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:0030896 | checkpoint clamp complex | 3 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0140513 | nuclear protein-containing complex | 2 | 8 |
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IIS7
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 8 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0007165 | signal transduction | 2 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0010564 | regulation of cell cycle process | 5 | 8 |
GO:0010948 | negative regulation of cell cycle process | 6 | 8 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0035556 | intracellular signal transduction | 3 | 8 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 8 |
GO:0045786 | negative regulation of cell cycle | 5 | 8 |
GO:0048519 | negative regulation of biological process | 3 | 8 |
GO:0048523 | negative regulation of cellular process | 4 | 8 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0051726 | regulation of cell cycle | 4 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 8 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 8 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0010212 | response to ionizing radiation | 4 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031573 | mitotic intra-S DNA damage checkpoint signaling | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 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:0044773 | mitotic DNA damage checkpoint signaling | 6 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 1 |
GO:0071478 | cellular response to radiation | 4 | 1 |
GO:0071479 | cellular response to ionizing radiation | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0104004 | cellular response to environmental stimulus | 3 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 306 | 310 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 581 | 585 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 695 | 699 | PF00656 | 0.589 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.645 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.809 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.764 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.525 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.430 |
DEG_Kelch_Keap1_1 | 530 | 535 | PF01344 | 0.727 |
DEG_SCF_FBW7_1 | 498 | 504 | PF00400 | 0.687 |
DEG_SCF_FBW7_1 | 657 | 664 | PF00400 | 0.649 |
DOC_CKS1_1 | 325 | 330 | PF01111 | 0.694 |
DOC_CKS1_1 | 498 | 503 | PF01111 | 0.686 |
DOC_CKS1_1 | 587 | 592 | PF01111 | 0.716 |
DOC_MAPK_MEF2A_6 | 47 | 55 | PF00069 | 0.459 |
DOC_MAPK_RevD_3 | 404 | 418 | PF00069 | 0.510 |
DOC_PP1_RVXF_1 | 622 | 629 | PF00149 | 0.695 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.564 |
DOC_PP2B_LxvP_1 | 351 | 354 | PF13499 | 0.677 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.600 |
DOC_PP2B_PxIxI_1 | 9 | 15 | PF00149 | 0.539 |
DOC_SPAK_OSR1_1 | 205 | 209 | PF12202 | 0.505 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 346 | 351 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 502 | 510 | PF00244 | 0.796 |
LIG_14-3-3_CanoR_1 | 591 | 599 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 623 | 627 | PF00244 | 0.739 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.437 |
LIG_BIR_III_4 | 309 | 313 | PF00653 | 0.709 |
LIG_BIR_III_4 | 615 | 619 | PF00653 | 0.676 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 624 | 628 | PF00533 | 0.662 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.457 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.466 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.516 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.486 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.522 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.524 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.574 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.690 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.505 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.360 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.668 |
LIG_GBD_Chelix_1 | 385 | 393 | PF00786 | 0.460 |
LIG_LIR_Apic_2 | 584 | 590 | PF02991 | 0.761 |
LIG_LIR_Gen_1 | 195 | 206 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 454 | 464 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 57 | 68 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 673 | 681 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 673 | 677 | PF02991 | 0.514 |
LIG_Pex14_1 | 173 | 177 | PF04695 | 0.451 |
LIG_Pex14_2 | 289 | 293 | PF04695 | 0.498 |
LIG_REV1ctd_RIR_1 | 296 | 304 | PF16727 | 0.446 |
LIG_SH2_CRK | 215 | 219 | PF00017 | 0.436 |
LIG_SH2_CRK | 587 | 591 | PF00017 | 0.744 |
LIG_SH2_NCK_1 | 681 | 685 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 681 | 684 | PF00017 | 0.597 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.731 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.622 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.533 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.586 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.679 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.736 |
LIG_SUMO_SIM_anti_2 | 597 | 604 | PF11976 | 0.748 |
LIG_SUMO_SIM_par_1 | 14 | 20 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 399 | 408 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 597 | 604 | PF11976 | 0.675 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.534 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.455 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.409 |
LIG_TRAF2_1 | 691 | 694 | PF00917 | 0.703 |
LIG_WRC_WIRS_1 | 456 | 461 | PF05994 | 0.432 |
MOD_CDC14_SPxK_1 | 344 | 347 | PF00782 | 0.737 |
MOD_CDC14_SPxK_1 | 44 | 47 | PF00782 | 0.591 |
MOD_CDK_SPK_2 | 341 | 346 | PF00069 | 0.739 |
MOD_CDK_SPK_2 | 497 | 502 | PF00069 | 0.709 |
MOD_CDK_SPK_2 | 586 | 591 | PF00069 | 0.718 |
MOD_CDK_SPxK_1 | 341 | 347 | PF00069 | 0.757 |
MOD_CDK_SPxK_1 | 41 | 47 | PF00069 | 0.485 |
MOD_CDK_SPxK_1 | 586 | 592 | PF00069 | 0.601 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.707 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.491 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.511 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.754 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.488 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.665 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.716 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.621 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.438 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.616 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.623 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.679 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.716 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.643 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.728 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.704 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.502 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.771 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.572 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.441 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.388 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.777 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.685 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.684 |
MOD_DYRK1A_RPxSP_1 | 301 | 305 | PF00069 | 0.521 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.707 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.505 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.454 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.679 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.685 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.674 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.706 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.674 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.668 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.646 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.712 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.604 |
MOD_GlcNHglycan | 39 | 43 | PF01048 | 0.448 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.527 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.695 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.454 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.513 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.707 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.479 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.806 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.742 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.472 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.723 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.755 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.743 |
MOD_GlcNHglycan | 682 | 685 | PF01048 | 0.620 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.465 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.653 |
MOD_GlcNHglycan | 75 | 80 | PF01048 | 0.698 |
MOD_GlcNHglycan | 92 | 97 | PF01048 | 0.541 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.454 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.551 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.550 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.430 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.456 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.523 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.558 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.760 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.704 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.585 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.652 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.718 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.369 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.655 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.676 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.648 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.645 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.700 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.633 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.752 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.613 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.706 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.661 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.670 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.701 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.521 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.718 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.610 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.728 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.797 |
MOD_N-GLC_2 | 227 | 229 | PF02516 | 0.566 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.419 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.576 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.477 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.589 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.385 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.753 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.685 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.752 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.564 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.442 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.563 |
MOD_NEK2_2 | 272 | 277 | PF00069 | 0.615 |
MOD_NEK2_2 | 665 | 670 | PF00069 | 0.701 |
MOD_PK_1 | 346 | 352 | PF00069 | 0.733 |
MOD_PKA_1 | 346 | 352 | PF00069 | 0.733 |
MOD_PKA_1 | 417 | 423 | PF00069 | 0.489 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.520 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.774 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.733 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.595 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.733 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.716 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.810 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.813 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.694 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.650 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.581 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.562 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.444 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.370 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.691 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.763 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.805 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.417 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.411 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.462 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.506 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.452 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.483 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.733 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.427 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.712 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.703 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.677 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.717 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.708 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.502 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.493 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.708 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.776 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.657 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.750 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.693 |
TRG_DiLeu_BaEn_2 | 699 | 705 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_3 | 399 | 405 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 508 | 513 | PF00026 | 0.723 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I126 | Leptomonas seymouri | 46% | 91% |
A0A1X0NTX6 | Trypanosomatidae | 23% | 97% |
A4H871 | Leishmania braziliensis | 73% | 96% |
A4HWJ6 | Leishmania infantum | 99% | 100% |
E9AQ97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 98% |
Q4QF86 | Leishmania major | 90% | 100% |