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 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q6T0
Term | Name | Level | Count |
---|---|---|---|
GO:0000245 | spliceosomal complex assembly | 7 | 2 |
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0050684 | regulation of mRNA processing | 7 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.526 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.709 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 607 | 609 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.713 |
DEG_APCC_DBOX_1 | 270 | 278 | PF00400 | 0.255 |
DEG_SCF_FBW7_1 | 296 | 303 | PF00400 | 0.358 |
DOC_ANK_TNKS_1 | 106 | 113 | PF00023 | 0.614 |
DOC_CKS1_1 | 297 | 302 | PF01111 | 0.332 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.234 |
DOC_MAPK_gen_1 | 181 | 189 | PF00069 | 0.299 |
DOC_MAPK_gen_1 | 414 | 423 | PF00069 | 0.241 |
DOC_MAPK_HePTP_8 | 411 | 423 | PF00069 | 0.241 |
DOC_MAPK_MEF2A_6 | 414 | 423 | PF00069 | 0.241 |
DOC_PP1_RVXF_1 | 161 | 168 | PF00149 | 0.241 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.695 |
DOC_PP4_FxxP_1 | 311 | 314 | PF00568 | 0.467 |
DOC_PP4_FxxP_1 | 529 | 532 | PF00568 | 0.241 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.600 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.594 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.643 |
DOC_USP7_UBL2_3 | 328 | 332 | PF12436 | 0.471 |
DOC_USP7_UBL2_3 | 340 | 344 | PF12436 | 0.445 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.595 |
DOC_USP7_UBL2_3 | 517 | 521 | PF12436 | 0.253 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.244 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.408 |
LIG_14-3-3_CanoR_1 | 319 | 327 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 347 | 351 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 669 | 678 | PF00244 | 0.523 |
LIG_APCC_ABBA_1 | 242 | 247 | PF00400 | 0.255 |
LIG_BRCT_BRCA1_1 | 618 | 622 | PF00533 | 0.674 |
LIG_Clathr_ClatBox_1 | 274 | 278 | PF01394 | 0.255 |
LIG_CtBP_PxDLS_1 | 476 | 480 | PF00389 | 0.255 |
LIG_deltaCOP1_diTrp_1 | 381 | 389 | PF00928 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 432 | 441 | PF00928 | 0.241 |
LIG_EH1_1 | 301 | 309 | PF00400 | 0.399 |
LIG_eIF4E_1 | 201 | 207 | PF01652 | 0.241 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.241 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.553 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.241 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.598 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.581 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.460 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.648 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.522 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.241 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.669 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.522 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.418 |
LIG_FHA_2 | 694 | 700 | PF00498 | 0.677 |
LIG_FHA_2 | 733 | 739 | PF00498 | 0.615 |
LIG_Integrin_RGD_1 | 361 | 363 | PF01839 | 0.614 |
LIG_LIR_Apic_2 | 413 | 419 | PF02991 | 0.241 |
LIG_LIR_Apic_2 | 425 | 430 | PF02991 | 0.241 |
LIG_LIR_Apic_2 | 528 | 532 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 182 | 189 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 387 | 397 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 403 | 407 | PF02991 | 0.178 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.194 |
LIG_LIR_Nem_3 | 552 | 557 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.404 |
LIG_MYND_3 | 531 | 535 | PF01753 | 0.234 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.264 |
LIG_PTB_Apo_2 | 153 | 160 | PF02174 | 0.393 |
LIG_PTB_Apo_2 | 629 | 636 | PF02174 | 0.570 |
LIG_PTB_Phospho_1 | 153 | 159 | PF10480 | 0.396 |
LIG_PTB_Phospho_1 | 629 | 635 | PF10480 | 0.576 |
LIG_Rb_pABgroove_1 | 236 | 244 | PF01858 | 0.278 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.339 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.241 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.437 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.234 |
LIG_SH2_CRK | 562 | 566 | PF00017 | 0.516 |
LIG_SH2_GRB2like | 490 | 493 | PF00017 | 0.321 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.255 |
LIG_SH2_NCK_1 | 596 | 600 | PF00017 | 0.686 |
LIG_SH2_SRC | 201 | 204 | PF00017 | 0.241 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.528 |
LIG_SUMO_SIM_anti_2 | 282 | 289 | PF11976 | 0.255 |
LIG_SUMO_SIM_anti_2 | 303 | 309 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 461 | 470 | PF11976 | 0.241 |
LIG_SUMO_SIM_anti_2 | 712 | 718 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 247 | 254 | PF11976 | 0.241 |
LIG_SUMO_SIM_par_1 | 428 | 435 | PF11976 | 0.234 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.570 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.635 |
LIG_TRAF2_1 | 735 | 738 | PF00917 | 0.580 |
LIG_TYR_ITIM | 503 | 508 | PF00017 | 0.388 |
LIG_UBA3_1 | 304 | 309 | PF00899 | 0.372 |
MOD_CDK_SPK_2 | 296 | 301 | PF00069 | 0.255 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.388 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.449 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.602 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.686 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.241 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.631 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.704 |
MOD_CK1_1 | 672 | 678 | PF00069 | 0.569 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.682 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.507 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.388 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.257 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.557 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.241 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.561 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.616 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.443 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.568 |
MOD_CK2_1 | 732 | 738 | PF00069 | 0.613 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.555 |
MOD_CMANNOS | 174 | 177 | PF00535 | 0.241 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.512 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.241 |
MOD_GlcNHglycan | 569 | 574 | PF01048 | 0.612 |
MOD_GlcNHglycan | 575 | 580 | PF01048 | 0.627 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.660 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.707 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.709 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.366 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.640 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.497 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.650 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.647 |
MOD_GSK3_1 | 672 | 679 | PF00069 | 0.573 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.693 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.296 |
MOD_N-GLC_1 | 631 | 636 | PF02516 | 0.568 |
MOD_N-GLC_2 | 218 | 220 | PF02516 | 0.366 |
MOD_N-GLC_2 | 399 | 401 | PF02516 | 0.241 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.701 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.255 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.452 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.241 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.568 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.627 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.467 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.575 |
MOD_PIKK_1 | 702 | 708 | PF00454 | 0.741 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.749 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.668 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.616 |
MOD_PKA_2 | 676 | 682 | PF00069 | 0.677 |
MOD_Plk_1 | 631 | 637 | PF00069 | 0.514 |
MOD_Plk_2-3 | 584 | 590 | PF00069 | 0.805 |
MOD_Plk_2-3 | 732 | 738 | PF00069 | 0.725 |
MOD_Plk_2-3 | 740 | 746 | PF00069 | 0.699 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.268 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.241 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.418 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.514 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.581 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.287 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.244 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.408 |
MOD_SUMO_for_1 | 290 | 293 | PF00179 | 0.241 |
MOD_SUMO_for_1 | 343 | 346 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 197 | 207 | PF00179 | 0.258 |
MOD_SUMO_rev_2 | 284 | 292 | PF00179 | 0.255 |
MOD_SUMO_rev_2 | 324 | 330 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 345 | 350 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 353 | 360 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 55 | 63 | PF00179 | 0.584 |
MOD_SUMO_rev_2 | 597 | 606 | PF00179 | 0.626 |
TRG_DiLeu_BaEn_1 | 666 | 671 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_2 | 524 | 530 | PF01217 | 0.255 |
TRG_DiLeu_BaEn_3 | 345 | 351 | PF01217 | 0.422 |
TRG_DiLeu_BaEn_4 | 626 | 632 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_4 | 673 | 679 | PF01217 | 0.655 |
TRG_DiLeu_LyEn_5 | 666 | 671 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.245 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.574 |
TRG_NLS_Bipartite_1 | 16 | 30 | PF00514 | 0.659 |
TRG_NLS_MonoExtC_3 | 24 | 29 | PF00514 | 0.647 |
TRG_NLS_MonoExtC_3 | 519 | 524 | PF00514 | 0.296 |
TRG_NLS_MonoExtN_4 | 23 | 30 | PF00514 | 0.653 |
TRG_NLS_MonoExtN_4 | 517 | 524 | PF00514 | 0.296 |
TRG_NLS_MonoExtN_4 | 605 | 611 | PF00514 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 498 | 502 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 669 | 673 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1H8 | Leptomonas seymouri | 81% | 100% |
A0A0S4JMD1 | Bodo saltans | 55% | 97% |
A0A1X0P1B0 | Trypanosomatidae | 60% | 100% |
A0A3R7KF70 | Trypanosoma rangeli | 59% | 100% |
A0A3S7X404 | Leishmania donovani | 95% | 100% |
A4HIU4 | Leishmania braziliensis | 84% | 100% |
A4I649 | Leishmania infantum | 94% | 100% |
C9ZRG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9B1D2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5B752 | Trypanosoma cruzi | 64% | 100% |