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: E9ASD2
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 | 354 | 358 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.406 |
CLV_PCSK_FUR_1 | 57 | 61 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.361 |
DEG_APCC_DBOX_1 | 360 | 368 | PF00400 | 0.381 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.569 |
DEG_ODPH_VHL_1 | 117 | 129 | PF01847 | 0.471 |
DOC_CDC14_PxL_1 | 394 | 402 | PF14671 | 0.486 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.541 |
DOC_CYCLIN_RxL_1 | 494 | 505 | PF00134 | 0.571 |
DOC_CYCLIN_yCln2_LP_2 | 430 | 436 | PF00134 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 556 | 562 | PF00134 | 0.500 |
DOC_MAPK_DCC_7 | 361 | 369 | PF00069 | 0.435 |
DOC_MAPK_DCC_7 | 427 | 436 | PF00069 | 0.425 |
DOC_MAPK_DCC_7 | 552 | 562 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 381 | 390 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 75 | 83 | PF00069 | 0.505 |
DOC_MAPK_HePTP_8 | 424 | 436 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 361 | 369 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 507 | 514 | PF00069 | 0.367 |
DOC_MAPK_RevD_3 | 90 | 104 | PF00069 | 0.410 |
DOC_PP1_RVXF_1 | 102 | 109 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 495 | 502 | PF00149 | 0.484 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 467 | 470 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.495 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.471 |
DOC_PP4_FxxP_1 | 299 | 302 | PF00568 | 0.555 |
DOC_PP4_FxxP_1 | 362 | 365 | PF00568 | 0.436 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 112 | 116 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 265 | 274 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 287 | 295 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.450 |
LIG_APCC_ABBA_1 | 560 | 565 | PF00400 | 0.281 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.473 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_2 | 33 | 39 | PF00533 | 0.462 |
LIG_deltaCOP1_diTrp_1 | 164 | 175 | PF00928 | 0.456 |
LIG_EH1_1 | 570 | 578 | PF00400 | 0.496 |
LIG_EVH1_1 | 285 | 289 | PF00568 | 0.494 |
LIG_EVH1_1 | 594 | 598 | PF00568 | 0.491 |
LIG_EVH1_2 | 186 | 190 | PF00568 | 0.603 |
LIG_FAT_LD_1 | 530 | 538 | PF03623 | 0.467 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.455 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.393 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.515 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.448 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.398 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.521 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.575 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.454 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.550 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.341 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.539 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.461 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.559 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 172 | 178 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 296 | 302 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 237 | 248 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 385 | 395 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 524 | 533 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 639 | 646 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 312 | 316 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 453 | 458 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 524 | 528 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 639 | 645 | PF02991 | 0.576 |
LIG_MLH1_MIPbox_1 | 274 | 278 | PF16413 | 0.545 |
LIG_MYND_1 | 398 | 402 | PF01753 | 0.501 |
LIG_MYND_1 | 555 | 559 | PF01753 | 0.505 |
LIG_PCNA_PIPBox_1 | 128 | 137 | PF02747 | 0.209 |
LIG_PCNA_PIPBox_1 | 304 | 313 | PF02747 | 0.456 |
LIG_PCNA_yPIPBox_3 | 128 | 142 | PF02747 | 0.260 |
LIG_Pex14_2 | 488 | 492 | PF04695 | 0.458 |
LIG_Pex14_2 | 642 | 646 | PF04695 | 0.537 |
LIG_Rb_pABgroove_1 | 323 | 331 | PF01858 | 0.460 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.424 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.402 |
LIG_SH2_CRK | 579 | 583 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 579 | 583 | PF00017 | 0.616 |
LIG_SH2_STAT3 | 406 | 409 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.386 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.527 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.557 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.450 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.491 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.495 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.640 |
LIG_SH3_5 | 198 | 202 | PF00018 | 0.387 |
LIG_SUMO_SIM_anti_2 | 244 | 249 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 68 | 75 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 241 | 246 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 291 | 296 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 347 | 354 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 558 | 565 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 91 | 96 | PF11976 | 0.452 |
LIG_TYR_ITIM | 577 | 582 | PF00017 | 0.484 |
LIG_UBA3_1 | 1 | 6 | PF00899 | 0.613 |
LIG_UBA3_1 | 430 | 437 | PF00899 | 0.433 |
LIG_UBA3_1 | 53 | 59 | PF00899 | 0.447 |
LIG_UBA3_1 | 536 | 543 | PF00899 | 0.572 |
LIG_WRC_WIRS_1 | 310 | 315 | PF05994 | 0.465 |
LIG_WRC_WIRS_1 | 498 | 503 | PF05994 | 0.484 |
MOD_CDK_SPxxK_3 | 298 | 305 | PF00069 | 0.546 |
MOD_CDK_SPxxK_3 | 459 | 466 | PF00069 | 0.493 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.515 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.479 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.525 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.379 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.364 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.457 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.680 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.503 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.458 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.568 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.413 |
MOD_Cter_Amidation | 249 | 252 | PF01082 | 0.465 |
MOD_Cter_Amidation | 47 | 50 | PF01082 | 0.494 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.579 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.447 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.551 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.275 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.448 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.277 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.408 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.702 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.765 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.699 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.658 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.692 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.403 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.339 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.483 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.469 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.389 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.465 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.488 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.413 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.350 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.590 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.639 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.571 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.531 |
MOD_N-GLC_2 | 255 | 257 | PF02516 | 0.299 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.422 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.499 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.410 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.548 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.584 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.408 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.688 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.634 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.686 |
MOD_NEK2_2 | 156 | 161 | PF00069 | 0.422 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.485 |
MOD_PIKK_1 | 619 | 625 | PF00454 | 0.771 |
MOD_PK_1 | 49 | 55 | PF00069 | 0.366 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.442 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.398 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.533 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.402 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.422 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.443 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.436 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.396 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.385 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.536 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.455 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.552 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.542 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.507 |
MOD_SUMO_rev_2 | 423 | 429 | PF00179 | 0.260 |
MOD_SUMO_rev_2 | 502 | 508 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 96 | 106 | PF00179 | 0.579 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_1 | 69 | 74 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_1 | 79 | 84 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_2 | 138 | 144 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 430 | 435 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 552 | 557 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 381 | 385 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 538 | 542 | PF00026 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P470 | Leptomonas seymouri | 65% | 100% |
A0A1X0P8C9 | Trypanosomatidae | 33% | 100% |
A0A3Q8IIL7 | Leishmania donovani | 92% | 100% |
A4HNM1 | Leishmania braziliensis | 78% | 99% |
A4ICX3 | Leishmania infantum | 92% | 100% |
F4I313 | Arabidopsis thaliana | 22% | 71% |
Q4Q264 | Leishmania major | 91% | 100% |
Q9C9H8 | Arabidopsis thaliana | 21% | 71% |