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: Q4QAE2
Term | Name | Level | Count |
---|---|---|---|
GO:0000079 | regulation of cyclin-dependent protein serine/threonine kinase activity | 6 | 7 |
GO:0001932 | regulation of protein phosphorylation | 7 | 7 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 7 |
GO:0019222 | regulation of metabolic process | 3 | 7 |
GO:0031323 | regulation of cellular metabolic process | 4 | 7 |
GO:0031399 | regulation of protein modification process | 6 | 7 |
GO:0042325 | regulation of phosphorylation | 7 | 7 |
GO:0043549 | regulation of kinase activity | 5 | 7 |
GO:0045859 | regulation of protein kinase activity | 6 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050790 | regulation of catalytic activity | 3 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 7 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 7 |
GO:0051246 | regulation of protein metabolic process | 5 | 7 |
GO:0051338 | regulation of transferase activity | 4 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0065009 | regulation of molecular function | 2 | 7 |
GO:0071900 | regulation of protein serine/threonine kinase activity | 7 | 7 |
GO:0080090 | regulation of primary metabolic process | 4 | 7 |
GO:1904029 | regulation of cyclin-dependent protein kinase activity | 5 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005515 | protein binding | 2 | 7 |
GO:0019899 | enzyme binding | 3 | 7 |
GO:0019900 | kinase binding | 4 | 7 |
GO:0019901 | protein kinase binding | 5 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.714 |
CLV_PCSK_FUR_1 | 363 | 367 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.623 |
CLV_PCSK_PC7_1 | 606 | 612 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.808 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.717 |
CLV_Separin_Metazoa | 130 | 134 | PF03568 | 0.622 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.527 |
DEG_SCF_FBW7_1 | 335 | 341 | PF00400 | 0.749 |
DEG_SCF_FBW7_1 | 78 | 84 | PF00400 | 0.744 |
DEG_SPOP_SBC_1 | 543 | 547 | PF00917 | 0.600 |
DOC_CKS1_1 | 335 | 340 | PF01111 | 0.748 |
DOC_CKS1_1 | 78 | 83 | PF01111 | 0.638 |
DOC_CYCLIN_yClb1_LxF_4 | 286 | 292 | PF00134 | 0.411 |
DOC_CYCLIN_yClb1_LxF_4 | 298 | 303 | PF00134 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 244 | 250 | PF00134 | 0.513 |
DOC_MAPK_gen_1 | 631 | 641 | PF00069 | 0.716 |
DOC_MAPK_MEF2A_6 | 201 | 208 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 298 | 304 | PF00149 | 0.595 |
DOC_PP2B_LxvP_1 | 521 | 524 | PF13499 | 0.811 |
DOC_PP2B_LxvP_1 | 648 | 651 | PF13499 | 0.798 |
DOC_PP2B_PxIxI_1 | 203 | 209 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.398 |
DOC_SPAK_OSR1_1 | 112 | 116 | PF12202 | 0.475 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.492 |
DOC_USP7_MATH_2 | 338 | 344 | PF00917 | 0.834 |
DOC_USP7_UBL2_3 | 213 | 217 | PF12436 | 0.411 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 404 | 409 | PF00244 | 0.815 |
LIG_14-3-3_CanoR_1 | 477 | 486 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 517 | 522 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 578 | 587 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 634 | 639 | PF00244 | 0.720 |
LIG_BIR_III_4 | 533 | 537 | PF00653 | 0.788 |
LIG_Clathr_ClatBox_1 | 505 | 509 | PF01394 | 0.761 |
LIG_EH1_1 | 290 | 298 | PF00400 | 0.563 |
LIG_eIF4E_1 | 248 | 254 | PF01652 | 0.499 |
LIG_EVH1_1 | 63 | 67 | PF00568 | 0.608 |
LIG_EVH1_1 | 648 | 652 | PF00568 | 0.797 |
LIG_FAT_LD_1 | 289 | 297 | PF03623 | 0.557 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.411 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.411 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.826 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.807 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.756 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.712 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.756 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.414 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.554 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.303 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.411 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.587 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.815 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.760 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.566 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.643 |
LIG_Integrin_RGD_1 | 511 | 513 | PF01839 | 0.730 |
LIG_LIR_Apic_2 | 110 | 116 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 219 | 223 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 309 | 314 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 274 | 281 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 290 | 297 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.352 |
LIG_MYND_1 | 61 | 65 | PF01753 | 0.736 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.411 |
LIG_Pex14_2 | 113 | 117 | PF04695 | 0.559 |
LIG_PTB_Apo_2 | 269 | 276 | PF02174 | 0.411 |
LIG_PTB_Apo_2 | 296 | 303 | PF02174 | 0.478 |
LIG_PTB_Phospho_1 | 296 | 302 | PF10480 | 0.480 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.476 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.454 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 576 | 580 | PF00017 | 0.569 |
LIG_SH2_PTP2 | 220 | 223 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.421 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.760 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.718 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.713 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.760 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.694 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.612 |
LIG_SH3_3 | 646 | 652 | PF00018 | 0.710 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.469 |
LIG_SUMO_SIM_anti_2 | 500 | 506 | PF11976 | 0.598 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.550 |
LIG_TRFH_1 | 77 | 81 | PF08558 | 0.605 |
LIG_TYR_ITIM | 216 | 221 | PF00017 | 0.411 |
LIG_WW_2 | 64 | 67 | PF00397 | 0.626 |
MOD_CDC14_SPxK_1 | 386 | 389 | PF00782 | 0.705 |
MOD_CDK_SPxK_1 | 383 | 389 | PF00069 | 0.704 |
MOD_CDK_SPxK_1 | 604 | 610 | PF00069 | 0.698 |
MOD_CDK_SPxxK_3 | 604 | 611 | PF00069 | 0.702 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.805 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.715 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.368 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.288 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.488 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.726 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.791 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.784 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.703 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.811 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.704 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.624 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.656 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.692 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.686 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.598 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.605 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.411 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.590 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.809 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.703 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.641 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.565 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.726 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.434 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.742 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.399 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.684 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.804 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.491 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.700 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.711 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.717 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.564 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.776 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.774 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.731 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.716 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.775 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.542 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.624 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.754 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.767 |
MOD_GlcNHglycan | 633 | 637 | PF01048 | 0.791 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.655 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.662 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.781 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.319 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.578 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.411 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.608 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.661 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.649 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.560 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.819 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.718 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.506 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.740 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.593 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.818 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.693 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.551 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.706 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.707 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.734 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.730 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.687 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.604 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.585 |
MOD_N-GLC_2 | 569 | 571 | PF02516 | 0.734 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.411 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.727 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.687 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.778 |
MOD_NEK2_2 | 204 | 209 | PF00069 | 0.411 |
MOD_NEK2_2 | 8 | 13 | PF00069 | 0.723 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.703 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.699 |
MOD_PK_1 | 365 | 371 | PF00069 | 0.704 |
MOD_PK_1 | 404 | 410 | PF00069 | 0.816 |
MOD_PK_1 | 515 | 521 | PF00069 | 0.717 |
MOD_PK_1 | 634 | 640 | PF00069 | 0.558 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.280 |
MOD_PKA_1 | 365 | 371 | PF00069 | 0.705 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.459 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.590 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.704 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.801 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.638 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.581 |
MOD_PKB_1 | 363 | 371 | PF00069 | 0.704 |
MOD_PKB_1 | 515 | 523 | PF00069 | 0.816 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.460 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.411 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.700 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.565 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.411 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.683 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.730 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.514 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.805 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.713 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.570 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.733 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.681 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.513 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.411 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.746 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.704 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.720 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.724 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.797 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.727 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.704 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.698 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.600 |
TRG_DiLeu_BaEn_1 | 110 | 115 | PF01217 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 537 | 542 | PF01217 | 0.764 |
TRG_DiLeu_BaLyEn_6 | 92 | 97 | PF01217 | 0.703 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.445 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.706 |
TRG_NES_CRM1_1 | 284 | 295 | PF08389 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 313 | 318 | PF00026 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0K2 | Leptomonas seymouri | 51% | 94% |
A0A3Q8IG93 | Leishmania donovani | 95% | 100% |
A4HDQ0 | Leishmania braziliensis | 77% | 93% |
A4I0Z6 | Leishmania infantum | 94% | 100% |
E9AX34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |