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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4H7D9
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006399 | tRNA metabolic process | 7 | 9 |
GO:0006400 | tRNA modification | 6 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008033 | tRNA processing | 8 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009451 | RNA modification | 5 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0031119 | tRNA pseudouridine synthesis | 7 | 6 |
GO:0034470 | ncRNA processing | 7 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034660 | ncRNA metabolic process | 6 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:1990481 | mRNA pseudouridine synthesis | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0009982 | pseudouridine synthase activity | 4 | 9 |
GO:0016853 | isomerase activity | 2 | 9 |
GO:0016866 | intramolecular transferase activity | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.446 |
CLV_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.749 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.732 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 666 | 668 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.441 |
CLV_PCSK_FUR_1 | 117 | 121 | PF00082 | 0.554 |
CLV_PCSK_FUR_1 | 695 | 699 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 210 | 212 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.800 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 697 | 699 | PF00082 | 0.354 |
CLV_PCSK_PC7_1 | 451 | 457 | PF00082 | 0.489 |
CLV_PCSK_PC7_1 | 667 | 673 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.796 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 752 | 756 | PF00082 | 0.476 |
CLV_Separin_Metazoa | 625 | 629 | PF03568 | 0.307 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.502 |
DEG_ODPH_VHL_1 | 308 | 320 | PF01847 | 0.540 |
DEG_SCF_FBW7_2 | 382 | 389 | PF00400 | 0.648 |
DOC_CYCLIN_RxL_1 | 152 | 161 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 499 | 509 | PF00134 | 0.475 |
DOC_MAPK_gen_1 | 116 | 126 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 36 | 44 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 727 | 735 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 749 | 757 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 119 | 128 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 193 | 202 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 727 | 735 | PF00069 | 0.360 |
DOC_MAPK_RevD_3 | 654 | 668 | PF00069 | 0.220 |
DOC_PP1_RVXF_1 | 314 | 321 | PF00149 | 0.650 |
DOC_PP1_RVXF_1 | 754 | 760 | PF00149 | 0.489 |
DOC_PP2B_LxvP_1 | 598 | 601 | PF13499 | 0.359 |
DOC_PP4_FxxP_1 | 562 | 565 | PF00568 | 0.400 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.692 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.162 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 181 | 189 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 533 | 538 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 568 | 574 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.489 |
LIG_Actin_WH2_2 | 301 | 318 | PF00022 | 0.612 |
LIG_Actin_WH2_2 | 654 | 669 | PF00022 | 0.220 |
LIG_Actin_WH2_2 | 741 | 758 | PF00022 | 0.477 |
LIG_AP2alpha_2 | 539 | 541 | PF02296 | 0.331 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.342 |
LIG_Clathr_ClatBox_1 | 176 | 180 | PF01394 | 0.476 |
LIG_deltaCOP1_diTrp_1 | 555 | 562 | PF00928 | 0.322 |
LIG_EH1_1 | 170 | 178 | PF00400 | 0.306 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.388 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.519 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.385 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.493 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.741 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.549 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.389 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.512 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.377 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.492 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.478 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.415 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.739 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.547 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.400 |
LIG_GBD_Chelix_1 | 731 | 739 | PF00786 | 0.343 |
LIG_LIR_Apic_2 | 285 | 289 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 165 | 176 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 468 | 477 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 511 | 519 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 685 | 692 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 511 | 517 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 685 | 689 | PF02991 | 0.307 |
LIG_LRP6_Inhibitor_1 | 656 | 662 | PF00058 | 0.220 |
LIG_LYPXL_yS_3 | 146 | 149 | PF13949 | 0.422 |
LIG_MYND_1 | 94 | 98 | PF01753 | 0.635 |
LIG_PCNA_yPIPBox_3 | 170 | 184 | PF02747 | 0.480 |
LIG_PTAP_UEV_1 | 327 | 332 | PF05743 | 0.543 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.353 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.451 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.410 |
LIG_SH2_GRB2like | 276 | 279 | PF00017 | 0.482 |
LIG_SH2_GRB2like | 514 | 517 | PF00017 | 0.307 |
LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.305 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.660 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.348 |
LIG_SH3_1 | 672 | 678 | PF00018 | 0.400 |
LIG_SH3_1 | 92 | 98 | PF00018 | 0.666 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.442 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.337 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.526 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.613 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.703 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.477 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.308 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.307 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.693 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.632 |
LIG_SUMO_SIM_anti_2 | 197 | 202 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 710 | 715 | PF11976 | 0.511 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.356 |
LIG_TRAF2_1 | 215 | 218 | PF00917 | 0.502 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.453 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.382 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.713 |
LIG_TRAF2_1 | 544 | 547 | PF00917 | 0.433 |
LIG_TRAF2_1 | 607 | 610 | PF00917 | 0.220 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.709 |
LIG_UBA3_1 | 637 | 643 | PF00899 | 0.307 |
LIG_WRC_WIRS_1 | 288 | 293 | PF05994 | 0.349 |
MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.541 |
MOD_CDK_SPxK_1 | 4 | 10 | PF00069 | 0.479 |
MOD_CDK_SPxxK_3 | 515 | 522 | PF00069 | 0.307 |
MOD_CDK_SPxxK_3 | 561 | 568 | PF00069 | 0.400 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.510 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.369 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.615 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.613 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.696 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.682 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.220 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.389 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.488 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.511 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.417 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.461 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.750 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.673 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.734 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.689 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.612 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.427 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.232 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.323 |
MOD_Cter_Amidation | 280 | 283 | PF01082 | 0.449 |
MOD_Cter_Amidation | 351 | 354 | PF01082 | 0.549 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.618 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.736 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.495 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.740 |
MOD_GlcNHglycan | 688 | 692 | PF01048 | 0.436 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.438 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.387 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.510 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.527 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.791 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.724 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.590 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.718 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.741 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.344 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.410 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.394 |
MOD_N-GLC_1 | 515 | 520 | PF02516 | 0.307 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.483 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.515 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.582 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.598 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.548 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.220 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.307 |
MOD_NEK2_2 | 524 | 529 | PF00069 | 0.400 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.499 |
MOD_NEK2_2 | 747 | 752 | PF00069 | 0.356 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.510 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.540 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.755 |
MOD_PIKK_1 | 722 | 728 | PF00454 | 0.289 |
MOD_PK_1 | 533 | 539 | PF00069 | 0.220 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.542 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.499 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.388 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.736 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.645 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.499 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.220 |
MOD_PKB_1 | 50 | 58 | PF00069 | 0.498 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.410 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.468 |
MOD_Plk_2-3 | 232 | 238 | PF00069 | 0.496 |
MOD_Plk_2-3 | 431 | 437 | PF00069 | 0.618 |
MOD_Plk_2-3 | 575 | 581 | PF00069 | 0.408 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.534 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.557 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.307 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.307 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.509 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.466 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.756 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.479 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.307 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.379 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.162 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.477 |
MOD_SUMO_rev_2 | 245 | 252 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 81 | 86 | PF00179 | 0.717 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.401 |
TRG_DiLeu_LyEn_5 | 248 | 253 | PF01217 | 0.401 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 686 | 689 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 694 | 696 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 727 | 729 | PF00400 | 0.480 |
TRG_NLS_Bipartite_1 | 345 | 365 | PF00514 | 0.718 |
TRG_NLS_MonoExtC_3 | 115 | 120 | PF00514 | 0.562 |
TRG_NLS_MonoExtC_3 | 453 | 459 | PF00514 | 0.489 |
TRG_NLS_MonoExtN_4 | 117 | 124 | PF00514 | 0.422 |
TRG_NLS_MonoExtN_4 | 345 | 350 | PF00514 | 0.710 |
TRG_NLS_MonoExtN_4 | 360 | 365 | PF00514 | 0.701 |
TRG_NLS_MonoExtN_4 | 451 | 458 | PF00514 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 502 | 507 | PF00026 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I609 | Leptomonas seymouri | 67% | 100% |
A0A3Q8IKM7 | Leishmania donovani | 80% | 100% |
A4I9K1 | Leishmania infantum | 80% | 100% |
D0A1W0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B4J9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q3H7 | Leishmania major | 81% | 100% |
V5B271 | Trypanosoma cruzi | 45% | 100% |