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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030896 | checkpoint clamp complex | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
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: E9AQ97
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 7 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0007165 | signal transduction | 2 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010564 | regulation of cell cycle process | 5 | 7 |
GO:0010948 | negative regulation of cell cycle process | 6 | 7 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 7 |
GO:0045786 | negative regulation of cell cycle | 5 | 7 |
GO:0048519 | negative regulation of biological process | 3 | 7 |
GO:0048523 | negative regulation of cellular process | 4 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 7 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 7 |
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 | 133 | 137 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.672 |
CLV_C14_Caspase3-7 | 565 | 569 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 681 | 685 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.675 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.821 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.776 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.594 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.454 |
DEG_Kelch_Keap1_1 | 514 | 519 | PF01344 | 0.762 |
DEG_SCF_FBW7_1 | 482 | 488 | PF00400 | 0.713 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.669 |
DEG_SPOP_SBC_1 | 640 | 644 | PF00917 | 0.627 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.725 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.713 |
DOC_CKS1_1 | 571 | 576 | PF01111 | 0.737 |
DOC_MAPK_MEF2A_6 | 47 | 55 | PF00069 | 0.428 |
DOC_MAPK_RevD_3 | 388 | 402 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 606 | 613 | PF00149 | 0.743 |
DOC_PP2B_LxvP_1 | 216 | 219 | PF13499 | 0.612 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.642 |
DOC_PP2B_PxIxI_1 | 9 | 15 | PF00149 | 0.588 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.540 |
DOC_SPAK_OSR1_1 | 190 | 194 | PF12202 | 0.550 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 696 | 700 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.837 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.720 |
LIG_14-3-3_CanoR_1 | 13 | 22 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 157 | 163 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 486 | 494 | PF00244 | 0.852 |
LIG_14-3-3_CanoR_1 | 607 | 611 | PF00244 | 0.794 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.458 |
LIG_BIR_III_4 | 295 | 299 | PF00653 | 0.742 |
LIG_BIR_III_4 | 675 | 679 | PF00653 | 0.506 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 608 | 612 | PF00533 | 0.742 |
LIG_EVH1_2 | 311 | 315 | PF00568 | 0.547 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.496 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.488 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.592 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.549 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.536 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.577 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.723 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.563 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.429 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.698 |
LIG_GBD_Chelix_1 | 369 | 377 | PF00786 | 0.490 |
LIG_LIR_Apic_2 | 568 | 574 | PF02991 | 0.780 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 57 | 68 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 659 | 667 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.732 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 659 | 663 | PF02991 | 0.571 |
LIG_Pex14_1 | 158 | 162 | PF04695 | 0.464 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.504 |
LIG_PTAP_UEV_1 | 432 | 437 | PF05743 | 0.472 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.568 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.470 |
LIG_SH2_CRK | 571 | 575 | PF00017 | 0.765 |
LIG_SH2_GRB2like | 183 | 186 | PF00017 | 0.339 |
LIG_SH2_NCK_1 | 667 | 671 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.594 |
LIG_SH3_1 | 313 | 319 | PF00018 | 0.551 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.757 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.577 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.741 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.702 |
LIG_SUMO_SIM_anti_2 | 581 | 588 | PF11976 | 0.802 |
LIG_SUMO_SIM_par_1 | 386 | 392 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 581 | 588 | PF11976 | 0.704 |
LIG_SUMO_SIM_par_1 | 63 | 69 | PF11976 | 0.562 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.569 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.448 |
LIG_TRAF2_1 | 677 | 680 | PF00917 | 0.701 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.488 |
LIG_WW_3 | 310 | 314 | PF00397 | 0.542 |
MOD_CDC14_SPxK_1 | 328 | 331 | PF00782 | 0.759 |
MOD_CDC14_SPxK_1 | 44 | 47 | PF00782 | 0.637 |
MOD_CDK_SPK_2 | 325 | 330 | PF00069 | 0.766 |
MOD_CDK_SPK_2 | 481 | 486 | PF00069 | 0.732 |
MOD_CDK_SPK_2 | 570 | 575 | PF00069 | 0.738 |
MOD_CDK_SPxK_1 | 325 | 331 | PF00069 | 0.765 |
MOD_CDK_SPxK_1 | 41 | 47 | PF00069 | 0.506 |
MOD_CDK_SPxxK_3 | 589 | 596 | PF00069 | 0.720 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.773 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.538 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.525 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.782 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.520 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.755 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.506 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.638 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.792 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.830 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.716 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.722 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.687 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.545 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.754 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.504 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.518 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.793 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.537 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.555 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.430 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.828 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.724 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.710 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.759 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.509 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.350 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.504 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.489 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.715 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.667 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.706 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.675 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.703 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.748 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.642 |
MOD_GlcNHglycan | 39 | 43 | PF01048 | 0.466 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.617 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.734 |
MOD_GlcNHglycan | 453 | 457 | PF01048 | 0.548 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.720 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.487 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.739 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.847 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.749 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.844 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.777 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.790 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.789 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.634 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.454 |
MOD_GlcNHglycan | 75 | 80 | PF01048 | 0.712 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.430 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.502 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.563 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.469 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.462 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.405 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.697 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.616 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.535 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.684 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.732 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.717 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.684 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.677 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.831 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.716 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.771 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.678 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.530 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.743 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.751 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.719 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.700 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.594 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.764 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.385 |
MOD_N-GLC_1 | 528 | 533 | PF02516 | 0.754 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.829 |
MOD_N-GLC_1 | 623 | 628 | PF02516 | 0.541 |
MOD_N-GLC_2 | 212 | 214 | PF02516 | 0.611 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.484 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.589 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.493 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.602 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.455 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.775 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.816 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.807 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.576 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.590 |
MOD_NEK2_2 | 258 | 263 | PF00069 | 0.634 |
MOD_NEK2_2 | 651 | 656 | PF00069 | 0.753 |
MOD_PK_1 | 330 | 336 | PF00069 | 0.761 |
MOD_PKA_1 | 330 | 336 | PF00069 | 0.761 |
MOD_PKA_1 | 401 | 407 | PF00069 | 0.517 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.806 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.761 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.616 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.833 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.746 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.751 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.828 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.744 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.668 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.611 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.532 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.465 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.793 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.818 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.831 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.542 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.488 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.484 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.529 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.486 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.539 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.761 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.545 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.756 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.690 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.746 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.764 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.414 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.520 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.464 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.734 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.834 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.735 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.503 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.720 |
TRG_DiLeu_BaEn_2 | 685 | 691 | PF01217 | 0.603 |
TRG_DiLeu_BaEn_3 | 383 | 389 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 401 | 403 | PF00400 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 492 | 497 | PF00026 | 0.775 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I126 | Leptomonas seymouri | 47% | 90% |
A0A3Q8IIS7 | Leishmania donovani | 88% | 98% |
A4H871 | Leishmania braziliensis | 73% | 97% |
A4HWJ6 | Leishmania infantum | 87% | 82% |
Q4QF86 | Leishmania major | 87% | 100% |