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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0033588 | elongator holoenzyme complex | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:0005819 | spindle | 5 | 1 |
Related structures:
AlphaFold database: A4HD08
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 2 |
GO:0002098 | tRNA wobble uridine modification | 8 | 2 |
GO:0002926 | tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation | 9 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006400 | tRNA modification | 6 | 2 |
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006475 | internal protein amino acid acetylation | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008033 | tRNA processing | 8 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016573 | histone acetylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0018393 | internal peptidyl-lysine acetylation | 8 | 1 |
GO:0018394 | peptidyl-lysine acetylation | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043007 | maintenance of rDNA | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0043570 | maintenance of DNA repeat elements | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 23 |
GO:0003676 | nucleic acid binding | 3 | 23 |
GO:0003723 | RNA binding | 4 | 23 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0016407 | acetyltransferase activity | 5 | 23 |
GO:0016740 | transferase activity | 2 | 23 |
GO:0016746 | acyltransferase activity | 3 | 23 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 23 |
GO:0043167 | ion binding | 2 | 23 |
GO:0043169 | cation binding | 3 | 23 |
GO:0046872 | metal ion binding | 4 | 23 |
GO:0051536 | iron-sulfur cluster binding | 3 | 23 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 23 |
GO:0051540 | metal cluster binding | 2 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0106261 | tRNA uridine(34) acetyltransferase activity | 6 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.430 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.222 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.579 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 414 | 422 | PF00400 | 0.418 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.324 |
DOC_MAPK_gen_1 | 109 | 120 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 241 | 249 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 546 | 555 | PF00069 | 0.401 |
DOC_MAPK_HePTP_8 | 107 | 123 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 241 | 249 | PF00069 | 0.375 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.277 |
DOC_PP4_FxxP_1 | 130 | 133 | PF00568 | 0.312 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.371 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.540 |
LIG_14-3-3_CanoR_1 | 202 | 208 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 225 | 231 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 448 | 455 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.242 |
LIG_14-3-3_CanoR_1 | 80 | 88 | PF00244 | 0.415 |
LIG_AP2alpha_1 | 454 | 458 | PF02296 | 0.275 |
LIG_BRCT_BRCA1_1 | 203 | 207 | PF00533 | 0.461 |
LIG_EH1_1 | 378 | 386 | PF00400 | 0.484 |
LIG_eIF4E_1 | 379 | 385 | PF01652 | 0.451 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.418 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.442 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.521 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.349 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.298 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.493 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.427 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.415 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.410 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.299 |
LIG_LIR_Apic_2 | 11 | 15 | PF02991 | 0.503 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.264 |
LIG_LIR_Apic_2 | 129 | 133 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 29 | 37 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 328 | 336 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 4 | 12 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 464 | 474 | PF02991 | 0.280 |
LIG_LIR_LC3C_4 | 116 | 121 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 4 | 8 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 512 | 516 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 602 | 607 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.360 |
LIG_Pex14_2 | 160 | 164 | PF04695 | 0.516 |
LIG_Pex14_2 | 330 | 334 | PF04695 | 0.321 |
LIG_Pex14_2 | 454 | 458 | PF04695 | 0.260 |
LIG_PTB_Apo_2 | 373 | 380 | PF02174 | 0.539 |
LIG_PTB_Apo_2 | 387 | 394 | PF02174 | 0.340 |
LIG_PTB_Phospho_1 | 373 | 379 | PF10480 | 0.539 |
LIG_PTB_Phospho_1 | 387 | 393 | PF10480 | 0.340 |
LIG_SH2_CRK | 513 | 517 | PF00017 | 0.275 |
LIG_SH2_CRK | 565 | 569 | PF00017 | 0.285 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 12 | 16 | PF00017 | 0.420 |
LIG_SH2_NCK_1 | 171 | 175 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 219 | 223 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.246 |
LIG_SH3_2 | 223 | 228 | PF14604 | 0.484 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.418 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.442 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.373 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 515 | 520 | PF11976 | 0.260 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.349 |
LIG_UBA3_1 | 506 | 515 | PF00899 | 0.325 |
LIG_WRPW_2 | 368 | 371 | PF00400 | 0.260 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.527 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.465 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.262 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.569 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.536 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.380 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.275 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.253 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.313 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.290 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.283 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.412 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.275 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.305 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.239 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.499 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.532 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.544 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.620 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.391 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.271 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.291 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.266 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.275 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.527 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.558 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.436 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.408 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.312 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.260 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.260 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.269 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.454 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.400 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.312 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.568 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.468 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.260 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.281 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.412 |
MOD_PIKK_1 | 473 | 479 | PF00454 | 0.409 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.380 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.210 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.134 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.294 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.190 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.247 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.397 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.296 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.404 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.328 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.319 |
MOD_Plk_1 | 599 | 605 | PF00069 | 0.660 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.295 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.348 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.269 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.334 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.432 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.564 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.278 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.330 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.584 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.517 |
MOD_SUMO_rev_2 | 11 | 21 | PF00179 | 0.481 |
TRG_DiLeu_BaEn_4 | 493 | 499 | PF01217 | 0.239 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.253 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.343 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.262 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.252 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.260 |
TRG_ER_diArg_1 | 550 | 552 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.268 |
TRG_ER_FFAT_2 | 250 | 260 | PF00635 | 0.239 |
TRG_NES_CRM1_1 | 260 | 273 | PF08389 | 0.275 |
TRG_NLS_MonoExtC_3 | 108 | 113 | PF00514 | 0.452 |
TRG_NLS_MonoExtN_4 | 109 | 114 | PF00514 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 228 | 232 | PF00026 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 399 | 403 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 89 | 94 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P567 | Leptomonas seymouri | 87% | 91% |
A0A0N1PFU7 | Leptomonas seymouri | 45% | 83% |
A0A0S4IQT9 | Bodo saltans | 68% | 96% |
A0A0S4KPU1 | Bodo saltans | 45% | 91% |
A0A1C7D1B7 | Dehalococcoides mccartyi (strain CBDB1) | 37% | 100% |
A0A1X0NG94 | Trypanosomatidae | 41% | 84% |
A0A1X0NX69 | Trypanosomatidae | 76% | 90% |
A0A3Q8ICG0 | Leishmania donovani | 45% | 81% |
A0A3R7KUY9 | Trypanosoma rangeli | 77% | 93% |
A0A3S7WXV4 | Leishmania donovani | 94% | 87% |
A0A422NDG5 | Trypanosoma rangeli | 44% | 83% |
A4H8F0 | Leishmania braziliensis | 44% | 81% |
A4HWS3 | Leishmania infantum | 45% | 81% |
A4I0J4 | Leishmania infantum | 93% | 87% |
C9ZVC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 93% |
C9ZW50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 91% |
D5VRB9 | Methanocaldococcus infernus (strain DSM 11812 / JCM 15783 / ME) | 36% | 100% |
E9AQI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 80% |
E9AWF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 88% |
O14023 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q02908 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
Q1ZXC6 | Dictyostelium discoideum | 33% | 100% |
Q23651 | Caenorhabditis elegans | 34% | 100% |
Q2KJ61 | Bos taurus | 33% | 100% |
Q4QB17 | Leishmania major | 94% | 100% |
Q4QEZ6 | Leishmania major | 45% | 100% |
Q58536 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 35% | 100% |
Q5HZM6 | Xenopus laevis | 33% | 100% |
Q5RIC0 | Danio rerio | 33% | 100% |
Q5ZHS1 | Gallus gallus | 35% | 100% |
Q60LW7 | Caenorhabditis briggsae | 33% | 100% |
Q6NVL5 | Xenopus tropicalis | 32% | 100% |
Q7X7L3 | Oryza sativa subsp. japonica | 35% | 100% |
Q93ZR1 | Arabidopsis thaliana | 34% | 100% |
Q9CZX0 | Mus musculus | 33% | 100% |
Q9H9T3 | Homo sapiens | 33% | 100% |
Q9VQZ6 | Drosophila melanogaster | 32% | 100% |
V5B5L2 | Trypanosoma cruzi | 43% | 91% |
V5BNQ5 | Trypanosoma cruzi | 76% | 92% |