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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032300 | mismatch repair complex | 2 | 8 |
GO:0032389 | MutLalpha complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: E9AEY8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006298 | mismatch repair | 6 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0003690 | double-stranded DNA binding | 5 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 8 |
GO:0016462 | pyrophosphatase activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 8 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 8 |
GO:0016887 | ATP hydrolysis activity | 7 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0030983 | mismatched DNA binding | 6 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140299 | small molecule sensor activity | 1 | 8 |
GO:0140612 | DNA damage sensor activity | 2 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 480 | 484 | PF00656 | 0.698 |
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.776 |
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.840 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 584 | 586 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 798 | 800 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.268 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 430 | 432 | PF00082 | 0.714 |
CLV_PCSK_PC1ET2_1 | 798 | 800 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.504 |
CLV_Separin_Metazoa | 600 | 604 | PF03568 | 0.505 |
DEG_APCC_DBOX_1 | 819 | 827 | PF00400 | 0.510 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.585 |
DEG_SPOP_SBC_1 | 461 | 465 | PF00917 | 0.807 |
DOC_CDC14_PxL_1 | 311 | 319 | PF14671 | 0.430 |
DOC_CKS1_1 | 238 | 243 | PF01111 | 0.619 |
DOC_CKS1_1 | 791 | 796 | PF01111 | 0.501 |
DOC_CYCLIN_RxL_1 | 359 | 369 | PF00134 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 699 | 705 | PF00134 | 0.376 |
DOC_MAPK_gen_1 | 783 | 791 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 798 | 804 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 37 | 45 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 566 | 574 | PF00069 | 0.675 |
DOC_PP1_RVXF_1 | 273 | 279 | PF00149 | 0.376 |
DOC_PP2B_LxvP_1 | 501 | 504 | PF13499 | 0.841 |
DOC_PP2B_LxvP_1 | 699 | 702 | PF13499 | 0.430 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.799 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.376 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.625 |
DOC_USP7_UBL2_3 | 645 | 649 | PF12436 | 0.471 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.837 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.831 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 790 | 795 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 165 | 169 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 259 | 268 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 297 | 305 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 346 | 351 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 407 | 414 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 416 | 424 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 806 | 814 | PF00244 | 0.498 |
LIG_BRCT_BRCA1_1 | 132 | 136 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.462 |
LIG_eIF4E_1 | 683 | 689 | PF01652 | 0.501 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.504 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.465 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.420 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.573 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.381 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.265 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.757 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.692 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.355 |
LIG_FHA_1 | 768 | 774 | PF00498 | 0.430 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.557 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.503 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.525 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.705 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.527 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.846 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.611 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.519 |
LIG_LIR_Apic_2 | 811 | 817 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.550 |
LIG_LYPXL_yS_3 | 595 | 598 | PF13949 | 0.634 |
LIG_MYND_1 | 500 | 504 | PF01753 | 0.836 |
LIG_Pex14_1 | 278 | 282 | PF04695 | 0.376 |
LIG_Pex14_2 | 657 | 661 | PF04695 | 0.376 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.430 |
LIG_SH2_CRK | 741 | 745 | PF00017 | 0.455 |
LIG_SH2_CRK | 748 | 752 | PF00017 | 0.390 |
LIG_SH2_CRK | 766 | 770 | PF00017 | 0.242 |
LIG_SH2_GRB2like | 477 | 480 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 748 | 752 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.675 |
LIG_SH2_STAP1 | 685 | 689 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.762 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.779 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.484 |
LIG_SH3_1 | 741 | 747 | PF00018 | 0.501 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.499 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.376 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.601 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.729 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.376 |
LIG_Sin3_3 | 611 | 618 | PF02671 | 0.532 |
LIG_SUMO_SIM_par_1 | 243 | 250 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 496 | 506 | PF11976 | 0.751 |
LIG_SUMO_SIM_par_1 | 828 | 833 | PF11976 | 0.457 |
LIG_TRAF2_1 | 366 | 369 | PF00917 | 0.348 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.404 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.476 |
LIG_TYR_ITIM | 746 | 751 | PF00017 | 0.376 |
LIG_TYR_ITIM | 764 | 769 | PF00017 | 0.376 |
LIG_WRC_WIRS_1 | 282 | 287 | PF05994 | 0.424 |
LIG_WRC_WIRS_1 | 472 | 477 | PF05994 | 0.679 |
MOD_CDK_SPxK_1 | 354 | 360 | PF00069 | 0.462 |
MOD_CDK_SPxxK_3 | 354 | 361 | PF00069 | 0.462 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.676 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.339 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.510 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.496 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.474 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.501 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.353 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.641 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.826 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.740 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.634 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.679 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.640 |
MOD_CK1_1 | 730 | 736 | PF00069 | 0.434 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.376 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.573 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.774 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.622 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.510 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.767 |
MOD_CK2_1 | 644 | 650 | PF00069 | 0.505 |
MOD_CK2_1 | 705 | 711 | PF00069 | 0.501 |
MOD_GlcNHglycan | 117 | 121 | PF01048 | 0.758 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.621 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.504 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.477 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.455 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.625 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.611 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.741 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.745 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.685 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.762 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.698 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.424 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.509 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.500 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.799 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.546 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.504 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.504 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.489 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.529 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.506 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.472 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.353 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.615 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.764 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.610 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.462 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.546 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.430 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.430 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.462 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.430 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.634 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.663 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.585 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.387 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.319 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.402 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.611 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.478 |
MOD_NEK2_2 | 586 | 591 | PF00069 | 0.703 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.787 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.420 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.695 |
MOD_PIKK_1 | 579 | 585 | PF00454 | 0.765 |
MOD_PIKK_1 | 617 | 623 | PF00454 | 0.747 |
MOD_PIKK_1 | 805 | 811 | PF00454 | 0.495 |
MOD_PK_1 | 566 | 572 | PF00069 | 0.675 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.592 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.486 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.376 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.531 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.757 |
MOD_PKA_2 | 730 | 736 | PF00069 | 0.501 |
MOD_PKA_2 | 785 | 791 | PF00069 | 0.376 |
MOD_PKA_2 | 805 | 811 | PF00069 | 0.242 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.383 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.573 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.438 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.430 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.421 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.464 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.556 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.721 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.376 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.465 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.707 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.627 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.376 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.612 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.462 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.607 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.794 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.838 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.690 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.390 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.575 |
MOD_ProDKin_1 | 790 | 796 | PF00069 | 0.501 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.838 |
MOD_SUMO_for_1 | 432 | 435 | PF00179 | 0.692 |
MOD_SUMO_rev_2 | 30 | 39 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 514 | 523 | PF00179 | 0.748 |
MOD_SUMO_rev_2 | 711 | 721 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 730 | 739 | PF00179 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 41 | 46 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 79 | 84 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 821 | 826 | PF01217 | 0.499 |
TRG_DiLeu_LyEn_5 | 497 | 502 | PF01217 | 0.760 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 748 | 751 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.527 |
TRG_NLS_Bipartite_1 | 345 | 364 | PF00514 | 0.268 |
TRG_NLS_MonoExtC_3 | 429 | 435 | PF00514 | 0.711 |
TRG_NLS_MonoExtN_4 | 358 | 364 | PF00514 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 556 | 560 | PF00026 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 629 | 634 | PF00026 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 652 | 656 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4H3 | Leptomonas seymouri | 62% | 100% |
A0A3Q8IM41 | Leishmania donovani | 94% | 100% |
A4HMI7 | Leishmania braziliensis | 82% | 100% |
A4IB67 | Leishmania infantum | 93% | 100% |
C9ZZH7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B644 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |