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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 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: E9AVN2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004707 | MAP kinase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 104 | 108 | PF00656 | 0.806 |
CLV_C14_Caspase3-7 | 639 | 643 | PF00656 | 0.557 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.343 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 621 | 623 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.343 |
CLV_Separin_Metazoa | 412 | 416 | PF03568 | 0.306 |
DEG_Kelch_Keap1_1 | 267 | 272 | PF01344 | 0.559 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.557 |
DEG_SCF_FBW7_2 | 576 | 583 | PF00400 | 0.343 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.640 |
DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.592 |
DEG_SPOP_SBC_1 | 547 | 551 | PF00917 | 0.309 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.550 |
DOC_CDC14_PxL_1 | 384 | 392 | PF14671 | 0.306 |
DOC_CYCLIN_RxL_1 | 591 | 603 | PF00134 | 0.293 |
DOC_MAPK_gen_1 | 341 | 350 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 383 | 392 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 482 | 491 | PF00069 | 0.503 |
DOC_MAPK_HePTP_8 | 380 | 392 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 383 | 392 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 485 | 493 | PF00069 | 0.484 |
DOC_PP1_RVXF_1 | 318 | 325 | PF00149 | 0.349 |
DOC_PP1_RVXF_1 | 326 | 333 | PF00149 | 0.269 |
DOC_PP2B_LxvP_1 | 438 | 441 | PF13499 | 0.372 |
DOC_PP2B_LxvP_1 | 675 | 678 | PF13499 | 0.397 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.232 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.616 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.367 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.229 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.293 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 120 | 130 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 423 | 431 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 465 | 470 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 482 | 491 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 622 | 629 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 695 | 703 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 331 | 346 | PF00022 | 0.293 |
LIG_Actin_WH2_2 | 402 | 417 | PF00022 | 0.306 |
LIG_Actin_WH2_2 | 490 | 508 | PF00022 | 0.212 |
LIG_Actin_WH2_2 | 630 | 648 | PF00022 | 0.364 |
LIG_AP2alpha_1 | 634 | 638 | PF02296 | 0.359 |
LIG_deltaCOP1_diTrp_1 | 402 | 406 | PF00928 | 0.306 |
LIG_eIF4E_1 | 385 | 391 | PF01652 | 0.306 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.630 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.306 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.343 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.488 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.805 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.594 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.306 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.318 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.312 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.293 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.343 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.506 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.418 |
LIG_Integrin_isoDGR_2 | 679 | 681 | PF01839 | 0.407 |
LIG_LIR_Apic_2 | 382 | 388 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 582 | 593 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 405 | 409 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.305 |
LIG_Pex14_1 | 595 | 599 | PF04695 | 0.293 |
LIG_Pex14_2 | 634 | 638 | PF04695 | 0.359 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.212 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.444 |
LIG_SH2_CRK | 585 | 589 | PF00017 | 0.293 |
LIG_SH2_NCK_1 | 160 | 164 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 698 | 702 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 698 | 702 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 698 | 701 | PF00017 | 0.388 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.666 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.343 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.518 |
LIG_SUMO_SIM_anti_2 | 606 | 613 | PF11976 | 0.286 |
LIG_SUMO_SIM_anti_2 | 84 | 90 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 55 | 62 | PF11976 | 0.385 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.372 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.343 |
LIG_UBA3_1 | 434 | 443 | PF00899 | 0.306 |
LIG_WRC_WIRS_1 | 403 | 408 | PF05994 | 0.306 |
MOD_CDK_SPK_2 | 281 | 286 | PF00069 | 0.691 |
MOD_CDK_SPxxK_3 | 37 | 44 | PF00069 | 0.456 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.666 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.593 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.675 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.544 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.612 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.654 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.629 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.624 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.739 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.693 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.444 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.408 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.219 |
MOD_CK1_1 | 658 | 664 | PF00069 | 0.636 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.602 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.306 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.285 |
MOD_CK2_1 | 576 | 582 | PF00069 | 0.343 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.293 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.343 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.620 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.363 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.696 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.778 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.679 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.674 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.672 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.537 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.782 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.672 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.323 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.306 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.491 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.240 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.293 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.343 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.571 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.600 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.426 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.823 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.622 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.646 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.527 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.644 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.455 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.643 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.778 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.646 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.634 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.721 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.306 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.331 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.330 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.283 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.735 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.222 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.688 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.538 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.773 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.330 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.630 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.495 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.341 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.629 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.306 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.306 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.212 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.343 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.735 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.647 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.372 |
MOD_PKA_1 | 621 | 627 | PF00069 | 0.293 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.709 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.685 |
MOD_PKA_2 | 414 | 420 | PF00069 | 0.315 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.454 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.212 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.282 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.342 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.590 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.330 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.318 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.374 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.306 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.366 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.482 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.426 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.563 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.711 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.747 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.506 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.306 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.306 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.229 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.321 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.293 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.632 |
MOD_SUMO_rev_2 | 550 | 559 | PF00179 | 0.339 |
TRG_DiLeu_BaEn_1 | 606 | 611 | PF01217 | 0.293 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.293 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.212 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 595 | 597 | PF00400 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 695 | 700 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU16 | Leptomonas seymouri | 51% | 100% |
A0A3Q8IC49 | Leishmania donovani | 90% | 99% |
A4HC95 | Leishmania braziliensis | 75% | 100% |
A4HZS7 | Leishmania infantum | 90% | 86% |
Q4QBU7 | Leishmania major | 91% | 100% |