_1 | 599 | 602 | PF00917 | 0.462 |
LIG_TRAF2_1 | 666 | 669 | PF00917 | 0.450 |
LIG_UBA3_1 | 377 | 386 | PF00899 | 0.440 |
LIG_WRC_WIRS_1 | 372 | 377 | PF05994 | 0.458 |
MOD_CDK_SPK_2 | 381 | 386 | PF00069 | 0.369 |
MOD_CDK_SPxxK_3 | 170 | 177 | PF00069 | 0.462 |
MOD_CDK_SPxxK_3 | 418 | 425 | PF00069 | 0.388 |
MOD_CDK_SPxxK_3 | 509 | 516 | PF00069 | 0.399 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.401 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.330 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.362 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.314 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.424 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.737 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.341 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.404 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.341 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.406 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.374 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.432 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.468 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.446 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.479 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.442 |
MOD_GlcNHglycan | 585 | 589 | PF01048 | 0.341 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.752 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.444 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.410 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.424 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.464 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.440 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.353 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.303 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.341 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.398 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.364 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.276 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.467 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.712 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.354 |
MOD_N-GLC_1 | 365 | 370 | PF02516 | 0.433 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.328 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.356 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.363 |
MOD_N-GLC_1 | 557 | 562 | PF02516 | 0.363 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.462 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.539 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.341 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.430 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.372 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.418 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.405 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.437 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.429 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.386 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.149 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.424 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.452 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.456 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.364 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.485 |
MOD_PIKK_1 | 603 | 609 | PF00454 | 0.485 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.491 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.462 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.462 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.429 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.412 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.432 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.486 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.341 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.420 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.341 |
MOD_PKB_1 | 97 | 105 | PF00069 | 0.401 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.401 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.354 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.342 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.397 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.391 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.455 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.358 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.348 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.434 |
MOD_Plk_1 | 662 | 668 | PF00069 | 0.477 |
MOD_Plk_2-3 | 371 | 377 | PF00069 | 0.462 |
MOD_Plk_2-3 | 566 | 572 | PF00069 | 0.388 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.419 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.481 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.375 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.486 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.369 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.368 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.387 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.348 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.452 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.296 |
MOD_SUMO_for_1 | 608 | 611 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 128 | 135 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 156 | 164 | PF00179 | 0.419 |
MOD_SUMO_rev_2 | 561 | 570 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_3 | 139 | 145 | PF01217 | 0.387 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 579 | 582 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.401 |
TRG_NES_CRM1_1 | 356 | 371 | PF08389 | 0.452 |
TRG_NES_CRM1_1 | 393 | 407 | PF08389 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 659 | 663 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDD3 | Leptomonas seymouri | 24% | 86% |
A0A0N1PEF0 | Leptomonas seymouri | 68% | 97% |
A0A0S4IUD0 | Bodo saltans | 24% | 100% |
A0A0S4IUZ2 | Bodo saltans | 34% | 82% |
A0A0S4JJU2 | Bodo saltans | 39% | 94% |
A0A0S4JRV7 | Bodo saltans | 25% | 87% |
A0A1X0NER7 | Trypanosomatidae | 24% | 100% |
A0A1X0P2S1 | Trypanosomatidae | 30% | 83% |
A0A1X0P4V9 | Trypanosomatidae | 47% | 100% |
A0A1X0P8H2 | Trypanosomatidae | 24% | 88% |
A0A3R7L0X2 | Trypanosoma rangeli | 27% | 87% |
A0A3S5H744 | Leishmania donovani | 25% | 88% |
A0A3S5H808 | Leishmania donovani | 93% | 100% |
A0A422NGS3 | Trypanosoma rangeli | 33% | 77% |
A0A422P1B1 | Trypanosoma rangeli | 48% | 100% |
A2Q0Z1 | Equus caballus | 24% | 100% |
A4H9P0 | Leishmania braziliensis | 25% | 88% |
A4HGY1 | Leishmania braziliensis | 25% | 100% |
A4HND7 | Leishmania braziliensis | 81% | 100% |
A4IC10 | Leishmania infantum | 94% | 100% |
A5A8V7 | Sus scrofa | 25% | 100% |
C9ZXL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 87% |
C9ZYJ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A590 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 89% |
E9AGQ5 | Leishmania infantum | 25% | 88% |
E9ARS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 88% |
E9B700 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
F4HQD4 | Arabidopsis thaliana | 26% | 87% |
F4JMJ1 | Arabidopsis thaliana | 25% | 83% |
O59838 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
O59855 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O74225 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 100% |
O88600 | Rattus norvegicus | 26% | 86% |
O93866 | Trichophyton rubrum | 24% | 100% |
O97125 | Drosophila melanogaster | 25% | 100% |
P02825 | Drosophila melanogaster | 25% | 100% |
P08418 | Schistosoma mansoni | 24% | 100% |
P0CB32 | Bos taurus | 26% | 100% |
P0DMV8 | Homo sapiens | 25% | 100% |
P0DMV9 | Homo sapiens | 25% | 100% |
P0DMW0 | Rattus norvegicus | 25% | 100% |
P0DMW1 | Rattus norvegicus | 25% | 100% |
P11142 | Homo sapiens | 24% | 100% |
P11145 | Trypanosoma brucei brucei | 25% | 100% |
P11147 | Drosophila melanogaster | 24% | 100% |
P16627 | Mus musculus | 25% | 100% |
P17066 | Homo sapiens | 25% | 100% |
P17879 | Mus musculus | 25% | 100% |
P18694 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 100% |
P19120 | Bos taurus | 24% | 100% |
P19378 | Cricetulus griseus | 23% | 100% |
P29843 | Drosophila melanogaster | 24% | 100% |
P32589 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P32590 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P34930 | Sus scrofa | 25% | 100% |
P34931 | Homo sapiens | 25% | 100% |
P34932 | Homo sapiens | 26% | 86% |
P36415 | Dictyostelium discoideum | 26% | 100% |
P40918 | Davidiella tassiana | 24% | 100% |
P41753 | Achlya klebsiana | 23% | 100% |
P41825 | Anopheles albimanus | 24% | 100% |
P41826 | Anopheles albimanus | 24% | 100% |
P41827 | Anopheles albimanus | 24% | 100% |
P47773 | Ictalurus punctatus | 23% | 100% |
P48720 | Blastocladiella emersonii | 25% | 100% |
P55063 | Rattus norvegicus | 25% | 100% |
P63017 | Mus musculus | 24% | 100% |
P63018 | Rattus norvegicus | 24% | 100% |
P82910 | Drosophila melanogaster | 25% | 100% |
P87047 | Paracoccidioides lutzii (strain ATCC MYA-826 / Pb01) | 25% | 100% |
Q00043 | Ajellomyces capsulatus | 25% | 100% |
Q01233 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 100% |
Q04967 | Sus scrofa | 25% | 100% |
Q05036 | Caenorhabditis elegans | 25% | 93% |
Q0IIM3 | Bos taurus | 29% | 84% |
Q0VA61 | Xenopus tropicalis | 30% | 100% |
Q10265 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
Q24789 | Echinococcus granulosus | 24% | 100% |
Q27965 | Bos taurus | 25% | 100% |
Q27975 | Bos taurus | 25% | 100% |
Q2TFN9 | Canis lupus familiaris | 28% | 86% |
Q4QDQ2 | Leishmania major | 25% | 88% |
Q4R888 | Macaca fascicularis | 25% | 100% |
Q4U0F3 | Bos mutus grunniens | 25% | 100% |
Q53RJ5 | Oryza sativa subsp. japonica | 24% | 100% |
Q566I3 | Xenopus laevis | 31% | 100% |
Q5B2V1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 100% |
Q5NVM9 | Pongo abelii | 24% | 100% |
Q5R7D3 | Pongo abelii | 25% | 100% |
Q5RDM4 | Pongo abelii | 26% | 86% |
Q5ZLK7 | Gallus gallus | 27% | 72% |
Q61316 | Mus musculus | 28% | 86% |
Q61696 | Mus musculus | 25% | 100% |
Q63617 | Rattus norvegicus | 31% | 72% |
Q6FJI3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 100% |
Q6S4N2 | Sus scrofa | 25% | 100% |
Q6TMK3 | Dictyostelium discoideum | 24% | 94% |
Q71U34 | Saguinus oedipus | 24% | 100% |
Q74ZJ0 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 24% | 100% |
Q75C78 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 24% | 100% |
Q7YQC6 | Canis lupus familiaris | 25% | 100% |
Q7ZUW2 | Danio rerio | 28% | 74% |
Q875P5 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 26% | 100% |
Q875V0 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 25% | 100% |
Q8INI8 | Drosophila melanogaster | 25% | 100% |
Q90473 | Danio rerio | 24% | 100% |
Q91233 | Oncorhynchus tshawytscha | 24% | 100% |
Q96W30 | Paracoccidioides lutzii (strain ATCC MYA-826 / Pb01) | 25% | 100% |
Q9BIR7 | Drosophila melanogaster | 25% | 100% |
Q9BIS2 | Drosophila melanogaster | 25% | 100% |
Q9GSU4 | Drosophila simulans | 25% | 100% |
Q9GSU7 | Drosophila simulans | 25% | 100% |
Q9JKR6 | Mus musculus | 31% | 72% |
Q9N1U2 | Saguinus oedipus | 24% | 100% |
Q9S7C0 | Arabidopsis thaliana | 26% | 87% |
Q9SAB1 | Arabidopsis thaliana | 23% | 95% |
Q9U639 | Manduca sexta | 25% | 100% |
Q9VG58 | Drosophila melanogaster | 25% | 100% |
Q9Y4L1 | Homo sapiens | 32% | 72% |
V5ARL4 | Trypanosoma cruzi | 46% | 100% |
V5DD81 | Trypanosoma cruzi | 31% | 89% |
V5DFF3 | Trypanosoma cruzi | 26% | 87% |