Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0034399 | nuclear periphery | 2 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: E9AT30
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902775 | mitochondrial large ribosomal subunit assembly | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 26 |
GO:0003676 | nucleic acid binding | 3 | 26 |
GO:0003824 | catalytic activity | 1 | 26 |
GO:0004386 | helicase activity | 2 | 26 |
GO:0005488 | binding | 1 | 26 |
GO:0005524 | ATP binding | 5 | 26 |
GO:0017076 | purine nucleotide binding | 4 | 26 |
GO:0030554 | adenyl nucleotide binding | 5 | 26 |
GO:0032553 | ribonucleotide binding | 3 | 26 |
GO:0032555 | purine ribonucleotide binding | 4 | 26 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 26 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 26 |
GO:0036094 | small molecule binding | 2 | 26 |
GO:0043167 | ion binding | 2 | 26 |
GO:0043168 | anion binding | 3 | 26 |
GO:0097159 | organic cyclic compound binding | 2 | 26 |
GO:0097367 | carbohydrate derivative binding | 2 | 26 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 26 |
GO:0140657 | ATP-dependent activity | 1 | 26 |
GO:1901265 | nucleoside phosphate binding | 3 | 26 |
GO:1901363 | heterocyclic compound binding | 2 | 26 |
GO:0003723 | RNA binding | 4 | 3 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0003724 | RNA helicase activity | 3 | 6 |
GO:0003743 | translation initiation factor activity | 4 | 5 |
GO:0008135 | translation factor activity, RNA binding | 3 | 5 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 6 |
GO:0045182 | translation regulator activity | 1 | 5 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.729 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 670 | 672 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 687 | 689 | PF00675 | 0.677 |
CLV_PCSK_FUR_1 | 668 | 672 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 687 | 689 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.387 |
CLV_PCSK_PC7_1 | 267 | 273 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.355 |
DEG_APCC_DBOX_1 | 134 | 142 | PF00400 | 0.365 |
DEG_APCC_DBOX_1 | 326 | 334 | PF00400 | 0.480 |
DEG_APCC_DBOX_1 | 421 | 429 | PF00400 | 0.408 |
DEG_APCC_DBOX_1 | 479 | 487 | PF00400 | 0.552 |
DEG_APCC_DBOX_1 | 61 | 69 | PF00400 | 0.435 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.495 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.492 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.464 |
DOC_CYCLIN_RxL_1 | 394 | 403 | PF00134 | 0.435 |
DOC_CYCLIN_RxL_1 | 412 | 420 | PF00134 | 0.572 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 2 | 8 | PF00134 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 428 | 434 | PF00134 | 0.590 |
DOC_CYCLIN_yCln2_LP_2 | 641 | 644 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 267 | 276 | PF00069 | 0.468 |
DOC_MAPK_JIP1_4 | 394 | 400 | PF00069 | 0.441 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.422 |
DOC_PP1_RVXF_1 | 496 | 502 | PF00149 | 0.287 |
DOC_PP1_RVXF_1 | 511 | 518 | PF00149 | 0.511 |
DOC_PP1_RVXF_1 | 573 | 580 | PF00149 | 0.430 |
DOC_PP1_SILK_1 | 131 | 136 | PF00149 | 0.374 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 641 | 644 | PF13499 | 0.409 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.498 |
DOC_PP4_FxxP_1 | 619 | 622 | PF00568 | 0.357 |
DOC_PP4_FxxP_1 | 663 | 666 | PF00568 | 0.526 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 676 | 681 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 28 | 34 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 359 | 365 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 43 | 50 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 436 | 446 | PF00244 | 0.760 |
LIG_14-3-3_CanoR_1 | 560 | 568 | PF00244 | 0.517 |
LIG_Actin_WH2_2 | 179 | 194 | PF00022 | 0.453 |
LIG_Actin_WH2_2 | 53 | 71 | PF00022 | 0.478 |
LIG_AP2alpha_1 | 654 | 658 | PF02296 | 0.529 |
LIG_APCC_ABBA_1 | 233 | 238 | PF00400 | 0.523 |
LIG_BIR_III_4 | 107 | 111 | PF00653 | 0.546 |
LIG_BIR_III_4 | 37 | 41 | PF00653 | 0.569 |
LIG_BRCT_BRCA1_1 | 301 | 305 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 419 | 423 | PF00533 | 0.383 |
LIG_CtBP_PxDLS_1 | 94 | 98 | PF00389 | 0.426 |
LIG_EH1_1 | 311 | 319 | PF00400 | 0.426 |
LIG_eIF4E_1 | 181 | 187 | PF01652 | 0.523 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.504 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.457 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.483 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.684 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.485 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.559 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.445 |
LIG_IRF3_LxIS_1 | 235 | 242 | PF10401 | 0.391 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 618 | 622 | PF02991 | 0.349 |
LIG_LIR_Apic_2 | 661 | 666 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 653 | 662 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 163 | 167 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 686 | 692 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.448 |
LIG_NRBOX | 185 | 191 | PF00104 | 0.480 |
LIG_OCRL_FandH_1 | 304 | 316 | PF00620 | 0.426 |
LIG_PCNA_PIPBox_1 | 694 | 703 | PF02747 | 0.542 |
LIG_Pex14_2 | 654 | 658 | PF04695 | 0.529 |
LIG_PTB_Apo_2 | 657 | 664 | PF02174 | 0.556 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.538 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.567 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.509 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 588 | 592 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.450 |
LIG_SH2_STAT3 | 649 | 652 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.551 |
LIG_SH3_2 | 666 | 671 | PF14604 | 0.582 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.517 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.495 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.514 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.556 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.571 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.771 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.687 |
LIG_SH3_3 | 663 | 669 | PF00018 | 0.540 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.568 |
LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 158 | 163 | PF11976 | 0.442 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.441 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.564 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.523 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.415 |
LIG_UBA3_1 | 186 | 192 | PF00899 | 0.533 |
LIG_UBA3_1 | 347 | 355 | PF00899 | 0.441 |
LIG_UBA3_1 | 384 | 390 | PF00899 | 0.422 |
LIG_UBA3_1 | 424 | 429 | PF00899 | 0.342 |
LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.426 |
LIG_WRC_WIRS_1 | 616 | 621 | PF05994 | 0.405 |
MOD_CDC14_SPxK_1 | 451 | 454 | PF00782 | 0.549 |
MOD_CDK_SPxK_1 | 448 | 454 | PF00069 | 0.541 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.446 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.736 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.428 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.593 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.708 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.449 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.496 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.448 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.442 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.443 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.600 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.426 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.430 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.681 |
MOD_DYRK1A_RPxSP_1 | 148 | 152 | PF00069 | 0.360 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.740 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.250 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.410 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.640 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.262 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.587 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.267 |
MOD_GlcNHglycan | 96 | 100 | PF01048 | 0.535 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.495 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.492 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.660 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.638 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.631 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.449 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.494 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.502 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.464 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.323 |
MOD_N-GLC_1 | 658 | 663 | PF02516 | 0.531 |
MOD_N-GLC_1 | 676 | 681 | PF02516 | 0.541 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.488 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.470 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.436 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.521 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.467 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.454 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.532 |
MOD_NEK2_1 | 658 | 663 | PF00069 | 0.511 |
MOD_NEK2_2 | 615 | 620 | PF00069 | 0.303 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.625 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.429 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.456 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.532 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.518 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.464 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.498 |
MOD_PKA_2 | 683 | 689 | PF00069 | 0.650 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.501 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.456 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.484 |
MOD_Plk_1 | 658 | 664 | PF00069 | 0.548 |
MOD_Plk_2-3 | 589 | 595 | PF00069 | 0.452 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.477 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.446 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.426 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.439 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.505 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.538 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.370 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.477 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.503 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.520 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.320 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.488 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.484 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.692 |
MOD_ProDKin_1 | 676 | 682 | PF00069 | 0.677 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.587 |
TRG_DiLeu_BaEn_1 | 285 | 290 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 394 | 399 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 358 | 360 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 668 | 671 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 687 | 689 | PF00400 | 0.646 |
TRG_NLS_MonoExtN_4 | 144 | 149 | PF00514 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 306 | 311 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 422 | 427 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I458 | Leptomonas seymouri | 76% | 100% |
A0A0N1I5R1 | Leptomonas seymouri | 22% | 89% |
A0A0S4IX79 | Bodo saltans | 24% | 97% |
A0A0S4JPF4 | Bodo saltans | 39% | 100% |
A0A1X0P7J3 | Trypanosomatidae | 57% | 100% |
A0A3Q8ID91 | Leishmania donovani | 26% | 100% |
A0A3Q8IF94 | Leishmania donovani | 25% | 100% |
A0A3Q8IG57 | Leishmania donovani | 92% | 90% |
A0A3S7WR01 | Leishmania donovani | 23% | 90% |
A4HGR1 | Leishmania braziliensis | 27% | 100% |
A4HK20 | Leishmania braziliensis | 25% | 100% |
A4HPB9 | Leishmania braziliensis | 88% | 100% |
A4HUC1 | Leishmania infantum | 23% | 90% |
A4I3T6 | Leishmania infantum | 26% | 100% |
A4I7K4 | Leishmania infantum | 25% | 100% |
A4ICF9 | Leishmania infantum | 93% | 100% |
D0A3C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AN20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q1G8 | Leishmania major | 93% | 100% |
Q4Q5P5 | Leishmania major | 25% | 100% |
Q4Q858 | Leishmania major | 26% | 100% |
V5D8J9 | Trypanosoma cruzi | 57% | 100% |