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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: E9B101
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 14 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0019538 | protein metabolic process | 3 | 14 |
GO:0036211 | protein modification process | 4 | 14 |
GO:0043170 | macromolecule metabolic process | 3 | 14 |
GO:0043412 | macromolecule modification | 4 | 14 |
GO:0044238 | primary metabolic process | 2 | 14 |
GO:0071704 | organic substance metabolic process | 2 | 14 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 14 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018095 | protein polyglutamylation | 7 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016874 | ligase activity | 2 | 14 |
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 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
GO:0016881 | acid-amino acid ligase activity | 4 | 1 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 1 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.496 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.374 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.195 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.439 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.311 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.556 |
CLV_Separin_Metazoa | 133 | 137 | PF03568 | 0.597 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.592 |
DOC_ANK_TNKS_1 | 567 | 574 | PF00023 | 0.439 |
DOC_CKS1_1 | 139 | 144 | PF01111 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 586 | 592 | PF00134 | 0.501 |
DOC_MAPK_FxFP_2 | 61 | 64 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 183 | 190 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 307 | 315 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 651 | 660 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 183 | 190 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 307 | 315 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 618 | 625 | PF00069 | 0.380 |
DOC_MAPK_NFAT4_5 | 308 | 316 | PF00069 | 0.435 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.313 |
DOC_PP2B_LxvP_1 | 427 | 430 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 663 | 666 | PF13499 | 0.571 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.463 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 672 | 676 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.267 |
DOC_USP7_MATH_2 | 224 | 230 | PF00917 | 0.434 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 213 | 217 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 57 | 62 | PF00244 | 0.441 |
LIG_Actin_WH2_2 | 35 | 52 | PF00022 | 0.624 |
LIG_BIR_III_4 | 457 | 461 | PF00653 | 0.345 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 541 | 545 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.417 |
LIG_deltaCOP1_diTrp_1 | 444 | 453 | PF00928 | 0.301 |
LIG_EH_1 | 526 | 530 | PF12763 | 0.434 |
LIG_eIF4E_1 | 297 | 303 | PF01652 | 0.418 |
LIG_eIF4E_1 | 689 | 695 | PF01652 | 0.369 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.591 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.554 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.679 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.516 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.424 |
LIG_FHA_1 | 698 | 704 | PF00498 | 0.323 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.498 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.557 |
LIG_GBD_Chelix_1 | 484 | 492 | PF00786 | 0.218 |
LIG_GBD_Chelix_1 | 554 | 562 | PF00786 | 0.258 |
LIG_LIR_Apic_2 | 220 | 224 | PF02991 | 0.434 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 128 | 135 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 268 | 276 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.334 |
LIG_MLH1_MIPbox_1 | 59 | 63 | PF16413 | 0.515 |
LIG_MYND_3 | 536 | 540 | PF01753 | 0.475 |
LIG_Pex14_2 | 635 | 639 | PF04695 | 0.284 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.343 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.441 |
LIG_SH2_PTP2 | 314 | 317 | PF00017 | 0.408 |
LIG_SH2_SRC | 455 | 458 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 292 | 295 | PF00017 | 0.435 |
LIG_SH2_STAT3 | 689 | 692 | PF00017 | 0.367 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 682 | 685 | PF00017 | 0.460 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 605 | 610 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 299 | 305 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 425 | 433 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 529 | 535 | PF11976 | 0.444 |
LIG_UBA3_1 | 272 | 279 | PF00899 | 0.499 |
LIG_WW_1 | 71 | 74 | PF00397 | 0.480 |
MOD_CDC14_SPxK_1 | 54 | 57 | PF00782 | 0.547 |
MOD_CDK_SPxK_1 | 51 | 57 | PF00069 | 0.571 |
MOD_CDK_SPxxK_3 | 234 | 241 | PF00069 | 0.392 |
MOD_CDK_SPxxK_3 | 51 | 58 | PF00069 | 0.566 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.498 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.515 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.653 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.454 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.522 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.533 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.780 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.647 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.435 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.435 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.623 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.643 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.552 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.427 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.499 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.475 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.423 |
MOD_Cter_Amidation | 305 | 308 | PF01082 | 0.243 |
MOD_Cter_Amidation | 412 | 415 | PF01082 | 0.355 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.159 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.722 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.582 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.780 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.648 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.639 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.592 |
MOD_GlcNHglycan | 662 | 666 | PF01048 | 0.425 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.319 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.618 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.543 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.523 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.697 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.725 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.451 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.444 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.581 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.541 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.623 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.447 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.651 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.518 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.392 |
MOD_N-GLC_1 | 384 | 389 | PF02516 | 0.493 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.358 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.588 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.279 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.481 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.463 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.673 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.349 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.465 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.425 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.418 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.566 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.375 |
MOD_NEK2_2 | 125 | 130 | PF00069 | 0.362 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.305 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.436 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.660 |
MOD_PIKK_1 | 688 | 694 | PF00454 | 0.330 |
MOD_PK_1 | 654 | 660 | PF00069 | 0.435 |
MOD_PKA_1 | 474 | 480 | PF00069 | 0.323 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.408 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.502 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.514 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.427 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.305 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.672 |
MOD_PKB_1 | 403 | 411 | PF00069 | 0.480 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.517 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.365 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.571 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.513 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.576 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.435 |
MOD_Plk_1 | 697 | 703 | PF00069 | 0.321 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.453 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.435 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.527 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.531 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.421 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.475 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.424 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.613 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.429 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.480 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.392 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.701 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.611 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.546 |
MOD_SUMO_rev_2 | 204 | 210 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 274 | 281 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 439 | 448 | PF00179 | 0.422 |
TRG_DiLeu_BaEn_1 | 226 | 231 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_1 | 31 | 36 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_1 | 483 | 488 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_1 | 690 | 695 | PF01217 | 0.341 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.317 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 298 | 303 | PF01217 | 0.418 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 190 | 192 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 414 | 416 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Q6 | Leptomonas seymouri | 57% | 98% |
A0A0S4ISF0 | Bodo saltans | 37% | 100% |
A0A1X0P1M0 | Trypanosomatidae | 41% | 100% |
A0A3Q8IDL7 | Leishmania donovani | 25% | 97% |
A0A3Q8IEC1 | Leishmania donovani | 90% | 100% |
A0A3R7LAU2 | Trypanosoma rangeli | 25% | 75% |
A0A3S5IS28 | Trypanosoma rangeli | 43% | 100% |
A4HIG0 | Leishmania braziliensis | 76% | 100% |
A4HYN9 | Leishmania infantum | 25% | 97% |
A4I5Q6 | Leishmania infantum | 90% | 100% |
A4Q9F0 | Mus musculus | 23% | 77% |
A8X9V4 | Caenorhabditis briggsae | 25% | 100% |
C9ZR25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AUL7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q09647 | Caenorhabditis elegans | 24% | 100% |
Q4Q765 | Leishmania major | 89% | 100% |
Q4QCW7 | Leishmania major | 25% | 100% |
Q6ZT98 | Homo sapiens | 25% | 79% |
V5BLC0 | Trypanosoma cruzi | 42% | 100% |