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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AIY2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006284 | base-excision repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004519 | endonuclease activity | 5 | 10 |
GO:0004527 | exonuclease activity | 5 | 7 |
GO:0005488 | binding | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003906 | DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 3 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008309 | double-stranded DNA exodeoxyribonuclease activity | 7 | 1 |
GO:0008311 | double-stranded DNA 3'-5' DNA exonuclease activity | 8 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 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:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
GO:0016829 | lyase activity | 2 | 2 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 2 |
GO:0140078 | class I DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.253 |
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.336 |
CLV_C14_Caspase3-7 | 679 | 683 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.391 |
CLV_PCSK_FUR_1 | 495 | 499 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 697 | 699 | PF00082 | 0.734 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.189 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.323 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.298 |
DEG_APCC_DBOX_1 | 323 | 331 | PF00400 | 0.336 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.298 |
DOC_CKS1_1 | 606 | 611 | PF01111 | 0.335 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.189 |
DOC_CYCLIN_RxL_1 | 403 | 413 | PF00134 | 0.256 |
DOC_CYCLIN_yCln2_LP_2 | 333 | 336 | PF00134 | 0.336 |
DOC_MAPK_gen_1 | 536 | 544 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 406 | 414 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 645 | 654 | PF00069 | 0.529 |
DOC_MAPK_RevD_3 | 67 | 82 | PF00069 | 0.189 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.298 |
DOC_PP1_RVXF_1 | 591 | 598 | PF00149 | 0.402 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.336 |
DOC_PP2B_PxIxI_1 | 203 | 209 | PF00149 | 0.391 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.189 |
DOC_PP4_FxxP_1 | 606 | 609 | PF00568 | 0.329 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.386 |
DOC_USP7_UBL2_3 | 256 | 260 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 700 | 705 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 709 | 714 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 411 | 419 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 536 | 546 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.223 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.298 |
LIG_BRCT_BRCA1_1 | 399 | 403 | PF00533 | 0.298 |
LIG_CtBP_PxDLS_1 | 353 | 357 | PF00389 | 0.336 |
LIG_deltaCOP1_diTrp_1 | 109 | 117 | PF00928 | 0.277 |
LIG_deltaCOP1_diTrp_1 | 244 | 251 | PF00928 | 0.214 |
LIG_EVH1_1 | 575 | 579 | PF00568 | 0.494 |
LIG_EVH1_2 | 576 | 580 | PF00568 | 0.511 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.225 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.454 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.243 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.380 |
LIG_FHA_1 | 726 | 732 | PF00498 | 0.503 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.253 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.288 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.282 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.274 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.274 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.542 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.493 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.298 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.278 |
LIG_Integrin_RGD_1 | 734 | 736 | PF01839 | 0.518 |
LIG_IRF3_LxIS_1 | 291 | 296 | PF10401 | 0.189 |
LIG_LIR_Apic_2 | 375 | 379 | PF02991 | 0.189 |
LIG_LIR_Apic_2 | 603 | 609 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 109 | 117 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 383 | 393 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 441 | 449 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 507 | 516 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 551 | 562 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 507 | 511 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.450 |
LIG_MYND_1 | 478 | 482 | PF01753 | 0.391 |
LIG_NRBOX | 228 | 234 | PF00104 | 0.391 |
LIG_OCRL_FandH_1 | 21 | 33 | PF00620 | 0.313 |
LIG_PCNA_yPIPBox_3 | 374 | 388 | PF02747 | 0.333 |
LIG_Pex14_1 | 247 | 251 | PF04695 | 0.195 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.298 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.314 |
LIG_PTB_Apo_2 | 569 | 576 | PF02174 | 0.486 |
LIG_PTB_Phospho_1 | 569 | 575 | PF10480 | 0.485 |
LIG_Rb_pABgroove_1 | 354 | 362 | PF01858 | 0.336 |
LIG_SH2_CRK | 385 | 389 | PF00017 | 0.332 |
LIG_SH2_CRK | 648 | 652 | PF00017 | 0.420 |
LIG_SH2_NCK_1 | 349 | 353 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 508 | 511 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.189 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 591 | 595 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.274 |
LIG_SH3_1 | 479 | 485 | PF00018 | 0.336 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.391 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.391 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.328 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.279 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.406 |
LIG_SH3_3 | 604 | 610 | PF00018 | 0.368 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.462 |
LIG_SUMO_SIM_par_1 | 204 | 210 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 73 | 80 | PF11976 | 0.189 |
LIG_SUMO_SIM_par_1 | 740 | 745 | PF11976 | 0.662 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.189 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.307 |
LIG_TRAF2_2 | 609 | 614 | PF00917 | 0.337 |
LIG_TYR_ITIM | 506 | 511 | PF00017 | 0.274 |
LIG_UBA3_1 | 36 | 43 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.229 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.325 |
LIG_WRC_WIRS_1 | 654 | 659 | PF05994 | 0.520 |
LIG_WRC_WIRS_1 | 706 | 711 | PF05994 | 0.575 |
LIG_WW_3 | 334 | 338 | PF00397 | 0.336 |
MOD_CDC14_SPxK_1 | 417 | 420 | PF00782 | 0.189 |
MOD_CDK_SPxK_1 | 414 | 420 | PF00069 | 0.189 |
MOD_CDK_SPxxK_3 | 67 | 74 | PF00069 | 0.189 |
MOD_CDK_SPxxK_3 | 709 | 716 | PF00069 | 0.481 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.337 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.333 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.333 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.342 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.375 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.426 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.400 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.403 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.470 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.609 |
MOD_CK1_1 | 708 | 714 | PF00069 | 0.728 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.395 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.240 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.489 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.189 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.668 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.177 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.298 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.264 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.357 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.391 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.412 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.403 |
MOD_GlcNHglycan | 398 | 402 | PF01048 | 0.391 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.343 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.688 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.688 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.271 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.292 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.305 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.397 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.321 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.414 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.389 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.240 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.247 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.430 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.751 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.625 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.395 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.274 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.253 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.291 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.280 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.373 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.237 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.368 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.267 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.393 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.336 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.417 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.587 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.333 |
MOD_NEK2_2 | 653 | 658 | PF00069 | 0.606 |
MOD_OFUCOSY | 484 | 490 | PF10250 | 0.335 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.370 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.306 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.189 |
MOD_PKA_1 | 536 | 542 | PF00069 | 0.475 |
MOD_PKA_1 | 82 | 88 | PF00069 | 0.211 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.328 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.189 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.455 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.280 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.640 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.344 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.274 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.200 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.314 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.333 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.522 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.280 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.232 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.480 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.391 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.334 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.391 |
MOD_ProDKin_1 | 700 | 706 | PF00069 | 0.602 |
MOD_ProDKin_1 | 709 | 715 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 35 | 45 | PF00179 | 0.274 |
MOD_SUMO_rev_2 | 637 | 647 | PF00179 | 0.573 |
MOD_SUMO_rev_2 | 678 | 686 | PF00179 | 0.627 |
TRG_AP2beta_CARGO_1 | 551 | 561 | PF09066 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 701 | 706 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 440 | 443 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 495 | 498 | PF00400 | 0.231 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 698 | 700 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 497 | 502 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB73 | Leptomonas seymouri | 63% | 100% |
A0A1X0P3V4 | Trypanosomatidae | 38% | 100% |
A0A3R7M024 | Trypanosoma rangeli | 42% | 100% |
A0A3S7XBT9 | Leishmania donovani | 79% | 100% |
A4IDU8 | Leishmania infantum | 79% | 100% |
D0A8S3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9ATW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q0N5 | Leishmania major | 80% | 99% |