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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 7 |
GO:0005929 | cilium | 4 | 8 |
GO:0042995 | cell projection | 2 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0099080 | supramolecular complex | 2 | 7 |
GO:0099081 | supramolecular polymer | 3 | 7 |
GO:0099512 | supramolecular fiber | 4 | 7 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4H8G3
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0018095 | protein polyglutamylation | 7 | 8 |
GO:0018193 | peptidyl-amino acid modification | 5 | 8 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 8 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
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:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 8 |
GO:0016881 | acid-amino acid ligase activity | 4 | 8 |
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:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
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:0070739 | protein-glutamic acid ligase activity | 3 | 2 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.275 |
CLV_PCSK_FUR_1 | 248 | 252 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.232 |
CLV_PCSK_PC7_1 | 11 | 17 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 696 | 700 | PF00082 | 0.264 |
DEG_SCF_FBW7_1 | 22 | 28 | PF00400 | 0.628 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.410 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.628 |
DOC_CYCLIN_yCln2_LP_2 | 76 | 82 | PF00134 | 0.552 |
DOC_MAPK_gen_1 | 536 | 544 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 536 | 544 | PF00069 | 0.491 |
DOC_MAPK_NFAT4_5 | 537 | 545 | PF00069 | 0.491 |
DOC_PP1_RVXF_1 | 624 | 631 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 694 | 700 | PF00149 | 0.458 |
DOC_PP4_FxxP_1 | 204 | 207 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 672 | 676 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.616 |
DOC_USP7_UBL2_3 | 39 | 43 | PF12436 | 0.550 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 174 | 183 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 335 | 339 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 375 | 380 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 621 | 639 | PF00022 | 0.473 |
LIG_APCC_ABBA_1 | 395 | 400 | PF00400 | 0.454 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.543 |
LIG_BIR_III_2 | 54 | 58 | PF00653 | 0.537 |
LIG_BIR_III_2 | 64 | 68 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 377 | 381 | PF00533 | 0.475 |
LIG_BRCT_BRCA1_1 | 493 | 497 | PF00533 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 274 | 279 | PF00928 | 0.364 |
LIG_eIF4E_1 | 526 | 532 | PF01652 | 0.454 |
LIG_eIF4E_1 | 653 | 659 | PF01652 | 0.454 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.638 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.616 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.740 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.454 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.454 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.553 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.588 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.434 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.450 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.479 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.479 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.496 |
LIG_FHA_2 | 678 | 684 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 388 | 392 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 501 | 507 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 274 | 282 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 331 | 341 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 558 | 569 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 547 | 552 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 649 | 653 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 727 | 732 | PF02991 | 0.389 |
LIG_MAD2 | 696 | 704 | PF02301 | 0.454 |
LIG_PCNA_PIPBox_1 | 576 | 585 | PF02747 | 0.454 |
LIG_PDZ_Class_2 | 729 | 734 | PF00595 | 0.363 |
LIG_Pex14_2 | 398 | 402 | PF04695 | 0.475 |
LIG_PTAP_UEV_1 | 5 | 10 | PF05743 | 0.535 |
LIG_PTB_Apo_2 | 624 | 631 | PF02174 | 0.454 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.456 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.390 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.454 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.491 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.461 |
LIG_SH2_CRK | 655 | 659 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 389 | 393 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 543 | 546 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 655 | 659 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.492 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.537 |
LIG_SH3_2 | 6 | 11 | PF14604 | 0.538 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.761 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.554 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.551 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.601 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.537 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.456 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.405 |
LIG_SH3_3 | 695 | 701 | PF00018 | 0.472 |
LIG_TYR_ITAM | 315 | 336 | PF00017 | 0.279 |
LIG_TYR_ITIM | 316 | 321 | PF00017 | 0.279 |
LIG_TYR_ITIM | 631 | 636 | PF00017 | 0.279 |
LIG_UBA3_1 | 608 | 614 | PF00899 | 0.218 |
LIG_WRC_WIRS_1 | 376 | 381 | PF05994 | 0.309 |
LIG_WRC_WIRS_1 | 445 | 450 | PF05994 | 0.309 |
LIG_WW_1 | 700 | 703 | PF00397 | 0.309 |
MOD_CDK_SPK_2 | 223 | 228 | PF00069 | 0.538 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.575 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.618 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.599 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.233 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.355 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.314 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.221 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.259 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.305 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.268 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.352 |
MOD_Cter_Amidation | 143 | 146 | PF01082 | 0.585 |
MOD_Cter_Amidation | 17 | 20 | PF01082 | 0.546 |
MOD_Cter_Amidation | 534 | 537 | PF01082 | 0.332 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.543 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.661 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.675 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.650 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.601 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.594 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.506 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.415 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.279 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.704 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.279 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.411 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.362 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.302 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.617 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.627 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.603 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.634 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.418 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.327 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.375 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.279 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.278 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.310 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.306 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.296 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.263 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.324 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.374 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.657 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.583 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.530 |
MOD_N-GLC_1 | 349 | 354 | PF02516 | 0.218 |
MOD_N-GLC_1 | 595 | 600 | PF02516 | 0.289 |
MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.281 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.574 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.312 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.287 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.307 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.341 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.279 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.279 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.281 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.279 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.575 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.517 |
MOD_NEK2_2 | 334 | 339 | PF00069 | 0.279 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.279 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.279 |
MOD_PIKK_1 | 720 | 726 | PF00454 | 0.317 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.560 |
MOD_PKA_1 | 145 | 151 | PF00069 | 0.603 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.309 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.787 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.603 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.616 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.386 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.310 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.279 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.510 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.229 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.253 |
MOD_Plk_2-3 | 102 | 108 | PF00069 | 0.543 |
MOD_Plk_2-3 | 646 | 652 | PF00069 | 0.310 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.294 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.316 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.313 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.610 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.637 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.544 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.564 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.387 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.279 |
MOD_SUMO_rev_2 | 260 | 270 | PF00179 | 0.490 |
TRG_AP2beta_CARGO_1 | 558 | 568 | PF09066 | 0.279 |
TRG_DiLeu_BaEn_1 | 45 | 50 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 527 | 532 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 681 | 686 | PF01217 | 0.279 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.190 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.309 |
TRG_ER_diArg_1 | 715 | 718 | PF00400 | 0.364 |
TRG_NES_CRM1_1 | 577 | 592 | PF08389 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 323 | 327 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 684 | 688 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 94 | 99 | PF00026 | 0.621 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDX5 | Leptomonas seymouri | 58% | 90% |
A0A3Q8IDL7 | Leishmania donovani | 24% | 100% |
A0A3S5H6X0 | Leishmania donovani | 72% | 90% |
A4HWT7 | Leishmania infantum | 72% | 90% |
A4HYN9 | Leishmania infantum | 24% | 100% |
E9AID0 | Leishmania braziliensis | 25% | 100% |
E9AQJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 90% |
E9AUL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4QCW7 | Leishmania major | 24% | 100% |
Q4QEY2 | Leishmania major | 71% | 100% |