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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: E9B2W6
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 5 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004518 | nuclease activity | 4 | 5 |
GO:0004527 | exonuclease activity | 5 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 479 | 483 | PF00656 | 0.732 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 672 | 674 | PF00675 | 0.229 |
CLV_PCSK_FUR_1 | 520 | 524 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.526 |
CLV_PCSK_PC7_1 | 522 | 528 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 704 | 708 | PF00082 | 0.247 |
CLV_Separin_Metazoa | 511 | 515 | PF03568 | 0.407 |
CLV_Separin_Metazoa | 517 | 521 | PF03568 | 0.450 |
DEG_APCC_DBOX_1 | 281 | 289 | PF00400 | 0.523 |
DEG_ODPH_VHL_1 | 448 | 459 | PF01847 | 0.770 |
DEG_SCF_FBW7_1 | 123 | 130 | PF00400 | 0.501 |
DEG_SCF_FBW7_1 | 243 | 250 | PF00400 | 0.616 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.739 |
DOC_CKS1_1 | 421 | 426 | PF01111 | 0.745 |
DOC_CKS1_1 | 86 | 91 | PF01111 | 0.722 |
DOC_CYCLIN_yCln2_LP_2 | 140 | 146 | PF00134 | 0.617 |
DOC_MAPK_DCC_7 | 138 | 148 | PF00069 | 0.728 |
DOC_MAPK_DCC_7 | 281 | 290 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 115 | 125 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 173 | 180 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 281 | 290 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 602 | 609 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 651 | 659 | PF00069 | 0.591 |
DOC_MAPK_NFAT4_5 | 602 | 610 | PF00069 | 0.591 |
DOC_MAPK_RevD_3 | 123 | 139 | PF00069 | 0.630 |
DOC_PP1_RVXF_1 | 604 | 610 | PF00149 | 0.591 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.716 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.742 |
DOC_PP2B_PxIxI_1 | 3 | 9 | PF00149 | 0.745 |
DOC_PP4_FxxP_1 | 244 | 247 | PF00568 | 0.741 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.747 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.713 |
DOC_USP7_MATH_2 | 259 | 265 | PF00917 | 0.527 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 262 | 267 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 298 | 306 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 469 | 473 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 530 | 535 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 689 | 698 | PF00244 | 0.591 |
LIG_Actin_WH2_2 | 498 | 516 | PF00022 | 0.310 |
LIG_Actin_WH2_2 | 574 | 592 | PF00022 | 0.517 |
LIG_APCC_ABBA_1 | 657 | 662 | PF00400 | 0.591 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.501 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.751 |
LIG_BRCT_BRCA1_1 | 634 | 638 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_1 | 741 | 745 | PF00533 | 0.564 |
LIG_EVH1_2 | 197 | 201 | PF00568 | 0.487 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.723 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.734 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.625 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.576 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.591 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.591 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.624 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.759 |
LIG_FHA_2 | 659 | 665 | PF00498 | 0.591 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.729 |
LIG_FXI_DFP_1 | 745 | 749 | PF00024 | 0.572 |
LIG_IRF3_LxIS_1 | 629 | 635 | PF10401 | 0.591 |
LIG_LIR_Apic_2 | 241 | 247 | PF02991 | 0.743 |
LIG_LIR_Apic_2 | 250 | 254 | PF02991 | 0.624 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 635 | 645 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 652 | 660 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 572 | 576 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 635 | 641 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 652 | 657 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 742 | 748 | PF02991 | 0.552 |
LIG_MYND_1 | 213 | 217 | PF01753 | 0.718 |
LIG_PCNA_yPIPBox_3 | 231 | 244 | PF02747 | 0.748 |
LIG_Pex14_1 | 528 | 532 | PF04695 | 0.405 |
LIG_Pex14_2 | 323 | 327 | PF04695 | 0.639 |
LIG_Pex14_2 | 95 | 99 | PF04695 | 0.519 |
LIG_PTAP_UEV_1 | 429 | 434 | PF05743 | 0.649 |
LIG_PTB_Apo_2 | 730 | 737 | PF02174 | 0.544 |
LIG_Rb_pABgroove_1 | 603 | 611 | PF01858 | 0.591 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.746 |
LIG_SH2_CRK | 573 | 577 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 573 | 577 | PF00017 | 0.591 |
LIG_SH2_PTP2 | 257 | 260 | PF00017 | 0.530 |
LIG_SH2_SRC | 257 | 260 | PF00017 | 0.756 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.591 |
LIG_SH2_STAT3 | 491 | 494 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 698 | 701 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.524 |
LIG_SH3_1 | 139 | 145 | PF00018 | 0.722 |
LIG_SH3_1 | 419 | 425 | PF00018 | 0.645 |
LIG_SH3_2 | 421 | 426 | PF14604 | 0.745 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.552 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.481 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.523 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.694 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.750 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.638 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.483 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.585 |
LIG_SH3_3 | 639 | 645 | PF00018 | 0.591 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.730 |
LIG_SUMO_SIM_par_1 | 545 | 553 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 566 | 572 | PF11976 | 0.577 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.660 |
LIG_TRFH_1 | 638 | 642 | PF08558 | 0.591 |
LIG_TYR_ITIM | 696 | 701 | PF00017 | 0.591 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.650 |
LIG_WW_2 | 213 | 216 | PF00397 | 0.677 |
LIG_WW_3 | 332 | 336 | PF00397 | 0.714 |
LIG_WW_3 | 423 | 427 | PF00397 | 0.754 |
MOD_CDC14_SPxK_1 | 332 | 335 | PF00782 | 0.708 |
MOD_CDC14_SPxK_1 | 593 | 596 | PF00782 | 0.502 |
MOD_CDK_SPK_2 | 641 | 646 | PF00069 | 0.429 |
MOD_CDK_SPxK_1 | 329 | 335 | PF00069 | 0.715 |
MOD_CDK_SPxK_1 | 420 | 426 | PF00069 | 0.748 |
MOD_CDK_SPxK_1 | 590 | 596 | PF00069 | 0.502 |
MOD_CDK_SPxxK_3 | 59 | 66 | PF00069 | 0.742 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.724 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.762 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.629 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.750 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.577 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.715 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.625 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.766 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.549 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.746 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.755 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.758 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.775 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.748 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.600 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.734 |
MOD_CK1_1 | 739 | 745 | PF00069 | 0.566 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.757 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.511 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.526 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.523 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.758 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.780 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.725 |
MOD_Cter_Amidation | 670 | 673 | PF01082 | 0.229 |
MOD_DYRK1A_RPxSP_1 | 59 | 63 | PF00069 | 0.738 |
MOD_DYRK1A_RPxSP_1 | 590 | 594 | PF00069 | 0.517 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.762 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.726 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.643 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.496 |
MOD_GlcNHglycan | 186 | 191 | PF01048 | 0.635 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.550 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.722 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.781 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.712 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.657 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.716 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.693 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.647 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.704 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.693 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.698 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.729 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.749 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.741 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.562 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.732 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.527 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.743 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.780 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.567 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.757 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.517 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.749 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.567 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.732 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.747 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.521 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.552 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.717 |
MOD_N-GLC_2 | 628 | 630 | PF02516 | 0.391 |
MOD_N-GLC_2 | 77 | 79 | PF02516 | 0.741 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.545 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.716 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.748 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.560 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.587 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.747 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.508 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.591 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.569 |
MOD_NEK2_2 | 276 | 281 | PF00069 | 0.639 |
MOD_NEK2_2 | 349 | 354 | PF00069 | 0.530 |
MOD_NEK2_2 | 649 | 654 | PF00069 | 0.591 |
MOD_OFUCOSY | 630 | 637 | PF10250 | 0.391 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.665 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.567 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.627 |
MOD_PK_1 | 530 | 536 | PF00069 | 0.660 |
MOD_PK_1 | 561 | 567 | PF00069 | 0.591 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.526 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.530 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.742 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.546 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.516 |
MOD_PKA_2 | 726 | 732 | PF00069 | 0.405 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.550 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.644 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.588 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.522 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.756 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.383 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.733 |
MOD_Plk_2-3 | 373 | 379 | PF00069 | 0.756 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.703 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.624 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.591 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.591 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.728 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.740 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.654 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.760 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.578 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.728 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.593 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.759 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.740 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.591 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.591 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.727 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 698 | 701 | PF00928 | 0.591 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.745 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 672 | 674 | PF00400 | 0.429 |
TRG_NES_CRM1_1 | 616 | 627 | PF08389 | 0.591 |
TRG_NLS_MonoExtN_4 | 134 | 141 | PF00514 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 282 | 287 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 689 | 693 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5Q4 | Leishmania donovani | 84% | 99% |
A4I804 | Leishmania infantum | 84% | 99% |
Q4Q590 | Leishmania major | 83% | 100% |