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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HK84
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.610 |
CLV_PCSK_FUR_1 | 160 | 164 | PF00082 | 0.738 |
CLV_PCSK_FUR_1 | 2 | 6 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 772 | 774 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 789 | 791 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 562 | 564 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 772 | 774 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.294 |
CLV_Separin_Metazoa | 506 | 510 | PF03568 | 0.546 |
DEG_APCC_DBOX_1 | 576 | 584 | PF00400 | 0.480 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.662 |
DEG_SPOP_SBC_1 | 214 | 218 | PF00917 | 0.767 |
DEG_SPOP_SBC_1 | 314 | 318 | PF00917 | 0.670 |
DOC_ANK_TNKS_1 | 410 | 417 | PF00023 | 0.439 |
DOC_CYCLIN_yCln2_LP_2 | 740 | 746 | PF00134 | 0.355 |
DOC_MAPK_gen_1 | 373 | 380 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 478 | 485 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 563 | 572 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 708 | 715 | PF00149 | 0.335 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.528 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.673 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.709 |
DOC_USP7_UBL2_3 | 443 | 447 | PF12436 | 0.581 |
DOC_USP7_UBL2_3 | 526 | 530 | PF12436 | 0.563 |
DOC_USP7_UBL2_3 | 608 | 612 | PF12436 | 0.257 |
DOC_USP7_UBL2_3 | 768 | 772 | PF12436 | 0.578 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 197 | 203 | PF00244 | 0.774 |
LIG_14-3-3_CanoR_1 | 269 | 276 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 5 | 14 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 509 | 519 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 548 | 552 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 733 | 737 | PF00244 | 0.336 |
LIG_14-3-3_CterR_2 | 826 | 828 | PF00244 | 0.658 |
LIG_APCC_ABBA_1 | 138 | 143 | PF00400 | 0.554 |
LIG_APCC_ABBA_1 | 591 | 596 | PF00400 | 0.227 |
LIG_BRCT_BRCA1_1 | 264 | 268 | PF00533 | 0.735 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.767 |
LIG_BRCT_BRCA1_1 | 714 | 718 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 766 | 770 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_2 | 766 | 772 | PF00533 | 0.561 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.686 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.646 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.568 |
LIG_FHA_1 | 792 | 798 | PF00498 | 0.560 |
LIG_FHA_1 | 805 | 811 | PF00498 | 0.397 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.629 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.662 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.295 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.398 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.613 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.740 |
LIG_LIR_Apic_2 | 550 | 554 | PF02991 | 0.571 |
LIG_LIR_Apic_2 | 637 | 643 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 569 | 579 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 716 | 726 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.770 |
LIG_LIR_Nem_3 | 513 | 518 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 694 | 699 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 715 | 721 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 804 | 809 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 820 | 825 | PF02991 | 0.651 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.723 |
LIG_Pex14_1 | 714 | 718 | PF04695 | 0.355 |
LIG_Pex14_2 | 692 | 696 | PF04695 | 0.447 |
LIG_Pex14_2 | 744 | 748 | PF04695 | 0.494 |
LIG_SH2_CRK | 539 | 543 | PF00017 | 0.617 |
LIG_SH2_CRK | 719 | 723 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 719 | 723 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 806 | 810 | PF00017 | 0.614 |
LIG_SH2_STAT3 | 606 | 609 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 806 | 809 | PF00017 | 0.590 |
LIG_SH3_2 | 239 | 244 | PF14604 | 0.707 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.685 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.703 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.676 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.746 |
LIG_TRAF2_1 | 172 | 175 | PF00917 | 0.693 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.703 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.581 |
LIG_TYR_ITIM | 717 | 722 | PF00017 | 0.227 |
LIG_TYR_ITSM | 586 | 593 | PF00017 | 0.447 |
LIG_WRC_WIRS_1 | 487 | 492 | PF05994 | 0.398 |
MOD_CDC14_SPxK_1 | 226 | 229 | PF00782 | 0.486 |
MOD_CDK_SPK_2 | 538 | 543 | PF00069 | 0.621 |
MOD_CDK_SPxK_1 | 223 | 229 | PF00069 | 0.495 |
MOD_CDK_SPxxK_3 | 262 | 269 | PF00069 | 0.737 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.692 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.650 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.671 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.601 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.665 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.652 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.532 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.595 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.490 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.588 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.566 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.425 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.694 |
MOD_CK1_1 | 804 | 810 | PF00069 | 0.591 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.630 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.698 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.720 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.664 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.513 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.679 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.704 |
MOD_Cter_Amidation | 439 | 442 | PF01082 | 0.402 |
MOD_DYRK1A_RPxSP_1 | 282 | 286 | PF00069 | 0.698 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.638 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.628 |
MOD_GlcNHglycan | 181 | 185 | PF01048 | 0.656 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.683 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.687 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.699 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.712 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.546 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.521 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.569 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.759 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.637 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.706 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.637 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.707 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.631 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.713 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.732 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.735 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.603 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.630 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.600 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.595 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.518 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.590 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.570 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.616 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.549 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.322 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.620 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.405 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.618 |
MOD_LATS_1 | 771 | 777 | PF00433 | 0.590 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.531 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.526 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.476 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.537 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.626 |
MOD_N-GLC_1 | 712 | 717 | PF02516 | 0.392 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.703 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.668 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.769 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.699 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.542 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.445 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.739 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.680 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.335 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.480 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.504 |
MOD_NEK2_2 | 232 | 237 | PF00069 | 0.529 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.680 |
MOD_NEK2_2 | 557 | 562 | PF00069 | 0.227 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.481 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.458 |
MOD_PK_1 | 376 | 382 | PF00069 | 0.501 |
MOD_PK_1 | 479 | 485 | PF00069 | 0.519 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.649 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.667 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.672 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.551 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.580 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.631 |
MOD_PKA_2 | 732 | 738 | PF00069 | 0.335 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.512 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.555 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.646 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.349 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.767 |
MOD_Plk_1 | 728 | 734 | PF00069 | 0.493 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.723 |
MOD_Plk_1 | 817 | 823 | PF00069 | 0.698 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.599 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.776 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.688 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.714 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.541 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.553 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.519 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.330 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.373 |
MOD_Plk_4 | 817 | 823 | PF00069 | 0.670 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.662 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.718 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.672 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.665 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.701 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.706 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.690 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.665 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.615 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.594 |
MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.359 |
MOD_SUMO_for_1 | 561 | 564 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 116 | 124 | PF00179 | 0.728 |
MOD_SUMO_rev_2 | 139 | 147 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 254 | 262 | PF00179 | 0.752 |
MOD_SUMO_rev_2 | 473 | 481 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 764 | 770 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 793 | 802 | PF00179 | 0.381 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.640 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.525 |
TRG_DiLeu_LyEn_5 | 152 | 157 | PF01217 | 0.709 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 719 | 722 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 160 | 163 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.628 |
TRG_NES_CRM1_1 | 754 | 766 | PF08389 | 0.345 |
TRG_NLS_MonoExtN_4 | 160 | 167 | PF00514 | 0.494 |
TRG_NLS_MonoExtN_4 | 438 | 445 | PF00514 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.698 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9E7 | Leptomonas seymouri | 64% | 100% |
A0A1X0NW98 | Trypanosomatidae | 42% | 100% |
A0A3Q8ID17 | Leishmania donovani | 78% | 100% |
A0A3R7KXA1 | Trypanosoma rangeli | 44% | 100% |
A4I7R9 | Leishmania infantum | 78% | 100% |
D0A9X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B2M7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q5I0 | Leishmania major | 78% | 98% |
V5BQQ4 | Trypanosoma cruzi | 45% | 100% |