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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0033557 | Slx1-Slx4 complex | 3 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
Related structures:
AlphaFold database: Q4Q9W0
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 2 |
GO:0000725 | recombinational repair | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006310 | DNA recombination | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004518 | nuclease activity | 4 | 7 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0004520 | DNA endonuclease activity | 5 | 7 |
GO:0004536 | DNA nuclease activity | 4 | 7 |
GO:0005488 | binding | 1 | 3 |
GO:0008821 | crossover junction DNA endonuclease activity | 7 | 2 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016888 | endodeoxyribonuclease activity, producing 5'-phosphomonoesters | 6 | 7 |
GO:0016889 | DNA endonuclease activity, producing 3'-phosphomonoesters | 6 | 2 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 7 |
GO:0016894 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters | 6 | 2 |
GO:0017108 | 5'-flap endonuclease activity | 7 | 7 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
GO:0048256 | flap endonuclease activity | 6 | 7 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 541 | 543 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 573 | 575 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 46 | 52 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.269 |
DEG_APCC_DBOX_1 | 469 | 477 | PF00400 | 0.342 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.456 |
DEG_SPOP_SBC_1 | 311 | 315 | PF00917 | 0.522 |
DOC_CKS1_1 | 180 | 185 | PF01111 | 0.572 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 212 | 215 | PF00134 | 0.411 |
DOC_MAPK_gen_1 | 537 | 545 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 85 | 92 | PF00069 | 0.437 |
DOC_PP2B_LxvP_1 | 212 | 215 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.572 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.661 |
DOC_PP4_FxxP_1 | 631 | 634 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 683 | 687 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 537 | 541 | PF12436 | 0.432 |
DOC_USP7_UBL2_3 | 596 | 600 | PF12436 | 0.487 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.768 |
LIG_14-3-3_CanoR_1 | 111 | 115 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 169 | 174 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 320 | 329 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 470 | 480 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 624 | 628 | PF00244 | 0.606 |
LIG_APCC_ABBA_1 | 220 | 225 | PF00400 | 0.366 |
LIG_CaM_IQ_9 | 549 | 565 | PF13499 | 0.418 |
LIG_Clathr_ClatBox_1 | 221 | 225 | PF01394 | 0.420 |
LIG_deltaCOP1_diTrp_1 | 286 | 292 | PF00928 | 0.620 |
LIG_deltaCOP1_diTrp_1 | 74 | 77 | PF00928 | 0.469 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.383 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.278 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.584 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.480 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.637 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.373 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.469 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.365 |
LIG_LIR_Apic_2 | 359 | 363 | PF02991 | 0.655 |
LIG_LIR_Apic_2 | 630 | 634 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 698 | 704 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 74 | 80 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.494 |
LIG_LYPXL_SIV_4 | 100 | 108 | PF13949 | 0.387 |
LIG_MYND_1 | 214 | 218 | PF01753 | 0.447 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.301 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.469 |
LIG_RPA_C_Fungi | 543 | 555 | PF08784 | 0.548 |
LIG_SH2_NCK_1 | 101 | 105 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 482 | 486 | PF00017 | 0.448 |
LIG_SH2_SRC | 482 | 485 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.304 |
LIG_SH3_1 | 303 | 309 | PF00018 | 0.600 |
LIG_SH3_1 | 514 | 520 | PF00018 | 0.415 |
LIG_SH3_2 | 414 | 419 | PF14604 | 0.520 |
LIG_SH3_2 | 508 | 513 | PF14604 | 0.601 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.618 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.418 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.637 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.801 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.571 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.565 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.728 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.391 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.768 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.339 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.567 |
LIG_SH3_3 | 622 | 628 | PF00018 | 0.595 |
LIG_SH3_CIN85_PxpxPR_1 | 410 | 415 | PF14604 | 0.610 |
LIG_SUMO_SIM_anti_2 | 275 | 280 | PF11976 | 0.504 |
LIG_SUMO_SIM_anti_2 | 89 | 94 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 689 | 695 | PF11976 | 0.611 |
LIG_SUMO_SIM_par_1 | 88 | 94 | PF11976 | 0.370 |
LIG_WRC_WIRS_1 | 357 | 362 | PF05994 | 0.621 |
LIG_WRC_WIRS_1 | 636 | 641 | PF05994 | 0.603 |
LIG_WW_2 | 183 | 186 | PF00397 | 0.630 |
LIG_WW_3 | 364 | 368 | PF00397 | 0.628 |
MOD_CDC14_SPxK_1 | 317 | 320 | PF00782 | 0.642 |
MOD_CDC14_SPxK_1 | 510 | 513 | PF00782 | 0.601 |
MOD_CDK_SPK_2 | 155 | 160 | PF00069 | 0.654 |
MOD_CDK_SPK_2 | 367 | 372 | PF00069 | 0.635 |
MOD_CDK_SPxK_1 | 314 | 320 | PF00069 | 0.637 |
MOD_CDK_SPxK_1 | 507 | 513 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 507 | 514 | PF00069 | 0.595 |
MOD_CDK_SPxxK_3 | 658 | 665 | PF00069 | 0.616 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.762 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.696 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.553 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.593 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.719 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.692 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.568 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.607 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.618 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.497 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.530 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.572 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.772 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.361 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.653 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.583 |
MOD_Cter_Amidation | 48 | 51 | PF01082 | 0.259 |
MOD_DYRK1A_RPxSP_1 | 624 | 628 | PF00069 | 0.659 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.402 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.542 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.654 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.715 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.619 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.567 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.304 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.575 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.605 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.434 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.655 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.608 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.685 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.638 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.599 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.648 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.541 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.583 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.573 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.604 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.742 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.364 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.547 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.633 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.346 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.620 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.696 |
MOD_NEK2_2 | 102 | 107 | PF00069 | 0.381 |
MOD_NEK2_2 | 465 | 470 | PF00069 | 0.409 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.653 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.615 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.500 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.460 |
MOD_PKA_1 | 573 | 579 | PF00069 | 0.599 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.426 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.567 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.712 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.310 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.606 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.583 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.375 |
MOD_PKB_1 | 51 | 59 | PF00069 | 0.304 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.339 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.569 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.574 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.572 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.237 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.608 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.444 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.443 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.506 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.411 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.670 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.654 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.601 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.505 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.614 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.711 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.601 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.749 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.663 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.600 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.635 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.634 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.652 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.456 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.768 |
MOD_SUMO_for_1 | 71 | 74 | PF00179 | 0.304 |
TRG_DiLeu_BaEn_1 | 698 | 703 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_4 | 434 | 440 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_4 | 698 | 704 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 512 | 514 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 554 | 557 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 580 | 583 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.380 |
TRG_NLS_MonoExtN_4 | 537 | 544 | PF00514 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 32 | 36 | PF00026 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7G5 | Leptomonas seymouri | 49% | 100% |
A0A3S7WZ95 | Leishmania donovani | 90% | 100% |
A4I1H7 | Leishmania infantum | 90% | 100% |
E9AIR5 | Leishmania braziliensis | 74% | 100% |
E9AXL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q9W0 | Leishmania major | 100% | 100% |