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: A4H871
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 | 149 | 153 | PF00656 | 0.717 |
CLV_C14_Caspase3-7 | 670 | 674 | PF00656 | 0.648 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.558 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.473 |
DEG_SCF_FBW7_1 | 561 | 566 | PF00400 | 0.566 |
DEG_SCF_FBW7_1 | 96 | 102 | PF00400 | 0.439 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.656 |
DEG_SPOP_SBC_1 | 629 | 633 | PF00917 | 0.592 |
DOC_CKS1_1 | 560 | 565 | PF01111 | 0.752 |
DOC_CKS1_1 | 96 | 101 | PF01111 | 0.452 |
DOC_CYCLIN_RxL_1 | 416 | 425 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 333 | 342 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 47 | 55 | PF00069 | 0.443 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.604 |
DOC_PP2B_LxvP_1 | 599 | 602 | PF13499 | 0.556 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.638 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.714 |
DOC_PP2B_PxIxI_1 | 9 | 15 | PF00149 | 0.576 |
DOC_PP4_FxxP_1 | 291 | 294 | PF00568 | 0.521 |
DOC_SPAK_OSR1_1 | 201 | 205 | PF12202 | 0.543 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.352 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.826 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 168 | 174 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 481 | 485 | PF00244 | 0.830 |
LIG_14-3-3_CanoR_1 | 603 | 611 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 654 | 660 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 71 | 75 | PF00244 | 0.604 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.481 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.314 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.461 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.511 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.543 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.676 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.513 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.520 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.557 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.528 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.561 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.531 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.378 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.655 |
LIG_GBD_Chelix_1 | 374 | 382 | PF00786 | 0.495 |
LIG_LIR_Apic_2 | 558 | 563 | PF02991 | 0.789 |
LIG_LIR_Gen_1 | 191 | 202 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 352 | 363 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 434 | 443 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 635 | 646 | PF02991 | 0.685 |
LIG_LIR_Gen_1 | 648 | 656 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 635 | 641 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 648 | 652 | PF02991 | 0.546 |
LIG_Pex14_1 | 169 | 173 | PF04695 | 0.488 |
LIG_Pex14_2 | 282 | 286 | PF04695 | 0.523 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.474 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.295 |
LIG_SH2_PTP2 | 560 | 563 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.662 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.763 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.389 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.566 |
LIG_SH3_3 | 613 | 619 | PF00018 | 0.737 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 570 | 577 | PF11976 | 0.785 |
LIG_SUMO_SIM_par_1 | 14 | 20 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 391 | 397 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 419 | 425 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 570 | 577 | PF11976 | 0.716 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.495 |
LIG_TRAF2_1 | 399 | 402 | PF00917 | 0.422 |
LIG_TRAF2_1 | 666 | 669 | PF00917 | 0.728 |
LIG_TRFH_1 | 63 | 67 | PF08558 | 0.365 |
LIG_WRC_WIRS_1 | 435 | 440 | PF05994 | 0.460 |
MOD_CDC14_SPxK_1 | 44 | 47 | PF00782 | 0.614 |
MOD_CDK_SPK_2 | 476 | 481 | PF00069 | 0.744 |
MOD_CDK_SPK_2 | 559 | 564 | PF00069 | 0.754 |
MOD_CDK_SPxK_1 | 41 | 47 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 578 | 585 | PF00069 | 0.712 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.748 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.529 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.546 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.756 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.493 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.540 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.540 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.697 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.345 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.517 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.663 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.657 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.686 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.745 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.736 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.709 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.744 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.695 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.557 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.507 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.734 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.602 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.539 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.804 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.551 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.561 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.478 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.409 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.804 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.708 |
MOD_CK2_1 | 655 | 661 | PF00069 | 0.743 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.676 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.747 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.535 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.484 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.541 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.726 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.717 |
MOD_GlcNHglycan | 39 | 43 | PF01048 | 0.483 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.738 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.705 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.622 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.725 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.464 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.814 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.757 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.706 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.797 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.767 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.460 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.681 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.448 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.580 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.494 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.525 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.542 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.662 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.569 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.592 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.710 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.674 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.666 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.739 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.689 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.777 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.654 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.752 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.717 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.744 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.692 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.551 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.663 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.351 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.815 |
MOD_N-GLC_2 | 223 | 225 | PF02516 | 0.606 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.467 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.589 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.511 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.592 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.426 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.559 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.653 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.708 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.571 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.738 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.797 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.624 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.481 |
MOD_NEK2_2 | 480 | 485 | PF00069 | 0.575 |
MOD_NEK2_2 | 640 | 645 | PF00069 | 0.770 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.810 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.635 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.753 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.758 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.766 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.819 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.661 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.594 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.570 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.482 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.711 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.810 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.815 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.624 |
MOD_Plk_2-3 | 663 | 669 | PF00069 | 0.556 |
MOD_Plk_2-3 | 92 | 98 | PF00069 | 0.648 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.468 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.456 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.506 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.562 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.488 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.520 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.520 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.520 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.768 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.706 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.729 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.759 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.520 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.517 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.618 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.430 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.746 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.822 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.698 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.793 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.461 |
MOD_SUMO_rev_2 | 360 | 368 | PF00179 | 0.311 |
TRG_DiLeu_BaEn_2 | 674 | 680 | PF01217 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 417 | 422 | PF01217 | 0.454 |
TRG_DiLeu_LyEn_5 | 389 | 394 | PF01217 | 0.337 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I126 | Leptomonas seymouri | 45% | 88% |
A0A1X0NTX6 | Trypanosomatidae | 22% | 92% |
A0A3Q8IIS7 | Leishmania donovani | 73% | 96% |
A4HWJ6 | Leishmania infantum | 73% | 80% |
E9AQ97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 98% |
Q4QF86 | Leishmania major | 73% | 100% |