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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0005635 | nuclear envelope | 4 | 2 |
GO:0005730 | nucleolus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0031967 | organelle envelope | 3 | 2 |
GO:0031975 | envelope | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0033588 | elongator holoenzyme complex | 3 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0140535 | intracellular protein-containing complex | 2 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
GO:0016020 | membrane | 2 | 1 |
GO:0005819 | spindle | 5 | 1 |
Related structures:
AlphaFold database: Q4QEZ6
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 3 |
GO:0002098 | tRNA wobble uridine modification | 8 | 3 |
GO:0002926 | tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation | 9 | 3 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006399 | tRNA metabolic process | 7 | 3 |
GO:0006400 | tRNA modification | 6 | 3 |
GO:0006473 | protein acetylation | 6 | 2 |
GO:0006475 | internal protein amino acid acetylation | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008033 | tRNA processing | 8 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009451 | RNA modification | 5 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016570 | histone modification | 5 | 2 |
GO:0016573 | histone acetylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0018393 | internal peptidyl-lysine acetylation | 8 | 2 |
GO:0018394 | peptidyl-lysine acetylation | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0034470 | ncRNA processing | 7 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034660 | ncRNA metabolic process | 6 | 3 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043007 | maintenance of rDNA | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0043570 | maintenance of DNA repeat elements | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0051276 | chromosome organization | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 19 |
GO:0003676 | nucleic acid binding | 3 | 19 |
GO:0003723 | RNA binding | 4 | 19 |
GO:0003824 | catalytic activity | 1 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0016407 | acetyltransferase activity | 5 | 19 |
GO:0016740 | transferase activity | 2 | 19 |
GO:0016746 | acyltransferase activity | 3 | 19 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 19 |
GO:0043167 | ion binding | 2 | 19 |
GO:0043169 | cation binding | 3 | 19 |
GO:0046872 | metal ion binding | 4 | 19 |
GO:0051536 | iron-sulfur cluster binding | 3 | 19 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 19 |
GO:0051540 | metal cluster binding | 2 | 19 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:0106261 | tRNA uridine(34) acetyltransferase activity | 6 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.337 |
CLV_C14_Caspase3-7 | 656 | 660 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.463 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.219 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 737 | 739 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 636 | 638 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 737 | 739 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 632 | 638 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 295 | 303 | PF00400 | 0.469 |
DOC_CDC14_PxL_1 | 28 | 36 | PF14671 | 0.420 |
DOC_CKS1_1 | 421 | 426 | PF01111 | 0.426 |
DOC_CKS1_1 | 560 | 565 | PF01111 | 0.274 |
DOC_CYCLIN_yClb1_LxF_4 | 228 | 233 | PF00134 | 0.426 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 478 | 487 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 175 | 185 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 226 | 233 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 242 | 249 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 292 | 301 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 453 | 462 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 84 | 93 | PF00069 | 0.416 |
DOC_MAPK_HePTP_8 | 450 | 462 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 292 | 301 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.421 |
DOC_PP1_RVXF_1 | 168 | 175 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 228 | 234 | PF00149 | 0.426 |
DOC_PP2B_PxIxI_1 | 457 | 463 | PF00149 | 0.525 |
DOC_PP4_FxxP_1 | 174 | 177 | PF00568 | 0.562 |
DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.525 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.249 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 687 | 695 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 726 | 730 | PF00244 | 0.495 |
LIG_APCC_ABBA_1 | 114 | 119 | PF00400 | 0.463 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_eIF4E_1 | 440 | 446 | PF01652 | 0.445 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.471 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.599 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.551 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.467 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.423 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.451 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.586 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.367 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.319 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.539 |
LIG_LIR_Apic_2 | 266 | 271 | PF02991 | 0.539 |
LIG_LIR_Apic_2 | 286 | 291 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 169 | 177 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 422 | 432 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 532 | 541 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 561 | 572 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 617 | 626 | PF02991 | 0.302 |
LIG_LIR_LC3C_4 | 181 | 186 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.286 |
LIG_MYND_3 | 31 | 35 | PF01753 | 0.431 |
LIG_NRBOX | 482 | 488 | PF00104 | 0.430 |
LIG_Pex14_1 | 203 | 207 | PF04695 | 0.426 |
LIG_Pex14_1 | 560 | 564 | PF04695 | 0.283 |
LIG_Pex14_2 | 199 | 203 | PF04695 | 0.268 |
LIG_PTAP_UEV_1 | 147 | 152 | PF05743 | 0.492 |
LIG_SH2_CRK | 579 | 583 | PF00017 | 0.324 |
LIG_SH2_CRK | 620 | 624 | PF00017 | 0.254 |
LIG_SH2_CRK | 640 | 644 | PF00017 | 0.495 |
LIG_SH2_CRK | 722 | 726 | PF00017 | 0.425 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 620 | 624 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 620 | 624 | PF00017 | 0.323 |
LIG_SH2_STAT3 | 418 | 421 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.399 |
LIG_SH3_1 | 206 | 212 | PF00018 | 0.426 |
LIG_SH3_1 | 692 | 698 | PF00018 | 0.477 |
LIG_SH3_2 | 291 | 296 | PF14604 | 0.525 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.703 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.414 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.451 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.493 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.479 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.361 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.491 |
LIG_SH3_3 | 700 | 706 | PF00018 | 0.463 |
LIG_Sin3_3 | 132 | 139 | PF02671 | 0.454 |
LIG_SUMO_SIM_anti_2 | 181 | 187 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 254 | 260 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 621 | 627 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 181 | 187 | PF11976 | 0.381 |
LIG_SxIP_EBH_1 | 692 | 705 | PF03271 | 0.525 |
LIG_TRAF2_1 | 116 | 119 | PF00917 | 0.564 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.249 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.249 |
LIG_TRAF2_1 | 750 | 753 | PF00917 | 0.439 |
LIG_UBA3_1 | 445 | 453 | PF00899 | 0.283 |
LIG_WW_3 | 289 | 293 | PF00397 | 0.210 |
MOD_CDK_SPxxK_3 | 153 | 160 | PF00069 | 0.580 |
MOD_CDK_SPxxK_3 | 517 | 524 | PF00069 | 0.162 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.469 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.603 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.688 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.559 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.315 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.645 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.284 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.262 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.302 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.324 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.570 |
MOD_CK2_1 | 747 | 753 | PF00069 | 0.546 |
MOD_DYRK1A_RPxSP_1 | 592 | 596 | PF00069 | 0.191 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.712 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.742 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.708 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.414 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.335 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.323 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.517 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.537 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.494 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.348 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.268 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.582 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.740 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.531 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.724 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.603 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.330 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.280 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.426 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.303 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.465 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.660 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.693 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.358 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.268 |
MOD_N-GLC_1 | 690 | 695 | PF02516 | 0.712 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.548 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.391 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.353 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.277 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.315 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.268 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.568 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.471 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.303 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.508 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.414 |
MOD_PIKK_1 | 618 | 624 | PF00454 | 0.439 |
MOD_PIKK_1 | 713 | 719 | PF00454 | 0.599 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.549 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.283 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.444 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.499 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.351 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.378 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.762 |
MOD_Plk_2-3 | 4 | 10 | PF00069 | 0.590 |
MOD_Plk_2-3 | 539 | 545 | PF00069 | 0.399 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.653 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.593 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.357 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.333 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.362 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.267 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.368 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.356 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.721 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.694 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.335 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.372 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.268 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.268 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.402 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.271 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.249 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.696 |
MOD_SUMO_rev_2 | 429 | 438 | PF00179 | 0.278 |
TRG_DiLeu_BaEn_3 | 52 | 58 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 603 | 608 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 638 | 643 | PF01217 | 0.368 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 524 | 526 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 551 | 554 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.570 |
TRG_NLS_MonoExtC_3 | 735 | 740 | PF00514 | 0.626 |
TRG_NLS_MonoExtC_3 | 80 | 85 | PF00514 | 0.477 |
TRG_NLS_MonoExtN_4 | 736 | 741 | PF00514 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 464 | 468 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFU7 | Leptomonas seymouri | 70% | 100% |
A0A0S4KPU1 | Bodo saltans | 60% | 100% |
A0A1X0NG94 | Trypanosomatidae | 59% | 100% |
A0A1X0NX69 | Trypanosomatidae | 45% | 100% |
A0A3Q8ICG0 | Leishmania donovani | 94% | 100% |
A0A3S7WXV4 | Leishmania donovani | 45% | 100% |
A0A422NDG5 | Trypanosoma rangeli | 60% | 100% |
A4H8F0 | Leishmania braziliensis | 83% | 100% |
A4HD08 | Leishmania braziliensis | 45% | 100% |
A4HWS3 | Leishmania infantum | 94% | 100% |
A4I0J4 | Leishmania infantum | 45% | 100% |
C9ZVC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZW50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AQI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
E9AWF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
O14023 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
Q1ZXC6 | Dictyostelium discoideum | 32% | 100% |
Q2KJ61 | Bos taurus | 33% | 100% |
Q4QB17 | Leishmania major | 45% | 100% |
Q5HZM6 | Xenopus laevis | 34% | 100% |
Q5RIC0 | Danio rerio | 34% | 100% |
Q5ZHS1 | Gallus gallus | 33% | 100% |
Q6NVL5 | Xenopus tropicalis | 32% | 100% |
Q9CZX0 | Mus musculus | 33% | 100% |
Q9H9T3 | Homo sapiens | 32% | 100% |
V5B5L2 | Trypanosoma cruzi | 58% | 100% |