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 |
Related structures:
AlphaFold database: A4H7D0
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031848 | protection from non-homologous end joining at telomere | 6 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0036297 | interstrand cross-link repair | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043247 | telomere maintenance in response to DNA damage | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0035312 | 5'-3' DNA exonuclease activity | 7 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 618 | 622 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 741 | 745 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 776 | 780 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 628 | 630 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 724 | 726 | PF00675 | 0.514 |
CLV_PCSK_FUR_1 | 722 | 726 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 724 | 726 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 739 | 741 | PF00082 | 0.640 |
CLV_PCSK_PC1ET2_1 | 739 | 741 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.334 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.497 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.487 |
DEG_SPOP_SBC_1 | 558 | 562 | PF00917 | 0.522 |
DEG_SPOP_SBC_1 | 666 | 670 | PF00917 | 0.534 |
DOC_ANK_TNKS_1 | 739 | 746 | PF00023 | 0.570 |
DOC_CKS1_1 | 163 | 168 | PF01111 | 0.442 |
DOC_CYCLIN_RxL_1 | 793 | 802 | PF00134 | 0.504 |
DOC_CYCLIN_RxL_1 | 95 | 106 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 149 | 155 | PF00134 | 0.317 |
DOC_CYCLIN_yCln2_LP_2 | 515 | 521 | PF00134 | 0.370 |
DOC_MAPK_DCC_7 | 438 | 447 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 7 | 16 | PF00069 | 0.481 |
DOC_MAPK_HePTP_8 | 534 | 546 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 109 | 117 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 304 | 313 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 33 | 41 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 438 | 447 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 537 | 546 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 7 | 16 | PF00069 | 0.481 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.401 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.479 |
DOC_PP2B_LxvP_1 | 542 | 545 | PF13499 | 0.511 |
DOC_PP2B_LxvP_1 | 712 | 715 | PF13499 | 0.511 |
DOC_PP2B_PxIxI_1 | 442 | 448 | PF00149 | 0.395 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.320 |
DOC_PP4_FxxP_1 | 163 | 166 | PF00568 | 0.359 |
DOC_PP4_FxxP_1 | 604 | 607 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 672 | 675 | PF00568 | 0.632 |
DOC_PP4_MxPP_1 | 733 | 736 | PF00568 | 0.534 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 785 | 789 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.322 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 343 | 348 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 517 | 526 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 724 | 733 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 759 | 765 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 796 | 801 | PF00244 | 0.519 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.239 |
LIG_BRCT_BRCA1_1 | 600 | 604 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 669 | 673 | PF00533 | 0.561 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.361 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.480 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.301 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.374 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.401 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.550 |
LIG_FHA_1 | 792 | 798 | PF00498 | 0.662 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.429 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.297 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.366 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.371 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.517 |
LIG_FHA_2 | 774 | 780 | PF00498 | 0.560 |
LIG_GBD_Chelix_1 | 322 | 330 | PF00786 | 0.306 |
LIG_HCF-1_HBM_1 | 199 | 202 | PF13415 | 0.341 |
LIG_Integrin_RGD_1 | 530 | 532 | PF01839 | 0.357 |
LIG_KLC1_Yacidic_2 | 199 | 204 | PF13176 | 0.337 |
LIG_LIR_Apic_2 | 437 | 443 | PF02991 | 0.429 |
LIG_LIR_Apic_2 | 601 | 607 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 669 | 675 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 143 | 153 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 338 | 348 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 727 | 736 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.490 |
LIG_MLH1_MIPbox_1 | 669 | 673 | PF16413 | 0.561 |
LIG_MYND_1 | 715 | 719 | PF01753 | 0.454 |
LIG_NRBOX | 241 | 247 | PF00104 | 0.451 |
LIG_PDZ_Class_2 | 804 | 809 | PF00595 | 0.632 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.396 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.364 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.359 |
LIG_SH2_GRB2like | 730 | 733 | PF00017 | 0.507 |
LIG_SH2_PTP2 | 146 | 149 | PF00017 | 0.305 |
LIG_SH2_SRC | 440 | 443 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 730 | 733 | PF00017 | 0.576 |
LIG_SH3_1 | 575 | 581 | PF00018 | 0.467 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.445 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 139 | 146 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 343 | 350 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 36 | 43 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 374 | 380 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 443 | 450 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 794 | 802 | PF11976 | 0.580 |
LIG_TRAF2_1 | 350 | 353 | PF00917 | 0.395 |
LIG_TRAF2_1 | 377 | 380 | PF00917 | 0.414 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.384 |
LIG_TRAF2_1 | 622 | 625 | PF00917 | 0.646 |
LIG_TYR_ITIM | 144 | 149 | PF00017 | 0.346 |
LIG_TYR_ITIM | 339 | 344 | PF00017 | 0.296 |
LIG_TYR_ITSM | 467 | 474 | PF00017 | 0.450 |
LIG_WRC_WIRS_1 | 189 | 194 | PF05994 | 0.373 |
LIG_WRC_WIRS_1 | 400 | 405 | PF05994 | 0.377 |
MOD_CDC14_SPxK_1 | 187 | 190 | PF00782 | 0.333 |
MOD_CDC14_SPxK_1 | 365 | 368 | PF00782 | 0.556 |
MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.354 |
MOD_CDK_SPxK_1 | 362 | 368 | PF00069 | 0.537 |
MOD_CDK_SPxxK_3 | 637 | 644 | PF00069 | 0.528 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.494 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.362 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.605 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.481 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.427 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.517 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.513 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.528 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.752 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.553 |
MOD_CK1_1 | 788 | 794 | PF00069 | 0.626 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.481 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.390 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.279 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.366 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.447 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.385 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.378 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.530 |
MOD_Cter_Amidation | 258 | 261 | PF01082 | 0.445 |
MOD_Cter_Amidation | 737 | 740 | PF01082 | 0.699 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.488 |
MOD_GlcNHglycan | 135 | 139 | PF01048 | 0.559 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.316 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.400 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.534 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.458 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.656 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.366 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.600 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.536 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.396 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.613 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.303 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.511 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.569 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.567 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.547 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.482 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.573 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.724 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.640 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.356 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.528 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.429 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.359 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.481 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.381 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.514 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.619 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.322 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.314 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.624 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.331 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.396 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.688 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.585 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.606 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.553 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.556 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.272 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.808 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.472 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.570 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.591 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.571 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.624 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.398 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.301 |
MOD_LATS_1 | 78 | 84 | PF00433 | 0.443 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.643 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.527 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.345 |
MOD_N-GLC_2 | 690 | 692 | PF02516 | 0.533 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.295 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.378 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.341 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.522 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.461 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.619 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.479 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.491 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.332 |
MOD_NEK2_1 | 726 | 731 | PF00069 | 0.524 |
MOD_NEK2_1 | 789 | 794 | PF00069 | 0.768 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.373 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.383 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.572 |
MOD_PIKK_1 | 591 | 597 | PF00454 | 0.591 |
MOD_PIKK_1 | 724 | 730 | PF00454 | 0.614 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.513 |
MOD_PKA_1 | 724 | 730 | PF00069 | 0.472 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.517 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.385 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.541 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.536 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.457 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.503 |
MOD_PKA_2 | 724 | 730 | PF00069 | 0.529 |
MOD_PKA_2 | 758 | 764 | PF00069 | 0.554 |
MOD_PKB_1 | 51 | 59 | PF00069 | 0.513 |
MOD_PKB_1 | 722 | 730 | PF00069 | 0.465 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.345 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.530 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.625 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.405 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.362 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.345 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.431 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.541 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.614 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.507 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.486 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.321 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.433 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.354 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.641 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.563 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.501 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.378 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.389 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.527 |
MOD_SUMO_for_1 | 765 | 768 | PF00179 | 0.628 |
MOD_SUMO_rev_2 | 618 | 627 | PF00179 | 0.646 |
TRG_DiLeu_BaEn_2 | 507 | 513 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_4 | 353 | 359 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 440 | 445 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 793 | 798 | PF01217 | 0.520 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 730 | 733 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 627 | 629 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 721 | 724 | PF00400 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 266 | 271 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 333 | 337 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 724 | 728 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAX7 | Leptomonas seymouri | 50% | 100% |
A0A3S5H6Q1 | Leishmania donovani | 74% | 100% |
A4HVS7 | Leishmania infantum | 74% | 100% |
E9APH3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QG05 | Leishmania major | 73% | 99% |