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 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IMH5
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.421 |
CLV_PCSK_PC7_1 | 20 | 26 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.334 |
DEG_COP1_1 | 79 | 89 | PF00400 | 0.417 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.397 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.438 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.443 |
DOC_ANK_TNKS_1 | 356 | 363 | PF00023 | 0.582 |
DOC_CYCLIN_RxL_1 | 520 | 528 | PF00134 | 0.317 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 174 | 180 | PF00134 | 0.500 |
DOC_MAPK_DCC_7 | 279 | 288 | PF00069 | 0.323 |
DOC_MAPK_DCC_7 | 33 | 42 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 340 | 349 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 340 | 349 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 57 | 64 | PF00149 | 0.327 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.373 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.419 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.383 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.386 |
DOC_USP7_MATH_2 | 323 | 329 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 544 | 548 | PF12436 | 0.468 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.543 |
LIG_14-3-3_CanoR_1 | 115 | 125 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 24 | 32 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 426 | 434 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 455 | 465 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 497 | 505 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 542 | 547 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 481 | 499 | PF00022 | 0.443 |
LIG_BIR_III_4 | 486 | 490 | PF00653 | 0.325 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.287 |
LIG_Clathr_ClatBox_1 | 180 | 184 | PF01394 | 0.434 |
LIG_deltaCOP1_diTrp_1 | 184 | 194 | PF00928 | 0.435 |
LIG_deltaCOP1_diTrp_1 | 558 | 563 | PF00928 | 0.285 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.693 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.410 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.525 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.390 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.359 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.390 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.382 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.313 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.437 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.410 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.411 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.470 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 431 | 437 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 301 | 310 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.349 |
LIG_LYPXL_SIV_4 | 196 | 204 | PF13949 | 0.391 |
LIG_PDZ_Class_2 | 586 | 591 | PF00595 | 0.445 |
LIG_Pex14_2 | 47 | 51 | PF04695 | 0.383 |
LIG_REV1ctd_RIR_1 | 491 | 501 | PF16727 | 0.379 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.396 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.327 |
LIG_SH2_GRB2like | 450 | 453 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 244 | 248 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 280 | 284 | PF00017 | 0.349 |
LIG_SH2_PTP2 | 222 | 225 | PF00017 | 0.477 |
LIG_SH2_SRC | 280 | 283 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.367 |
LIG_SH3_1 | 279 | 285 | PF00018 | 0.470 |
LIG_SH3_2 | 311 | 316 | PF14604 | 0.458 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.587 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.494 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.455 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.463 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.381 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.289 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.519 |
LIG_SUMO_SIM_par_1 | 284 | 293 | PF11976 | 0.314 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.553 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.348 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.438 |
LIG_TRAF2_1 | 562 | 565 | PF00917 | 0.467 |
LIG_TRFH_1 | 63 | 67 | PF08558 | 0.296 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.391 |
LIG_UBA3_1 | 492 | 501 | PF00899 | 0.330 |
LIG_WRC_WIRS_1 | 98 | 103 | PF05994 | 0.382 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.406 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.571 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.461 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.549 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.336 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.527 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.394 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.418 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.345 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.505 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.487 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.501 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.439 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.427 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.725 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.356 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.320 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.293 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.357 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.381 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.328 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.269 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.505 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.403 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.596 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.443 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.555 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.499 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.459 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.468 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.458 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.473 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.330 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.433 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.483 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.368 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.407 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.361 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.551 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.445 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.443 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.357 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.283 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.401 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.427 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.477 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.267 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.395 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.374 |
MOD_NEK2_2 | 53 | 58 | PF00069 | 0.373 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.605 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.564 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.327 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.386 |
MOD_PKA_1 | 74 | 80 | PF00069 | 0.425 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.557 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.386 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.575 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.317 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.361 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.425 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.622 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.464 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.347 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.383 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.593 |
MOD_Plk_2-3 | 461 | 467 | PF00069 | 0.362 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.424 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.419 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.369 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.359 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.489 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.499 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.407 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.410 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.380 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.393 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.333 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 282 | 287 | PF01217 | 0.360 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 582 | 585 | PF00400 | 0.273 |
TRG_NES_CRM1_1 | 486 | 498 | PF08389 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.220 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILV6 | Leptomonas seymouri | 79% | 100% |
A0A0S4J9M2 | Bodo saltans | 49% | 100% |
A0A1X0NIM0 | Trypanosomatidae | 57% | 100% |
A0A3R7LDW9 | Trypanosoma rangeli | 60% | 100% |
A4HD80 | Leishmania braziliensis | 90% | 100% |
D0A6Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9AH35 | Leishmania infantum | 100% | 100% |
E9AWL3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O22466 | Solanum lycopersicum | 24% | 100% |
O22467 | Arabidopsis thaliana | 24% | 100% |
O22468 | Arabidopsis thaliana | 24% | 100% |
O22469 | Arabidopsis thaliana | 22% | 100% |
O22607 | Arabidopsis thaliana | 23% | 100% |
O93377 | Xenopus laevis | 25% | 100% |
P0CS36 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 100% |
P0CS37 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 100% |
P13712 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P90916 | Caenorhabditis elegans | 25% | 100% |
P90917 | Caenorhabditis elegans | 25% | 100% |
Q09028 | Homo sapiens | 25% | 100% |
Q10G81 | Oryza sativa subsp. japonica | 24% | 100% |
Q16576 | Homo sapiens | 24% | 100% |
Q24572 | Drosophila melanogaster | 25% | 100% |
Q2UA71 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 23% | 100% |
Q3MHL3 | Bos taurus | 25% | 100% |
Q3SWX8 | Bos taurus | 24% | 100% |
Q4I7L0 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 24% | 100% |
Q4P553 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 100% |
Q4QAV7 | Leishmania major | 98% | 100% |
Q4R304 | Macaca fascicularis | 24% | 100% |
Q4WEI5 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 100% |
Q54SD4 | Dictyostelium discoideum | 22% | 100% |
Q5M7K4 | Xenopus tropicalis | 25% | 100% |
Q5R654 | Pongo abelii | 24% | 100% |
Q5RF92 | Pongo abelii | 25% | 100% |
Q60972 | Mus musculus | 25% | 100% |
Q60973 | Mus musculus | 24% | 100% |
Q61Y48 | Caenorhabditis briggsae | 24% | 100% |
Q6C7Q4 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 22% | 100% |
Q6INH0 | Xenopus laevis | 25% | 100% |
Q6P315 | Xenopus tropicalis | 24% | 100% |
Q6P3H7 | Danio rerio | 25% | 100% |
Q71UF4 | Rattus norvegicus | 24% | 100% |
Q7S7N3 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 22% | 100% |
Q7ZTY4 | Danio rerio | 25% | 100% |
Q8AVH1 | Xenopus laevis | 25% | 100% |
Q9I8G9 | Gallus gallus | 24% | 100% |
Q9W7I5 | Gallus gallus | 25% | 100% |
Q9Y825 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
V5BAV4 | Trypanosoma cruzi | 58% | 100% |