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: A4I0J4
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 | 11 | 13 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.667 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 643 | 645 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 495 | 497 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.616 |
DEG_APCC_DBOX_1 | 474 | 482 | PF00400 | 0.430 |
DEG_APCC_DBOX_1 | 495 | 503 | PF00400 | 0.430 |
DOC_MAPK_gen_1 | 190 | 201 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 322 | 330 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.512 |
DOC_MAPK_HePTP_8 | 188 | 204 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 322 | 330 | PF00069 | 0.385 |
DOC_PIKK_1 | 97 | 105 | PF02985 | 0.465 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.526 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.297 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.192 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.642 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 306 | 312 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 540 | 548 | PF00244 | 0.259 |
LIG_AP2alpha_1 | 535 | 539 | PF02296 | 0.293 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.515 |
LIG_EH1_1 | 459 | 467 | PF00400 | 0.495 |
LIG_eIF4E_1 | 460 | 466 | PF01652 | 0.464 |
LIG_EVH1_1 | 25 | 29 | PF00568 | 0.528 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.430 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.445 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.349 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.282 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.333 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.440 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.427 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.422 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.316 |
LIG_LIR_Apic_2 | 203 | 208 | PF02991 | 0.276 |
LIG_LIR_Apic_2 | 210 | 214 | PF02991 | 0.429 |
LIG_LIR_Apic_2 | 92 | 96 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 110 | 118 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 434 | 445 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 545 | 555 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 683 | 692 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 85 | 93 | PF02991 | 0.498 |
LIG_LIR_LC3C_4 | 197 | 202 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 276 | 280 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 557 | 563 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 593 | 597 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 694 | 698 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 85 | 89 | PF02991 | 0.484 |
LIG_PCNA_yPIPBox_3 | 174 | 188 | PF02747 | 0.426 |
LIG_PDZ_Class_3 | 704 | 709 | PF00595 | 0.470 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.529 |
LIG_Pex14_2 | 411 | 415 | PF04695 | 0.328 |
LIG_Pex14_2 | 535 | 539 | PF04695 | 0.277 |
LIG_PTB_Apo_2 | 454 | 461 | PF02174 | 0.544 |
LIG_PTB_Phospho_1 | 454 | 460 | PF10480 | 0.544 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.382 |
LIG_SH2_CRK | 594 | 598 | PF00017 | 0.293 |
LIG_SH2_CRK | 646 | 650 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 300 | 304 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 93 | 97 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 685 | 689 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.262 |
LIG_SH3_2 | 304 | 309 | PF14604 | 0.495 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.571 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.430 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.532 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.454 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.431 |
LIG_SUMO_SIM_anti_2 | 197 | 203 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 266 | 272 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 197 | 203 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 596 | 601 | PF11976 | 0.277 |
LIG_TRAF2_1 | 572 | 575 | PF00917 | 0.363 |
LIG_UBA3_1 | 587 | 596 | PF00899 | 0.341 |
LIG_WRC_WIRS_1 | 685 | 690 | PF05994 | 0.685 |
LIG_WRC_WIRS_1 | 692 | 697 | PF05994 | 0.585 |
LIG_WRPW_2 | 449 | 452 | PF00400 | 0.277 |
MOD_CDK_SPK_2 | 699 | 704 | PF00069 | 0.442 |
MOD_CDK_SPxK_1 | 699 | 705 | PF00069 | 0.444 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.470 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.403 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.279 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.758 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.544 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.503 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.496 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.540 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.293 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.271 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.330 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.307 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.321 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.300 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.496 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.523 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.367 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.693 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.300 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.319 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.266 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.500 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.543 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.503 |
MOD_GlcNHglycan | 681 | 685 | PF01048 | 0.589 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.418 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.300 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.305 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.283 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.230 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.356 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.277 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.678 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.584 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.407 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.417 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.473 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.323 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.286 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.311 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.285 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.456 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.499 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.348 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.549 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.586 |
MOD_NEK2_1 | 698 | 703 | PF00069 | 0.678 |
MOD_NEK2_2 | 275 | 280 | PF00069 | 0.277 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.293 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.411 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.392 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.225 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.114 |
MOD_PK_1 | 60 | 66 | PF00069 | 0.539 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.402 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.300 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.278 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.451 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.283 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.404 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.341 |
MOD_Plk_1 | 653 | 659 | PF00069 | 0.356 |
MOD_Plk_1 | 680 | 686 | PF00069 | 0.676 |
MOD_Plk_2-3 | 313 | 319 | PF00069 | 0.312 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.347 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.292 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.337 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.437 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.277 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.340 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.449 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.601 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.638 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.530 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.558 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.451 |
MOD_SUMO_rev_2 | 92 | 102 | PF00179 | 0.500 |
TRG_DiLeu_BaEn_4 | 574 | 580 | PF01217 | 0.266 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 380 | 385 | PF01217 | 0.264 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 646 | 649 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.642 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.279 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 474 | 477 | PF00400 | 0.251 |
TRG_ER_diArg_1 | 507 | 510 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 563 | 566 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 642 | 644 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 703 | 705 | PF00400 | 0.614 |
TRG_ER_FFAT_2 | 331 | 341 | PF00635 | 0.266 |
TRG_NES_CRM1_1 | 341 | 354 | PF08389 | 0.293 |
TRG_NLS_MonoExtC_3 | 11 | 16 | PF00514 | 0.485 |
TRG_NLS_MonoExtC_3 | 189 | 194 | PF00514 | 0.411 |
TRG_NLS_MonoExtN_4 | 12 | 17 | PF00514 | 0.491 |
TRG_NLS_MonoExtN_4 | 190 | 195 | PF00514 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 170 | 175 | PF00026 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 309 | 313 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 480 | 484 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 660 | 664 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P567 | Leptomonas seymouri | 86% | 100% |
A0A0N1PFU7 | Leptomonas seymouri | 45% | 95% |
A0A0S4IQT9 | Bodo saltans | 69% | 100% |
A0A0S4KPU1 | Bodo saltans | 46% | 100% |
A0A1X0NG94 | Trypanosomatidae | 42% | 96% |
A0A1X0NX69 | Trypanosomatidae | 76% | 100% |
A0A3Q8ICG0 | Leishmania donovani | 46% | 93% |
A0A3R7KUY9 | Trypanosoma rangeli | 77% | 100% |
A0A3S7WXV4 | Leishmania donovani | 100% | 100% |
A0A422NDG5 | Trypanosoma rangeli | 42% | 95% |
A4H8F0 | Leishmania braziliensis | 45% | 93% |
A4HD08 | Leishmania braziliensis | 93% | 100% |
A4HWS3 | Leishmania infantum | 46% | 93% |
C9ZVC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 77% | 100% |
C9ZW50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
D5VRB9 | Methanocaldococcus infernus (strain DSM 11812 / JCM 15783 / ME) | 36% | 100% |
E9AQI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 92% |
E9AWF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O14023 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q02908 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
Q1ZXC6 | Dictyostelium discoideum | 33% | 100% |
Q23651 | Caenorhabditis elegans | 34% | 100% |
Q2KJ61 | Bos taurus | 32% | 100% |
Q4QB17 | Leishmania major | 96% | 100% |
Q4QEZ6 | Leishmania major | 45% | 93% |
Q58536 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 36% | 100% |
Q5HZM6 | Xenopus laevis | 33% | 100% |
Q5RIC0 | Danio rerio | 33% | 100% |
Q5ZHS1 | Gallus gallus | 33% | 100% |
Q60LW7 | Caenorhabditis briggsae | 35% | 100% |
Q6NVL5 | Xenopus tropicalis | 32% | 100% |
Q7X7L3 | Oryza sativa subsp. japonica | 35% | 100% |
Q93ZR1 | Arabidopsis thaliana | 33% | 100% |
Q9CZX0 | Mus musculus | 31% | 100% |
Q9H9T3 | Homo sapiens | 32% | 100% |
Q9VQZ6 | Drosophila melanogaster | 33% | 100% |
V5B5L2 | Trypanosoma cruzi | 43% | 100% |
V5BNQ5 | Trypanosoma cruzi | 77% | 100% |