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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: A0A3Q8IEC1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 18 |
GO:0008152 | metabolic process | 1 | 18 |
GO:0019538 | protein metabolic process | 3 | 18 |
GO:0036211 | protein modification process | 4 | 18 |
GO:0043170 | macromolecule metabolic process | 3 | 18 |
GO:0043412 | macromolecule modification | 4 | 18 |
GO:0044238 | primary metabolic process | 2 | 18 |
GO:0071704 | organic substance metabolic process | 2 | 18 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 18 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0018095 | protein polyglutamylation | 7 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016874 | ligase activity | 2 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 4 |
GO:0016881 | acid-amino acid ligase activity | 4 | 4 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 2 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 348 | 352 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.419 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.448 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.253 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.510 |
CLV_Separin_Metazoa | 132 | 136 | PF03568 | 0.635 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.623 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.578 |
DOC_ANK_TNKS_1 | 566 | 573 | PF00023 | 0.442 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 585 | 591 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 668 | 674 | PF00134 | 0.322 |
DOC_MAPK_FxFP_2 | 60 | 63 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 182 | 189 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 306 | 314 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 182 | 189 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 306 | 314 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 617 | 624 | PF00069 | 0.392 |
DOC_MAPK_NFAT4_5 | 307 | 315 | PF00069 | 0.474 |
DOC_PP2B_LxvP_1 | 662 | 665 | PF13499 | 0.578 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.315 |
DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.412 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.416 |
DOC_USP7_MATH_2 | 223 | 229 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 278 | 282 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 199 | 203 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 285 | 293 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 423 | 429 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.392 |
LIG_Actin_WH2_2 | 34 | 51 | PF00022 | 0.594 |
LIG_BIR_III_4 | 456 | 460 | PF00653 | 0.412 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 540 | 544 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.366 |
LIG_BRCT_BRCA1_1 | 655 | 659 | PF00533 | 0.719 |
LIG_EH_1 | 525 | 529 | PF12763 | 0.453 |
LIG_eIF4E_1 | 296 | 302 | PF01652 | 0.431 |
LIG_eIF4E_1 | 688 | 694 | PF01652 | 0.384 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.604 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.539 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.555 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.455 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.475 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.446 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.621 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.341 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.520 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.516 |
LIG_FXI_DFP_1 | 142 | 146 | PF00024 | 0.416 |
LIG_GBD_Chelix_1 | 483 | 491 | PF00786 | 0.242 |
LIG_GBD_Chelix_1 | 553 | 561 | PF00786 | 0.282 |
LIG_Integrin_isoDGR_2 | 421 | 423 | PF01839 | 0.449 |
LIG_Integrin_RGD_1 | 381 | 383 | PF01839 | 0.572 |
LIG_LIR_Apic_2 | 219 | 223 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 59 | 63 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 127 | 134 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 267 | 275 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 656 | 662 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.383 |
LIG_MLH1_MIPbox_1 | 58 | 62 | PF16413 | 0.473 |
LIG_MYND_3 | 535 | 539 | PF01753 | 0.498 |
LIG_Pex14_2 | 634 | 638 | PF04695 | 0.326 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.485 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.472 |
LIG_SH2_PTP2 | 313 | 316 | PF00017 | 0.434 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 97 | 101 | PF00017 | 0.326 |
LIG_SH2_STAT3 | 291 | 294 | PF00017 | 0.464 |
LIG_SH2_STAT3 | 688 | 691 | PF00017 | 0.382 |
LIG_SH2_STAT3 | 73 | 76 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 681 | 684 | PF00017 | 0.353 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.508 |
LIG_SUMO_SIM_anti_2 | 604 | 609 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 298 | 304 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 461 | 467 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 528 | 534 | PF11976 | 0.482 |
LIG_UBA3_1 | 271 | 278 | PF00899 | 0.511 |
LIG_WW_1 | 70 | 73 | PF00397 | 0.446 |
MOD_CDC14_SPxK_1 | 53 | 56 | PF00782 | 0.530 |
MOD_CDK_SPxK_1 | 467 | 473 | PF00069 | 0.440 |
MOD_CDK_SPxK_1 | 50 | 56 | PF00069 | 0.523 |
MOD_CDK_SPxxK_3 | 199 | 206 | PF00069 | 0.439 |
MOD_CDK_SPxxK_3 | 467 | 474 | PF00069 | 0.557 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.532 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.503 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.391 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.664 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.513 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.543 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.554 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.802 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.655 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.692 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.474 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.611 |
MOD_CK1_1 | 655 | 661 | PF00069 | 0.651 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.525 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.488 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.520 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.509 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.498 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.411 |
MOD_Cter_Amidation | 304 | 307 | PF01082 | 0.294 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.407 |
MOD_DYRK1A_RPxSP_1 | 199 | 203 | PF00069 | 0.376 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.621 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.504 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.791 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.679 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.677 |
MOD_GlcNHglycan | 654 | 658 | PF01048 | 0.553 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.478 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.663 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.556 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.554 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.704 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.779 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.481 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.593 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.483 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.626 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.414 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.590 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.444 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.437 |
MOD_N-GLC_1 | 576 | 581 | PF02516 | 0.613 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.480 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.504 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.380 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.472 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.442 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.556 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.625 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.675 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.467 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.406 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.352 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.453 |
MOD_PIKK_1 | 576 | 582 | PF00454 | 0.493 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.635 |
MOD_PIKK_1 | 687 | 693 | PF00454 | 0.342 |
MOD_PKA_1 | 473 | 479 | PF00069 | 0.359 |
MOD_PKA_1 | 56 | 62 | PF00069 | 0.389 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.411 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.524 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.510 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.445 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.516 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.364 |
MOD_PKB_1 | 402 | 410 | PF00069 | 0.525 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.445 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.498 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.607 |
MOD_Plk_1 | 696 | 702 | PF00069 | 0.341 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.500 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.494 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.521 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.729 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.425 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.486 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.348 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.597 |
MOD_Plk_4 | 677 | 683 | PF00069 | 0.507 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.513 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.439 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.628 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.572 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.514 |
MOD_SUMO_for_1 | 651 | 654 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 273 | 280 | PF00179 | 0.503 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_1 | 298 | 303 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_1 | 482 | 487 | PF01217 | 0.534 |
TRG_DiLeu_BaEn_1 | 689 | 694 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 99 | 104 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.306 |
TRG_ER_diArg_1 | 108 | 110 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 622 | 625 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Q6 | Leptomonas seymouri | 56% | 98% |
A0A0S4ISF0 | Bodo saltans | 37% | 100% |
A0A1X0P1M0 | Trypanosomatidae | 40% | 100% |
A0A3Q8IDL7 | Leishmania donovani | 25% | 100% |
A0A3R7LAU2 | Trypanosoma rangeli | 25% | 75% |
A0A3S5IS28 | Trypanosoma rangeli | 41% | 100% |
A4HIG0 | Leishmania braziliensis | 76% | 100% |
A4HYN9 | Leishmania infantum | 25% | 100% |
A4I5Q6 | Leishmania infantum | 100% | 100% |
A4Q9F0 | Mus musculus | 25% | 77% |
A8X9V4 | Caenorhabditis briggsae | 24% | 100% |
C9ZR25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AID0 | Leishmania braziliensis | 28% | 94% |
E9AUL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B101 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q765 | Leishmania major | 93% | 100% |
Q4QCW7 | Leishmania major | 27% | 100% |
Q8NHH1 | Homo sapiens | 24% | 88% |
V5BLC0 | Trypanosoma cruzi | 42% | 100% |