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: A0A3Q8IC49
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 | 109 | 113 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.498 |
CLV_C14_Caspase3-7 | 644 | 648 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.705 |
CLV_PCSK_FUR_1 | 7 | 11 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 626 | 628 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.331 |
CLV_Separin_Metazoa | 417 | 421 | PF03568 | 0.299 |
DEG_SCF_FBW7_2 | 581 | 588 | PF00400 | 0.331 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.620 |
DEG_SPOP_SBC_1 | 209 | 213 | PF00917 | 0.502 |
DEG_SPOP_SBC_1 | 255 | 259 | PF00917 | 0.608 |
DEG_SPOP_SBC_1 | 551 | 555 | PF00917 | 0.303 |
DOC_CDC14_PxL_1 | 389 | 397 | PF14671 | 0.299 |
DOC_CYCLIN_RxL_1 | 596 | 608 | PF00134 | 0.287 |
DOC_MAPK_gen_1 | 346 | 355 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 388 | 397 | PF00069 | 0.309 |
DOC_MAPK_gen_1 | 4 | 14 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 487 | 496 | PF00069 | 0.358 |
DOC_MAPK_HePTP_8 | 385 | 397 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 388 | 397 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 490 | 498 | PF00069 | 0.358 |
DOC_PP1_RVXF_1 | 323 | 330 | PF00149 | 0.351 |
DOC_PP1_RVXF_1 | 331 | 338 | PF00149 | 0.269 |
DOC_PP2B_LxvP_1 | 443 | 446 | PF13499 | 0.358 |
DOC_PP2B_LxvP_1 | 680 | 683 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 566 | 569 | PF00568 | 0.304 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.584 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.349 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 665 | 670 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 20 | 27 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 428 | 436 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 470 | 475 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 627 | 634 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 700 | 708 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 9 | 15 | PF00244 | 0.648 |
LIG_Actin_WH2_2 | 336 | 351 | PF00022 | 0.287 |
LIG_Actin_WH2_2 | 407 | 422 | PF00022 | 0.299 |
LIG_AP2alpha_1 | 639 | 643 | PF02296 | 0.369 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.560 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.530 |
LIG_deltaCOP1_diTrp_1 | 407 | 411 | PF00928 | 0.299 |
LIG_eIF4E_1 | 390 | 396 | PF01652 | 0.299 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.607 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.347 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.331 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.304 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.657 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.617 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.299 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.337 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.303 |
LIG_FHA_2 | 606 | 612 | PF00498 | 0.287 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.331 |
LIG_FHA_2 | 694 | 700 | PF00498 | 0.423 |
LIG_Integrin_isoDGR_2 | 684 | 686 | PF01839 | 0.471 |
LIG_LIR_Apic_2 | 387 | 393 | PF02991 | 0.299 |
LIG_LIR_Apic_2 | 564 | 569 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 314 | 324 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 587 | 598 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 410 | 414 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 584 | 589 | PF02991 | 0.299 |
LIG_Pex14_1 | 600 | 604 | PF04695 | 0.287 |
LIG_Pex14_2 | 639 | 643 | PF04695 | 0.369 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.424 |
LIG_SH2_CRK | 590 | 594 | PF00017 | 0.287 |
LIG_SH2_NCK_1 | 165 | 169 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 703 | 707 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 703 | 707 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.424 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.568 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.733 |
LIG_SH3_3 | 631 | 637 | PF00018 | 0.331 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.516 |
LIG_SUMO_SIM_anti_2 | 610 | 618 | PF11976 | 0.290 |
LIG_SUMO_SIM_anti_2 | 89 | 95 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 10 | 15 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 154 | 160 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 60 | 67 | PF11976 | 0.368 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.358 |
LIG_TRAF2_1 | 502 | 505 | PF00917 | 0.331 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.331 |
LIG_UBA3_1 | 439 | 448 | PF00899 | 0.299 |
LIG_WRC_WIRS_1 | 408 | 413 | PF05994 | 0.299 |
MOD_CDK_SPK_2 | 286 | 291 | PF00069 | 0.678 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.557 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.627 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.547 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.586 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.597 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.585 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.639 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.449 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.236 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.388 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.229 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.612 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.333 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.331 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.287 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.331 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.595 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.424 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.649 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.647 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.709 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.714 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.606 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.551 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.476 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.644 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.644 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.323 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.299 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.358 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.287 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.331 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.557 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.494 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.476 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.684 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.475 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.697 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.623 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.560 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.677 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.565 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.299 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.236 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.329 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.270 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.216 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.604 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.650 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.299 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.644 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.640 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.316 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.669 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.505 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.300 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.299 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.331 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.618 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.358 |
MOD_PK_1 | 10 | 16 | PF00069 | 0.553 |
MOD_PKA_1 | 626 | 632 | PF00069 | 0.287 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.640 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.674 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.636 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.299 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.436 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.287 |
MOD_PKA_2 | 654 | 660 | PF00069 | 0.506 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.570 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.553 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.299 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.645 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.320 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.299 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.417 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.553 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.447 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.667 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.648 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.756 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.608 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.299 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.299 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.311 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.287 |
MOD_ProDKin_1 | 665 | 671 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 555 | 565 | PF00179 | 0.327 |
TRG_DiLeu_BaEn_1 | 611 | 616 | PF01217 | 0.287 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.287 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 600 | 602 | PF00400 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 700 | 705 | PF00026 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU16 | Leptomonas seymouri | 51% | 100% |
A4HC95 | Leishmania braziliensis | 77% | 100% |
A4HZS7 | Leishmania infantum | 99% | 100% |
E9AVN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QBU7 | Leishmania major | 93% | 100% |