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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: Q4Q264
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004672 | protein kinase activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005524 | ATP binding | 5 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.491 |
CLV_MEL_PAP_1 | 109 | 115 | PF00089 | 0.479 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.361 |
DEG_APCC_DBOX_1 | 361 | 369 | PF00400 | 0.381 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.562 |
DEG_ODPH_VHL_1 | 117 | 129 | PF01847 | 0.468 |
DEG_SPOP_SBC_1 | 12 | 16 | PF00917 | 0.402 |
DOC_CDC14_PxL_1 | 395 | 403 | PF14671 | 0.484 |
DOC_CKS1_1 | 300 | 305 | PF01111 | 0.533 |
DOC_CYCLIN_RxL_1 | 495 | 506 | PF00134 | 0.569 |
DOC_CYCLIN_yCln2_LP_2 | 431 | 437 | PF00134 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 557 | 563 | PF00134 | 0.493 |
DOC_MAPK_DCC_7 | 362 | 370 | PF00069 | 0.434 |
DOC_MAPK_DCC_7 | 553 | 563 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 382 | 391 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 75 | 83 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 362 | 370 | PF00069 | 0.348 |
DOC_MAPK_MEF2A_6 | 426 | 435 | PF00069 | 0.405 |
DOC_MAPK_RevD_3 | 90 | 104 | PF00069 | 0.412 |
DOC_PP1_RVXF_1 | 102 | 109 | PF00149 | 0.414 |
DOC_PP1_RVXF_1 | 496 | 503 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.435 |
DOC_PP2B_LxvP_1 | 468 | 471 | PF13499 | 0.504 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 300 | 303 | PF00568 | 0.548 |
DOC_PP4_FxxP_1 | 363 | 366 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.646 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 112 | 116 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 266 | 275 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 288 | 296 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 639 | 645 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.448 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 522 | 526 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_2 | 33 | 39 | PF00533 | 0.462 |
LIG_deltaCOP1_diTrp_1 | 164 | 175 | PF00928 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 621 | 630 | PF00928 | 0.555 |
LIG_EH1_1 | 571 | 579 | PF00400 | 0.488 |
LIG_EVH1_1 | 286 | 290 | PF00568 | 0.495 |
LIG_EVH1_2 | 188 | 192 | PF00568 | 0.556 |
LIG_FAT_LD_1 | 531 | 539 | PF03623 | 0.463 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.452 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.403 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.514 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.447 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.379 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.523 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.570 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.401 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.537 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.553 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.409 |
LIG_LIR_Apic_2 | 172 | 178 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 297 | 303 | PF02991 | 0.559 |
LIG_LIR_Apic_2 | 621 | 627 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 238 | 249 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 386 | 396 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 523 | 534 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 642 | 650 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 487 | 491 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 642 | 648 | PF02991 | 0.587 |
LIG_MLH1_MIPbox_1 | 275 | 279 | PF16413 | 0.548 |
LIG_MYND_1 | 399 | 403 | PF01753 | 0.498 |
LIG_MYND_1 | 556 | 560 | PF01753 | 0.496 |
LIG_MYND_1 | 627 | 631 | PF01753 | 0.676 |
LIG_PCNA_PIPBox_1 | 305 | 314 | PF02747 | 0.446 |
LIG_Pex14_2 | 489 | 493 | PF04695 | 0.453 |
LIG_Pex14_2 | 645 | 649 | PF04695 | 0.556 |
LIG_PROFILIN_1 | 594 | 600 | PF00235 | 0.530 |
LIG_Rb_pABgroove_1 | 324 | 332 | PF01858 | 0.458 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.424 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.400 |
LIG_SH2_CRK | 580 | 584 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 407 | 411 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.602 |
LIG_SH2_STAT3 | 407 | 410 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.385 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.523 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.551 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.447 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.491 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.640 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.701 |
LIG_SH3_5 | 198 | 202 | PF00018 | 0.389 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 68 | 75 | PF11976 | 0.511 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 242 | 247 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 292 | 297 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 348 | 355 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 91 | 96 | PF11976 | 0.460 |
LIG_TYR_ITIM | 578 | 583 | PF00017 | 0.474 |
LIG_UBA3_1 | 1 | 6 | PF00899 | 0.607 |
LIG_UBA3_1 | 431 | 438 | PF00899 | 0.428 |
LIG_UBA3_1 | 53 | 59 | PF00899 | 0.446 |
LIG_UBA3_1 | 537 | 544 | PF00899 | 0.563 |
LIG_WRC_WIRS_1 | 499 | 504 | PF05994 | 0.483 |
MOD_CDK_SPxxK_3 | 299 | 306 | PF00069 | 0.539 |
MOD_CDK_SPxxK_3 | 460 | 467 | PF00069 | 0.494 |
MOD_CDK_SPxxK_3 | 543 | 550 | PF00069 | 0.519 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.531 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.461 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.397 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.527 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.379 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.355 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.484 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.692 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.511 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.567 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.432 |
MOD_Cter_Amidation | 250 | 253 | PF01082 | 0.470 |
MOD_Cter_Amidation | 47 | 50 | PF01082 | 0.489 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.600 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.457 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.472 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.459 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.423 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.409 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.720 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.783 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.703 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.679 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.687 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.402 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.408 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.481 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.376 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.464 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.420 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.544 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.672 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.606 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.650 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.578 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.527 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.526 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.429 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.376 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.499 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.599 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.556 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.675 |
MOD_NEK2_2 | 156 | 161 | PF00069 | 0.421 |
MOD_NEK2_2 | 565 | 570 | PF00069 | 0.459 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.484 |
MOD_PIKK_1 | 622 | 628 | PF00454 | 0.773 |
MOD_PK_1 | 49 | 55 | PF00069 | 0.362 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.439 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.395 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.532 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.524 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.486 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.364 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.421 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.442 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.390 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.395 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.385 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.522 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.448 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.572 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.438 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.518 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.536 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.508 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.524 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.563 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.612 |
MOD_SUMO_rev_2 | 96 | 106 | PF00179 | 0.566 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_1 | 69 | 74 | PF01217 | 0.446 |
TRG_DiLeu_BaEn_1 | 79 | 84 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_2 | 138 | 144 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 321 | 326 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 431 | 436 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 444 | 449 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 474 | 479 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 553 | 558 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 539 | 543 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P470 | Leptomonas seymouri | 71% | 100% |
A0A1X0P8C9 | Trypanosomatidae | 33% | 100% |
A0A3Q8IIL7 | Leishmania donovani | 92% | 100% |
A4HNM1 | Leishmania braziliensis | 76% | 100% |
A4ICX3 | Leishmania infantum | 92% | 100% |
E9ASD2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F4I313 | Arabidopsis thaliana | 22% | 71% |
Q9C9H8 | Arabidopsis thaliana | 21% | 72% |