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: 20 |
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 |
Related structures:
AlphaFold database: E9B048
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 12 |
GO:0009889 | regulation of biosynthetic process | 4 | 12 |
GO:0010468 | regulation of gene expression | 5 | 12 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 12 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 12 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0031323 | regulation of cellular metabolic process | 4 | 12 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051252 | regulation of RNA metabolic process | 5 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 12 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 12 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004402 | histone acetyltransferase activity | 4 | 12 |
GO:0008080 | N-acetyltransferase activity | 6 | 12 |
GO:0016407 | acetyltransferase activity | 5 | 12 |
GO:0016410 | N-acyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 12 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 12 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
GO:0140110 | transcription regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 144 | 148 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.569 |
CLV_C14_Caspase3-7 | 625 | 629 | PF00656 | 0.756 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.399 |
CLV_PCSK_FUR_1 | 240 | 244 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.671 |
CLV_PCSK_PC7_1 | 521 | 527 | PF00082 | 0.192 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 665 | 669 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.380 |
CLV_Separin_Metazoa | 743 | 747 | PF03568 | 0.414 |
DEG_APCC_DBOX_1 | 220 | 228 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.562 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.496 |
DEG_SPOP_SBC_1 | 659 | 663 | PF00917 | 0.548 |
DEG_SPOP_SBC_1 | 678 | 682 | PF00917 | 0.478 |
DOC_ANK_TNKS_1 | 355 | 362 | PF00023 | 0.358 |
DOC_ANK_TNKS_1 | 609 | 616 | PF00023 | 0.602 |
DOC_CYCLIN_RxL_1 | 382 | 395 | PF00134 | 0.445 |
DOC_MAPK_DCC_7 | 72 | 81 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 540 | 547 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 664 | 670 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.400 |
DOC_PP1_RVXF_1 | 733 | 740 | PF00149 | 0.396 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 730 | 733 | PF13499 | 0.349 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.364 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.608 |
DOC_USP7_UBL2_3 | 554 | 558 | PF12436 | 0.585 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 673 | 678 | PF00397 | 0.778 |
LIG_14-3-3_CanoR_1 | 126 | 135 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 337 | 343 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 370 | 375 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 644 | 654 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 721 | 728 | PF00244 | 0.464 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.359 |
LIG_DLG_GKlike_1 | 5 | 12 | PF00625 | 0.471 |
LIG_eIF4E_1 | 247 | 253 | PF01652 | 0.531 |
LIG_eIF4E_1 | 278 | 284 | PF01652 | 0.409 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.568 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.648 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.509 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.627 |
LIG_FHA_2 | 692 | 698 | PF00498 | 0.584 |
LIG_LIR_Apic_2 | 328 | 333 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 225 | 236 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 340 | 347 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 738 | 745 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.413 |
LIG_LYPXL_S_1 | 36 | 40 | PF13949 | 0.415 |
LIG_LYPXL_yS_3 | 37 | 40 | PF13949 | 0.415 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.475 |
LIG_NRBOX | 709 | 715 | PF00104 | 0.364 |
LIG_PCNA_yPIPBox_3 | 19 | 30 | PF02747 | 0.431 |
LIG_Pex14_2 | 330 | 334 | PF04695 | 0.339 |
LIG_Pex14_2 | 433 | 437 | PF04695 | 0.444 |
LIG_PTB_Apo_2 | 282 | 289 | PF02174 | 0.411 |
LIG_PTB_Apo_2 | 405 | 412 | PF02174 | 0.469 |
LIG_PTB_Phospho_1 | 282 | 288 | PF10480 | 0.408 |
LIG_Rb_pABgroove_1 | 735 | 743 | PF01858 | 0.378 |
LIG_SH2_CRK | 153 | 157 | PF00017 | 0.380 |
LIG_SH2_GRB2like | 267 | 270 | PF00017 | 0.380 |
LIG_SH2_NCK_1 | 496 | 500 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 496 | 500 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 741 | 745 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 736 | 739 | PF00017 | 0.386 |
LIG_SH3_1 | 463 | 469 | PF00018 | 0.554 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.373 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.421 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.575 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.433 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.571 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.491 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.488 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.451 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.552 |
LIG_SUMO_SIM_anti_2 | 590 | 598 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 578 | 583 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 590 | 598 | PF11976 | 0.517 |
LIG_TRAF2_1 | 360 | 363 | PF00917 | 0.435 |
LIG_TRAF2_1 | 639 | 642 | PF00917 | 0.535 |
LIG_TYR_ITIM | 35 | 40 | PF00017 | 0.407 |
LIG_UBA3_1 | 389 | 394 | PF00899 | 0.478 |
LIG_WW_2 | 89 | 92 | PF00397 | 0.502 |
LIG_WW_3 | 479 | 483 | PF00397 | 0.438 |
MOD_CDK_SPxK_1 | 504 | 510 | PF00069 | 0.481 |
MOD_CDK_SPxxK_3 | 615 | 622 | PF00069 | 0.533 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.470 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.518 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.518 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.506 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.551 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.599 |
MOD_CK1_1 | 763 | 769 | PF00069 | 0.686 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.599 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.548 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.463 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.626 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.583 |
MOD_CK2_1 | 746 | 752 | PF00069 | 0.368 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.497 |
MOD_Cter_Amidation | 457 | 460 | PF01082 | 0.281 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.723 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.666 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.485 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.420 |
MOD_GlcNHglycan | 190 | 194 | PF01048 | 0.686 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.534 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.245 |
MOD_GlcNHglycan | 471 | 475 | PF01048 | 0.522 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.548 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.563 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.541 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.586 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.536 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.356 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.505 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.511 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.636 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.592 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.587 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.495 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.537 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.704 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.720 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.497 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.572 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.560 |
MOD_LATS_1 | 42 | 48 | PF00433 | 0.515 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.471 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.244 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.537 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.496 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.568 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.528 |
MOD_NEK2_1 | 760 | 765 | PF00069 | 0.425 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.744 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.589 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.481 |
MOD_PIKK_1 | 687 | 693 | PF00454 | 0.475 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.481 |
MOD_PKA_1 | 459 | 465 | PF00069 | 0.637 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.449 |
MOD_PKA_1 | 622 | 628 | PF00069 | 0.660 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.593 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.377 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.484 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.576 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.618 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.593 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.705 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.445 |
MOD_PKA_2 | 720 | 726 | PF00069 | 0.486 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.545 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.556 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.599 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.410 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.510 |
MOD_Plk_1 | 747 | 753 | PF00069 | 0.401 |
MOD_Plk_2-3 | 628 | 634 | PF00069 | 0.626 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.366 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.397 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.469 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.444 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.604 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.662 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.570 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.434 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.516 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.481 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.532 |
MOD_ProDKin_1 | 673 | 679 | PF00069 | 0.777 |
MOD_SUMO_for_1 | 629 | 632 | PF00179 | 0.636 |
MOD_SUMO_rev_2 | 138 | 148 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 395 | 402 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 550 | 560 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 608 | 618 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 625 | 631 | PF00179 | 0.633 |
TRG_DiLeu_BaEn_4 | 640 | 646 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_4 | 705 | 711 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 524 | 526 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 539 | 541 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.386 |
TRG_NLS_Bipartite_1 | 610 | 627 | PF00514 | 0.531 |
TRG_NLS_MonoExtC_3 | 621 | 626 | PF00514 | 0.651 |
TRG_NLS_MonoExtN_4 | 619 | 626 | PF00514 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 485 | 489 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIW1 | Leptomonas seymouri | 55% | 100% |
A0A1X0NS80 | Trypanosomatidae | 41% | 100% |
A0A2D1QVA5 | Leishmania donovani | 91% | 100% |
A4H7H5 | Leishmania braziliensis | 28% | 100% |
A4HGT1 | Leishmania braziliensis | 78% | 100% |
A4HVV6 | Leishmania infantum | 28% | 100% |
A4I3V8 | Leishmania infantum | 91% | 100% |
D7RTH9 | Leishmania donovani | 28% | 100% |
E9APK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4Q837 | Leishmania major | 90% | 100% |