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 | yes | yes: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016592 | mediator complex | 3 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q7B6
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 2 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 2 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.498 |
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.592 |
CLV_PCSK_FUR_1 | 141 | 145 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 144 | 150 | PF00082 | 0.471 |
CLV_PCSK_PC7_1 | 325 | 331 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.692 |
DEG_APCC_DBOX_1 | 328 | 336 | PF00400 | 0.278 |
DEG_APCC_DBOX_1 | 590 | 598 | PF00400 | 0.656 |
DEG_COP1_1 | 385 | 393 | PF00400 | 0.204 |
DOC_CKS1_1 | 405 | 410 | PF01111 | 0.335 |
DOC_CYCLIN_RxL_1 | 111 | 120 | PF00134 | 0.500 |
DOC_CYCLIN_RxL_1 | 446 | 456 | PF00134 | 0.314 |
DOC_CYCLIN_yClb1_LxF_4 | 62 | 67 | PF00134 | 0.496 |
DOC_MAPK_gen_1 | 137 | 147 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 268 | 276 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 329 | 337 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 347 | 356 | PF00069 | 0.222 |
DOC_MAPK_gen_1 | 590 | 597 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 590 | 597 | PF00069 | 0.578 |
DOC_PP1_RVXF_1 | 331 | 338 | PF00149 | 0.338 |
DOC_PP1_RVXF_1 | 561 | 567 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 468 | 471 | PF13499 | 0.398 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.414 |
DOC_PP4_FxxP_1 | 372 | 375 | PF00568 | 0.404 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.270 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.687 |
DOC_USP7_MATH_2 | 489 | 495 | PF00917 | 0.204 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 412 | 416 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 533 | 540 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 569 | 574 | PF00244 | 0.426 |
LIG_Actin_WH2_1 | 320 | 335 | PF00022 | 0.426 |
LIG_Actin_WH2_2 | 348 | 365 | PF00022 | 0.335 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.677 |
LIG_BRCT_BRCA1_1 | 368 | 372 | PF00533 | 0.349 |
LIG_deltaCOP1_diTrp_1 | 434 | 442 | PF00928 | 0.271 |
LIG_EH1_1 | 325 | 333 | PF00400 | 0.267 |
LIG_eIF4E_1 | 326 | 332 | PF01652 | 0.404 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.674 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.329 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.322 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.541 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.462 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.600 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.342 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.411 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.267 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.313 |
LIG_Integrin_RGD_1 | 260 | 262 | PF01839 | 0.569 |
LIG_LIR_Apic_2 | 369 | 375 | PF02991 | 0.404 |
LIG_LIR_Apic_2 | 414 | 420 | PF02991 | 0.271 |
LIG_LIR_Apic_2 | 472 | 476 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.566 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.292 |
LIG_SH2_NCK_1 | 473 | 477 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.550 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.365 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.344 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.561 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.285 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.684 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.404 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.417 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 454 | 462 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 517 | 523 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 593 | 599 | PF11976 | 0.584 |
LIG_UBA3_1 | 441 | 449 | PF00899 | 0.433 |
LIG_UBA3_1 | 460 | 466 | PF00899 | 0.314 |
LIG_WW_3 | 487 | 491 | PF00397 | 0.292 |
LIG_WW_3 | 61 | 65 | PF00397 | 0.461 |
MOD_CDK_SPxK_1 | 58 | 64 | PF00069 | 0.516 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.556 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.621 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.705 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.594 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.314 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.425 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.609 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.486 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.358 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.379 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.291 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.311 |
MOD_Cter_Amidation | 141 | 144 | PF01082 | 0.456 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.668 |
MOD_GlcNHglycan | 161 | 165 | PF01048 | 0.543 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.512 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.614 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.705 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.289 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.280 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.378 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.472 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.558 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.502 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.522 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.541 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.660 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.578 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.714 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.632 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.314 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.336 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.284 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.640 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.435 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.349 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.545 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.636 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.357 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.487 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.552 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.780 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.555 |
MOD_NEK2_2 | 272 | 277 | PF00069 | 0.602 |
MOD_OFUCOSY | 336 | 342 | PF10250 | 0.335 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.700 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.271 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.270 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.271 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.354 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.516 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.512 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.616 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.413 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.521 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.530 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.693 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.568 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.645 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.335 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.271 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.516 |
MOD_SUMO_for_1 | 82 | 85 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 105 | 113 | PF00179 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 561 | 564 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 524 | 528 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 563 | 567 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJY2 | Leptomonas seymouri | 48% | 96% |
A0A1X0P246 | Trypanosomatidae | 30% | 100% |
A0A3S5H7N0 | Leishmania donovani | 93% | 100% |
A0A422P3I6 | Trypanosoma rangeli | 30% | 100% |
A4H934 | Leishmania braziliensis | 76% | 100% |
A4I5K5 | Leishmania infantum | 93% | 100% |
C9ZQY2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B0V0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5DQL7 | Trypanosoma cruzi | 30% | 100% |