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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4QET2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.389 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 640 | 642 | PF00675 | 0.374 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 662 | 664 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.441 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.709 |
DOC_ANK_TNKS_1 | 348 | 355 | PF00023 | 0.533 |
DOC_CKS1_1 | 153 | 158 | PF01111 | 0.594 |
DOC_CYCLIN_yCln2_LP_2 | 166 | 172 | PF00134 | 0.502 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 193 | PF00134 | 0.605 |
DOC_MAPK_gen_1 | 215 | 224 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 272 | 282 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 439 | 447 | PF00069 | 0.397 |
DOC_MAPK_HePTP_8 | 212 | 224 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 215 | 224 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 442 | 449 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 646 | 655 | PF00069 | 0.355 |
DOC_PP1_RVXF_1 | 176 | 183 | PF00149 | 0.617 |
DOC_PP1_RVXF_1 | 195 | 202 | PF00149 | 0.560 |
DOC_PP1_RVXF_1 | 264 | 270 | PF00149 | 0.528 |
DOC_PP1_RVXF_1 | 415 | 422 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 166 | 169 | PF13499 | 0.650 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.630 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.721 |
DOC_USP7_UBL2_3 | 397 | 401 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.824 |
LIG_14-3-3_CanoR_1 | 100 | 110 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.389 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.700 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.728 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.575 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.413 |
LIG_CaM_IQ_9 | 282 | 297 | PF13499 | 0.520 |
LIG_deltaCOP1_diTrp_1 | 558 | 565 | PF00928 | 0.393 |
LIG_DLG_GKlike_1 | 275 | 282 | PF00625 | 0.577 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.459 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.564 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.400 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.413 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.413 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.472 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.598 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.586 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.393 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.413 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.400 |
LIG_FXI_DFP_1 | 572 | 576 | PF00024 | 0.358 |
LIG_GBD_Chelix_1 | 430 | 438 | PF00786 | 0.358 |
LIG_GBD_Chelix_1 | 477 | 485 | PF00786 | 0.393 |
LIG_Integrin_RGD_1 | 465 | 467 | PF01839 | 0.424 |
LIG_LIR_Apic_2 | 132 | 138 | PF02991 | 0.684 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.691 |
LIG_LIR_Apic_2 | 179 | 185 | PF02991 | 0.616 |
LIG_LIR_Apic_2 | 539 | 545 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 278 | 285 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 432 | 440 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 432 | 436 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 657 | 661 | PF02991 | 0.388 |
LIG_LYPXL_SIV_4 | 381 | 389 | PF13949 | 0.543 |
LIG_PDZ_Class_2 | 679 | 684 | PF00595 | 0.623 |
LIG_Pex14_2 | 469 | 473 | PF04695 | 0.413 |
LIG_PTB_Apo_2 | 501 | 508 | PF02174 | 0.413 |
LIG_REV1ctd_RIR_1 | 199 | 207 | PF16727 | 0.659 |
LIG_RPA_C_Fungi | 20 | 32 | PF08784 | 0.570 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.499 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.619 |
LIG_SH2_CRK | 658 | 662 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 279 | 282 | PF00017 | 0.553 |
LIG_SH2_SRC | 452 | 455 | PF00017 | 0.413 |
LIG_SH2_SRC | 529 | 532 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 606 | 610 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 644 | 648 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.323 |
LIG_SH3_1 | 135 | 141 | PF00018 | 0.629 |
LIG_SH3_2 | 156 | 161 | PF14604 | 0.656 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.584 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.629 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.559 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.671 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.438 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.356 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.525 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.664 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.323 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.794 |
LIG_SH3_CIN85_PxpxPR_1 | 173 | 178 | PF14604 | 0.626 |
LIG_Sin3_3 | 232 | 239 | PF02671 | 0.599 |
LIG_SUMO_SIM_par_1 | 357 | 363 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 651 | 657 | PF11976 | 0.413 |
LIG_TRAF2_1 | 368 | 371 | PF00917 | 0.593 |
LIG_TRAF2_1 | 595 | 598 | PF00917 | 0.393 |
LIG_TYR_ITIM | 431 | 436 | PF00017 | 0.348 |
LIG_TYR_ITIM | 656 | 661 | PF00017 | 0.413 |
LIG_WRC_WIRS_1 | 461 | 466 | PF05994 | 0.355 |
MOD_CDC14_SPxK_1 | 347 | 350 | PF00782 | 0.595 |
MOD_CDK_SPK_2 | 173 | 178 | PF00069 | 0.626 |
MOD_CDK_SPK_2 | 344 | 349 | PF00069 | 0.586 |
MOD_CDK_SPxK_1 | 344 | 350 | PF00069 | 0.586 |
MOD_CDK_SPxxK_3 | 63 | 70 | PF00069 | 0.663 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.683 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.629 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.574 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.616 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.624 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.479 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.469 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.379 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.413 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.481 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.678 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.774 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.659 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.698 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.724 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.631 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.589 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.591 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.400 |
MOD_Cter_Amidation | 195 | 198 | PF01082 | 0.536 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.706 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.641 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.589 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.668 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.560 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.637 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.275 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.636 |
MOD_GlcNHglycan | 45 | 49 | PF01048 | 0.725 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.499 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.434 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.800 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.669 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.573 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.743 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.654 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.392 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.510 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.640 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.513 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.358 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.679 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.413 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.385 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.358 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.406 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.750 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.434 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.598 |
MOD_N-GLC_1 | 637 | 642 | PF02516 | 0.459 |
MOD_N-GLC_2 | 41 | 43 | PF02516 | 0.691 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.680 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.665 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.368 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.290 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.380 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.330 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.413 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.708 |
MOD_PKA_1 | 316 | 322 | PF00069 | 0.631 |
MOD_PKA_1 | 662 | 668 | PF00069 | 0.413 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.572 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.389 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.413 |
MOD_PKA_2 | 671 | 677 | PF00069 | 0.497 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.590 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.413 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.412 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.598 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.382 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.360 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.413 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.744 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.687 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.589 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.661 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.660 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.539 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.689 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.643 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.826 |
MOD_SUMO_for_1 | 304 | 307 | PF00179 | 0.562 |
MOD_SUMO_for_1 | 500 | 503 | PF00179 | 0.323 |
MOD_SUMO_for_1 | 548 | 551 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 402 | 412 | PF00179 | 0.459 |
TRG_DiLeu_BaEn_1 | 408 | 413 | PF01217 | 0.249 |
TRG_DiLeu_BaLyEn_6 | 182 | 187 | PF01217 | 0.635 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.612 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.568 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 137 | 142 | PF00026 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 410 | 414 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 646 | 650 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE38 | Leptomonas seymouri | 66% | 100% |
A0A0S4JLW5 | Bodo saltans | 36% | 90% |
A0A3S5H6X9 | Leishmania donovani | 94% | 100% |
A4H8L1 | Leishmania braziliensis | 76% | 100% |
A4HWY3 | Leishmania infantum | 94% | 100% |
C9ZW20 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AQP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |