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: E9AWF5
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 | 0.492 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.124 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.281 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.136 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.686 |
CLV_PCSK_PC1ET2_1 | 493 | 495 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.605 |
DEG_APCC_DBOX_1 | 472 | 480 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 493 | 501 | PF00400 | 0.418 |
DOC_ANK_TNKS_1 | 171 | 178 | PF00023 | 0.265 |
DOC_CYCLIN_RxL_1 | 374 | 384 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 50 | 56 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 188 | 199 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 320 | 328 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 338 | 348 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 625 | 634 | PF00069 | 0.401 |
DOC_MAPK_HePTP_8 | 186 | 202 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 320 | 328 | PF00069 | 0.376 |
DOC_PIKK_1 | 95 | 103 | PF02985 | 0.457 |
DOC_PP2B_LxvP_1 | 50 | 53 | PF13499 | 0.446 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.278 |
DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.309 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.614 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 159 | 167 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 304 | 310 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 538 | 546 | PF00244 | 0.243 |
LIG_AP2alpha_1 | 533 | 537 | PF02296 | 0.276 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.533 |
LIG_Clathr_ClatBox_1 | 419 | 423 | PF01394 | 0.307 |
LIG_EH1_1 | 457 | 465 | PF00400 | 0.484 |
LIG_eIF4E_1 | 458 | 464 | PF01652 | 0.452 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.418 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.443 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.349 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.579 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.326 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.428 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.415 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.410 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.331 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.299 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.349 |
LIG_LIR_Apic_2 | 18 | 24 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 201 | 206 | PF02991 | 0.265 |
LIG_LIR_Apic_2 | 208 | 212 | PF02991 | 0.328 |
LIG_LIR_Apic_2 | 90 | 94 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 407 | 415 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 432 | 443 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 543 | 553 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 626 | 636 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 681 | 690 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 83 | 91 | PF02991 | 0.489 |
LIG_LIR_LC3C_4 | 195 | 200 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 543 | 549 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 555 | 561 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 591 | 595 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 692 | 696 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 83 | 87 | PF02991 | 0.474 |
LIG_PCNA_yPIPBox_3 | 172 | 186 | PF02747 | 0.420 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.516 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.315 |
LIG_Pex14_2 | 533 | 537 | PF04695 | 0.260 |
LIG_PTB_Apo_2 | 452 | 459 | PF02174 | 0.540 |
LIG_PTB_Phospho_1 | 452 | 458 | PF10480 | 0.540 |
LIG_Rb_pABgroove_1 | 244 | 252 | PF01858 | 0.324 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.381 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.276 |
LIG_SH2_CRK | 644 | 648 | PF00017 | 0.286 |
LIG_SH2_NCK_1 | 250 | 254 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 298 | 302 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 683 | 687 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.246 |
LIG_SH3_2 | 302 | 307 | PF14604 | 0.484 |
LIG_SH3_2 | 53 | 58 | PF14604 | 0.442 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.519 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.418 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.442 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.421 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.615 |
LIG_SUMO_SIM_anti_2 | 195 | 201 | PF11976 | 0.368 |
LIG_SUMO_SIM_anti_2 | 264 | 270 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 195 | 201 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 594 | 599 | PF11976 | 0.260 |
LIG_TRAF2_1 | 570 | 573 | PF00917 | 0.349 |
LIG_UBA3_1 | 585 | 594 | PF00899 | 0.325 |
LIG_WRC_WIRS_1 | 683 | 688 | PF05994 | 0.607 |
LIG_WRC_WIRS_1 | 690 | 695 | PF05994 | 0.560 |
LIG_WRPW_2 | 447 | 450 | PF00400 | 0.260 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.476 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.392 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.263 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.733 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.564 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.533 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.509 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.551 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.276 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.254 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.314 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.290 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.236 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.284 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.284 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.520 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.365 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.540 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.394 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.276 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.306 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.240 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.548 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.496 |
MOD_GlcNHglycan | 679 | 683 | PF01048 | 0.543 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.449 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.272 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.291 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.266 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.210 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.347 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.666 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.276 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.556 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.417 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.482 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.313 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.260 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.260 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.269 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.448 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.337 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.434 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.579 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.648 |
MOD_NEK2_2 | 273 | 278 | PF00069 | 0.260 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.282 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.409 |
MOD_PIKK_1 | 596 | 602 | PF00454 | 0.380 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.210 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.135 |
MOD_PK_1 | 58 | 64 | PF00069 | 0.530 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.407 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.294 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.248 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.448 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.296 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.329 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.346 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.648 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.295 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.348 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.450 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.270 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.334 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.427 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.278 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.356 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.564 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.541 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.532 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.522 |
MOD_SUMO_rev_2 | 90 | 100 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_4 | 572 | 578 | PF01217 | 0.240 |
TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.253 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.632 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 320 | 323 | PF00400 | 0.263 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.128 |
TRG_ER_diArg_1 | 472 | 475 | PF00400 | 0.253 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 561 | 564 | PF00400 | 0.260 |
TRG_ER_diArg_1 | 640 | 642 | PF00400 | 0.268 |
TRG_ER_FFAT_2 | 329 | 339 | PF00635 | 0.240 |
TRG_NES_CRM1_1 | 339 | 352 | PF08389 | 0.276 |
TRG_NLS_MonoExtC_3 | 11 | 16 | PF00514 | 0.510 |
TRG_NLS_MonoExtC_3 | 187 | 192 | PF00514 | 0.416 |
TRG_NLS_MonoExtN_4 | 12 | 17 | PF00514 | 0.512 |
TRG_NLS_MonoExtN_4 | 188 | 193 | PF00514 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 478 | 482 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 658 | 662 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P567 | Leptomonas seymouri | 83% | 100% |
A0A0N1PFU7 | Leptomonas seymouri | 45% | 94% |
A0A0S4IQT9 | Bodo saltans | 69% | 100% |
A0A0S4KPU1 | Bodo saltans | 45% | 100% |
A0A1X0NG94 | Trypanosomatidae | 41% | 95% |
A0A1X0NX69 | Trypanosomatidae | 76% | 100% |
A0A3Q8ICG0 | Leishmania donovani | 46% | 92% |
A0A3R7KUY9 | Trypanosoma rangeli | 77% | 100% |
A0A3S7WXV4 | Leishmania donovani | 95% | 99% |
A0A422NDG5 | Trypanosoma rangeli | 42% | 94% |
A4H8F0 | Leishmania braziliensis | 45% | 92% |
A4HD08 | Leishmania braziliensis | 94% | 100% |
A4HWS3 | Leishmania infantum | 46% | 92% |
A4I0J4 | Leishmania infantum | 95% | 99% |
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% | 91% |
O14023 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
Q02908 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
Q1ZXC6 | Dictyostelium discoideum | 33% | 100% |
Q23651 | Caenorhabditis elegans | 34% | 100% |
Q2KJ61 | Bos taurus | 33% | 100% |
Q4QB17 | Leishmania major | 95% | 100% |
Q4QEZ6 | Leishmania major | 45% | 92% |
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 | 34% | 100% |
Q6NVL5 | Xenopus tropicalis | 32% | 100% |
Q7X7L3 | Oryza sativa subsp. japonica | 35% | 100% |
Q93ZR1 | Arabidopsis thaliana | 33% | 100% |
Q9CZX0 | Mus musculus | 32% | 100% |
Q9H9T3 | Homo sapiens | 33% | 100% |
Q9VQZ6 | Drosophila melanogaster | 33% | 100% |
V5B5L2 | Trypanosoma cruzi | 42% | 100% |
V5BNQ5 | Trypanosoma cruzi | 76% | 100% |