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 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
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: A4HB44
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031848 | protection from non-homologous end joining at telomere | 6 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0036297 | interstrand cross-link repair | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043247 | telomere maintenance in response to DNA damage | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0035312 | 5'-3' DNA exonuclease activity | 7 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 499 | 505 | PF00089 | 0.493 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.639 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.754 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 578 | 580 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.376 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.354 |
DEG_SCF_FBW7_1 | 20 | 27 | PF00400 | 0.254 |
DEG_SCF_FBW7_2 | 362 | 368 | PF00400 | 0.503 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.458 |
DEG_SPOP_SBC_1 | 586 | 590 | PF00917 | 0.496 |
DEG_SPOP_SBC_1 | 601 | 605 | PF00917 | 0.527 |
DOC_CKS1_1 | 362 | 367 | PF01111 | 0.500 |
DOC_CYCLIN_RxL_1 | 152 | 159 | PF00134 | 0.371 |
DOC_MAPK_gen_1 | 154 | 162 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 211 | 220 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 227 | 234 | PF00069 | 0.236 |
DOC_MAPK_gen_1 | 276 | 285 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 154 | 162 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.368 |
DOC_MAPK_RevD_3 | 330 | 345 | PF00069 | 0.418 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.499 |
DOC_PP2B_LxvP_1 | 451 | 454 | PF13499 | 0.442 |
DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.333 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.338 |
DOC_PP4_FxxP_1 | 470 | 473 | PF00568 | 0.442 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.469 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 452 | 461 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 511 | 516 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 557 | 563 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 567 | 577 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 597 | 606 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 645 | 651 | PF00244 | 0.463 |
LIG_BIR_III_2 | 236 | 240 | PF00653 | 0.485 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.350 |
LIG_Dynein_DLC8_1 | 177 | 183 | PF01221 | 0.229 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.432 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.412 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.568 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.447 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.661 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.731 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.501 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.284 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.642 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.543 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.602 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.688 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.694 |
LIG_GBD_Chelix_1 | 347 | 355 | PF00786 | 0.493 |
LIG_LIR_Apic_2 | 106 | 110 | PF02991 | 0.396 |
LIG_LIR_Apic_2 | 164 | 170 | PF02991 | 0.318 |
LIG_LIR_Apic_2 | 385 | 390 | PF02991 | 0.368 |
LIG_LIR_Apic_2 | 92 | 97 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 422 | 432 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 610 | 620 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.350 |
LIG_MLH1_MIPbox_1 | 72 | 76 | PF16413 | 0.251 |
LIG_MYND_1 | 327 | 331 | PF01753 | 0.429 |
LIG_Pex14_1 | 103 | 107 | PF04695 | 0.333 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.475 |
LIG_Pex14_2 | 286 | 290 | PF04695 | 0.444 |
LIG_Pex14_2 | 71 | 75 | PF04695 | 0.246 |
LIG_PTAP_UEV_1 | 133 | 138 | PF05743 | 0.304 |
LIG_PTB_Apo_2 | 390 | 397 | PF02174 | 0.484 |
LIG_PTB_Phospho_1 | 390 | 396 | PF10480 | 0.474 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.458 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.445 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.460 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.535 |
LIG_SH2_CRK | 448 | 452 | PF00017 | 0.431 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.527 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.231 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.316 |
LIG_SH3_2 | 362 | 367 | PF14604 | 0.500 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.537 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.617 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.398 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.543 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 183 | 190 | PF11976 | 0.226 |
LIG_SUMO_SIM_anti_2 | 425 | 431 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 425 | 431 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 587 | 596 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 649 | 657 | PF11976 | 0.600 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.499 |
LIG_TRAF2_1 | 617 | 620 | PF00917 | 0.482 |
LIG_TYR_ITIM | 394 | 399 | PF00017 | 0.399 |
LIG_WRC_WIRS_1 | 72 | 77 | PF05994 | 0.248 |
LIG_WW_2 | 109 | 112 | PF00397 | 0.405 |
LIG_WW_3 | 208 | 212 | PF00397 | 0.467 |
LIG_WW_3 | 96 | 100 | PF00397 | 0.392 |
MOD_CDC14_SPxK_1 | 273 | 276 | PF00782 | 0.346 |
MOD_CDK_SPK_2 | 301 | 306 | PF00069 | 0.553 |
MOD_CDK_SPxK_1 | 270 | 276 | PF00069 | 0.323 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.500 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.254 |
MOD_CDK_SPxxK_3 | 513 | 520 | PF00069 | 0.518 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.492 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.685 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.697 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.724 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.593 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.619 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.388 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.637 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.522 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.571 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.536 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.335 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.662 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.422 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.632 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.578 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.572 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.579 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.454 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.507 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.601 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.782 |
MOD_GlcNHglycan | 368 | 372 | PF01048 | 0.799 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.382 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.703 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.489 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.665 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.537 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.497 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.425 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.565 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.365 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.702 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.452 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.477 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.731 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.345 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.530 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.616 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.654 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.652 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.556 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.320 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.602 |
MOD_N-GLC_1 | 558 | 563 | PF02516 | 0.581 |
MOD_N-GLC_2 | 61 | 63 | PF02516 | 0.330 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.319 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.547 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.516 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.359 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.573 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.623 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.641 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.645 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.666 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.313 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.332 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.393 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.485 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.631 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.461 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.579 |
MOD_PIKK_1 | 624 | 630 | PF00454 | 0.601 |
MOD_PK_1 | 511 | 517 | PF00069 | 0.652 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.325 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.546 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.734 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.544 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.401 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.519 |
MOD_PKB_1 | 276 | 284 | PF00069 | 0.262 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.294 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.702 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.510 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.453 |
MOD_Plk_1 | 532 | 538 | PF00069 | 0.523 |
MOD_Plk_1 | 558 | 564 | PF00069 | 0.482 |
MOD_Plk_2-3 | 374 | 380 | PF00069 | 0.480 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.552 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.252 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.223 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.347 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.357 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.284 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.688 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.730 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.552 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.377 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.289 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.467 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.353 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.755 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.585 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.517 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.469 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.528 |
TRG_DiLeu_BaEn_1 | 379 | 384 | PF01217 | 0.499 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_2 | 462 | 468 | PF01217 | 0.266 |
TRG_DiLeu_BaLyEn_6 | 275 | 280 | PF01217 | 0.353 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.384 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.379 |
TRG_NLS_MonoExtC_3 | 577 | 583 | PF00514 | 0.750 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 353 | 357 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB91 | Leptomonas seymouri | 47% | 75% |
A0A0S4INP1 | Bodo saltans | 27% | 86% |
A0A1X0P9Y1 | Trypanosomatidae | 31% | 89% |
A0A3Q8IHR3 | Leishmania donovani | 66% | 99% |
A0A3R7MJM0 | Trypanosoma rangeli | 32% | 93% |
A4IA93 | Leishmania infantum | 66% | 81% |
C9ZM02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 91% |
E9B5B5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 98% |
Q4Q2L8 | Leishmania major | 66% | 99% |
V5BQH0 | Trypanosoma cruzi | 33% | 92% |